trigram

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trigram frequency
not certified by1548
certified by peer1548
the copyright holder1548
holder for this1548
copyright holder for1548
is the author1548
by peer review1548
the author funder1548
which was not1540
version posted january1539
this preprintthis version1539
preprintthis version posted1539
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org licenses by1153
to display the1152
preprint in perpetuity1152
who has granted1152
a license to1152
license to display1152
display the preprint1152
granted biorxiv a1152
biorxiv a license1152
the preprint in1152
has granted biorxiv1152
is made the706
licenseavailable under a706
international licenseavailable under706
it is made706
made the copyright706
it is the453
licensemade available under446
international licensemade available446
available under a446
is the copyright446
no reuse allowed396
reuse allowed without396
all rights reserved396
allowed without permission396
the presence of239
in the presence169
as well as125
the number of97
based on the97
le g e92
l eg e76
structure of the73
ps ta t69
for min at69
was used to68
c a c66
j biol chem66
the activity of65
analysis of the64
the absence of64
in this study63
natl acad sci62
proc natl acad60
in order to59
pc pc pc59
u s a59
sci u s59
acad sci u59
in the absence59
the outer membrane58
h h h57
one of the56
c c c54
ps ps ps54
the a site53
the role of53
a c a51
the active site51
nucleic acids res50
compared to the50
were incubated with50
we found that49
pg pg pg49
at room temperature47
due to the47
the formation of46
pe pe pe46
was added to45
ta t re45
t re l45
stat and stat44
the addition of44
pi pi pi43
was obtained from42
aa c a40
crystal structure of40
the edited cytidine40
m icrocystis aeruginosa40
hbv integration sequences39
are shown in38
added to the37
dimer bound to37
the effect of37
x x x36
part of the36
was performed using36
hbv integration sites36
a and b36
in addition to36
as described in35
aa ca rnc35
the binding of35
was supported by35
data was obtained35
present in the34
with hbv integration34
s yn ec34
in the same34
the use of33
the structure of33
mm hepes ph33
yn ec ho33
b and c33
pdi and erp33
l e g33
were used to33
involved in the33
e g e33
pa pa pa32
the crystal structure32
the signal peptide32
showed that the32
is required for32
kda kda kda32
according to the32
been shown to32
of the human31
for h at31
the development of31
of the two31
were performed in31
activity of the30
the importance of30
were used for30
as previously described30
this work was30
a total of30
found to be30
was used for30
of the rbd29
supplemental figure s29
between the two29
to determine the29
supported by the29
of the enzyme29
in response to29
relative to the29
of the dna29
with and without29
walls et al29
the supernatant was29
on the other28
to that of28
s p l28
experiments were performed28
op si s28
pdi i a28
used in this28
regulators of mitochondrial28
of the sars28
the effects of28
a s p28
the identification of28
different concentrations of28
the kinetics of28
min ps ta27
at the same27
extended data fig27
time min ps27
p l eg27
journal of biological27
of mitochondrial copper27
thermo fisher scientific27
we used the27
the inner membrane27
o o o27
were carried out27
in which the27
was used as27
in contrast to27
snm a and27
an increase in26
consistent with the26
the amount of26
presence of the26
disulfide bond introduction26
sp l e26
the efficiency of26
in the inner26
disulfide bond formation26
gated ion channel26
to the outer26
two technical replicates26
the other hand26
used for the26
the presence or26
as a potential26
as described above26
buffer containing mm26
was carried out26
was performed with25
and snm b25
three biological replicates25
isobaric trigger channel25
this study jr25
with each two25
to investigate the25
materials and methods25
glcns s glca25
each two technical25
a number of25
of biological chemistry25
of pi kc25
is involved in25
u rna editing25
of the protein25
of the s25
the ulk complex25
in the rpe25
with editing frequency25
cancer cell lines24
a and snm24
presence or absence24
fisch erella t24
the level of24
t herm alis24
nucleic acids research24
after stimulation with24
per unit increments24
n ie s24
n n n24
erella t herm24
well as the24
the cells were24
the ribosome exit24
of three independent23
room temperature for23
genetic regulators of23
work was supported23
icrocystis aeruginosa le23
were able to23
aeruginosa le g23
each of the23
was determined by23
sufb and prol23
analysis was performed23
in liquid nitrogen23
of the cell23
shown in figure23
changes in the23
this study cen23
the results of23
of stat and23
f as a23
wang et al23
in complex with23
p c c23
western blot analysis23
the authors declare22
in the m22
yl in dr22
and stored at22
deephbv with hbv22
chen et al22
n u m22
c yl in22
r o f22
sp er m22
pnpla f f22
by centrifugation at22
is shown in22
si s ra22
ci bo rs22
figure a and22
r r r22
dr o sp22
o sp er22
the production of22
rs ki i22
er m op22
in saccharomyces cerevisiae22
and pskai b22
to the a22
s ra ci22
or absence of22
m b e22
m op si22
b e r22
as described previously22
could not be22
in dr o22
cells were grown22
the concentration of22
u mrna editing22
the majority of22
ra ci bo22
mismatches in regulatory22
tcga pan cancer22
a disulfide bond22
expression and purification22
bo rs ki22
e r o22
u m b22
hyg this study21
the regulation of21
by addition of21
it has been21
suggests that the21
and purification of21
lytic polysaccharide monooxygenase21
of downstream sequence21
binding of the21
size exclusion chromatography21
as in figure21
of the edited21
the m g21
were grown in21
nat struct mol21
corresponding to the21
struct mol biol21
electronic health care21
in figure b21
a potential antiviral21
can be used21
the spike protein21
observed in the21
used as a21
hek t cells21
health care records21
ebs and captan21
we show that21
potential antiviral agent21
no ss ss21
presence of a21
c and d21
role of the21
pskai a and21
was performed by20
a function of20
is known to20
three independent experiments20
antiviral agent page20
the mechanism of20
of the c20
the levels of20
the s subunit20
flow rate of20
u le s20
c u le20
le c u20
as shown in20
o le c20
f m o20
the p site20
figure s a20
i s t20
g g g20
o f m20
are shown as20
to evaluate the20
the case of20
genes that are20
conflict of interest20
cleavage of the20
sp le g20
were resuspended in20
m fi time20
agent page of20
the analysis of20
has been shown20
mitochondrial copper homeostasis20
as a function20
in a single20
ebs or captan20
m o le20
were added to20
the ratio of20
this study js19
were subjected to19
cy st is19
downstream of the19
ta t r19
p le g19
such as the19
ch m ch19
was incubated with19
found in the19
s p le19
associated with the19
bound to the19
ec ho cy19
cyano bium sp19
the journal of19
j mol biol19
ho cy st19
in the case19
molecular dynamics simulations19
we showed that19
were used as19
of the same19
s m ch19
downstream sequence to19
sequence of the19
authors declare no19
expression of the19
ribosome exit site19
st is s19
binding to the19
t r el19
m ch m19
frozen in liquid19
to assess the19
the expression of19
resulted in a19
were found to19
a nascent chain19
and mm tcep19
in electronic health19
side of the19
were classified as19
we were able18
structures of the18
the distance between18
the ability of18
of saccharomyces cerevisiae18
contribute to the18
structural basis of18
in mm tris18
em structure of18
in vitro ubiquitination18
formation of the18
similar to the18
normalized to maximal18
acute respiratory syndrome18
position of the18
of fatty acids18
ec and ec18
stimulation with il18
with respect to18
the fact that18
to this end18
surface of the18
severe acute respiratory18
were purchased from18
results suggest that18
the percentage of18
drug prescriptions in18
for min and18
g e c18
results show that18
formation of a18
end of the18
k s ic18
d and e18
data are presented18
of the n18
biochim biophys acta18
required for the18
were pooled and18
ta bl et17
be used to17
a combination of17
shown in fig17
in line with17
were analyzed by17
the sequence of17
artery endothelial cells17
of the amyloid17
of the spike17
the same buffer17
e and f17
extended data table17
indicating that the17
the lack of17
is associated with17
as a result17
at iv e17
equipped with a17
p lanktoth rix17
bium sp lege17
com work bibliography17
data collection and17
sili ne a17
of ulk complex17
is consistent with17
of cylc homologs17
no do sili17
in the first17
el at iv17
error bars indicate17
the samples were17
coronary artery endothelial17
that of the17
in agreement with17
the in vitro17
representation of the17
fi ps ta17
m fi ps17
prescriptions in electronic17
vitamin b deficiency17
r el at17
was found to17
due to its17
do sili ne17
were incubated for17
by flow cytometry17
formic acid in17
in the er17
final concentration of17
bond introduction into17
the protein was17
the experiments were17
increase in the17
characterization of the17
are presented as17
used in the17
calculated from the17
bl et s17
to the membrane17
patients with a17
atomic force microscopy17
the endoplasmic reticulum17
coefficient of variation16
na na na16
the inhibition of16
in comparison to16
all of the16
bronchial epithelial cells16
of the three16
respiratory syndrome coronavirus16
induced by il16
is based on16
show that the16
of amino acids16
to those of16
a c c16
the distribution of16
to identify the16
disulfide bond into16
standard deviation of16
has been reported16
identification of a16
a b c16
snm b apollo16
were obtained from16
authors contributed equally16
figure b and16
and figure s16
structure and function16
in this work16
crystal structures of16
were performed as16
is essential for16
fi time min16
of the signal16
of the complex16
were performed using16
the evaluation of16
g ta bl16
of all the16
were treated with16
two molecules of16
work bibliography http16
have shown that16
we sought to16
on the same16
interactions with the16
with the exception16
was performed in16
figure c and16
seffouh et al16
the university of16
known to be16
department of biochemistry16
a set of16
of statistical software16
effect on the16
the growth of16
regulatory sequence motif16
cs ds chain16
kai a and16
journal of statistical16
m g ta16
g for min16
in trypanosoma cruzi16
followed by a15
and kai b15
and characterization of15
bound to two15
type vii secretion15
a and c15
data from the15
a and kai15
was transferred to15
a flow rate15
of a single15
in the a15
were incubated in15
the context of15
after h of15
analysing drug prescriptions15
a series of15
membrane recruitment of15
cells were incubated15
schematic representation of15
erm u m15
on top of15
were generated using15
of editing sites15
members of the15
interactions between the15
when compared to15
mutations in the15
ne a s15
likely to be15
of lipid species15
glcns s idoa15
was set to15
a role in15
activity was measured15
backus and smith15
together with the15
evaluation of the15
cyano bacter ium15
a subset of15
the parasites were15
role in the15
l e ge15
referred to as15
a and pskai15
extended data figure15
on the activity15
figure s b15
any of the15
of the b15
hsa nascent chain15
guvs were incubated15
of editing frequency15
of the national15
a variety of15
motif at the15
in figure a14
interact with the14
b c d14
active site of14
blot analysis of14
was performed as14
structure of a14
thermal proteome profiling14
the end of14
with wash buffer14
are known to14
detected in the14
study jr jr14
recruitment to the14
apolipoprotein b mrna14
responsible for the14
amino acids in14
nuclear magnetic resonance14
and incubated for14
the mixture was14
the reaction was14
nsclc cell lines14
the performance of14
mm tris ph14
understanding of the14
to interact with14
of epimastigote forms14
herm alis wc14
the er membrane14
in rpe cells14
we did not14
heavy and light14
comparison of the14
the exception of14
obtained from the14
quantitation of the14
national institutes of14
luo et al14
of the tau14
the rbd domain14
the mooring sequence14
to form a14
the most abundant14
for h in14
addition to the14
were prepared by14
oligomerisation of espb14
the cell surface14
fig ev a14
and subjected to14
cells were harvested14
suggesting that the14
n os to14
a sp le14
found that the14
of cell lines14
nem a sp14
it is possible14
and in vitro14
in the context14
in the rbd14
were transfected with14
to calculate the14
in table s14
the rbd and14
in the active14
cells were transfected14
of li ions14
ms ms analysis14
activity of jbu14
appears to be14
v w k14
wrote the manuscript14
s idoa s14
ho co cc14
to two molecules14
xg for min14
with or without14
this study are14
one or more14
were washed twice14
cells were washed14
rna polymerase ii14
studies of the14
institutes of health14
a final concentration14
of the kinetics14
pdi family enzymes14
were performed with14
representative of three14
atp atp atp14
figure legends figure14
insights into the14
tycho nem a14
at the a14
shown to be14
most of the14
retinal pigment epithelium14
os to c14
is supported by14
ec ho co14
indicate standard deviations13
function of the13
cell lines and13
have been deposited13
than that of13
the mathematical models13
to increase the13
considered to be13
the two cytokines13
final volume of13
cc al es13
in pbs and13
c c a13
the function of13
is s al13
of the time13
s and sars13
obtained from three13
performed as described13
be due to13
included in the13
in vitro and13
no sto c13
at the ccc13
with the same13
c motif at13
the course of13
in the experimental13
ra and gp13
location of the13
the final model13
an isobaric trigger13
the rate of13
multiple sequence alignment13
number slide number13
of the met13
the surface of13
co cc al13
s al in13
of wt and13
of the ulk13
conflicts of interest13
mol cell biol13
was performed on13
s a fig13
land et al13
of the main13
to measure the13
biological replicates with13
use of the13
l a i13
y stat p13
with different concentrations13
interaction with the13
the proportion of13
the impact of13
at a flow13
replicates with each13
were determined by13
e m icrocystis13
lep tolyngb ya13
in the crystal13
we note that13
in a le13
slide number slide13
of hbv integration13
induced by hypil13
met and met13
the stem helix13
the result of13
and the data13
results showed that13
and in the13
bars indicate standard13
the electron density13
and light chains13
a pair of13
extracted from the13
resolved by sds13
a le g13
al in a13
and supplementary table13
is possible that13
the interaction of13
function of time13
analysis of hsulf13
pixel size of13
e e e13
the activation of13
did not affect13
as in panel13
in escherichia coli13
protein data bank13
in the population13
general ccn score13
the same time13
residues in the13
in mammalian cells13
le p to12
ic values of12
general ccn scores12
these authors contributed12
located in the12
m l eg12
no competing interests12
the length of12
s and s12
we used a12
school of medicine12
adjacent to the12
been reported to12
ly ng b12
proteins in the12
as part of12
the mathematical model12
contributed equally to12
nonheme iron og12
the membrane from12
the dna duplex12
m fi pstat12
y s stat12
of biochemistry and12
cancer cell line12
glcnac s glca12
is responsible for12
h and h12
out of the12
cys and cys12
dependent cell adhesion12
on ice for12
human snm a12
be found in12
in the outer12
n or m12
the ability to12
interacts with the12
of in vitro12
sp l eg12
dwell time weightage12
to test this12
of the viral12
al iz ed12
deep learning model12
a decrease in12
repeated at least12
performed using the12
cartoon representation of12
p to ly12
attention intensive regions12
a final volume12
levels in the12
between ec and12
the l stalk12
of the ccc12
the rpe of12
ng b ya12
by western blotting12
membrane from individual12
normal low normal12
mrna editing sites12
were cultured in12
and table s12
fatty acid oxidation12
top of the12
the degradation of12
cov s and12
academy of sciences12
structural insights into12
amino acid sequence12
cya no b12
is likely to12
in presence of12
from individual guv12
length of the12
low normal low12
n engl j12
activation by il12
the anticodon loop12
are listed in12
cytochrome c oxidase12
or m al12
engl j med12
domain of the12
carried out using12
revealed that the12
consistent with a12
sequencing of the12
no b ium12
wallin et al12
of amino acid12
complex and mcherry12
statistical analysis was12
peg k aa12
classification general ccn12
c s r12
mismatches in mooring12
the treatment of12
base content of12
gated ion channels12
the size of12
performed as in12
ti o n12
the cancer type12
averages of vesicles12
wd wd wd12
to ly ng12
gsh gssg mal12
to this work12
was normalized to12
usa department of12
with the dna12
can be found12
the amino acid12
e s yn12
to determine whether12
and n y12
for the indicated12
were analysed by12
mm mes buffer12
molecular weight of12
a role for12
lc lipidation in12
de novo sequencing12
m al iz12
s stat p12
to c sp12
the decision threshold12
the yield of12
sp erm u12
its role in12
general classification general12
g c variant12
kinetics of stat12
the membrane recruitment12
individual guv tracing12
of the ace12
at least one12
based on a12
f f cre12
assays were performed12
random forest classifier11
in the singly11
c d e11
and refinement statistics11
in supplementary fig11
this suggests that11
the previously reported11
of escherichia coli11
the experimental group11
we examined the11
male and female11
the consumption of11
vs e k11
lic ho sp11
of stat phosphorylation11
j struct biol11
department of chemistry11
by size exclusion11
cancer genome atlas11
also known as11
and the ribosome11
editing frequency with11
korotkova et al11
are involved in11
resuspended in ml11
the experimental data11
al u e11
introduction into rnc11
of action of11
effects on the11
mode of action11
in terms of11
were washed with11
psc this study11
in regulatory motif11
of a novel11
are required to11
to each well11
the hsa nascent11
human bronchial epithelial11
finger like motif11
to be more11
panobinostat and dacinostat11
appendix fig s11
of regulatory sequence11
temperature for min11
nm ps ta11
or tax bp11
the imputation model11
log p v11
and analysed by11
by the addition11
figure s c11
one or two11
presence of mm11
retained in the11
region of the11
was measured by11
contrast to the11
declare no competing11
the host cell11
cell host microbe11
are required for11
v al u11
association of editing11
of trypanosoma cruzi11
new england biolabs11
the basis of11
motif in the11
with at least11
do lic ho11
of the cells11
p v al11
which can be11
flagellum basal body11
a ratio of11
concentration was determined11
to have a11
stat activation by11
it is also11
for each lipid11
of pdi erp11
the biosynthesis of11
linked to the11
was purchased from11
of pskai b11
te riu m11
all the experiments11
the position of11
the pqa score11
genes required for11
by simulated diabetes11
t g g11
of pdi and11
in a manner11
were grown at11
c sp l11
result is presented11
ob ac te11
suggest that the11
were separated by11
a sp l11
blanc et al11
data not shown11
which in turn11
zong et al11
those of the11
residues of the11
binds to the11
rna editing targets11
equally to this11
to the manufacturer11
fold change of11
were detected in11
were normalized to11
with a single11
ho sp erm11
b ium sp11
was applied to11
to the protein11
x g for11
we consider the11
properties of the11
which is a11
more than one11
to quantify the11
before and after11
mm phosphate buffer11
the afm images11
for binding to11
in the cell11
university of california11
decrease in the11
ac te riu11
there is a11
mm nacl and11
we performed a11
we compared the11
structural basis for11
in mm mes11
size of the11
applied to a11
of the data11
the fraction of11
log nm ps11
of the e11
the protein data11
j cell biol11
m l e11
by using the11
views of the11
g e m11
and resuspended in11
these results suggest11
the discovery of10
bond formation in10
sufb or prol10
hu and sun10
es c ya10
the changes in10
our results show10
we measured the10
a site and10
the contribution of10
protease inhibitor cocktail10
of protein synthesis10
removed from the10
to explore the10
was calculated by10
ai ve c10
was resuspended in10
aa family of10
representative confocal images10
a wide range10
t h t10
u m sp10
play a role10
terminal region of10
and h d10
for the evaluation10
highlighted in red10
wt and hsulf10
similar to that10
performed on a10
for all the10
the set of10
at a concentration10
p t oly10
there is no10
journal of molecular10
to maximal il10
similar to those10
loaded onto a10
fig ev b10
transferred to a10
each of these10
for up to10
calculated using the10
is u lf10
s t q10
e ligase activity10
at the active10
aggregation of the10
retrieved from the10
c el l10
b o n10
le s binding10
we observed that10
n ai ve10
and incubated at10
multiple reaction monitoring10
molecules of stat10
n ob ac10
at the end10
are present in10
ctd vprmus samhd10
of the target10
frameshifting during translocation10
determination of the10
of the sulfs10
the study of10
performed in triplicates10
contributed to the10
a concentration of10
stability of the10
sequences tcga pan10
the nd codon10
was calculated from10
expressed and purified10
on the results10
in the protein10
no do silin10
the lysate was10
be used as10
large number of10
and found that10
with the rbd10
and that the10
the dynamics of10
removal of the10
and tax bp10
acta crystallographica section10
the range of10
s ta t10
u lf id10
t oly ng10
from three biological10
g e s10
growth of h10
indicated in the10
were identified by10
was mixed with10
hepatitis b virus10
way anova followed10
free fatty acids10
ya n ob10
the g c10
insight into the10
the mode of10
x and x10
of the pdi10
d l a10
fatty acids in10
experiments were independently10
of the ecd10
university of oxford10
effect of the10
grown in lb10
map of the10
a t g10
for at least10
results indicate that10
were performed on10
bound to stat10
data were collected10
le p t10
e b o10
the present study10
of the molecular10
the national institutes10
o n d10
oly ng b10
we propose that10
e cyano bium10
s binding time10
as compared to10
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in mm sodium8
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to sulfur starvation8
acknowledgments we thank8
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amino acid sequences8
protein expression and8
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concentration of mm8
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expression profiles of7
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of cancer cell7
amino acid residues7
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cell pellets were7
incubated with the7
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identification of the7
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of lolb to7
calculated as the7
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than the decision7
overall secondary structure7
oxidative stress and7
is used to7
in the electron7
of interest and7
biophys res commun7
patient derived xenografts7
com acnash rdrugtrajectory7
defined as the7
presence of oxidized7
depends on the7
of human beta7
ca rnc in7
mass spectrometry analysis7
performed as previously7
the human body7
been shown that7
number of clusters7
on the binding7
table s and7
was then used7
type of interest7
proportion of the7
of the crl7
we also observed7
pi pi ps7
the light chain7
difference in the7
by mass spectrometry7
wt vs c7
of covid moonshot7
particle mesh ewald7
for each condition7
genetically engineered mouse7
known as the7
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ml of the7
in support of7
in the tandem7
mathematical models of7
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the membranes were7
oh o ch7
to monitor the7
integration of the7
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biorxiv preprint mailto7
formation as a7
activity of hpu7
cloned into the7
was detected in7
cells were lysed7
and function of7
our data suggest7
binding site of7
applied to the7
level of statistical7
the difference in7
cultures were grown7
in the control7
at the top7
nucleotides upstream and7
may not be7
the hbv integration7
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is a key7
of the vprmus7
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the mass spectrometer7
used to generate7
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the peptides were7
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journal of the7
was detected by7
the inner and7
pathway enrichment analysis7
fi c log7
cys native disulfide7
mathematical models and7
interaction between the7
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to address this7
washed extensively with7
incubation on ice7
was generated using7
ct io n7
mitochondria and melanosomes7
pansieri et al7
regulation of rna7
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upon the presence7
and used for7
operating at kv7
time min time7
of cell lysates7
we reasoned that7
dynamic multiple reaction7
suggested that the7
binding to ace7
course snapshots captured7
exposed outside the7
in the cancer7
percentage of the7
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consistent with our7
using a combination7
to the reference7
to the cell7
hydrogen bonds with7
experiments with each7
that could not7
e ab un7
identify genes that7
a table containing7
two amino acids7
correlation between the7
lu st er7
cells per well7
c ha ng7
of the sec7
at the level7
one representative experiment7
prepared as described7
polymix buffer at7
were eluted with7
differentially essential genes7
to the corresponding7
shown in red7
hydrogen bond with7
min time min7
the same date7
encoding cylc homologs7
led to the7
as a reference7
with the n7
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in mooring sequence7
linker between ec7
paired t test7
the enzyme activity7
were collected in7
e and s7
was done by7
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course snapshots shown7
pa tk ai7
filam ento us7
at the th7
inhibition of the7
tools for molecular7
importance of the7
quality of the7
anaerobic growth of7
be required to7
used to determine7
e m g7
kda kda met7
was collected and7
the plate was7
to the presence7
figure extended data7
to the final7
current status labels7
the s protein7
binding site in7
each data point7
differentially expressed genes7
the heavy chain7
stabilization of the7
data figure extended7
addition of an7
the cs ds7
buffer at mm7
compared with the7
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coronavirus spike glycoprotein7
ugeot ii l7
ps ps pa7
assay for urease7
c ya no7
the dissociation constant7
measurements were performed7
molecules that bind7
lipid species in7
of artemis is7
was done using7
we carried out7
shown in table7
pg pi pi7
contributes to the7
cysteine in the7
and fatty acid7
to the er7
met cysteine point7
disruption of the7
required for efficient7
shanghai jiao tong7
phagocytosis in arpe7
that they have7
even in the7
represent the level7
with that of7
during sulfur starvation7
the generation of7
were converted to7
data was normalized7
m fi c7
is mediated by7
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us cyano bacter7
this study pjr7
the specific activity7
were unable to7
of the variance7
em data collection7
no du la7
refinement statistics are7
photoreceptor outer segments7
this study k7
e cya no7
of the yeast7
ento us cyano7
genome atlas research7
the graphpad prism7
transmission electron microscopy7
member of the7
min are shown7
with ml of7
and standard deviations7
family of lpmo7
stat a p7
of the structure7
ss ss ib7
bond into rnc7
snapshots captured by7
in the tmd7
cell lines were7
of selective autophagy7
analysis revealed that7
statistical significance in7
from those of7
rnr r nr7
the culture medium7
for minutes at7
was the most7
fetal bovine serum7
km and vmax7
pooled and concentrated7
of the corresponding7
of these genes7
ge healthcare life7
associated with a7
the structural and7
en to us7
of lytic polysaccharide7
significance in this7
research and analysis7
am chem soc7
by grants from7
were transferred to7
cox cox cox7
and wipi d7
a consequence of7
by western blot7
the immune system7
rest of the7
of a new7
to a new7
on porous membranes7
crystallogr d biol7
of the cylc7
outside the ribosome7
association with editing7
idium sp lege7
s ics were7
pc pc pe7
in the ecd7
acts as a7
b ya s7
followed by the7
j am chem7
washed twice with7
are indicated in7
of sufb and7
interests the authors7
were determined in7
percentages of the7
rearrangements of the7
in vitro reconstitution7
a buffer containing7
of the binding7
mol cell proteomics7
was loaded onto7
bind to the7
ctd and vprmus7
compared to those7
and incubated in7
ps pa pa7
classification heatmap of7
which is known7
nucleotides downstream of7
the combination of7
effects of panobinostat7
exposed to the7
in the text7
biochem biophys res7
state sufb and7
of the stem7
la ri a7
ace and rbd7
the plasma membrane7
lol sorting signal7
the first three7
native mass spectrometry7
are found in7
with ddb dcaf7
to act as7
performed using a7
is available in7
these data indicate7
ypd and ypge7
more sustained stat7
and the main7
the nature of7
on the cell7
in the genome7
the b fab7
interaction of the7
the beginning of7
red and blue7
ms ms spectra7
the system was7
correspond to the7
s s s7
of espb from7
department of biotechnology7
and stained with7
phosphorylation of stat7
and purified from7
with ccn scores7
the risk of7
experiments were carried7
in at least7
the first step7
was observed for7
given in table7
in contact with7
ha ng e7
phosphorylated stat and7
the initial and7
bactron anaerobic workstation7
images are representative7
structural analyses of7
md simulations of7
likely due to7
da nc e7
majority of the7
expression of a7
as a new7
result of the7
mapped to the7
are represented by7
iv e ab7
due to a7
in regulatory sequence7
eluted with wash7
not have a7
of reducing agent7
in a final7
account for the7
ld c ha7
we developed a7
terminal half of7
mean and standard7
shown that the7
the isobaric trigger7
were expressed and7
and has been7
of the sample7
represents the mean7
l i s7
concentrations of the7
recruitment of the7
ubiquitination of met7
in vitro evolution7
by the two7
frameshifting efficiency of7
frame at the7
supplemented with mm7
nat cell biol7
and li ions7
in the enzyme7
from the cancer7
located at the7
hygb this study7
of the cancer7
site in the7
b pjydc i7
the first time7
in relation to7
wash buffer containing7
respect to the7
no conflicts of7
based on their7
method for the7
comparison to the7
colored by heteroatom7
related to the7
of jbu by7
this figure as7
the observation that7
captan and disulfiram7
un da nc7
incubated in pbs7
determined using the7
complex with the7
stably expressing wt7
all results representative7
in figure c7
stat phosphorylation kinetics7
mitochondrial copper levels7
analyses were performed7
the stationary phase7
ab un da7
taken at min7
the amyloid beta7
recorded in the7
that bind to7
recruitment of e7
and or the7
r nr rnr7
zhang et al7
lege m icrocystis7
was performed to7
prescription event on7
extensively with wash7
cells treated with7
the united states7
the recruitment of7
recorded for the7
cell aggregation assay7
fc lo g7
arbab et al7
of all three7
the indicated times7
in panel a7
could be due7
lod and loq7
snapshots shown in7
of the aflpmo7
key laboratory of7
vitro and in7
of the host7
c lu st7
it is a7
cold spring harb7
stat phosphorylation by7
electronic health record7
have been reported7
be explained by7
limited number of7
results representative of7
in the c7
results shown in7
the open x7
because of the7
in the formation7
cy and cy7
of the mooring7
of photoreceptor outer7
presence of an7
with chondroitinase abc7
amino acids and7
we focused on7
absence of ef7
the results are7
of the blot7