1 oadly conserved portions of the regions that
we interrogated.
2 Here
we interrogate 0.9 million genetic variants in 939 CFM c
3 Here,
we interrogated 119 human blood samples for transcripts
4 We interrogated 120 regions flanked by segmental duplica
5 Here
we interrogated 156 single-nucleotide polymorphisms (SNP
6 f effect, and total genetic burden of MEIS1,
we interrogated 188 case subjects and 182 control subjec
7 We interrogated 2000 unverified protein-coding genes usi
8 We interrogated 385 pancreatic cancer genomes to define
9 We interrogated 54 to 70 genes in 442 patients with CUP
10 vitamin D deficiency might worsen outcomes,
we interrogated 703 primary melanoma transcriptomes to u
11 eny and establish trait-allele associations,
we interrogated 75 M. bovis and 61 M. tuberculosis genom
12 In this study
we interrogate 752 NDMM patients using whole genome sequ
13 23 unique pairs of genetic alterations that
we interrogated,
9 were able to induce HCC.
14 We interrogate a (88)Sr(+) ion with our stimulated Brill
15 Here
we interrogate a complex-mediated change in the substrat
16 Here
we interrogate a unique class of excitatory neurons in t
17 Here,
we interrogated a comprehensive RNA-sequencing database
18 Therefore,
we interrogated a customized small interfering RNA (siRN
19 We interrogated a library of FDA-approved drugs for thei
20 h-throughput high-content screening (HTHCS),
we interrogated a number of oncogenic mechanisms of TFE3
21 As an example,
we interrogated a protein microarray formed by a commerc
22 Here,
we interrogated a rich data set of neuroectodermal enhan
23 Building on this foundation,
we interrogated a small-molecule library for compounds t
24 Using a 2,304-element microarray,
we interrogated a total of 250 sera from Michigan lung c
25 early stages of the pathway to cyclopamine,
we interrogated a V. californicum RNA-seq dataset using
26 functional identity of this venom component,
we interrogated a venom gland EST database for the saw-s
27 We interrogated A-domain 2-keto and 2-hydroxy acid activ
28 To this end,
we interrogated Abeta polymorphism with amyloid conforma
29 -promoting effects of GPNMB in this context,
we interrogated activated pathways in tumors derived fro
30 To address this,
we interrogated activated signaling pathways in a compar
31 In addition,
we interrogated an 840-member novel oxime library for re
32 In this study,
we interrogated an aberrant miR-based regulatory network
33 We interrogated an M. avium subsp. paratuberculosis Delt
34 First,
we interrogate and justify the relevance of bead endocyt
35 Here,
we interrogate and quantitatively model how proliferatio
36 ion is seen after acute kidney injury (AKI),
we interrogated another bone fide AKI marker, Kim1 and n
37 To address this issue
we interrogated AR signaling in AD and recurrent prostat
38 We interrogated at massive scale the structural properti
39 We interrogated at single-cell resolution how these alte
40 Here,
we interrogate axial patterning mechanisms in the human
41 We interrogated baseline single photon emission computed
42 To characterize this evolutionary process,
we interrogated,
by whole genome sequencing, 25 samples
43 Here,
we interrogate CD22BBz CAR signaling in response to low
44 histocompatibility complex class I tetramer,
we interrogated CD8(+) T cell responses during CHIKV inf
45 Using a novel strategy,
we interrogated CLL membrane-specific autologous immunog
46 In this study,
we interrogated clonal relationships between CD4(+) T ce
47 Finally,
we interrogated CNVs in the Clinical Genome Resource, fi
48 We interrogated common SNPs (minor allele frequency >5%)
49 Here, using single-cell technology,
we interrogate complex patterning defects and define a H
50 ern the regenerative capacity of hair cells,
we interrogated custom human cDNA microarrays with senso
51 Here,
we interrogate cytosine methylation patterns in sperm ob
52 Finally,
we interrogated differences in cardiac gene expression r
53 Here,
we interrogated differential molecular mechanisms depend
54 We interrogated DNA methylation at baseline and 3 hours
55 order to gain insight into these questions,
we interrogate dynamic size-growth behavior of single ce
56 We interrogated E(2)-induced apoptosis by analysis of ge
57 gut-restricted for oral administration, and
we interrogated efficacy and mechanism using in vitro an
58 te with anxiety induction in human subjects,
we interrogated emotion-state-dependent olfactory proces
59 We interrogated FCMR contributions to B cell function by
60 Using mathematical modeling
we interrogated four alternative explanatory models for
61 Here
we interrogate functional interaction between BRCA1 and
62 Here
we interrogated functions of hepatic stellate cells (HSC
63 n tissue is not available from most samples,
we interrogated gene expression in lymphoblasts from 244
64 , to discover novel therapeutic GSC targets,
we interrogated gene expression profiles from GSCs, diff
65 We interrogated genes of interest in an interval on mous
66 We interrogated genome-wide association, exome sequencin
67 In this paper
we interrogate glycolytic and mitochondrial functional c
68 and may undergo mesenchymal differentiation,
we interrogated GSC potential to generate vascular peric
69 We interrogated &
gt;1.5 million genetic variants in EoE cas
70 Here,
we interrogated &
gt;50 RAD51C missense variants, finding th
71 Here,
we interrogate how cancer cells harboring distinct alter
72 Here,
we interrogate how IR deletion in ICs impacts antibacter
73 Here
we interrogate how one MYC co-factor, host cell factor (
74 framework with classical nucleation theory,
we interrogate how solution conditions influence the mul
75 Moreover,
we interrogate how their distribution-and abundance rela
76 imaging and transcriptional profiling tools,
we interrogated how distinct microenvironments in the gu
77 Here,
we interrogate human IFP-derived MSC (IFP-MSC) reaction
78 To investigate this model,
we interrogate human platelets using approaches that inc
79 We interrogated human tumor tissue for immunofluorescenc
80 We interrogated innate pathways governing APP stability
81 accepted clinical tool CAPRA-S in the cases
we interrogated irrespective of Gleason grade, prostate-
82 de insights on the biological role of CEB25,
we interrogated its structural features.
83 Here,
we interrogated known EGFR-MAPK signaling intermediates
84 We interrogated known microarray data sets to define NAM
85 We interrogated large databases and found that sonic hed
86 and lipidomic-wide systems genetic approach,
we interrogated lipid regulatory networks in 107 genetic
87 Here
we interrogated locus- and family-specific methylation p
88 Here
we interrogate LOH of polymorphisms in essential genes a
89 Next,
we interrogated mechanisms of insulin-associated hepatoc
90 Here,
we interrogated mechanisms of Trm cell function in prima
91 between oncogenic PIK3CA and OGDH function,
we interrogated metabolic requirements and found an incr
92 We interrogated more than 2 million single nucleotide po
93 We interrogated more than 9000 transcripts at 6 time poi
94 We interrogated mutants impaired in the Fe homeostasis r
95 Finally,
we interrogate nanodiamonds as small as 40 nm in diamete
96 ted NanoString molecular barcoding approach,
we interrogate neuroinflammatory dysregulation and heter
97 From an initial 630 ILBC primary tumors,
we interrogated oncogenic substitutions and insertions a
98 We interrogated our mandatory administrative database fo
99 We interrogated our model by investigating changes in th
100 In addition,
we interrogated our screening results to find novel host
101 tudy of two closely related macaque species,
we interrogated potential causal factors for their diffe
102 Here
we interrogated preNMDAR functions pharmacologically to
103 We interrogated publically available 18S rRNA gene datas
104 We interrogated purified sorted tumor fractions from the
105 otinib, dasatinib, ponatinib, and DCC-2036),
we interrogated response of CML cell lines and primary C
106 We interrogated RNA-Seq data from 3,775 malignant neopla
107 ather than complete loss of SBDS expression,
we interrogated SDS patient cells for defects in ribosom
108 he role of the Wnt family of genes in NSCLP,
we interrogated seven Wnt genes (Wnt3, Wnt3A, Wnt5A, Wnt
109 Here
we interrogated signal transducer and activator of trans
110 Specifically,
we interrogated site-specific binding by the transcripti
111 Here
we interrogate sites of MRN-dependent processing by iden
112 Here,
we interrogated small RNA data from the aphid, Myzus per
113 For fine mapping
we interrogated SNPs within +/- 250 kb flanking regions
114 immunoprecipitation (eCLIP) of desired RBPs,
we interrogate specific RNA-protein complexes, such as h
115 We interrogate submitted items with energetic neutrons,
116 Here,
we interrogated superenhancer landscapes of primary glio
117 Here,
we interrogate survivorship hypotheses using data from a
118 Here
we interrogate synaptic connections between afferent pat
119 Experimentally,
we interrogate system dynamics under three groups of per
120 We interrogated tagraxofusp resistance in patients and e
121 le signaling nodes at the single-cell level,
we interrogate TCR signaling dynamics in control C57BL/6
122 he common mechanism of hepatocarcinogenesis,
we interrogated temporal gene expression profiles in a g
123 Here
we interrogate the Adolescent Brain Cognitive Developmen
124 Here
we interrogate the alternative splicing landscape of ped
125 Here
we interrogate the appropriateness of a range of previou
126 Here,
we interrogate the behavioral functions of VP(GABA) neur
127 Here,
we interrogate the biochemical activity and nucleic acid
128 Here,
we interrogate the biochemical mechanism of procaspase-3
129 Here
we interrogate the cellular responses to target cell inf
130 Here,
we interrogate the complete ORN population of the Drosop
131 In this study,
we interrogate the complexity in cAMP/PKA-MAPK/ERK1&2 cr
132 In this study,
we interrogate the compositional systematics of ~ 3500 C
133 Here
we interrogate the consequences of chronic necroptosis o
134 ergent anatomical and functional approaches,
we interrogate the contribution to fear of basal amygdal
135 gh sensitivity (picomolar detection limits),
we interrogate the detection mechanism via complementary
136 Here,
we interrogate the DNA methylation state of the genomic
137 Here,
we interrogate the effects of targeting EphB4 and ephrin
138 igenetic, proteomic and functional analyses,
we interrogate the ensuing chromatin and transcriptional
139 Here
we interrogate the epigenetic landscape of enhancer elem
140 In order to address this,
we interrogate the evolutionary history of the entire SA
141 scriptional program from regulation by SOX2,
we interrogate the expression of newly-identified trache
142 Here,
we interrogate the function of RBPs in cancer using pool
143 Here,
we interrogate the genome of Aspergillus fresenii to rev
144 Here
we interrogate the genomes of 7,651 diverse human cancer
145 Here,
we interrogate the gut microbiome of mother-child dyads
146 he glycosylated and nonglycosylated species,
we interrogate the hormone biosynthesis.
147 Here,
we interrogate the impact of a BRCA1 mutation-associated
148 Here,
we interrogate the impact of dietary iron deficiency (ID
149 Here,
we interrogate the impact of siRNA knockdown of ARID1a c
150 Here,
we interrogate the importance of CenDNA in centromere sp
151 Here,
we interrogate the interplay between folded and disorder
152 In the current study,
we interrogate the intersection of TLR4 signaling, epith
153 Here,
we interrogate the local structure of the M(III) surface
154 Here,
we interrogate the mechanism by which the white-opaque s
155 Here,
we interrogate the MNK-eIF4E axis in diffuse large B-cel
156 Here
we interrogate the molecular consequences of CRISPR/Cas9
157 Here,
we interrogate the molecular programs of isotype-specifi
158 Here
we interrogate the nanoscale assembly of lignocellulosic
159 Here,
we interrogate the NC-GRN in the lamprey, taking advanta
160 f samples analysed so far, to our knowledge,
we interrogate the noncoding transcriptome, alternative
161 We interrogate the psychological and neural basis of thi
162 Herein,
we interrogate the reactivity of thiooxime esters and id
163 Here,
we interrogate the relationship between population-based
164 By using the SCBC,
we interrogate the response of human-derived glioblastom
165 Here,
we interrogate the retrotransposition efficiency and epi
166 Here,
we interrogate the role of galectin-3, a GBP that contro
167 teraction calls with nascent gene expression
we interrogate the role of promoter hubs and super-enhan
168 Here,
we interrogate the role of the caspase recruitment domai
169 Here,
we interrogate the role of tRNA anticodon modifications
170 We interrogate the soil MCP concept by investigating the
171 Here,
we interrogate the striking correlation of FOA with retr
172 Here
we interrogate the structurally dense (1.64 mcbits/ angs
173 Here
we interrogate the structure and biophysical properties
174 Here,
we interrogate the structure of the prototype pinholin b
175 Here,
we interrogate the transcriptional features and cellular
176 Here
we interrogate the transcriptome of 113 single CTCs from
177 Here,
we interrogate the tumor microenvironment at single-cell
178 ional susceptibility loci for breast cancer,
we interrogated the 2q35 gene desert for chromatin archi
179 Using NicE-viewSeq,
we interrogated the accessibility of chromatin in a cell
180 Here,
we interrogated the activities and structures of two DUF
181 First,
we interrogated the activity of SAOUHSC_02373 against a
182 We interrogated the activity of the PSMA-PI3K axis throu
183 Furthermore,
we interrogated the AluJb-LIN28B candidate: the genetic
184 In the work reported herein,
we interrogated the amyloidogenesis mechanism of human b
185 Using a systems biology approach,
we interrogated the AR-regulated proteome and identified
186 We interrogated the architecture of the complete Dengue
187 To explore the pathogenesis,
we interrogated the beta-cell transcriptomes from donors
188 on and critical for rational vaccine design,
we interrogated the biochemical properties of 9,888 MHC
189 Therefore,
we interrogated the biological effects of class I HDAC i
190 We interrogated the bronchoalveolar lavage and blood vir
191 We interrogated the CARDIoGRAMplusC4D (Coronary ARtery D
192 Here,
we interrogated the cerebral and peripheral pathology of
193 In this study
we interrogated the chemistry of the PCSK9 active site a
194 In the present study,
we interrogated the clonal architecture by mutation-spec
195 Using UK10K exome sequencing data,
we interrogated the coding regions of KAR and NETO genes
196 ns in PanIN 3 lesions and pancreatic tumors,
we interrogated the comparative ability of adult pancrea
197 We interrogated the complexity of serum using multiple c
198 Here,
we interrogated the contribution of common polygenic var
199 Here,
we interrogated the contribution of the SWI/SNF subunit
200 We interrogated the contribution of these two processes
201 n PLX-4032-induced responses and resistance,
we interrogated the contributions of anti-apoptotic BCL-
202 on between these 2 cancer driving processes,
we interrogated the cytidine deaminase family of protein
203 Using molecular dynamics simulations,
we interrogated the DNA-binding domain of murine ETS1 al
204 We interrogated the dual functions of beta-catenin in re
205 In this study,
we interrogated the effect of decreased Ag amount/durati
206 Here,
we interrogated the effect of HSV-1 infection on EV biog
207 We interrogated the effect of reduced endogenous estroge
208 rophysiological, and behavioral experiments,
we interrogated the effects of short interfering RNA-med
209 Using FRET reporters,
we interrogated the effects of soluble beta-glucan on in
210 We interrogated the electronic health record (EHR) infor
211 Accordingly,
we interrogated the enzymatic, biophysical, and function
212 Here,
we interrogated the epigenetic and transcriptional respo
213 We interrogated the evolution of the phosphotriesterase
214 n reported in the chicken embryo as a whole,
we interrogated the existence or absence of genomic impr
215 We interrogated the expression and regulation of 226 tra
216 Here,
we interrogated the expression of all ETS family members
217 ding may influence cellular protein folding,
we interrogated the folding landscape of a model beta-ri
218 In a second set of experiments,
we interrogated the function of each level of the hypoth
219 Here,
we interrogated the function of the basolateral amygdala
220 hospholipid bilayer on GPCR activation, here
we interrogated the functional, pharmacological, and bio
221 for the heme-dependent regulation of hrg-1,
we interrogated the hrg-1 promoter.
222 Here,
we interrogated the importance of IDE-mediated catabolis
223 Here,
we interrogated the in vivo kinetics of lymphocytes in C
224 Here,
we interrogated the in vivo relevance of this cell popul
225 In this work,
we interrogated the intrinsic ability of Ras to self-ass
226 Here,
we interrogated the major signaling pathways deregulated
227 In the current investigation,
we interrogated the mechanisms underlying sialylation-de
228 Then
we interrogated the microarrays with cholera toxin, anti
229 We interrogated the molecular signature and electrophysi
230 using a complementary, multi-omics approach,
we interrogated the monoterpene indole alkaloid (MIA) bi
231 Here,
we interrogated the parts of the PI(4,5)P(2) head group
232 Here
we interrogated the pathways involved.
233 We interrogated the pattern of expression of esophagus-s
234 arallel, by comparing with parental genomes,
we interrogated the phasing of these deletions with the
235 c Ag-specific TCR-transgenic CD8(+) T cells,
we interrogated the phenotype, functionality, and recall
236 ependent increase in sub-RPE deposit height,
we interrogated the potential of CFH as a previously uni
237 Here
we interrogated the proteome during stepwise differentia
238 Further,
we interrogated the proteome of three different wild-typ
239 Here,
we interrogated the regulation of RE1-silencing transcri
240 We interrogated the role of a neuronal cell adhesion mol
241 Here,
we interrogated the role of adenosine-to-inosine (A-to-I
242 Here,
we interrogated the role of AEG-1 in NTIS in the context
243 In the current study,
we interrogated the role of aSMA(+) CAFs in a genetic mo
244 nate receptor for CD154 during alloimmunity,
we interrogated the role of CD154:CD11b interactions in
245 In this article,
we interrogated the role of GRP78 in the tumor microenvi
246 Here,
we interrogated the role of microRNAs (miRs) in CD8 T ce
247 ward a proneural glioblastoma (GBM) subtype,
we interrogated the role of PDGFRs in intratumoral GBM h
248 We interrogated the role of the ATX-LPA pathway in aller
249 Here,
we interrogated the roles of Brahma/SWI2-related gene 1
250 Here
we interrogated the roles of individual Rpb1 and Spt5 CT
251 We interrogated the root transcriptome of the resistant
252 We interrogated the Smc3p subunit of cohesin by random i
253 eir subcellular distribution and regulation,
we interrogated the spatiotemporal regulation of Ras uti
254 single-centre, cross-sectional cohort study
we interrogated the structural and functional relationsh
255 essential component of NF-kappaB activation,
we interrogated the susceptibility of mice lacking the A
256 Using doxycycline-inducible ES cell lines,
we interrogated the TGF-beta signaling pathway by expres
257 Here,
we interrogated the therapeutic plasticity of neural ste
258 Here
we interrogated the transcriptional effects of BETi and
259 In addition,
we interrogated the transcriptional regulation of primar
260 Here,
we interrogated the transcriptome and several histone mo
261 Here
we interrogated the transcriptome of individuals carryin
262 We interrogated the transcriptome, genome, proteome, and
263 molecular determinants of (18)FDG retention,
we interrogated the transcriptomes of human-cancer cell
264 3-enhanced, post-receptor IL1beta signaling,
we interrogated the TRB3 interactome using coimmunopreci
265 the pristine surface of a newborn CF airway,
we interrogated the viability of individual bacteria imm
266 We interrogated the viral antibody repertoire before and
267 We interrogated the Wap super-enhancer, generating mice
268 We interrogated the well-described mechanism of MEK/ERK
269 We interrogated the whole-transcriptome in human umbilic
270 ific 'CAG' factors (Cdx2, Arid3a and Gata3),
we interrogate their chromosomal target occupancies, mod
271 ine the interaction of MOZ and BMI1 in vivo,
we interrogated their role in regulating Hox genes and b
272 o determine the functions of these proteins,
we interrogated their transfer DNA insertion mutants wit
273 ing time-resolved fluorescence spectroscopy,
we interrogate these emitters at the single-molecule lev
274 Here,
we interrogated these compartments in hepatocellular car
275 luripotent stem cells (hPSCs) as a paradigm,
we interrogated these dynamics by performing RNA sequenc
276 irect product of the [4 + 2]-cycloaddition),
we interrogated thiopeptide pyridine synthases using a c
277 We interrogate this coincidence by global analysis using
278 nal TGFbeta receptor I (ALK5) knockout mice,
we interrogate this mechanism.
279 Here,
we interrogate this pathway with genetic screens, target
280 We interrogate this series of molecules with pulsed elec
281 Here,
we interrogate this simple but crucial prediction utiliz
282 We interrogated this network in gp78(-/-) mouse embryoni
283 We interrogated this region by conducting a meta-analysi
284 Here,
we interrogated three components of the starvation respo
285 Here,
we interrogate tissue healing across eleven rodents and
286 We interrogated tissue-specific methylome databases to i
287 also modulates transcription of many genes,
we interrogated transcriptional profiles of LT-treated i
288 Here,
we interrogate transcriptome data from primary breast tu
289 We interrogated transcriptomes under multiple conditions
290 Here
we interrogated,
using three separate but complementary
291 We interrogated vaccinia-reactive CD4 in vitro T cell li
292 tivity of UCOEs has remained poorly defined,
we interrogated various CBX3 subfragments in the context
293 Here
we interrogate whether Hh signaling is required for PGC
294 Here,
we interrogate whether the gut microbiota can be conside
295 Herein,
we interrogated whether and how SARS-CoV-2 causes hyperg
296 Here,
we interrogated whether fermented food bioactivity relat
297 Here,
we interrogated whether nucleocapsid-specific antibodies
298 Here,
we interrogated whether PGC-1alpha is involved in tumor
299 Here
we interrogated whether the receptor for advanced glycat
300 Hence, in this study,
we interrogated whole retinal vascular transcriptomic ch