1 with pathogenic ncRNAs, using comprehensive
transcriptome analyses.
2 abases that incorporate information from the
transcriptome analyses.
3 r genes was examined using double mutant and
transcriptome analyses.
4 dosage effects have been confirmed by recent
transcriptome analyses.
5 r 2 h (R2) and 48 h (R48)), were sampled for
transcriptome analyses.
6 We collected colons from mice and performed
transcriptome analyses.
7 were identified in prior work by comparative
transcriptome analyses.
8 rwent identical clamp procedures and hepatic
transcriptome analyses.
9 in profiles with ex vivo islet secretome and
transcriptome analyses.
10 y mask the direct impact of those factors in
transcriptome analyses.
11 ed explicitly in other published gpa1 mutant
transcriptome analyses.
12 lated mature mRNAs are the focus of standard
transcriptome analyses.
13 y a combination of metabolome, proteome, and
transcriptome analyses.
14 Based on
transcriptome analyses across 36 environmental condition
15 Transcriptome analyses across nonhuman primates and huma
16 Genome sequences and
transcriptome analyses allow the correlation between gen
17 ese data with previous microarray and global
transcriptome analyses allowed us to expand the putative
18 Transcriptome analyses also showed that some genes are a
19 Lastly, quantitative data from
transcriptome analyses and gene ontology partitioning we
20 By using whole-
transcriptome analyses and phenotypic screenings of the
21 Genetic and
transcriptome analyses associated a mutation in the vinc
22 Transcriptome analyses before and during nivolumab thera
23 he complete molecular signatures of cells by
transcriptome analyses but also the cascade of events th
24 Transcriptome analyses by RNA-seq were conducted as a fu
25 of Sub1A-1-mediated tolerance, we performed
transcriptome analyses comparing the temporal submergenc
26 We performed
transcriptome analyses comparing wild-type (WT) EHEC and
27 Genome-wide protein localization and
transcriptome analyses demonstrate overlapping gene regu
28 Recent
transcriptome analyses demonstrated a high number of cis
29 mmunoprecipitation-sequencing, with parallel
transcriptome analyses determined by RNA sequencing.
30 etically deficient mouse strains, and global
transcriptome analyses failed to associate the protectiv
31 We employed these models in conjunction with
transcriptome analyses following cyclophosphamide treatm
32 Previous
transcriptome analyses have identified candidate molecul
33 Interestingly,
transcriptome analyses have identified SOCS2 as being pr
34 Transcriptome analyses have recently identified PARP12,
35 Advances in high-throughput
transcriptome analyses have revealed hundreds of antisen
36 cularly true for non-coding RNAs where whole
transcriptome analyses have revealed that the much of th
37 Recent
transcriptome analyses have shown the differential expre
38 Transcriptome analyses have typically disregarded nucleo
39 Subsequent mRNA
transcriptome analyses highlighted several genes induced
40 nt reads improves the accuracy of genome and
transcriptome analyses,
however lack of consensus betwee
41 Transcriptome analyses identified a small number of gene
42 Genome-wide
transcriptome analyses identified an uncharacterized tri
43 Transcriptome analyses identified markedly different gen
44 Whole-
transcriptome analyses identified multiple splicing chan
45 Our
transcriptome analyses identify the interleukin 21 (IL21
46 Cell biologic and
transcriptome analyses implicate dysregulation of ciliog
47 nce-associated secretory phenotype and whole-
transcriptome analyses implicated the p38 MAPK/IL8 pathw
48 Using cell-type-specific
transcriptome analyses in a rodent model of chronic dopa
49 Adipose tissue
transcriptome analyses in children indicate that humans
50 We also performed comparative genome-wide
transcriptome analyses in livers of MLL3, MLL4, and MLL3
51 Using co-culture experiments and mouse
transcriptome analyses in syngeneic mouse models, we pro
52 To identify these genes, we performed
transcriptome analyses in the striatum in 6-hydroxydopam
53 Transcriptome analyses indicate a highly specific tempor
54 Transcriptome analyses indicate dynamic and orchestrated
55 Phenotypic, functional, and
transcriptome analyses indicate that 2 degrees effectors
56 es, the red/far-red photoreceptors; however,
transcriptome analyses indicate that the gene regulatory
57 Transcriptome analyses indicated that FixK positively re
58 phila melanogaster (fruit fly) genetics with
transcriptome analyses it was found that the beneficial
59 idual X-linked genes and by microarray-based
transcriptome analyses,
it was challenged by a recent st
60 After comparing the published data from
transcriptome analyses,
mutant studies, and exogenous ho
61 Using a combination of
transcriptome analyses,
mutants, and reporter constructs
62 Using single-base methylation maps and
transcriptome analyses of a colitis-induced mouse colon
63 ent of gene expression variation through the
transcriptome analyses of a large maize-teosinte experim
64 Unexpectedly, unbiased whole-
transcriptome analyses of adipose macrophages revealed t
65 Transcriptome analyses of At vip2 suggest that VIP2 is l
66 In addition,
transcriptome analyses of Brassica homologues of Arabido
67 Here, through integrated epigenome and
transcriptome analyses of cell lines, genotyped clinical
68 ns of both KAP1 and associated histones, and
transcriptome analyses of cells deficient in KAP1.
69 Transcriptome analyses of CIP-deficient hearts revealed
70 Transcriptome analyses of CLL and the main normal B cell
71 Genome-wide
transcriptome analyses of conditional heart-specific p53
72 Transcriptome analyses of DFU tissue showed induction of
73 with the general CDK inhibitor flavopiridol,
transcriptome analyses of FIT-039-treated cells revealed
74 s 336 proteins not previously represented in
transcriptome analyses of guard cells and 52 proteins cl
75 We report here the
transcriptome analyses of highly expressed genes that ar
76 survival genes has been investigated through
transcriptome analyses of highly responsive, primary bon
77 nrichment platform and conducted large-scale
transcriptome analyses of human cytomegalovirus (HCMV) i
78 Transcriptome analyses of Kap1-deleted B splenocytes rev
79 Transcriptome analyses of laser-capture microdissected n
80 We performed cross-species
transcriptome analyses of mouse and human neurofibromas
81 We performed high-throughput
transcriptome analyses of multiple placenta samples from
82 as been a recent burst of articles reporting
transcriptome analyses of Mycobacterium tuberculosis, in
83 Whole
transcriptome analyses of next generation RNA sequencing
84 bb but not neuroglobin or cytoglobin mRNA in
transcriptome analyses of nigral dopaminergic neurons.
85 Transcriptome analyses of overexpressing hairy roots and
86 We present
transcriptome analyses of primary cultures of human feta
87 MCs) in the adult thymus, we performed whole
transcriptome analyses of primary thymic, bone, and skin
88 Previous
transcriptome analyses of seed development in grape reve
89 Genome-wide
transcriptome analyses of several bacterial species have
90 Until recently,
transcriptome analyses of single cells have been confine
91 study provide a starting point for detailed
transcriptome analyses of stem cells.
92 Here, we integrate metabolome and
transcriptome analyses of Stevia to explore the biosynth
93 Transcriptome analyses of T cells identified Foxo1-regul
94 We present the first genome and
transcriptome analyses of the cinereous vulture compared
95 Transcriptome analyses of the EBB1 transgenics identifie
96 Here, we report the use of genome-wide
transcriptome analyses of the marine diatom Thalassiosir
97 Transcriptome analyses of these cells suggest that Lb1 i
98 ata on linkage, whole-genome sequencing, and
transcriptome analyses of these dogs compared to severel
99 igated tumorigenesis and metastasis of MM in
transcriptome analyses of three distinct cell lines that
100 Upon tumor formation, phenotypic and
transcriptome analyses of tumor cells revealed salient O
101 Recent whole-genome and
transcriptome analyses of Y chromosomes in humans and ot
102 Transcriptome analyses often have focused on housekeepin
103 We conducted
transcriptome analyses on 835 obese subjects with mean B
104 Global
transcriptome analyses on neural tubes isolated from E9.
105 transformed cell lines, we performed global
transcriptome analyses on resting B cells and on EBV and
106 thology and multigene family classification,
transcriptome analyses,
phylogenetic analyses, and patho
107 Here, we show that comparative
transcriptome analyses predict remodeling of extracellul
108 Through global
transcriptome analyses,
proteasomal inhibition showed co
109 Our
transcriptome analyses reveal that only a fraction of or
110 Transcriptome analyses reveal that SAR establishment in
111 Transcriptome analyses revealed a consistent up-regulati
112 Transcriptome analyses revealed distinct gene expression
113 Transcriptome analyses revealed expression of genes enco
114 Genome-wide
transcriptome analyses revealed that 89 apoptosis-associ
115 Subsequent whole-genome
transcriptome analyses revealed that genes associated wi
116 Additional experiments motivated by the
transcriptome analyses revealed that growth on a surface
117 High-resolution
transcriptome analyses revealed that reduced PRPF6 alter
118 Transcriptome analyses revealed that ROR1 x TCL1 leukemi
119 Genome-wide
transcriptome analyses revealed that Th1-polarized infla
120 Transcriptome analyses revealed that the clustered regul
121 Transcriptome analyses revealed that the sigA(G336C) sub
122 Transcriptome analyses revealed that, in the absence of
123 shared by all Brassicaceae, cytogenetic and
transcriptome analyses revealed two younger WGD events t
124 enome-wide chromatin immunoprecipitation and
transcriptome analyses (
RNA-Seq), we identified a subset
125 Transcriptome analyses show that DFPM also stimulates ex
126 Transcriptome analyses show that expression of extracell
127 More importantly,
transcriptome analyses show that MM-401 induces changes
128 In agreement with these findings,
transcriptome analyses showed a strong DG172-mediated re
129 Transcriptome analyses showed changes in mRNA levels for
130 Transcriptome analyses showed that 11,328 of the oligonu
131 Global
transcriptome analyses showed that ChlR controls the exp
132 Transcriptome analyses showed that Foxo proteins regulat
133 In vivo and in vitro
transcriptome analyses showed that NPC-secreted factors
134 Combined genetic and
transcriptome analyses showed that Rsf-1 (HBXAPalpha) wa
135 Transcriptome analyses showed that the expression of gen
136 Transcriptome analyses showed that the protective effect
137 s method is routinely used to validate whole
transcriptome analyses such as DNA microarrays, suppress
138 Our previous genome-wide microRNA and mRNA
transcriptome analyses suggest a key role for miR-153 in
139 Transcriptome analyses suggest TWSG1 is produced during
140 Transcriptome analyses suggested a possible role for ver
141 transcription polymerase chain reaction and
transcriptome analyses suggested nonsense mRNA decay as
142 Transcriptome analyses supported these physiologic findi
143 Transcriptome analyses supported this synergy and sugges
144 We report here whole-
transcriptome analyses that characterize CcpA-dependent,
145 We here report whole
transcriptome analyses that characterize glucose-depende
146 However, in
transcriptome analyses,
the majority of their predicted
147 ng to be available and will be necessary for
transcriptome analyses to become routine tests in the cl
148 We used morphological, functional, and
transcriptome analyses to benchmark maturation of EHM.
149 ied by only a single amino acid in CovS, and
transcriptome analyses to characterize the impact of Cov
150 We used global
transcriptome analyses to determine if these physiologic
151 We have used
transcriptome analyses to gain insights into the scope o
152 We performed
transcriptome analyses to identify genes controlled by t
153 nt the duck genome sequence and perform deep
transcriptome analyses to investigate immune-related gen
154 t the feasibility of integrating genomic and
transcriptome analyses to map critical neurodevelopmenta
155 port single cell RNA sequencing and unbiased
transcriptome analyses to reveal major distinctions betw
156 In a previous study, we used comparative-
transcriptome analyses to select a group of genes that w
157 We used
transcriptome analyses to show that MYCN-amplified neuro
158 Transcriptome analyses under different salt growth condi
159 The
transcriptome analyses used microarray hybridization and
160 Transcriptome analyses using GeneChip and RNA-sequencing
161 Using sensitive
transcriptome analyses we identified 2263 cellular genes
162 Through the use of high-resolution global
transcriptome analyses,
we demonstrated a female-biased
163 On the basis of whole-
transcriptome analyses,
we identify many genes that are
164 Using unbiased
transcriptome analyses,
we show a pronounced separation
165 In this study, using detailed genomic and
transcriptome analyses,
we show that CenH3 was lost inde
166 yping, and genotyping, and blood samples for
transcriptome analyses were obtained within 24 hours of
167 Transcriptome analyses were used to address the relation
168 Comparative
transcriptome analyses were used to identify potential c
169 Genome-wide genetic and
transcriptome analyses were used to investigate the orig
170 his striking difference was reflected in the
transcriptome analyses,
which revealed enrichment of cel
171 By combining whole-genome
transcriptome analyses with (live) imaging mass spectrom
172 We combined comparative genome and
transcriptome analyses with the experimental tools avail