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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

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