quadgram

This is a table of type quadgram and their frequencies. Use it to search & browse the list to learn more about your study carrel.

quadgram	frequency
in the presence of	217
to the plasma membrane	173
of the golgi apparatus	158
to the cell surface	150
of the golgi complex	105
in the golgi apparatus	98
to the golgi apparatus	90
in the absence of	85
in the golgi complex	83
has been shown to	80
to the golgi complex	78
in the endoplasmic reticulum	71
the cytoplasmic domain of	69
from the endoplasmic reticulum	69
of the secretory pathway	67
in the case of	62
at the plasma membrane	58
on the other hand	57
severe acute respiratory syndrome	55
the golgi apparatus and	53
have been shown to	52
the rough endoplasmic reticulum	52
the role of the	52
the presence of the	51
between the er and	51
been shown to be	51
on the cell surface	50
of mouse hepatitis virus	49
of vesicular stomatitis virus	48
in the formation of	48
the endoplasmic reticulum and	48
at the cell surface	45
from the er to	45
in the secretory pathway	44
the formation of the	43
the lumen of the	42
of the golgi stack	42
african swine fever virus	42
the early secretory pathway	41
in the context of	41
acute respiratory syndrome coronavirus	41
the er and the	40
the er to the	40
of the endoplasmic reticulum	39
was found to be	39
er and the golgi	38
it is possible that	38
in the cytoplasmic domain	38
play a role in	37
the cytoplasmic tail of	37
guanine nucleotide exchange factor	37
through the secretory pathway	37
as well as the	35
the endoplasmic reticulum to	35
is required for the	35
as shown in fig	34
and the golgi apparatus	34
of the e protein	34
it has been shown	34
the presence of a	33
in contrast to the	32
endoplasmic reticulum to the	32
with the plasma membrane	32
the er and golgi	32
through the golgi complex	32
er to the golgi	31
similar to that of	31
retained in the golgi	31
has been shown that	30
through the golgi apparatus	30
guanine nucleotide exchange factors	30
the lumenal domain of	29
it has been suggested	29
to be involved in	29
in the golgi region	29
in the lumen of	29
the golgi complex and	28
vesicular stomatitis virus g	28
in addition to the	28
the golgi apparatus of	28
retention in the golgi	28
of the ga in	27
side of the golgi	27
of semliki forest virus	27
the golgi to the	27
is consistent with the	27
has been suggested that	27
the surface of the	27
the golgi apparatus is	26
transported to the cell	26
the plasma membrane and	26
in cells infected with	26
the organization of the	26
s d and s	26
the transmembrane domain of	26
of the m protein	26
the function of the	25
of the plasma membrane	25
from the golgi apparatus	25
as a result of	25
herpes simplex virus type	25
at the same time	25
to that of the	25
the structure of the	25
the golgi complex in	25
the golgi apparatus in	25
the cytoplasmic face of	24
the presence or absence	24
from the plasma membrane	24
a golgi retention signal	24
the fact that the	24
the yeast golgi apparatus	24
of the b protein	24
also been shown to	24
to the endoplasmic reticulum	24
the presence of bfa	24
of herpes simplex virus	23
cisternae of the golgi	23
the regulated secretory pathway	23
presence or absence of	23
domain of dpap a	23
endoplasmic reticulum and golgi	23
secretory proteins in the	23
de haan et al	23
these results suggest that	23
in vitro and in	23
an important role in	23
the e glycoprotein of	23
an integral membrane protein	22
and the golgi complex	22
from the golgi complex	22
at the end of	22
proteins in the endoplasmic	22
for the retention of	22
organization of the golgi	22
from the golgi to	22
endoplasmic reticulum and the	22
retained in the er	21
exit from the tgn	21
the level of the	21
golgi complex to the	21
in the presence or	21
transport through the golgi	21
and function of the	21
by the addition of	21
stomatitis virus g protein	21
the transmembrane segment of	21
as well as in	21
the golgi complex to	21
proteins into the er	21
localized to the golgi	21
the periphery of the	20
reticulum to the golgi	20
the kre p tmd	20
has been implicated in	20
the formation of a	20
d and s d	20
structure and function of	20
transport to the cell	20
the hydrophobic thickness of	20
along the secretory pathway	20
the top of the	20
the yeast secretory pathway	20
its retention in the	20
it is likely that	20
the assembly of the	20
similar results were obtained	20
between the endoplasmic reticulum	20
domain of dpap b	20
on the surface of	20
it is clear that	20
golgi retention signal in	20
the golgi complex is	19
of the cytoplasmic domain	19
of the transmembrane domain	19
the morphology of the	19
for the formation of	19
in polarized epithelial cells	19
to the formation of	19
expressed in cos cells	19
at the level of	19
associated with the golgi	19
amino acids of the	19
the golgi apparatus to	19
er to golgi transport	19
the possibility that the	19
of severe acute respiratory	19
are involved in the	19
with the golgi apparatus	19
been suggested to be	19
by the presence of	19
is known about the	19
the case of the	19
the length of the	19
of a number of	18
in the transport of	18
j cell biol doi	18
the plasma membrane of	18
the cells were fixed	18
a large number of	18
of the n protein	18
the plasma membrane in	18
of secretory proteins in	18
has been suggested to	18
into the er in	18
a final concentration of	18
identification and characterization of	18
the ability of the	18
reticulum and the golgi	18
of the cytoplasmic tail	18
the total number of	18
see materials and methods	18
of coronavirus e protein	18
cells were infected with	18
coronavirus mouse hepatitis virus	18
within the golgi apparatus	18
on the basis of	17
cells were treated with	17
in materials and methods	17
with respect to the	17
in cells treated with	17
described in materials and	17
in of the cells	17
by the fact that	17
labeled with s methionine	17
was shown to be	17
the cytosolic domain of	17
mouse hepatitis virus strain	17
is likely to be	17
and the plasma membrane	17
transmembrane proteins in the	17
retention signal in a	17
cytoplasmic domain of the	17
of the elementary unit	16
cytoplasmic face of the	16
from the cell surface	16
and is required for	16
in the regulation of	16
under the control of	16
in the early secretory	16
a wide range of	16
at a dilution of	16
presence of mm caffeine	16
and analyzed by sds	16
is targeted to the	16
transported to the plasma	16
to the golgi network	16
of african swine fever	16
cytoplasmic domain of dpap	16
on the plasma membrane	16
of the early secretory	16
was added to the	16
in the plasma membrane	16
washed three times with	16
the er in the	16
are thought to be	16
the presence of mm	16
signal in a membrane	16
of a membrane protein	16
has also been shown	16
had no effect on	16
transport to the golgi	16
m and e proteins	15
the severe acute respiratory	15
transport of secretory proteins	15
the presence of caffeine	15
golgi structure and function	15
the vesicular stomatitis virus	15
the center of the	15
of the s protein	15
the majority of the	15
the vsv g protein	15
are shown in fig	15
the membrane of the	15
are transported to the	15
by the observation that	15
side of the membrane	15
the protein to the	15
proteins to the golgi	15
the nature of the	15
of m and s	15
is not required for	15
the gbf gea and	15
the amino terminus of	15
as described in materials	15
out of the er	15
spanning domain of coronavirus	15
after min of chase	15
nucleotide exchange factor gbf	15
the trans golgi network	15
these results indicate that	15
golgi apparatus to the	15
vesicular stomatitis virus glycoprotein	15
hepatitis virus strain a	15
little is known about	15
the absence of the	15
back to the er	15
did not affect the	15
the host immune response	14
in er to golgi	14
purification and characterization of	14
the ii cytoplasmic tail	14
in the cytoplasmic tail	14
terminal amino acids of	14
gea and big sec	14
this work was supported	14
transported to the golgi	14
through er and golgi	14
proteins from the er	14
a potent inhibitor of	14
gbf gea and big	14
the location of the	14
the structure and function	14
in the er and	14
the localization of the	14
the membrane spanning domain	14
to occur in the	14
fragmentation of the golgi	14
a role in the	14
is localized to the	14
of the er membrane	14
be due to the	14
it is not clear	14
in a number of	14
no effect on the	14
of the murine coronavirus	14
membrane proteins of the	14
the size of the	14
have shown that the	14
transport of vesicular stomatitis	14
the site of budding	14
in the synthesis of	14
with the golgi network	14
as described in the	14
transport of semliki forest	14
cells were fixed and	14
are present in the	14
on the cytoplasmic side	14
of the rough endoplasmic	14
the amino acid sequence	14
vitro and in vivo	14
fragmentation of the ga	14
at the nonpermissive temperature	13
to the vacuolar membrane	13
the cell surface and	13
is similar to that	13
the hydrophobic length of	13
the control of the	13
the end of the	13
the cytoplasmic tails of	13
the cells were then	13
may play a role	13
the addition of the	13
to changes in the	13
one possibility is that	13
to determine whether the	13
m and s proteins	13
the rsv env gene	13
rough endoplasmic reticulum and	13
play an important role	13
at the restrictive temperature	13
er in the presence	13
and in revised form	13
was found in the	13
the observation that the	13
the thickness of the	13
to a final concentration	13
in the liquid crystalline	13
is transported to the	13
of regulated secretory proteins	13
fhx p in the	13
on the role of	13
to be required for	13
the product of the	13
of the golgi stacks	13
morphology of the golgi	13
proteins in the er	13
has been reported to	13
in the transmembrane domain	13
site of budding of	13
exit from the endoplasmic	13
isolation and characterization of	13
it should be noted	13
of the budding compartment	13
remains to be determined	13
by the endoplasmic reticulum	13
low density lipoprotein receptor	13
on the cytoplasmic face	13
form of s d	13
into the lumen of	13
exit from the er	13
is supported by the	13
the coronavirus mouse hepatitis	13
of the intermediate compartment	13
these data indicate that	13
at the exit from	13
endoplasmic reticulum to golgi	13
cells were transfected with	13
the effect of bfa	13
the transmembrane domains of	13
for the treatment of	12
required for the formation	12
when the cells were	12
in vps mutant cells	12
necessary and sufficient for	12
and characterization of a	12
at the cell periphery	12
cells were incubated with	12
of m s complexes	12
lumen of the golgi	12
of the vsv g	12
coronavirus infectious bronchitis virus	12
of the golgi ribbon	12
of proteins to the	12
hydrophobic thickness of the	12
the rate of bulk	12
of vsv g protein	12
to the periphery of	12
exit from the trans	12
there is evidence that	12
at the golgi complex	12
effect of bfa on	12
used at a dilution	12
arf guanine nucleotide exchange	12
been shown that the	12
at g for min	12
for the presence of	12
cells infected with mhv	12
that the kre p	12
the cells were incubated	12
protein was found to	12
kd protein associated with	12
manuscript submitted for publication	12
of the vesicular stomatitis	12
are targeted to the	12
the liquid crystalline phase	12
the crystal structure of	12
to the transmembrane segment	12
rate of bulk flow	12
in the number of	12
is thought to be	12
the transmembrane region of	12
the cytoplasmic side of	12
hydrophobic length of the	12
membrane protein of the	12
protein exit from the	12
the golgi exclusion zone	12
in the biosynthesis of	12
the herpes simplex virus	12
the synthesis of the	12
of the influenza virus	12
is sufficient for golgi	12
are retained in the	12
work was supported by	12
bulk flow from the	12
to be due to	12
is shown in fig	12
it is not known	12
of bulk flow from	12
to be present in	12
transport from the endoplasmic	12
of mm caffeine at	12
with the m protein	12
membrane glycoproteins to the	12
in the yeast secretory	12
redistribution of golgi proteins	12
been implicated in the	12
from the rer to	12
the bulk of the	11
of the dpap a	11
the golgi stack and	11
from the er and	11
in the sorting of	11
it has been proposed	11
at h after infection	11
were found to be	11
is dependent on the	11
should be noted that	11
amino acid sequence of	11
results were obtained with	11
cytoplasmic domain of tgn	11
domain of coronavirus e	11
have been found to	11
cells were incubated for	11
the ends of the	11
has been proposed that	11
cytoplasmic side of the	11
nucleotide exchange factor for	11
the intracellular transport of	11
the exit from the	11
proteins to the endoplasmic	11
have been suggested to	11
the e protein is	11
are likely to be	11
from the tgn to	11
as a consequence of	11
the average number of	11
association with the golgi	11
cells were fixed with	11
to the surface of	11
within and adjacent to	11
face of the golgi	11
localization of ibv m	11
of the coronavirus mouse	11
protein transport from the	11
rer to the golgi	11
the plasma membrane by	11
membrane association of the	11
membrane spanning domain of	11
the absence of a	11
the biogenesis of lysosomes	11
and the cells were	11
of the fusion proteins	11
the rer to the	11
and characterization of the	11
collected for subcellular fractionation	11
elements of the ga	11
of the er and	11
adjacent to the transmembrane	11
of the protein to	11
transport to the plasma	11
incubated in the presence	11
in close proximity to	11
at the site of	11
does not appear to	11
of transmembrane proteins in	11
the rough er and	11
membrane proteins from the	11
the cell surface in	11
the addition of galactose	11
signal in the cytoplasmic	11
in ergic golgi membranes	11
journal of cell biology	11
with the exception of	11
within the secretory pathway	11
and adjacent to the	11
the secretory pathway and	11
one of the most	11
murine coronavirus spike protein	11
association of m and	11
be associated with the	11
it seems likely that	11
maintenance of the golgi	11
have also been shown	11
transport from the golgi	11
were collected for subcellular	11
have been implicated in	11
the rate at which	11
golgi to the plasma	11
of the protein was	11
at the endoplasmic reticulum	11
the low density lipoprotein	11
that is required for	11
budding of progeny virions	11
been found to be	11
of golgi proteins into	11
golgi proteins into the	11
the ii transmembrane region	11
was not affected by	11
to the golgi and	11
and the golgi stack	11
for min and chased	11
treated with brefeldin a	11
may be involved in	11
retinas were collected for	11
in the amount of	11
the cells were washed	11
we have previously shown	11
the g protein of	11
are a number of	10
on the localization of	10
of type i astrocytes	10
referred to as the	10
the tgn to the	10
secretory vesicles from the	10
than that of the	10
and cytoplasmic domains of	10
crystal structure of the	10
semliki forest virus membrane	10
to interact with the	10
with that of the	10
data indicate that the	10
in the er or	10
of the g protein	10
was inserted into the	10
type ii membrane protein	10
first site of budding	10
the cytoplasmic domains of	10
ribophorins i and ii	10
involved in protein transport	10
terminal domain of the	10
respiratory syndrome coronavirus envelope	10
golgi retention of a	10
characterization of a novel	10
studies have shown that	10
vacuoles operate in the	10
and sorting by the	10
sialyltransferase specify golgi retention	10
the distribution of the	10
the first site of	10
are localized to the	10
expressed on the cell	10
in the present study	10
raises the possibility that	10
the golgi apparatus the	10
golgi network of att	10
it has been demonstrated	10
transport to the vacuole	10
the membranes of the	10
sequences within and adjacent	10
to the basolateral surface	10
the transport of semliki	10
of the lumenal domain	10
there is no evidence	10
network of att cells	10
operate in the transport	10
at the top of	10
kre p cytoplasmic tail	10
of the fusion protein	10
the secretory pathway of	10
presence of brefeldin a	10
the constitutive and regulated	10
for the sorting of	10
to the cell periphery	10
the presence of monensin	10
that the presence of	10
of the yeast golgi	10
has been localized to	10
of proteins into the	10
a member of the	10
important role in the	10
of membrane proteins in	10
the murine coronavirus spike	10
cells were grown in	10
proteins in the golgi	10
in different cell types	10
very similar to that	10
a change in the	10
the context of a	10
the secretory pathway in	10
during the cell cycle	10
the m protein is	10
the intracellular localization of	10
length of the peptide	10
transported through the golgi	10
golgi apparatus and the	10
caffeine at reduced temperature	10
there are a number	10
was performed as described	10
of the gbf gea	10
is involved in the	10
of the nlrp inflammasome	10
to the cis golgi	10
the absence of other	10
the class e compartment	10
thickness of the bilayer	10
in the assembly of	10
the presence of castanospermine	10
of the host cell	10
lumenal domain of dpap	10
may be important for	10
proteins have been shown	10
proteins through the golgi	10
with s methionine and	10
the unfolded protein response	10
the guanine nucleotide exchange	10
was present in the	10
transport of proteins into	10
transmembrane and cytoplasmic domains	10
be involved in the	10
of luminal er proteins	10
to localize to the	10
are required for the	10
proteins in the tgn	10
of the sars coronavirus	10
the dpap a cytosolic	10
transport between the er	10
a regulated secretory pathway	10
the presence of brefeldin	10
glycoproteins to the cell	10
of proteins from the	10
involved in the formation	10
a component of the	10
for its retention in	10
a guanine nucleotide exchange	10
protein is required for	10
were shown to be	10
transport and sorting by	10
from golgi to er	10
to be associated with	10
and the formation of	10
syndrome coronavirus envelope protein	10
in a variety of	10
the yeast saccharomyces cerevisiae	10
disruption of the golgi	10
the s protein is	10
national institutes of health	10
in vivo and in	10
surface of the er	10
dpap a cytosolic domain	10
of the rough er	10
transmembrane domain of the	9
in the form of	9
results suggest that the	9
from the secretory pathway	9
in agreement with the	9
condensed secretory proteins at	9
epidermal growth factor receptor	9
of class i and	9
by the finding that	9
membrane and secretory proteins	9
motif in the cytoplasmic	9
for the synthesis of	9
to the apical membrane	9
top of the stacking	9
to the endocytic pathway	9
that the cytoplasmic domain	9
on the cell type	9
for retention of transmembrane	9
quality control in the	9
the extent to which	9
with s methionine for	9
retrograde transport of proteins	9
the er to golgi	9
proteins destined for the	9
at in the presence	9
coronavirus from condensed secretory	9
to the er and	9
golgi cisternae and or	9
the action of the	9
of the lipid bilayer	9
of the protein is	9
during the course of	9
kd form of s	9
site of addition of	9
darby canine kidney cells	9
that are required for	9
the presence of an	9
of influenza virus hemagglutinin	9
plays a role in	9
be retained in the	9
of the rsv env	9
exit site of the	9
an er recycling pathway	9
en route to the	9
be located in the	9
from condensed secretory proteins	9
chinese hamster ovary cells	9
the activation of the	9
fusion with the plasma	9
domain of kre p	9
vesicles from the tgn	9
the specificity of the	9
it is important to	9
the context of the	9
in the field of	9
at a multiplicity of	9
critical reading of the	9
vivo and in vitro	9
is mediated by the	9
is believed to be	9
of the golgi cisternae	9
the plasma membrane was	9
the secretory pathway is	9
protein transport and sorting	9
the presence of tunicamycin	9
of the stacking gel	9
back to the golgi	9
the subcellular localization of	9
of a consensus motif	9
and the role of	9
an increase in the	9
subcellular localization of the	9
of coronavirus el protein	9
proteins accumulate in the	9
secretory proteins at the	9
fibrosis transmembrane conductance regulator	9
of arf and arf	9
signal prevents secretion of	9
to be important for	9
of the env gene	9
of protein exit from	9
glycoprotein of mouse hepatitis	9
determination of the first	9
p is required for	9
golgi vacuoles operate in	9
galactose and sialic acid	9
golgi localization of the	9
terminal signal prevents secretion	9
vesicles from the trans	9
and the presence of	9
sufficient for golgi retention	9
across the endoplasmic reticulum	9
targeted to the plasma	9
and has been shown	9
were infected with mhv	9
retention of transmembrane proteins	9
membrane proteins in the	9
back to the tgn	9
both arf and arf	9
of the severe acute	9
oligonucleotides and were used	9
of the first site	9
within the cytoplasmic domain	9
an essential role in	9
forest virus membrane glycoproteins	9
in addition to its	9
plays an important role	9
transport from the er	9
of golgi structure and	9
in the biogenesis of	9
retrieval from a post	9
sorting at the exit	9
transport from the rer	9
the e protein ic	9
of big and big	9
the carboxy terminus of	9
beyond the site of	9
a role for the	9
has been demonstrated that	9
in the vicinity of	9
the effects of pdmp	9
cis side of the	9
is required for its	9
in the generation of	9
of bfa on the	9
was fused to the	9
both in vitro and	9
proteins are involved in	9
proteins at the exit	9
cells treated with brefeldin	9
complexes with each other	9
that are involved in	9
residue transmembrane domain of	9
baby hamster kidney cells	9
the endoplasmic reticulum the	9
in the yeast golgi	9
the golgi localization of	9
the journal of cell	9
part of the golgi	9
intracellular transport of secretory	9
a number of other	9
in the same buffer	9
numbers of transition vesicles	9
site of the golgi	9
protein sorting in the	9
g ml of bfa	9
periphery of the cell	9
as an integral membrane	9
of budding of progeny	9
of newly synthesized proteins	9
cystic fibrosis transmembrane conductance	9
membrane cycling from golgi	9
of the signal peptide	9
of viral membrane proteins	9
is not known whether	9
of the regulated secretory	9
as indicated by the	9
was isolated from the	9
the kre p cytoplasmic	9
reading of the manuscript	9
were washed three times	9
to play a role	9
in the electron microscope	9
a marker for the	9
and intracellular transport of	9
biosynthetic protein transport and	9
this is consistent with	9
the endoplasmic reticulum by	9
occurs in the golgi	9
the ga in processes	9
a member of a	9
the cis side of	9
may be related to	9
the apical or basolateral	8
cells expressing s d	8
the endoplasmic reticulum in	8
cytoplasm to vacuole targeting	8
of dpap a is	8
er and golgi apparatus	8
were analyzed by sds	8
e glycoprotein of mouse	8
cytoplasmic tail of the	8
the first amino acids	8
of the transferrin receptor	8
sensitive to endo h	8
mutational analysis of the	8
and maintenance of the	8
the formation of secretory	8
of cargo from the	8
the mechanism by which	8
structure of the golgi	8
the importance of the	8
time retinas were collected	8
did not inhibit the	8
of the kre p	8
membrane traffic between the	8
the association of m	8
were collected from the	8
intravitreally with s methionine	8
been shown to interact	8
the rate of transport	8
cytosolic domain of dpap	8
via the plasma membrane	8
the golgi and the	8
progeny coronavirus from condensed	8
has not yet been	8
the catalytic sec domain	8
proteins of the golgi	8
exchange factor for arf	8
can be divided into	8
to be responsible for	8
at least in part	8
vesicle budding and fusion	8
that transport from the	8
kindly provided by dr	8
subfamilies of arf gefs	8
of the e glycoprotein	8
a consensus motif for	8
the er in cells	8
er plus golgi mixed	8
has been made in	8
it will be interesting	8
the centers of syncytia	8
budding compartment of mouse	8
was transported to the	8
which is involved in	8
can be used to	8
transit through the golgi	8
injected intravitreally with s	8
is responsible for the	8
min and chased for	8
a type ii membrane	8
lumenal domain of the	8
was detected in the	8
a major role in	8
vesicles budding from the	8
the cisternal maturation model	8
accumulate in the golgi	8
disassembly of the golgi	8
in support of this	8
the exit site of	8
in the golgi compartment	8
the env gene product	8
sorting of progeny coronavirus	8
membrane origin for autophagy	8
signal for golgi retention	8
prevents secretion of luminal	8
of the nuclear envelope	8
in the secretion of	8
present in the golgi	8
in the processing of	8
the appearance of the	8
may be due to	8
deletion of amino acids	8
p r o o	8
it has also been	8
evidence for membrane cycling	8
for the existence of	8
avian coronavirus infectious bronchitis	8
formed in the presence	8
to be localized to	8
of infectious bronchitis virus	8
suggests an er recycling	8
the transmembrane and cytoplasmic	8
were prepared as described	8
j o u r	8
on the presence of	8
low levels of expression	8
a result of the	8
in the localization of	8
to the cytoplasmic face	8
depending on the cell	8
were carried out as	8
through the golgi stack	8
protein correlates with its	8
virus membrane glycoproteins to	8
transmembrane domain of a	8
in the er membrane	8
g protein of vesicular	8
by cona sepharose chromatography	8
secretion of luminal er	8
cells were labeled with	8
motif for retention of	8
role of the cytoplasmic	8
to the apical surface	8
in the cytosolic domain	8
membranes of the golgi	8
found to be a	8
is also involved in	8
for membrane cycling from	8
the activity of the	8
a single amino acid	8
replication of coronavirus mhv	8
our understanding of the	8
a l p r	8
of protein secretion in	8
the relocated golgi enzymes	8
at the exit site	8
h at room temperature	8
at the indicated times	8
the catalytic domain of	8
between the rough endoplasmic	8
enzymes involved in the	8
localized to the plasma	8
transport of newly synthesized	8
one face of a	8
membrane protein correlates with	8
from the rough endoplasmic	8
the golgi complex the	8
the budding compartment of	8
identification of a consensus	8
in the elementary unit	8
found to interact with	8
of the mouse hepatitis	8
been localized to the	8
of fhx p in	8
the first step in	8
l p r e	8
to the er in	8
o u r n	8
sorting by the endoplasmic	8
compartments of the secretory	8
the hepatitis c virus	8
of progeny coronavirus from	8
are derived from the	8
in some cell types	8
is possible that the	8
derived from the er	8
number of er buds	8
the existence of a	8
shown to be a	8
hepatitis c virus rna	8
domain of coronavirus el	8
branches of the secretory	8
has been found to	8
is the site of	8
and processed for immunofluorescence	8
cycling from golgi to	8
sorting within the regulated	8
would be expected to	8
out of the cell	8
a model for the	8
a membrane protein correlates	8
amino terminus of the	8
the process of protein	8
as shown by the	8
were transported to the	8
the position of the	8
protein of vesicular stomatitis	8
elements of the golgi	8
used to replace the	8
r n a l	8
assembly of vaccinia virus	8
the cell surface to	8
of golgi membrane proteins	8
were labeled with s	8
compartments of the golgi	8
top of the gradient	8
the cells were treated	8
r o o f	8
oligomerization of a membrane	8
found in the er	8
rapid redistribution of golgi	8
purification and properties of	8
in the golgi cisternae	8
the ph of the	8
complex to the endoplasmic	8
will be interesting to	8
e protein ic activity	8
of the newly synthesized	8
of addition of n	8
of protein transport from	8
u r n a	8
of brefeldin a suggests	8
was used at a	8
a multiplicity of infection	8
consensus motif for retention	8
with its retention in	8
the cell surface is	8
signal peptidase cleavage site	8
control of protein exit	8
these observations suggest that	8
retrieval from the pvc	8
at which time retinas	8
it is unlikely that	8
its transport to the	8
n a l p	8
glycoproteins from the er	8
at each time point	8
a suggests an er	8
been proposed that the	8
of hepatitis c virus	8
have been proposed to	8
brefeldin a suggests an	8
budding from the er	8
at the ends of	8
grown in the presence	8
membrane protein sorting in	8
the first transmembrane domain	8
been shown to form	8
was retained in the	8
is not essential for	8
appears to be the	8
well as in the	8
of some of the	8
of the herpes simplex	8
by the action of	8
correlates with its retention	8
effect on the localization	8
have been reported to	8
to be a potent	8
acid sequence of the	8
face of the er	8
which time retinas were	8
truncated forms of kexlp	7
the p cytoplasmic tail	7
at the periphery of	7
the idea that the	7
is composed of a	7
is essential for the	7
in vitro translation product	7
in the release of	7
which is known to	7
the transmissible gastroenteritis coronavirus	7
is unclear whether the	7
in the same golgi	7
to the basolateral membrane	7
proteins to the cell	7
be a potent inhibitor	7
a possible role for	7
were maintained in darkness	7
the golgi complex was	7
by the formation of	7
first amino acids of	7
of mhc class i	7
delivered to the vacuole	7
both necessary and sufficient	7
that there is a	7
in the center of	7
a decrease in the	7
localization to the golgi	7
did not prevent the	7
at er exit sites	7
it remains to be	7
class i and class	7
first transmembrane domain of	7
induce the formation of	7
from er to golgi	7
of the endocytic pathway	7
hr at which time	7
rna replication depends on	7
golgi complex in the	7
was added to a	7
targeted to the cis	7
a small number of	7
it was suggested that	7
specifies trans golgi localization	7
was similar to that	7
the early stages of	7
of each of the	7
the biosynthesis of the	7
located in the golgi	7
be localized to the	7
the rous sarcoma virus	7
of human chorionic gonadotropin	7
signals for transmembrane proteins	7
rsv env gene product	7
of secretory granules in	7
in the range of	7
h after infection with	7
that the transmembrane domain	7
this result suggests that	7
plasma membrane of the	7
a new class of	7
traffic and organelle structure	7
treatment of cells with	7
and then chased for	7
kre p mnt p	7
protein was shown to	7
the m s complexes	7
of the process of	7
the mechanisms by which	7
of proteins through the	7
the efficiency of the	7
results indicate that the	7
retention of golgi enzymes	7
the amino acid sequences	7
be transported to the	7
type iii secretion system	7
the study of the	7
localized in the golgi	7
of the biosynthesis of	7
been reported to be	7
to the e glycoprotein	7
to be retained in	7
between the tgn and	7
of cholesterol to the	7
view of the golgi	7
of the gal promoter	7
the integrity of the	7
that proteins destined for	7
for the localization of	7
sequences serve as retention	7
of dpap b is	7
in the treatment of	7
is a type ii	7
viral rna replication in	7
within the regulated secretory	7
as demonstrated by the	7
as a mechanism for	7
glycoprotein is required for	7
evidence that transport from	7
secreted from the cell	7
the secretory pathway to	7
of a variety of	7
mouse hepatitis virus a	7
the trans golgi apparatus	7
a mutation in the	7
found to be localized	7
reticulum and golgi apparatus	7
for the first time	7
is located in the	7
endoplasmic reticulum exit sites	7
is the number of	7
been shown to inhibit	7
constitutive and regulated secretion	7
cisterna of the golgi	7
of the protein in	7
required for its retention	7
is required for golgi	7
a late golgi compartment	7
linked oligosaccharides on the	7
of transmembrane proteins to	7
er in cells treated	7
for their ability to	7
cells were incubated in	7
the golgi apparatus a	7
of the interaction between	7
of s d and	7
as part of the	7
from the tgn is	7
in the rough endoplasmic	7
surface of the protein	7
the golgi stacks and	7
the removal of the	7
has been known to	7
the course of the	7
of the avian coronavirus	7
and results in the	7
the oligosaccharide chains of	7
the presence of galactose	7
the fusion protein was	7
elements of the endoplasmic	7
p in the elementary	7
a number of studies	7
from mung bean seedlings	7
thickness of a bilayer	7
the addition of n	7
this protein in the	7
the control of membrane	7
short cytoplasmic sequences serve	7
at the ultrastructural level	7
the golgi complex by	7
sufficient for golgi localization	7
in the golgi and	7
and the effects of	7
present in the er	7
a central role in	7
is one of the	7
domain is sufficient for	7
after the addition of	7
the subcellular distribution of	7
from a patient with	7
the er in yeast	7
secretory and plasma membrane	7
membrane traffic and organelle	7
cytoplasmic sequences serve as	7
the localization of ibv	7
by centrifugation at g	7
it is unclear whether	7
golgi apparatus is a	7
amino acids in the	7
cisternae and or tgn	7
nih t cells were	7
residues of fhx p	7
different from that of	7
to the replication complex	7
krijnse locker et al	7
of the mhv infection	7
protein secretion in eukaryotes	7
that the majority of	7
and s d are	7
golgi proteins to the	7
the sequence of the	7
aspects of the process	7
for golgi retention of	7
of the rous sarcoma	7
in infected cells the	7
a single arf protein	7
proteins from the golgi	7
protein associated with a	7
on the integrity of	7
export from the endoplasmic	7
mechanism of action of	7
and their role in	7
the major capsid protein	7
newly synthesized lysosomal enzymes	7
the m and e	7
to the presence of	7
replication of mouse hepatitis	7
the cytoplasm to vacuole	7
the signal peptidase cleavage	7
retention in the er	7
the default pathway for	7
from the nucleus to	7
protein to the cell	7
the signal recognition particle	7
centrifugation at g for	7
residues in the transmembrane	7
min in the presence	7
protein translocation across the	7
in health and disease	7
on one face of	7
by a monoclonal antibody	7
chains of fhx p	7
have been identified in	7
terminal sialic acid residues	7
is determined by the	7
of the high mannose	7
plus golgi mixed extracts	7
localized to the trans	7
for viral replication and	7
protein transport through the	7
a bilayer of di	7
for the replication of	7
for critical reading of	7
an open reading frame	7
rate of transport of	7
along the exocytic pathway	7
is the presence of	7
proteins have been identified	7
golgi localization of glycosyltransferases	7
formation of secretory granules	7
maintenance of golgi structure	7
to be derived from	7
collected from the top	7
serve as retention signals	7
hydrophobic thickness of a	7
of cells infected with	7
as well as a	7
pc in the liquid	7
has also been reported	7
resistant to endo h	7
the e protein of	7
the retention of golgi	7
in baby hamster kidney	7
the cystic fibrosis transmembrane	7
the cisternae of the	7
it is interesting to	7
been shown to contain	7
the first amino acid	7
compartment of mouse hepatitis	7
is known to be	7
concentration of g ml	7
the effects of bfa	7
that some of the	7
of the golgi membrane	7
targeting of proteins to	7
the cytosolic tail of	7
induces the formation of	7
of the yeast vacuolar	7
be part of the	7
the mhv m protein	7
and functional analysis of	7
on the golgi complex	7
characterization of the budding	7
membrane proteins to the	7
cells were grown on	7
to endo h digestion	7
and is involved in	7
conformational change in the	7
potent inhibitor of the	7
region of the cell	7
the truncated ribophorin i	7
from a number of	7
to the golgi region	7
effects of brefeldin a	7
proteins of the secretory	7
avian infectious bronchitis virus	7
for transmembrane proteins in	7
infectious bronchitis virus e	7
via the cell surface	7
other components of the	7
distribution of the intermediate	7
been suggested that the	7
and plasma membrane proteins	7
the glycan portion of	7
might be involved in	7
as described for the	7
newly synthesized membrane proteins	7
form complexes with each	7
replication depends on gbf	7
as retention signals for	7
core of the bilayer	7
transported out of the	7
compartment at the cis	7
is mediated by a	7
treated with endo h	7
in mislocalization to the	7
to be mediated by	7
were incubated for h	7
stages of the secretory	7
transitional elements of the	7
a number of different	7
to be located in	7
were present in the	7
for min in the	7
to examine the role	7
the large arf gefs	7
play important roles in	7
to be able to	7
a consequence of the	7
from the trans golgi	7
to the er membrane	7
to the accumulation of	7
in the yeast saccharomyces	7
secretory and membrane proteins	7
export from the er	7
cells were washed three	7
has been known for	7
model for the retention	7
viral replication and morphogenesis	7
of the oligosaccharide chain	7
the expansion of the	7
be due to a	7
dependent retrograde transport of	7
in the function of	7
maintained in darkness for	7
s methionine for min	7
the plasma membrane to	7
has been proposed to	7
the expression of the	7
retention signals for transmembrane	7
the formation of dolichyl	6
localization of components involved	6
of cd and cd	6
to the endo h	6
activation of the nlrp	6
endocytic compartment where they	6
has led to the	6
in response to a	6
solubilized with triton x	6
is required for viral	6
secretory pathway of eukaryotic	6
is not sufficient to	6
factors v and viii	6
requires polar residues on	6
were washed once with	6
and lumenal domains of	6
into secretory granules in	6
was used to determine	6
by nilsson et al	6
reticulum and golgi complex	6
side of the er	6
organization of the er	6
domain of the protein	6
the m and s	6
the m glycoprotein of	6
this is supported by	6
the lipid fatty acyl	6
to be transported to	6
cis face of the	6
site of virion budding	6
of low molecular weight	6
the nucleus to the	6
is attached to the	6
golgi complex beyond the	6
face of a predicted	6
in our understanding of	6
luminal er proteins are	6
from the intermediate compartment	6
a small percentage of	6
also been implicated in	6
pathway of eukaryotic cells	6
the elementary unit of	6
of endosomes and lysosomes	6
located in the er	6
of brefeldin a on	6
the absence of caffeine	6
is in agreement with	6
in the ii cytoplasmic	6
replication in association with	6
and its role in	6
binding proteins to exocytic	6
added to a final	6
in the golgi stack	6
a wide variety of	6
residue sequence of st	6
across the er membrane	6
for min followed by	6
major histocompatibility complex class	6
in the maintenance of	6
carboxy terminus of the	6
out of the golgi	6
was cloned into the	6
of the big sec	6
as a measure of	6
terminal portion of the	6
to accumulate in the	6
retrograde transport from the	6
his leu leu lys	6
components involved in protein	6
as determined by the	6
of the stem region	6
the apical and basolateral	6
at low levels of	6
the elementary unit in	6
the vaccinia virus a	6
enzymes in hela cells	6
lumen of the er	6
oligosaccharide chains of fhx	6
of the translocation apparatus	6
and embedded in epon	6
events in the yeast	6
transmembrane segment of p	6
functional characterization of the	6
of the host immune	6
the signal for golgi	6
that the e protein	6
to be important in	6
with the idea that	6
it is difficult to	6
g protein to the	6
proteins that interact with	6
are not essential for	6
h after infection at	6
by brefeldin a of	6
it cannot be excluded	6
a limited number of	6
budding from the tgn	6
the golgi complex requires	6
were incubated with the	6
of the copi coat	6
the surface of cells	6
of man ii in	6
then inserted into the	6
required for viral replication	6
this raises the possibility	6
evidence for the existence	6
at the surface of	6
that luminal er proteins	6
for a review see	6
of kre p was	6
the conformation of the	6
protein in the golgi	6
block the formation of	6
the polarized epithelial cell	6
a monoclonal antibody against	6
the localization of p	6
the mouse hepatitis virus	6
in mixtures of di	6
incubated at c for	6
transport and processing through	6
in membrane traffic and	6
processed with a half	6
the african swine fever	6
mouse hepatitis virus replicase	6
golgi complex and the	6
the gene for the	6
granules of the regulated	6
from the fact that	6
of the cystic fibrosis	6
the collapse of the	6
as described above for	6
coronavirus m proteins accumulate	6
is an integral membrane	6
are associated with the	6
cell surface expression of	6
with regard to the	6
these results demonstrate that	6
early secretory pathway in	6
to the yeast tgn	6
rate of secretion of	6
of the glycoprotein processing	6
in the retention of	6
the cytoplasmic and transmembrane	6
of the small gtpase	6
vitro and in cells	6
in the golgi membrane	6
the accumulation of glycoproteins	6
biology of membrane trafficking	6
and regulated secretion of	6
retention of a cis	6
the golgi stack in	6
the course of an	6
either immediately or after	6
helix in the transmembrane	6
placed under the control	6
secreted proteins in a	6
protein transport and processing	6
and the cell surface	6
m proteins accumulate in	6
elements operating in er	6
exposed on the cytoplasmic	6
kre p tmd is	6
are also involved in	6
a small amount of	6
requires only one vesicular	6
sites of virus replication	6
of components involved in	6
is clear that the	6
translocation across the endoplasmic	6
between m and s	6
is accompanied by a	6
the avian coronavirus infectious	6
localization signal in the	6
with uranyl acetate and	6
rats were injected intravitreally	6
of the gene encoding	6
leu leu leu gly	6
gea p and gea	6
of plasma membrane proteins	6
the golgi complex as	6
caused by mutations in	6
the n protein was	6
as well as other	6
these data suggest that	6
infected cells were labeled	6
did not result in	6
the small g proteins	6
an antibody specific for	6
mutations in the cytoplasmic	6
or absence of mm	6
membrane trafficking in human	6
are referred to as	6
for localization to the	6
is required for normal	6
a crucial role in	6
could be due to	6
glucosidase i and glucosidase	6
first step in the	6
of the gm activator	6
between the rough er	6
amino acid residues of	6
shown to interact with	6
may be part of	6
of st is sufficient	6
by the method of	6
cells in the presence	6
acid residues of the	6
and shown to be	6
the site of virion	6
vesicle budding from the	6
the rate of secretion	6
a subunit of the	6
prevalent but still unrecognized	6
golgi enzymes in hela	6
the intermediate elements operating	6
might be expected to	6
derivatives of ras l	6
the fusion of the	6
processing through the yeast	6
regulated secretion of proteins	6
of the polarized epithelial	6
to the bilayer normal	6
added to the cells	6
middle east respiratory syndrome	6
to determine if the	6
and the endoplasmic reticulum	6
golgi protein requires polar	6
c virus rna replication	6
data suggest that the	6
the limiting membrane of	6
in viral rna synthesis	6
for golgi ribbon formation	6
in the membrane of	6
cells were washed once	6
terminal half of the	6
were fixed with paraformaldehyde	6
secretory granules in att	6
very similar to those	6
of the low density	6
vesicular stomatitis virus in	6
the amount of radioactivity	6
was used as a	6
closely associated with the	6
in the perinuclear region	6
mhc class i molecules	6
m and n proteins	6
shown to be required	6
der meer et al	6
linked oligosaccharides of the	6
processing in the golgi	6
the external domain of	6
studies have indicated that	6
of the intermediate elements	6
retention of membrane proteins	6
the big sec subfamily	6
medial golgi enzymes in	6
of guanine nucleotide exchange	6
lumenal domain of p	6
sorting of lysosomal enzymes	6
dissecting the role of	6
from the top of	6
nitrogen in the ring	6
the effects of the	6
operating in er to	6
membrane versions of ras	6
lipid fatty acyl chains	6
in cultured rat hepatocytes	6
is no evidence that	6
gtp binding and hydrolysis	6
association with cellular membranes	6
the tgn and the	6
that the ii cytoplasmic	6
class i and ii	6
transport of cholesterol to	6
the endoplasmic reticulum membrane	6
with the lipid bilayer	6
from the e r	6
the cell periphery and	6
to the center of	6
structural features of the	6
transport of lysosomal enzymes	6
of the arf proteins	6
protein encoded by the	6
and vps mutant cells	6
are part of the	6
these results show that	6
golgi and the golgi	6
of the sample was	6
despite the fact that	6
is interesting to note	6
essentially as described by	6
trafficking in human disease	6
in darkness for hr	6
domain of a coronavirus	6
interesting to note that	6
induced retrograde movement of	6
the maturation of the	6
does not seem to	6
of nascent secretory vesicles	6
of the glycan portion	6
cell biology of membrane	6
with semliki forest virus	6
as well as for	6
occurs in the trans	6
is due to the	6
for the development of	6
was supported by grants	6
of the stacked cisternae	6
with the help of	6
a new type of	6
in the culture medium	6
of secretory and plasma	6
insights into the control	6
the surface expression of	6
structure of arf in	6
and membrane association of	6
i and glucosidase ii	6
protein to the plasma	6
leu leu gly leu	6
in spite of the	6
proteins are sorted from	6
the identification of the	6
type i membrane proteins	6
may be responsible for	6
er proteins are sorted	6
to the fact that	6
and were used to	6
hepatitis c virus replication	6
american type culture collection	6
the mechanism of action	6
type of viral glycoprotein	6
for the study of	6
rna replication in association	6
proteins to exocytic and	6
similar to those of	6
under the electron microscope	6
one side of the	6
can be attributed to	6
rain at room temperature	6
be interesting to see	6
were kindly provided by	6
will be discussed in	6
in thin sections of	6
in the production of	6
have previously shown that	6
the coxsackievirus b protein	6
segment of p o	6
in the distribution of	6
used in this study	6
s and he proteins	6
that m and s	6
found in the pellet	6
in association with the	6
but not in the	6
the plasma membrane where	6
appear to occur in	6
van der meer et	6
the gbf gea subfamily	6
to the early golgi	6
polar residues on one	6
a direct role in	6
the addition of a	6
p and gea p	6
continuous with the golgi	6
during the assembly of	6
of an avian coronavirus	6
the ph domain of	6
appears to be a	6
in the process of	6
in the structure of	6
translocation of the ga	6
residues on one face	6
the b protein of	6
a golgi membrane protein	6
and the release of	6
dispersal of the golgi	6
of newly synthesized membrane	6
a kind gift of	6
evidence that luminal er	6
of a bilayer of	6
surface area of the	6
intermediate elements operating in	6
glycosyltransferase complexes in eukaryotes	6
sorted from secreted proteins	6
a resident of the	6
for the organization of	6
type ii integral membrane	6
in protein transport and	6
context of cisternal maturation	6
to the tgn and	6
were found in the	6
integral membrane versions of	6
a part of the	6
of the iicr chimera	6
domain of vsv g	6
golgi complex requires only	6
kd subunit of the	6
glycoprotein of an avian	6
to be localized in	6
constitutive and regulated secretory	6
and then incubated with	6
the m protein was	6
reasonable to assume that	6
of anterograde and retrograde	6
lumen of the rer	6
the vicinity of the	6
the ibv e protein	6
be found in the	6
total number of er	6
pathways of protein secretion	6
control of the gal	6
in association with cellular	6
in golgi structure formation	6
were added to the	6
a number of membrane	6
the presence of swainsonine	6
low molecular weight gtp	6
methionine for min and	6
the sorting of the	6
and is essential for	6
gillingham and munro b	6
to the golgi membranes	6
we were able to	6
have been linked to	6
center of the syncytia	6
to distinguish between these	6
structural proteins during the	6
of the chimeric proteins	6
is not clear whether	6
accumulated in the golgi	6
carried out as described	6
the interface between the	6
the processing of the	6
er and golgi complex	6
will be required to	6
of the hepatitis c	6
formed in the absence	6
staining of the ga	6
cytoplasmic and transmembrane domains	6
kre p tmd in	6
used in this paper	6
and membrane topology of	6
the context of cisternal	6
sorting of secretory and	6
has been identified as	6
in the gene encoding	6
into the control of	6
that most of the	6
fixed and processed for	6
compartment of the golgi	6
take place in the	6
a number of cell	6
complex beyond the site	6
the maintenance of the	6
transported from the er	6
components of the cellular	6
the regulation of the	6
linked oligosaccharide chains of	6
of interest to determine	6
of a subset of	6
complex requires only one	6
retention signal in the	6
seen in cells infected	6
with the fact that	6
are sorted from secreted	6
between medial golgi enzymes	6
difference between the two	6
one vesicular transport step	6
it was concluded that	6
effects of bfa on	6
in the gel phase	6
is restricted to the	6
man ii was found	6
the sec family of	6
as well as by	6
the el glycoprotein of	6
are transported through the	6
to a lesser extent	6
effects of monensin on	6
were injected intravitreally with	6
produced in the presence	6
of membrane trafficking in	6
transmembrane domain of st	6
mutant forms of kexlp	6
is both necessary and	6
only one vesicular transport	6
the influenza virus hemagglutinin	6
vesicular compartment at the	6
described in the results	6
of the ga and	6
cloning and expression of	6
de groot et al	6
gives rise to the	6
similar to those observed	6
is required for efficient	6
to the budding compartment	6
the constitutive exocytic pathway	6
can be found in	6
the coronavirus spike protein	6
were metabolically labeled for	6
protein requires polar residues	6
a conformational change in	6
region of the golgi	6
from secreted proteins in	6
intracellular transport of the	6
mannose residues of fhx	6
for hr at which	6
activator protein for secretion	6
can be achieved by	6
transported to the vacuole	6
through the yeast golgi	6
after removal of the	6
that many of the	6
retrieved back to the	6
cells were pulse labeled	6
to note that the	6
of the protein that	6
examine the role of	6
regulated secretory proteins in	6
length of the transmembrane	6
the secretory granules of	6
incubated for min at	6
leu gly leu val	6
and processing through the	6
in the tgn of	5
golgi matrix protein gm	5
for rain on ice	5
characterization of the fusion	5
rough surface of the	5
of the nervous system	5
rough er and the	5
of the sugar chains	5
be derived from the	5
truncated ribophorin i molecules	5
stained by antibodies to	5
and in some cases	5
antibody specific for the	5
effect of caffeine on	5
the polarization of the	5
deletion mutants of the	5
the retention of p	5
centrifuged at g for	5
the linear density of	5
suggesting that they are	5
factors at the golgi	5
of the t cell	5
that this may be	5
of an integral membrane	5
could serve as a	5
of dpap b was	5
inhibitor of jack bean	5
movement of the protein	5
the secretory pathway by	5
in the appearance of	5
across the golgi stack	5
role of the arf	5
both s d and	5
virions in the golgi	5
do membranes hold the	5
this has not been	5
mislocalization to the vacuole	5
were expressed in cos	5
the basolateral surface of	5
their transport to the	5
in the budding of	5
domain of the cd	5
it has been speculated	5
the functioning of the	5
of the vacuolar membrane	5
the vesicular transport model	5
protein in the er	5
domain of the e	5
is not affected by	5
into the ecori site	5
the disorder of the	5
with a diameter of	5
st is sufficient for	5
treated with bfa for	5
protein of the er	5
a role in golgi	5
in place of the	5
stem regions of the	5
the presence of high	5
vesicle formation from the	5
the influenza virus ha	5
the intensity of the	5
to an increase in	5
ser ser ile arg	5
been known to be	5
domains of the vacuolar	5
of the vacuolar h	5
ceacam a cells were	5
mutation in the gene	5
regulating organelle structure and	5
fixed at h p	5
inhibition of protein trafficking	5
sars coronavirus envelope protein	5
for regulating organelle structure	5
portion of the fusion	5
densely packed membrane vesicles	5
which is similar to	5
takes place at double	5
the in vitro translation	5
be important for the	5
may function in glycosylation	5
tail of dpap a	5
trans side of the	5
complex to the er	5
the cis face of	5
of arf in complex	5
the synthesis of dolichyl	5
to the vacuole by	5
generally referred to as	5
the outside of the	5
higher levels of expression	5
infected with semliki forest	5
of the m glycoprotein	5
of murine hepatitis virus	5
demonstration of an extensive	5
shown to inhibit the	5
terminus of the protein	5
remains to be elucidated	5
the numbers of transition	5
it was shown that	5
be of interest to	5
anterograde and retrograde traffic	5
synthesized in the er	5
a amino acid long	5
is complicated by the	5
modification of intracellular membrane	5
proteins are retained in	5
and processing of the	5
of the arf gefs	5
region of the bilayer	5
have been used to	5
granules in the golgi	5
the m protein of	5
the enzyme to the	5
the elementary unit was	5
at an early stage	5
that resides in the	5
a consequence of a	5
formation of the viral	5
in the tgn and	5
plasma membrane where it	5
by antibodies to gait	5
at a final concentration	5
then transported to the	5
example of this is	5
the coronavirus m protein	5
is also consistent with	5
nature of the golgi	5
protein sorting events defined	5
the alkaline phosphatase treatment	5
a great deal of	5
the apical surface of	5
fixed and prepared for	5
sample was treated with	5
may each act to	5
product of herpes simplex	5
each act to localize	5
the transport of the	5
proteins and lipids from	5
the transmembrane and luminal	5
plays a central role	5
these findings suggest that	5
presence of caffeine at	5
in protein transport from	5
transport of protein between	5
inhibit the formation of	5
is provided by the	5
multiplicity of infection of	5
a recombinant vaccinia virus	5
can be seen in	5
leu leu lys gly	5
the ibv m protein	5
are found in the	5
the difference between the	5
cytoplasmic tail and transmembrane	5
compartment where they are	5
to the permissive temperature	5
in much the same	5
is referred to as	5
metabolically radiolabeled for min	5
er to golgi traffic	5
the components of the	5
immature secretory granules from	5
in a late golgi	5
to one of the	5
m and s associate	5
the conclusion that the	5
be consistent with the	5
the erm family proteins	5
the molar ratio of	5
for rain at room	5
darkness for hr at	5
secretory granules in the	5
to exocytic and endocytic	5
characterization of the coronavirus	5
nature of the carbohydrate	5
the question of whether	5
the cell biology of	5
and the appearance of	5
egress through er and	5
traverse the secretory pathway	5
is also possible that	5
situ and in vitro	5
pathway for membrane proteins	5
blood group a and	5
of great interest to	5
tail and transmembrane region	5
regulated secretory proteins are	5
transmembrane segment of a	5
progeny virions site of	5
components back to the	5
transport of membrane proteins	5
of viral proteins and	5
we refer to as	5
contents of cellular origin	5
has not been possible	5
from rat liver golgi	5
in the host cell	5
golgi membranes to the	5
a general mechanism for	5
saturation of the retention	5
of the mutant proteins	5
stomatitis virus glycoprotein is	5
on the secretion of	5
targeted to the golgi	5
in the course of	5
proteins during the assembly	5
the intracellular sites of	5
of a set of	5
of the transmissible gastroenteritis	5
have not yet been	5
hela cells expressing gml	5
the field of intracellular	5
that the protein is	5
e ects of the	5
there is increasing evidence	5
of viral proteins in	5
open reading frame of	5
cells were harvested and	5
enzyme to the golgi	5
antibodies directed against the	5
localization of galactosyltransferase in	5
do not have the	5
eluates were applied to	5
formation utilizes components of	5
the golgi apparatus are	5
transmembrane domain of n	5
arg lys met t	5
replaced by that of	5
that of the wild	5
it is apparent that	5
there appears to be	5
have been observed in	5
prepared for indirect immunofluorescence	5
and fuse with the	5
the golgi cisternae and	5
in mouse hepatitis virus	5
sars cov e protein	5
on the organization of	5
the presence of viral	5
packaged into secretory granules	5
detected at the cell	5
linked oligosaccharides occurs in	5
a negative regulator of	5
across the rer membrane	5
of this protein in	5
incubated for min in	5
important to note that	5
consistent with the idea	5
transfer of a membrane	5
a small fraction of	5
intracellular membrane structures for	5
not transported to the	5
arf at the plasma	5
the iicr rm chimera	5
distribution of man ii	5
is initiated in the	5
in terms of the	5
at the amino acid	5
the cellular secretory pathway	5
proteins were transported to	5
fused to the transmembrane	5
exocytic and endocytic compartments	5
g proteins of the	5
secretory granules of the	5
sec portion of the	5
for h and then	5
the golgi region and	5
protein in which the	5
granules in att cells	5
the perinuclear region of	5
modification and vacuolar protein	5
golgi apparatus of the	5
sialyltransferase is sufficient for	5
does not affect the	5
as illustrated in fig	5
the dilated rims of	5
of the viral glycoproteins	5
high levels of expression	5
apical or basolateral domains	5
processing of the oligosaccharide	5
at c for h	5
has also been implicated	5
the cytoplasmic domain is	5
studies suggest that the	5
physical interaction between the	5
in the trans golgi	5
coronavirus rna replication depends	5
by the prototype serum	5
a functional role for	5
specific transmembrane domain of	5
minute virus of mice	5
and chased for various	5
gml or vsv g	5
with a variety of	5
and luminal domains of	5
were washed with pbs	5
have yet to be	5
an integral membrane glycoprotein	5
uranyl acetate and lead	5
through the golgi is	5
a critical role in	5
the formation of hybrid	5
to the ergic and	5
is distinct from the	5
involved in the synthesis	5
seems likely that the	5
cannot be excluded that	5
virus takes place at	5
stomatitis virus g glycoprotein	5
type tr and chimeric	5
and composition of the	5
sars coronavirus e protein	5
a compartment for sorting	5
gain access to the	5
intracellular aspects of the	5
by grants from the	5
lys gly leu leu	5
in the m protein	5
been shown to regulate	5
polarization of the ga	5
the poliovirus replication complex	5
this leads to the	5
that of wild type	5
cleavage of structural proteins	5
as shown in table	5
the center of syncytia	5
the carbohydrate portion of	5
isolated from natural sources	5
kin recognition between medial	5
of the elh prohormone	5
the cytoplasmic surface of	5
cov e protein ic	5
progress has been made	5
the ends of transmembrane	5
and functional characterization of	5
of the isolation membrane	5
the ga and the	5
residues within the membrane	5
the unglycosylated form of	5
trafficking through the golgi	5
this indicates that the	5
the effects of monensin	5
the site of assembly	5
in pbs for h	5
rna replication of mouse	5
bar corresponds to mm	5
a membrane protein of	5
the results of the	5
targeted derivatives of ras	5
the significance of the	5
in addition to a	5
applied to rca agarose	5
network continuous with the	5
as well as with	5
have been detected in	5
were washed twice with	5
a specific transmembrane domain	5
in saccharomyces cerevisiae the	5
it would be interesting	5
role of the b	5
flow from the golgi	5
protein to the vacuole	5
very little is known	5
of apical and basolateral	5
to be incorporated into	5
under the same conditions	5
has the potential to	5
of the iicr rm	5
important insights into the	5
within the golgi stack	5
absence of the drug	5
the loss of the	5
a significant amount of	5
the addition of o	5
artifact to center stage	5
branch of the secretory	5
recognition between medial golgi	5
the middle of the	5
within the golgi cisternae	5
the role of these	5
described by nilsson et	5
associated with the er	5
intact ribophorin i molecules	5
that appear to be	5
of condensed secretory proteins	5
coronavirus replication complex formation	5
involved in the processing	5
the e protein was	5
localization with vat p	5
of the luminal domain	5
the cell surface via	5
for transport of vesicular	5
to be independent of	5
more than of the	5
caffeine at degrees c	5
even in the absence	5
proteins of the early	5
the cell surface the	5
expression of a dominant	5
has shown that the	5
hepatitis c virus p	5
that the site of	5
the transmembrane ot helices	5
elementary unit of fibroin	5
to vacuole targeting pathway	5
act to localize the	5
is linked to the	5
were transfected with a	5
in a later section	5
to show that the	5
de planque et al	5
is likely that the	5
protein from the tgn	5
are inserted into the	5
the polymeric immunoglobulin receptor	5
the formation of constitutive	5
are distinct from the	5
support the conclusion that	5
the golgi apparatus maintains	5
localization of low molecular	5
tgn suggest a general	5
average number of buds	5
to their final destination	5
glycosylation in the golgi	5
cytoplasmic tail of p	5
the n protein is	5
suggested to be the	5
to an endocytic compartment	5
that s d and	5
vesicles and the golgi	5
of dpap a to	5
is regulated by the	5
of the head of	5
it would appear that	5
from artifact to center	5
has been the subject	5
in the cytoplasm and	5
the bottom of the	5
primary cultures of rat	5
of the viral envelope	5
in the rough er	5
to h after infection	5
assembly of the head	5
dpap a and dpap	5
the er retention of	5
in the pancreatic exocrine	5
regions of the golgi	5
been the subject of	5
of avian infectious bronchitis	5
components of the translocation	5
on the type of	5
lys met t his	5
ser ser ser ile	5
scale bars correspond to	5
gene product of herpes	5
the b protein has	5
of heterotrimeric g proteins	5
man ii to the	5
were performed as described	5
of the viral genome	5
reaches the cell surface	5
the head of bacteriophage	5
through the formation of	5
are localized in the	5
dpap a to the	5
and then inserted into	5
retention of a trans	5
cells infected with the	5
number of buds per	5
of exit from the	5
is based on the	5
protein modification and vacuolar	5
only of the cells	5
bypass the golgi apparatus	5
absence of mm caffeine	5
localization of the fusion	5
vacuolar protein sorting events	5
localizes to the tgn	5
a portion of the	5
n protein and the	5
protein transport between the	5
retention of dpap a	5
small g proteins of	5
western blotting with the	5
this suggests that the	5
function depends on the	5
the ic has been	5
the effects of brefeldin	5
a and a pol	5
hepatitis virus takes place	5
the total amount of	5
for up to min	5
in the processing pathway	5
have been identified that	5
it may be that	5
nascent secretory vesicles from	5
to the transmembrane and	5
the amount of the	5
signal anchor and stem	5
in the class e	5
translocation across the er	5
and used to replace	5
the addition of bfa	5
are consistent with the	5
due to the fact	5
is necessary for the	5
protein transport to the	5
and chased for h	5
sorting in the golgi	5
the regulated secretory proteins	5
the complexity of the	5
of the er in	5
of autophagic vacuoles in	5
of the presence of	5
of glycoproteins from the	5
of the exocytic pathway	5
on the extracellular side	5
of membrane traffic and	5
glycosylation and secretion of	5
val val ile leu	5
the plasma membrane is	5
of the membrane protein	5
and or transport of	5
cytoplasmic domain of gp	5
the golgi apparatus was	5
but does not prevent	5
b protein is a	5
it is also possible	5
localize the enzyme to	5
determined by the subcellular	5
codistribution with thiamine pyrophosphatase	5