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1 ommonly observed, SPE is highly genotype and tissue specific.
2 ulatory and signaling architecture is highly tissue specific.
3 disc, ASP and myoblasts, whereas others are tissue-specific.
8 the majority of promoters and enhancers have tissue-specific accessibility, and we discover regulator
14 e features of adenoviral vectors that enable tissue specific and efficient delivery of the CRISPR-Cas
15 mited conditionally significant results: non-tissue-specific and brain-specific Basenji-H3K4me3 for a
20 functional in zebrafish, allow imputation of tissue-specific and shared patterns of transcription fac
23 ation in peripheral tissues, and exacerbates tissue-specific and whole-body insulin resistance in hig
25 iled investigations of our results highlight tissue-specific associations, drug validation opportunit
28 Caspian seals Pusa caspica by age, sex, and tissue-specific bioaccumulation, and compared with that
31 er establish the utility of breast milk as a tissue-specific biospecimen for investigations of breast
34 on article summarizes the recent advances on tissue-specific carcinogens and their complex crosstalk
37 factor, plays a crucial role in determining tissue-specific cell fate, including differentiation of
39 resource for chronic social stress-induced, tissue-specific changes in proteins, lipids, and metabol
43 posed by a biological, tissue-level control; tissue-specific chemical variation is most likely to sur
45 orms and show that isoform mixing influences tissue-specific clathrin activity in neurons, which requ
46 l effects of different RAS mutations and the tissue-specific clinical implications are complex and nu
51 single-cell transcriptomics, we identified a tissue-specific core signature of snMacs and two spatial
52 tudies indicating the existence of cell- and tissue-specific cysteine-omes, further emphasizing the n
53 al during clinical sepsis, and contribute to tissue-specific cytokine responses that are protective a
55 possibly smoking cessation, although larger, tissue-specific datasets are required to confirm these r
56 se over 15 entities caused by generalized or tissue-specific defects in enzymes of glycogen metabolis
59 We investigated metabolites from mice with tissue-specific deletion of VDR in intestinal epithelial
62 es that suggests a potential role of 5hmC in tissue-specific development; as well as a resource to fa
63 types of autophagy, a clear understanding of tissue-specific differences in their activity and regula
64 vitro plants revealed temperature-dependent, tissue-specific differential distribution of various phe
66 ngle-cell RNA-seq tissue atlas to generate a tissue-specific DNA methylation reference matrix, allowi
67 research is warranted to evaluate how these tissue-specific DNAm markers classify and predict asthma
69 abolic subsequences, we generated an adipose tissue-specific DRP1 knockout model (Adipo-Drp1(flx/flx)
70 standing the biological barriers that hinder tissue-specific drug delivery and strategies to overcome
71 scuss key advances and emerging concepts for tissue-specific drug delivery approaches and their clini
72 ciferase assay (ETSLA) system to investigate tissue-specific dynamics of circadian gene expression.
73 cover transcriptional networks that maintain tissue-specific EC identity and to identify novel angioc
75 ed potential angiocrine interactions between tissue-specific ECs and other cell types by analyzing li
77 clustering algorithm, we found that certain tissue-specific ECs cluster strongly by tissue (eg, live
79 ed variability, including either systemic or tissue-specific effects across multiple organ systems, w
80 studies map to non-coding sequence and their tissue-specific effects influence transcriptional regula
86 otent cells, they can transition into active tissue-specific enhancers during development, highlighti
88 rogression better than others; compared with tissue-specific enhancers, pleiotropic enhancers show st
89 us to predict 461,141 putative developmental tissue-specific enhancers, the human orthologues of whic
90 To this end, we systematically performed a tissue-specific enrichment analysis using our recently d
91 ers to putative target genes and demonstrate tissue-specific enrichments of sequence variants associa
94 ative 3' back-splicing, and both of them are tissue-specific, especially enriched in brain tissues.
98 ome a crucial component of gene and regulate tissue-specific expression during mouse tissue developme
101 y is predicted largely by the divergence and tissue-specific expression of the human co-orthologs, i.
103 on of tissue-specific genes and change their tissue-specific expression patterns during evolution.
106 an orange carrot (genotype DH1) and compared tissue-specific expression profiles and in vitro product
107 operties with TCDD and BNF, and the distinct tissue-specific expression profiles indicate different f
109 antage of the newly emerged, genome-wide and tissue-specific expression quantitative trait loci (eQTL
111 family of covalently circularized RNAs with tissue-specific expression, were recently demonstrated t
112 eractors of ULK1 and ULK2 all have different tissue-specific expressions partially contributing to di
115 w evidence that nutrient availability shapes tissue-specific fate programs via alphaKG-dependent diox
118 ichments of shared high-posterior SNPs in 53 tissue-specific functional categories and find evidence
119 idermis, mesophyll, and vascular bundle, its tissue-specific functions in thermomorphogenesis are not
123 g motifs of transcription factors related to tissue-specific functions, and marked genes functionally
126 s thaliana seedlings were investigated using tissue-specific GA inactivation in wild-type (Col-0) or
127 cal techniques, tissue ablation, microscopy, tissue-specific gene and enzyme activity expression with
128 hat our single blind study using eight liver tissue-specific gene biomarkers (e.g. AMBP and AHSG) is
130 phenotypic, microscopic, transcriptomic, and tissue-specific gene expression analyses, we demonstrate
131 ge, we developed a framework for integrating tissue-specific gene expression and epigenomic maps to o
132 could have a significant role in regulating tissue-specific gene expression and transcript splicing.
133 position as a common feature associated with tissue-specific gene expression changes in the heart.
135 s of regulatory element evolution that shape tissue-specific gene expression programs and defines reg
137 his analysis revealed a dramatic increase in tissue-specific gene expression, concurrent with slowed
140 tively, our results indicate a rich layer of tissue-specific gene regulation at the level of alternat
141 t sites are found to drive the expression of tissue-specific genes and change their tissue-specific e
144 latory architectures of germline and somatic tissue-specific genes, uncover regulatory rules for gene
145 tigation such as biotherapeutic development, tissue-specific genetic engineering, and genetic disease
150 ciated with regulatory motif alterations and tissue-specific histone marks consistent with these vari
154 Although research into the induction of tissue-specific immunity by vaccines and with age is sti
157 or post-thymic gammadeltaT17 development and tissue-specific imprinting, which is essential for infec
163 ation, gene predictors were trained using 19 tissue-specific J. regia transcriptomes aligned to the g
167 that observed in Arabidopsis is reported and tissue-specific localization in the epidermis and mesoph
168 spite growing interest in the development of tissue-specific lymphatics, the cellular origin of bone
170 integrins expressed in parental cells, in a tissue specific manner, as a key step of cancer progress
173 Its functional properties are regulated in a tissue-specific manner through co-assembly with beta sub
174 ncRNAs are distributed across the body in a tissue-specific manner with some also being sexually dim
176 components (genetic and environmental), in a tissue-specific manner, to trigger or sustain a disease
188 h a dietary trace element to shed light on a tissue-specific mechanism of disease risk based on impai
189 associated with reinfection, suggesting that tissue-specific mechanisms govern the development of imm
190 ians reveals that most fossil specimens show tissue-specific melanosome chemistries that differ from
191 the transcription factor TBX3 as a candidate tissue-specific member of the beta-catenin transcription
193 e whether murine CD8alphaalpha binds only to tissue-specific MHC-Ib molecules or also to ubiquitously
194 onserved cnidarian feature, and evidence for tissue-specific microRNA arm switching as found in Bilat
196 onsiderably different, PUMA captures similar tissue-specific miRNA-target regulatory interactions in
197 We generated a doxycycline-inducible adipose tissue-specific MMP14 overexpression model to study its
198 ugh the generation and analysis of cell- and tissue-specific models using transcriptomic, proteomic,
200 d-elbow gating mechanism elucidates distinct tissue-specific modulations, pharmacology, and disease p
201 ach cell type were then analyzed to retrieve tissue-specific molecular information and to generate cl
202 anner, but also provide a blueprint of how a tissue-specific molecule might be constructed for applic
203 nalyzed single-cell RNA sequencing data from tissue-specific mouse ECs generated by the Tabula Muris
205 expression in testis, which illustrates the tissue-specific nature of cis-regulatory evolution bypas
208 n antibody-mediated toxin neutralization and tissue-specific neutrophilic inflammation preserve tissu
213 uencing, we identified a large repertoire of tissue-specific p53 genes and a common p53 transcription
214 heral vs. lymphoid organs, revealing a novel tissue-specific paradigm for the reactivation of memory
215 l adenomatous polyposis), by changing only 2 tissue-specific parameters: the number of stem cells in
217 ht the consequences of chronic infection for tissue-specific pathology and identify open questions in
220 issue sites from 60 individuals, we identify tissue-specific patterns of NK cell subset distribution,
221 how that this simple theory predicts complex tissue-specific patterns of segregation in mouse experim
226 otein targets of ROS modification that drive tissue-specific physiology in vivo are largely unknown.
227 bserved in all organs examined, highlighting tissue-specific prenatal molecular phenotypes in SMA.
229 r, we failed to reveal biologically relevant tissue-specific processes subjected to miRNA-mediated re
230 MA we identified miRNAs regulating important tissue-specific processes that, when mutated, may result
235 four transgenic lines that express Cre under tissue-specific promoters of the pancreas, mammary gland
236 This approach depends on the availability of tissue-specific promoters, and it does not allow further
237 om ATP generation by uncoupling protein 1, a tissue-specific protein present in mitochondria of brown
238 demonstrate the important contribution of a tissue-specific protein to the polyQ protein-mediated se
240 ially contribute to organogenesis, including tissue-specific regulation between male and female inflo
243 findings represent a clear demonstration of tissue-specific regulation of organelle protein import a
244 d-like proteins (MBNL) belong to a family of tissue-specific regulators of RNA metabolism that contro
246 We report that 42% of the 285 significant tissue-specific regulatory interactions we identify were
248 ing private clonotypes, which tended to form tissue-specific repertoires, especially in the periphera
250 ults demonstrate a mechanism that allows for tissue-specific resistance against stress and could aid
252 es (ROS) are signaling molecules produced by tissue-specific respiratory burst oxidase homolog (RBOH)
253 i) conditions highlight the need to consider tissue-specific responses in strategies targeting regene
255 ing approaches to demonstrate a reproductive tissue-specific role for CEPR1 in controlling yield and
256 ene-trait associations, but also detects the tissue-specific role of candidate target genes in comple
259 tely required in spermatogenesis, indicating tissue-specific roles in centriole and basal body format
260 sceral regions may shed new light on adipose tissue-specific roles in systemic metabolic perturbation
261 In this review, we discuss the expression, tissue-specific roles, and substrate specificities of th
262 levels per sample, we find highly consistent tissue specific RP mRNA signatures in normal and tumor s
264 , rhizome fortification, stress response and tissue-specific secondary metabolites biosynthesis.
265 st peripherally encountered antigens such as tissue-specific self-antigens that are regionally draine
266 strategy to screen hundreds of sequences for tissue-specific silencer activity in whole Drosophila em
271 GAL4 GFP enhancer trap system, we describe a tissue-specific split luciferase assay for non-invasive
272 elopment inectodermal and mesodermal-derived tissue-specific stem and progenitor cells and then, foll
273 The horizontal basal cell (HBC) is a dormant tissue-specific stem cell presumed to only be forced int
276 rectal and LN tissue suggest that different tissue-specific strategies may be required to eliminate
277 ons of clock emergence, its concordance with tissue-specific structure/function, the interdependence
279 eogenic peptides are well suited for current tissue-specific therapeutic paradigms to augment the end
280 "core" set of TOP mRNAs, but also identifies tissue-specific TOP mRNAs produced via alternative trans
281 tocyte nuclear factor-1beta (HNF-1beta) is a tissue-specific transcription factor that is required fo
288 scriptional response in vivo, revealing both tissue-specific transcriptomes and a unique signature, w
289 ol in the roots of L. frutescens and compare tissue-specific transcriptomes with existing data from E
291 ion of Drosophila copper homeostasis by ATP7 tissue-specific transgenic expression caused alterations
292 us de novo mutations in EEF1A2, encoding the tissue-specific translation elongation factor eEF1A2, ha
293 ilitate TE survival and rapid proliferation: tissue-specific transposition and minimization of negati
296 ceptibility gene type 1 or 2 (BRCA1/2) poses tissue-specific variations in cancer risks and primarily
297 entify DNAm smoking effects that are unique (tissue-specific) vs. shared between tissues (tissue-shar
300 in regulatory sequence can therefore lead to tissue-specific Y-Chromosome-driven sex biases in expres