1 We report here that 20 weeks of RET also restores muscle
2 We report here that a common genetic variation of the no
3 We report here that a mild pro-oxidant intracellular mil
4 We report here that a nucleotide excision repair (NER)-a
5 We report here that a plasma protease cascade, the facto
6 We report here that a population of human beta2-adrenerg
7 We report here that a pro-brain-derived neurotrophic fac
8 We report here that a single acute infusion of insulin i
9 We report here that a single additional trans-Hoogsteen
10 We report here that a specific arrangement of Yippee dom
11 IMPORTANCE
We report here that a stable full-length enterovirus 71
12 We report here that a tetra-substituted naphthalene-diim
13 We report here that a type I strain of Toxoplasma inhibi
14 We report here that Abeta3pE-42 has an enhanced capacity
15 We report here that ablation of mTOR complex 1 (mTORC1)
16 We report here that ablation of Nf1 in bone-forming cell
17 We report here that actinomycin D and RG7787 act synergi
18 We report here that activation of cell death by avirulen
19 We report here that activation of ILC2s by IL-33 is suff
20 idered the key DNA-binding domain of PARP-2,
we report here that all three domains of PARP-2 collecti
21 mass spectrometry based proteomics approach,
we report here that all three neurotoxins, BoNT/A2, /F4,
22 Using a human-Her2 self-antigen mouse model,
we report here that alpha-4-1BB significantly enhanced C
23 We report here that alphaE-catenin inhibits beta4 integr
24 We report here that although the cytokines interferon-al
25 We report here that amino acid substitutions in a thromb
26 We report here that an adapter protein, ArgBP2, is a com
27 We report here that an Arabidopsis oligopeptide transpor
28 We report here that antigen-specific proliferative respo
29 We report here that,
as in the patients, Zc3h14 is not e
30 We report here that AT-101, a derivative of gossypol in
31 We report here that auditory hair cells contain two mole
32 We report here that AURKA expression is driven by beta-c
33 We report here that autophagy was dynamically regulated
34 We report here that BACE1 regulates neuronal excitabilit
35 We report here that begomovirus and curtovirus AL2/C2 pr
36 We report here that besides PTC events, translation kine
37 We report here that beta-lapachone is a potent, reversib
38 We report here that between 16 and 30 h after puparium f
39 We report here that Blm10 is required for the maintenanc
40 We report here that BMI1 has a role in G2/M checkpoint a
41 We report here that both LANA1 and EBNA1 undergo highly
42 We report here that both RIG-I and MDA5 efficiently disp
43 We report here that both VEGF receptor 2 (VEGFR2)-positi
44 We report here that Brg1 controls a transcriptional prog
45 We report here that bromodomain-containing protein 7 (BR
46 We report here that BTA-EG4 decreases Abeta levels, alte
47 We report here that budding yeast Rif1 (Rap1-interacting
48 We report here that C6 ceramide increases serum-stimulat
49 We report here that capsaicin nasal spray is effective i
50 We report here that CARMIL2 (capping protein, Arp2/3, my
51 We report here that CAS expression itself is up-regulate
52 We report here that CD44 (ADAM10 substrate), a receptor
53 We report here that CD74 and MIF are markedly increased
54 We report here that CD8(+) T-cell frequency and function
55 We report here that Cdc45 from budding yeast binds tight
56 he ATP-dependent RNA helicase UPF1 in vitro,
we report here that cellular TumiD requires UPF1.
57 We report here that CNIs compromise the overall Treg imm
58 We report here that condensin, a conserved protein compl
59 We report here that constitutive expression of soybean o
60 We report here that COPII-coated transport carriers trav
61 We report here that corticostriatal cocultures prepared
62 We report here that current techniques for small RNA det
63 Using fission yeast as a model,
we report here that DBAN delays G1-S transition.
64 We report here that decreasing O-GlcNAcylation enhances
65 We report here that deficiency in bax exerted broad neur
66 We report here that deficiency in IRF8 results in dimini
67 We report here that deletion of the p63 C-terminus in mi
68 We report here that depending on the type of the spine,
69 We report here that dFBr inhibits human muscle (alphabet
70 We report here that differential ERK signaling controls
71 We report here that distinct regulatory miRNA networks o
72 We report here that DLG5 functions as an evolutionarily
73 We report here that efficient stacking occurs in the abs
74 Consistent with previous work on RSV Gag,
we report here that electrostatic interactions provide t
75 We report here that elevated FAM83B expression increases
76 man HSCs and human progenitor cells (HSPCs),
we report here that elevated levels of CCND1-CDK4 comple
77 hrough characterization of the emb14 mutant,
we report here that Emb14 gene encodes a circular permut
78 We report here that Emicro-directed expression of the an
79 We report here that erythro-myeloid progenitors in mice
80 We report here that ESX-1-dependent cell membrane lysis
81 We report here that eukaryotic elongation factor-2 kinas
82 We report here that expression of alphaB-crystallin was
83 We report here that expression of BRAF(V600E) in human n
84 We report here that expression of human cadherin-related
85 We report here that expression of huntingtin (Htt) exon
86 We report here that expression of KLF12, a member of the
87 We report here that FlnB and Fmn1 physically interact, a
88 We report here that floral temperature often differs bet
89 We report here that foragers of different native Asian h
90 We report here that fungal and human septins are able to
91 We report here that Gap1 is also down-regulated when cel
92 We report here that glial App plays a role in physiology
93 g experimental mouse models of Parkinsonism,
we report here that global p11 knockout (KO) mice develo
94 We report here that glycosylation at Asn-297 is critical
95 We report here that GRK5 nuclear accumulation is depende
96 We report here that growth signals reciprocally regulate
97 We report here that haploinsufficiency of murine Adamts9
98 We report here that HBc expressed in a mammalian cell ly
99 We report here that HFs mobilize ectopic progenitors fro
100 We report here that highly invasive prostate cancer cell
101 We report here that Hippo pathway components in Drosophi
102 We report here that HIV Vpu failed to degrade IRF3 in in
103 We report here that HIV-1 infection in human monocytes e
104 We report here that host range restriction peptidase (hr
105 We report here that human CFTR is also phosphorylated by
106 We report here that human pluripotent stem cell (hPSC)-d
107 We report here that (
i) the degradation of ICP0 is not i
108 We report here that (
i) the ESR1 promoter region contain
109 We report here that IDH1(R132H) exhibits a growth-inhibi
110 We report here that IFN-gamma stimulation induces a tran
111 We report here that IL-1alpha and -beta were degraded in
112 We report here, that immunodominance of known sequences
113 We report here that in a spermidine-deficient B. subtili
114 By contrast,
we report here that in a well-established transplantable
115 We report here that in addition to the production of the
116 We report here that in an immortalized mouse hepatocyte
117 We report here that in rat and human neuroprogenitor cel
118 We report here that in rats approximately 50% of granule
119 We report here that in rats at 24 h withdrawal from syst
120 We report here that in Sprague Dawley rat, the MOP recep
121 We report here that in the absence of LKB1 in beta cells
122 We report here that in utero TBC1D24 knockdown in the ra
123 on force-clamp optical tweezers experiments
we report here that,
in a paradoxical violation of mecha
124 We report here that,
in the guinea pig model, a human is
125 We report here that insulin can amplify action potential
126 We report here that intranasal vaccination with these pe
127 We report here that IOS1 is also required for full susce
128 sp70 is stress-inducible, but paradoxically,
we report here that JB12 was degraded by the proteasome
129 We report here that JQ1, a small molecule inhibitor of b
130 We report here that JQ1-induced BET inhibition modulated
131 We report here that K17 interacts with the RNA-binding p
132 We report here that Kaposi's sarcoma-associated herpesvi
133 We report here that knock-out of CK2 in striatonigral ne
134 We report here that knock-out of the C. elegans nicalin
135 Using a rat model of radiation dermatitis,
we report here that Krt17 expression initially is down-r
136 We report here that KSHV vIRF4 targets the beta-catenin/
137 We report here that LAM lesions and angiomyolipomas over
138 We report here that let-7 family members are expressed i
139 Using an optogenetic approach,
we report here that LFS of two interneuron subtypes and,
140 We report here that,
like alpha- and betaherpesviruses,
141 We report here that liver BVRA protects against hepatic
142 We report here that Lmf1 expression is induced by ER str
143 We report here that loss of SOD2 correlates with the ove
144 We report here that LVs carrying shorter CTs expressed h
145 We report here that MCL-1 downregulation is associated w
146 We report here that members of the prototype galectin fa
147 We report here that mice lacking AC6 (AC6(-/-)) have inc
148 We report here that mice with embryonic neural stem-cell
149 We report here that mimicking this development switch in
150 We report here that miR-874 down-regulates the major G1/
151 We report here that missense mutations in the epigenetic
152 We report here that mitochondria are functionally segreg
153 We report here that mixing ZnCl2 with TPPO precipitates
154 er under endogenous corticosterone exposure,
we report here that monomeric GR interaction with a half
155 We report here that movement of helical residues 120-122
156 We report here that MPK4 is found in complexes in vivo w
157 We report here that MRE11 is also phosphorylated by ATM
158 We report here that MSO neurons in gerbil also have reso
159 We report here that mTOR complex 1 (mTORC1) in TECs play
160 We report here that mTOR kinase complexes 1 and 2 (mTORC
161 We report here that mTORC1 activation is accompanied by
162 We report here that mTORC1 and mTORC2 are activated in r
163 We report here that multiple reaction monitoring assay u
164 We report here that multiple system atrophy (MSA) is cau
165 We report here that murine embryonic fibroblast cells fr
166 V variation as a proxy for mutational input,
we report here that mutational spectra differ substantia
167 We report here that nascent HSCs are resistant to the JA
168 We report here that Ndj1, a previously known meiosis-spe
169 We report here that neurofibromin, a Ras-GAP encoded by
170 We report here that Nf2-deficient cells display elevated
171 dipeptide component in the cytosol by NOD2,
we report here that NLRP3 inflammasome activation is cau
172 ng a novel antibody to detect active NOTCH3,
we report here that NOTCH3 signals constitutively in a p
173 We report here that novel Tyrosine kinase 2 (Tyk2) gene
174 We report here that of two translesion synthesis polymer
175 We report here that OGT glycosylates aspartate much fast
176 We report here that one manner in which environmental fa
177 We report here that open reading frame (ORF) R17 encodes
178 We report here that PDE3 and PDE4 expression levels are
179 Using a mouse model system,
we report here that perinatal and juvenile neuronal abla
180 We report here that periodic diaphragm contraction via p
181 We report here that pharmacological inhibition or geneti
182 We report here that photoinitiated electron flow involvi
183 We report here that planar cell polarity (PCP) proteins
184 We report here that podocyte-specific deletion of Vangl2
185 We report here that point deletions and insertions withi
186 We report here that PqqE activity is dependent on the ac
187 We report here that primary rat embryo fibroblasts (REF5
188 We report here that pro-brain-derived neurotrophic facto
189 We report here that products of both genes are found at
190 We report here that PRRSV infection of MARC-145 cells an
191 We report here that pyruvate reacts readily in the prese
192 We report here that quiescence exit kinetics are differe
193 We report here that quiescence induced by heat stress re
194 We report here that Rad23 is extensively phosphorylated
195 We report here that ratiometric calcium imaging reveals
196 cross-linked by engineered disulfide bonds,
we report here that residues 59 to 79 cannot, suggesting
197 We report here that retinas devoid of MG rip apart, a de
198 We report here that Rga6 is another fission yeast Cdc42
199 We report here that rice retinoblastoma-related protein-
200 We report here that RLIP76 was required for expression a
201 iction of Nesprin1 in the context of the NE,
we report here that rootletin recruits Nesprin1alpha at
202 We report here that RyR2 undergoes post-translational mo
203 We report here that S. aureus-infected mice generate VH3
204 We report here that Salmonella strains with mutations of
205 Broadening this narrow vision,
we report here that SaPIs ensure their promiscuous trans
206 By a genetic strategy,
we report here that selective deletion of gp96 from CD11
207 We report here that sequence-specific binding of the con
208 We report here that serum components, as discovered duri
209 However,
we report here that serum lactate levels in LT-treated m
210 We report here that several factors affected glycolytic
211 We report here that silencing of the deubiquitinase cyli
212 We report here that single intranasal immunization with
213 We report here that Six2 is required to maintain express
214 ine nucleotide exchange factor for RhoA, but
we report here that SmgGDS does not mediate GDP/GTP exch
215 model of human intestinal cryptosporidiosis,
we report here that some of these C. parvum RNA transcri
216 We report here that Sonic Hedgehog (Shh)-Smoothened sign
217 We report here that specific downregulation of miRNA-107
218 mbination of ex vivo and in vivo approaches,
we report here that stage-specific reciprocal dorso-vent
219 In contrast,
we report here that STING potently suppresses inflammati
220 We report here that sulforaphane treatment fails to acti
221 We report here that SYTA localized to ER-PM contact site
222 We report here that T-cell-specific deletion of mTOR res
223 We report here that T1L, but not T3D, mu2 localizes to n
224 We report here that TAF1 phosphorylates p53 at Thr55, le
225 We report here that targeted chemogenetic activation of
226 We report here that targeted deletion of both the Hdac1
227 We report here that targeting a completely different pro
228 We report here that Tat uses unexpected regulatory mecha
229 We report here that TbetaRI interacts with the SH3 domai
230 We report here that TCDD-induced TiPARP also targets PEP
231 We report here that TDP-43 is a substrate of MEK, a cent
232 We report here that TGF-beta directly regulates alternat
233 We report here that TH cell somata, tapering and varicos
234 We report here that THADA knockout flies are obese, hype
235 We report here that the activities of two Dnmt2 homologs
236 We report here that the Arg kinase domain interacts dire
237 We report here that the B cell response to IAV is altere
238 We report here that the CDC listeriolysin O (LLO), secre
239 We report here that the degree of drug conjugation per p
240 We report here that the distribution of release time is
241 We report here that the DNA polymerase III holoenzyme in
242 We report here that the EBV type 2 (EBV-2) strain displa
243 We report here that the echolocating bat controls the fe
244 We report here that the ELF domain of FANCL is required
245 We report here that the endocytic adaptor protein Numb l
246 We report here that the engineered oncolytic vaccinia vi
247 We report here that the eriophyid mite-transmitted Wheat
248 We report here that the evolved VLV vector engineered to
249 We report here that the first three amino acids of this
250 We report here that the Gbg dimer directly partners with
251 We report here that the H. pylori CheZ, CheZ(HP), locali
252 We report here that the highly pathogenic HIV R3A effici
253 for assessing disease progression.IMPORTANCE
We report here that the HIV/SIV-associated B cell dysfun
254 We report here that the ID injection of DNA vectors usin
255 We report here that the initiation of bud growth after s
256 We report here that the intestine-specific homeobox prot
257 We report here that the kAE1 cytoplasmic N terminus actu
258 We report here that the levels of miR1 and miR133a decre
259 We report here that the lincRNA gene lincRNA-Tnfaip3, lo
260 We report here that the mTORC2 obligate cofactor Rictor
261 We report here that the N-terminal leader of two insect
262 We report here that the Nedd4 family HECT E3, WWP1, asse
263 We report here that the newly sighted children, ranging
264 We report here that the PERK/eIF2alpha/ATF4 signaling br
265 We report here that the protein RibR counteracts the FMN
266 We report here that the Ptrh2 knockout mouse model recap
267 We report here that the redox molecule NADH binds the 26
268 We report here that the redundant casein kinases Yck1p a
269 We report here that the regions surrounding the first th
270 Finally,
we report here that the restriction of target cell avail
271 More importantly,
we report here that the Ru(IV) horizontal lineO(2+) form
272 We report here that the SOMATIC EMBRYOGENESIS RECEPTOR K
273 We report here that the somatic mating type locus contai
274 We report here that the species identity of fly eggs can
275 We report here that the Wilms tumor protein, WT1, which
276 Indeed,
we report here that there are strong species differences
277 We report here that these 14-3-3 FKO mice display other
278 We report here that these formaldehyde formulations can
279 We report here that these molecules are widespread throu
280 that antagonize the OAS-RNase L pathway, and
we report here that these proteins are furthermore conse
281 rescence spectroscopy and X-Ray diffraction,
we report here that this disparity is instead due to dif
282 We report here that this property emerges during early d
283 We report here that through the design of the chromophor
284 We report here that TIPE3 (TNFAIP8L3) is the transfer pr
285 We report here that TLR10 suppressed the production of a
286 We report here that tobacco-specific nitrosamines (TSNAs
287 We report here that TOE1 can function as an inhibitor of
288 We report here that transcription repressor Growth facto
289 We report here that translation of nanos1 after fertiliz
290 rmatophagoides farinae-induced asthma model,
we report here that TRPV4-knockout mice were protected f
291 We report here that two aspects of cAMP-induced differen
292 We report here that UL37 of herpes simplex virus 1 (HSV-
293 We report here that upon cross-species transmission and
294 We report here that USP8/UBPY, a deubiquitinating enzyme
295 In contrast,
we report here that Vibrio cholerae lacking DacA-1, a PB
296 We report here that when amphetamine enters dopamine neu
297 We report here that wild-type alpha-syn from cell lines,
298 We report here that within the adult endocrine pancreas,
299 We report here that Wnt/beta-catenin signaling increases
300 We report here that Zfx facilitates the development of e