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 eny and establish trait-allele associations,
we interrogated 75 M. bovis and 61 M. tuberculosis genom
11 Therefore,
we interrogated a customized small interfering RNA (siRN
12 We interrogated a library of FDA-approved drugs for thei
13 As an example,
we interrogated a protein microarray formed by a commerc
14 Building on this foundation,
we interrogated a small-molecule library for compounds t
15 Using a 2,304-element microarray,
we interrogated a total of 250 sera from Michigan lung c
16 early stages of the pathway to cyclopamine,
we interrogated a V. californicum RNA-seq dataset using
17 functional identity of this venom component,
we interrogated a venom gland EST database for the saw-s
18 We interrogated A-domain 2-keto and 2-hydroxy acid activ
19 To address this,
we interrogated activated signaling pathways in a compar
20 In addition,
we interrogated an 840-member novel oxime library for re
21 We interrogated an M. avium subsp. paratuberculosis Delt
22 First,
we interrogate and justify the relevance of bead endocyt
23 Here,
we interrogate and quantitatively model how proliferatio
24 ion is seen after acute kidney injury (AKI),
we interrogated another bone fide AKI marker, Kim1 and n
25 To address this issue
we interrogated AR signaling in AD and recurrent prostat
26 We interrogated at massive scale the structural properti
27 We interrogated at single-cell resolution how these alte
28 We interrogated baseline single photon emission computed
29 Using a novel strategy,
we interrogated CLL membrane-specific autologous immunog
30 In this study,
we interrogated clonal relationships between CD4(+) T ce
31 We interrogated common SNPs (minor allele frequency >5%)
32 ern the regenerative capacity of hair cells,
we interrogated custom human cDNA microarrays with senso
33 Here,
we interrogate cytosine methylation patterns in sperm ob
34 We interrogated DNA methylation at baseline and 3 hours
35 We interrogated E(2)-induced apoptosis by analysis of ge
36 te with anxiety induction in human subjects,
we interrogated emotion-state-dependent olfactory proces
37 We interrogated FCMR contributions to B cell function by
38 Using mathematical modeling
we interrogated four alternative explanatory models for
39 Here
we interrogate functional interaction between BRCA1 and
40 n tissue is not available from most samples,
we interrogated gene expression in lymphoblasts from 244
41 We interrogated genome-wide association, exome sequencin
42 and may undergo mesenchymal differentiation,
we interrogated GSC potential to generate vascular peric
43 We interrogated &
gt;1.5 million genetic variants in EoE cas
44 imaging and transcriptional profiling tools,
we interrogated how distinct microenvironments in the gu
45 To investigate this model,
we interrogate human platelets using approaches that inc
46 We interrogated human tumor tissue for immunofluorescenc
47 accepted clinical tool CAPRA-S in the cases
we interrogated irrespective of Gleason grade, prostate-
48 de insights on the biological role of CEB25,
we interrogated its structural features.
49 We interrogated known microarray data sets to define NAM
50 We interrogated large databases and found that sonic hed
51 Next,
we interrogated mechanisms of insulin-associated hepatoc
52 between oncogenic PIK3CA and OGDH function,
we interrogated metabolic requirements and found an incr
53 We interrogated more than 2 million single nucleotide po
54 We interrogated more than 9000 transcripts at 6 time poi
55 We interrogated mutants impaired in the Fe homeostasis r
56 From an initial 630 ILBC primary tumors,
we interrogated oncogenic substitutions and insertions a
57 We interrogated our mandatory administrative database fo
58 Here
we interrogated preNMDAR functions pharmacologically to
59 We interrogated publically available 18S rRNA gene datas
60 otinib, dasatinib, ponatinib, and DCC-2036),
we interrogated response of CML cell lines and primary C
61 We interrogated RNA-Seq data from 3,775 malignant neopla
62 ather than complete loss of SBDS expression,
we interrogated SDS patient cells for defects in ribosom
63 he role of the Wnt family of genes in NSCLP,
we interrogated seven Wnt genes (Wnt3, Wnt3A, Wnt5A, Wnt
64 Here
we interrogated signal transducer and activator of trans
65 Specifically,
we interrogated site-specific binding by the transcripti
66 For fine mapping
we interrogated SNPs within +/- 250 kb flanking regions
67 We interrogate submitted items with energetic neutrons,
68 Here
we interrogate synaptic connections between afferent pat
69 le signaling nodes at the single-cell level,
we interrogate TCR signaling dynamics in control C57BL/6
70 Here
we interrogate the appropriateness of a range of previou
71 Here,
we interrogate the biochemical activity and nucleic acid
72 Here,
we interrogate the biochemical mechanism of procaspase-3
73 Here
we interrogate the cellular responses to target cell inf
74 In this study,
we interrogate the complexity in cAMP/PKA-MAPK/ERK1&2 cr
75 Here
we interrogate the consequences of chronic necroptosis o
76 Here
we interrogate the epigenetic landscape of enhancer elem
77 Here
we interrogate the genomes of 7,651 diverse human cancer
78 he glycosylated and nonglycosylated species,
we interrogate the hormone biosynthesis.
79 Here,
we interrogate the local structure of the M(III) surface
80 Here,
we interrogate the mechanism by which the white-opaque s
81 Here,
we interrogate the MNK-eIF4E axis in diffuse large B-cel
82 Here
we interrogate the molecular consequences of CRISPR/Cas9
83 Here,
we interrogate the NC-GRN in the lamprey, taking advanta
84 f samples analysed so far, to our knowledge,
we interrogate the noncoding transcriptome, alternative
85 We interrogate the psychological and neural basis of thi
86 By using the SCBC,
we interrogate the response of human-derived glioblastom
87 Here,
we interrogate the role of the caspase recruitment domai
88 Here,
we interrogate the structure of the prototype pinholin b
89 ional susceptibility loci for breast cancer,
we interrogated the 2q35 gene desert for chromatin archi
90 We interrogated the activity of the PSMA-PI3K axis throu
91 In the work reported herein,
we interrogated the amyloidogenesis mechanism of human b
92 We interrogated the architecture of the complete Dengue
93 on and critical for rational vaccine design,
we interrogated the biochemical properties of 9,888 MHC
94 Therefore,
we interrogated the biological effects of class I HDAC i
95 We interrogated the CARDIoGRAMplusC4D (Coronary ARtery D
96 In this study
we interrogated the chemistry of the PCSK9 active site a
97 In the present study,
we interrogated the clonal architecture by mutation-spec
98 ns in PanIN 3 lesions and pancreatic tumors,
we interrogated the comparative ability of adult pancrea
99 Here,
we interrogated the contribution of common polygenic var
100 Here,
we interrogated the contribution of the SWI/SNF subunit
101 We interrogated the contribution of these two processes
102 n PLX-4032-induced responses and resistance,
we interrogated the contributions of anti-apoptotic BCL-
103 In this study,
we interrogated the effect of decreased Ag amount/durati
104 We interrogated the effect of reduced endogenous estroge
105 Using FRET reporters,
we interrogated the effects of soluble beta-glucan on in
106 We interrogated the evolution of the phosphotriesterase
107 n reported in the chicken embryo as a whole,
we interrogated the existence or absence of genomic impr
108 We interrogated the expression and regulation of 226 tra
109 Here,
we interrogated the expression of all ETS family members
110 ding may influence cellular protein folding,
we interrogated the folding landscape of a model beta-ri
111 In a second set of experiments,
we interrogated the function of each level of the hypoth
112 for the heme-dependent regulation of hrg-1,
we interrogated the hrg-1 promoter.
113 Here,
we interrogated the importance of IDE-mediated catabolis
114 Here,
we interrogated the in vivo relevance of this cell popul
115 In this work,
we interrogated the intrinsic ability of Ras to self-ass
116 Then
we interrogated the microarrays with cholera toxin, anti
117 We interrogated the pattern of expression of esophagus-s
118 arallel, by comparing with parental genomes,
we interrogated the phasing of these deletions with the
119 c Ag-specific TCR-transgenic CD8(+) T cells,
we interrogated the phenotype, functionality, and recall
120 ependent increase in sub-RPE deposit height,
we interrogated the potential of CFH as a previously uni
121 We interrogated the role of a neuronal cell adhesion mol
122 Here,
we interrogated the role of AEG-1 in NTIS in the context
123 In this article,
we interrogated the role of GRP78 in the tumor microenvi
124 ward a proneural glioblastoma (GBM) subtype,
we interrogated the role of PDGFRs in intratumoral GBM h
125 We interrogated the role of the ATX-LPA pathway in aller
126 Here
we interrogated the roles of individual Rpb1 and Spt5 CT
127 We interrogated the root transcriptome of the resistant
128 We interrogated the Smc3p subunit of cohesin by random i
129 essential component of NF-kappaB activation,
we interrogated the susceptibility of mice lacking the A
130 Using doxycycline-inducible ES cell lines,
we interrogated the TGF-beta signaling pathway by expres
131 Here,
we interrogated the therapeutic plasticity of neural ste
132 Here
we interrogated the transcriptional effects of BETi and
133 In addition,
we interrogated the transcriptional regulation of primar
134 Here,
we interrogated the transcriptome and several histone mo
135 Here
we interrogated the transcriptome of individuals carryin
136 molecular determinants of (18)FDG retention,
we interrogated the transcriptomes of human-cancer cell
137 the pristine surface of a newborn CF airway,
we interrogated the viability of individual bacteria imm
138 We interrogated the Wap super-enhancer, generating mice
139 We interrogated the whole-transcriptome in human umbilic
140 ific 'CAG' factors (Cdx2, Arid3a and Gata3),
we interrogate their chromosomal target occupancies, mod
141 ine the interaction of MOZ and BMI1 in vivo,
we interrogated their role in regulating Hox genes and b
142 o determine the functions of these proteins,
we interrogated their transfer DNA insertion mutants wit
143 ing time-resolved fluorescence spectroscopy,
we interrogate these emitters at the single-molecule lev
144 Here,
we interrogated these compartments in hepatocellular car
145 We interrogate this coincidence by global analysis using
146 We interrogate this series of molecules with pulsed elec
147 Here,
we interrogate this simple but crucial prediction utiliz
148 We interrogated this network in gp78(-/-) mouse embryoni
149 We interrogated this region by conducting a meta-analysi
150 We interrogated tissue-specific methylome databases to i
151 We interrogated transcriptomes under multiple conditions
152 Here
we interrogated,
using three separate but complementary
153 We interrogated vaccinia-reactive CD4 in vitro T cell li
154 tivity of UCOEs has remained poorly defined,
we interrogated various CBX3 subfragments in the context
155 Here
we interrogate whether Hh signaling is required for PGC