ライフサイエンスコーパス: cell-specific

1 e been described, some of which are host and cell specific.

2 Loss of HAPLESS 2/GENERATIVE CELL SPECIFIC 1 (HAP2/GCS1) proteins results in gamete f

3 e found that the increase in Treg cells in T cell-specific A20-deficient mice was already observed in

4 eficient mice fed a high-cholesterol diet, T cell-specific ABCG1 deficiency protected against atheros

5 In vivo, T-cell-specific ablation of murine Gclc prevented autoimmu

6 Here we show that B cell-specific ablation of Nfat2 leads to the loss of the

7 In the thymus, T cell-specific ablation of the Roquin paralogs leads to a

8 Using optogenetics, cell-specific ablation, whole cell patch-clamp and immun

9 Akt3/+S472 in triple-negative breast cancer cells, specific ablation of Akt3/-S472 enhanced, whereas

10 ly, we have shown that villin, an epithelial cell-specific actin-binding protein functions as an anti

11 We hypothesized that cell-specific actions of Smad3 regulate repair and remod

12 This study provides evidence that the cell-specific activities of different PKM isoforms gener

13 We conclude that this cell-specific alpha-tubulin isotype dictates the hallmar

14 city of the kinesin-2 OSM-3/KIF17, whereas a cell-specific alpha-tubulin isotype regulates ciliary ul

15 Thus, PV-cell-specific alternative splicing of neurexins is criti

16 The cell-specific and common downregulated genes were charac

17 stmitotic neurons, where its accumulation is cell-specific and correlated with gene expression.

18 We used perivascular-cell-specific and pericyte-specific lineage-tracing mode

19 ether, this provides proof-of-concept that a cell-specific and region-specific gene expression approa

20 Here, a cell-specific and region-specific transcriptomics approa

21 ational approach for identifying effectively cell-specific and stimulation-specific promoter and enha

22 gulates mitochondrial function; however, the cell-specific and temporal role of DRP1 in AKI in vivo i

23 aracrine ATP signalling enhances firing in a cell-specific and tonotopically-determined manner.

24 unohistochemically by antibodies that target cell-specific antigens in the cytosol or plasma membrane

25 stimulate lymphocyte proliferation and tumor cell-specific antitumor immune responses.

26 d rescued Par-4-mediated induction of cancer cell-specific apoptosis.

27 creted protein biomarkers and trigger cancer-cell-specific apoptosis.

28 Finally, genetic engineering and cell-specific application of extracellular vesicles coul

29 ll surface glycan by taking advantage of the cell-specific aptamer, and the lectin-functionalized gol

30 tosterone (DHT)-induced PCOS with global and cell-specific AR-resistant (ARKO) mice to investigate th

31 B cell-specific ATM deficiency attenuated the establishmen

32 Thus, our study defines a proviral role of B cell-specific ATM expression during chronic gammaherpesv

33 gammaherpesvirus tropism for B-1 B cells, B cell-specific ATM expression was necessary to support vi

34 In summary, we identified a novel role for B cell-specific, BAFF-dependent transmembrane activator an

35 the cost of high technical noise, including cell-specific biases in capture efficiency and library g

36 Endothelial cell-specific, but not macrophage-specific Adora2a delet

37 Germ cell-specific, but not Sertoli cell-specific Nhe8 disrup

38 l reprogramming by introducing individual TS cell-specific 'CAG' factors (Cdx2, Arid3a and Gata3), we

39 Cardiac function significantly declined in T-cell-specific CD4-Cre(+/)(-)CD73(flox/flox) mice identic

40 aortic constriction (TAC) using global and T-cell-specific CD73(-)(/-) mice.

41 d a model of specific antibody deficiency, B cell-specific CD79a-Cre x XBP1 (X-box binding protein-1)

42 Nectin-like 4 (NECL4, CADM4) is a Schwann cell-specific cell adhesion molecule that promotes axo-g

43 ional variants that precisely co-locate with cell-specific chromatin domains and pancreatic islet enh

44 -specific control module governed by a renal cell-specific chromatin structure located distal to Cyp2

45 hment of neuronal fate with the formation of cell-specific ciliary structures in Caenorhabditis elega

46 od was applied to the quantification of four cell-specific cluster of differentiation (CD) proteins u

47 A library screening, we identified an immune cell-specific, co-stimulatory receptor B7.2 (CD86) as a

48 n TNFR1 under the control of the mesenchymal cell-specific CollagenVI promoter.

49 Both global and NK-cell-specific conditional deletion of A2AR enhanced prop

50 cells (DCs) from female mice with dendritic cell-specific conditional knockout of Prdm1 (CKO mice) a

51 Here, we characterized the cell-specific connectivity of VTA dopamine neurons, thei

52 We suggest that cell-specific control of MT glutamylation may be a conse

53 his research question, we have generated a T cell-specific Coronin 1a knock-out mouse (Coro1a(fl/fl)

54 RPE cells, we used two different mature RPE cell-specific Cre recombinase drivers to inactivate eith

55 or neuron apoptosis, which can be rescued by cell-specific CRE-mediated expression of wild-type FUS w

56 concentrations in the blood of sensitized T cell-specific Cyp27b1-KO mice support a lymphocyte-drive

57 Here, we engineer human beta-cell-specific cytotoxic T lymphocytes and demonstrate th

58 When calibrated to cell-specific data, executable network models can reveal

59 Queries across cell-specific databases revealed that a majority of the

60 24-miR-221-beclin-1 loop in mediating cancer cell-specific death.

61 B-cell-specific deficiency in FcmuR enhanced the spontaneo

62 We further show that T-cell-specific deficiency of Fabp4 and Fabp5 (Fabp4/Fabp5

63 T cell-specific deficiency of the genome organizer Satb1 i

64 Using mice with Foxp3(+) Treg-cell specific deletion of Blimp1 and other approaches, h

65 We show that T cell-specific deletion and early pharmaceutical inhibiti

66 nticancer functions in vivo, and mice with T cell-specific deletion of Atg5 have reduced tumour outgr

67 and regulatory (Treg) cells, and mice with T cell-specific deletion of Blimp1 (Blimp1CKO mice) sponta

68 The cell-specific deletion of CXCR4 in arterial endothelial

69 Mice with T-cell-specific deletion of GATA3 did not develop colitis

70 nesulfonic acid to control mice, mice with T-cell-specific deletion of GATA3, and mice with deletion

71 Treg cell-specific deletion of genes that regulate TH17 cell

72 on of G-protein receptor kinase 3 (GRK3) nor cell-specific deletion of GRK3/arrestin-dependent p38alp

73 we created mice harboring liver parenchymal cell-specific deletion of HOIP (Hoip(Deltahep) mice) by

74 rt here that mice with embryonic neural stem-cell-specific deletion of Llgl1 (Nestin-Cre/Llgl1(fl/fl)

75 ucosal damage, we engineered mice carrying a cell-specific deletion of Nod2 in villin and Lyz2-expres

76 Using mice with an intestinal epithelial cell-specific deletion of PPARdelta, we show that intest

77 In addition, we studied AAI in mice with a T cell-specific deletion of recombination signal-binding p

78 We in this study report that B cell-specific deletion of relb led to only a slight decr

79 B cell-specific deletion of T-bet was also associated with

80 T cell-specific deletion of talin in Tln1(fl/fl)Cd4(Cre) m

81 mice with a cardiomyocyte- or smooth muscle cell-specific deletion of the BK (CMBK or SMBK knockouts

82 stigation of mice with intestinal epithelial cell-specific deletion of the p38alpha gene, we find tha

83 equired for the acquisition of the dendritic-cell-specific demethylation and expression signature, fo

84 Regulatory T cell-specific demethylation region (TSDR) demethylation,

85 r genotype; however, PG shows photosynthetic cell-specific differential localization depending on the

86 rolling a core transcriptional programme for cell-specific differentiation.

87 Mice with ductal cell-specific disruption of Pten but not control mice de

88 In analyses of mice with ductal cell-specific disruption of Pten, with or without activa

89 atory SNPs depend on inadequate knowledge of cell-specific DNA binding motifs.

90 xpanded minor clones and obtained epithelial cell-specific DNA/RNA for quantitative NGS analysis.

91 Transcription factor control of cell-specific downstream targets can be significantly al

92 pirical Bayes approach to reliably model the cell-specific dropout rates and amplification bias by us

93 estigated associations in this study between cell-specific dynamic signaling pathways and drug sensit

94 Moreover, cell-specific effects of CXCR4 in the arterial wall and

95 Due to its many functions and cell-specific effects, the consequences of TGF-beta sign

96 ingly, mice with gastrointestinal epithelial cell-specific Egfr deletion demonstrated no differences

97 tion-induced cytidine deaminase (AID) is a B-cell-specific enzyme that targets immunoglobulin genes t

98 Here, we show that PGE2 uses cell-specific EP2 receptor-mediated increases in Ca(2+)

99 Here, using a beta-cell specific epidermal growth factor receptor (EGFR) nu

100 LigA (LK90) based B-cell specific epitopes were predicted and synthesised as

101 T cell-specific Etv5-deficient and littermate control mice

102 We constructed cell-specific executable models of the signaling axis, c

103 ranscripts were validated by qPCR to confirm cell specific expression in microdissected tissues, as w

104 Cell-specific expression levels, pathway cross-talk, and

105 Treg-cell-specific expression of an Akt-insensitive Foxo1 mut

106 its primary islet cell counterpart including cell-specific expression of beta (e.g., Pdx1) and alpha

107 We found that T cell-specific expression of Bim during early/cortical, b

108 ration of transgenic mice with smooth muscle cell-specific expression of either USP20 or its catalyti

109 Mice with acinar cell-specific expression of Kras(G12D) were crossed with

110 he first in vivo genetic evidence of sensory cell-specific expression of this unusual co-receptor and

111 However, only few genes with egg cell-specific expression or defects have been identified

112 Many cell-specific factors may be at play, including higher K

113 transcriptional start sites of B-cell- and T-cell-specific factors.

114 B cell-specific Fcmr(-/-) mice lacked robust clonal expans

115 tivity (R (2) = 0.74) without the use of any cell-specific fitting parameters.

116 mproved vascular permeability of endothelial cell-specific Fli1-knockout mice by increasing the expre

117 flammatory components of SSc and endothelial cell-specific Fli1-knockout mice recapitulating SSc vasc

118 CR transgenic model of GVHD, wherein TS1 CD4 cells specific for a model minor histocompatibility Ag (

119 TRAPeS with transcriptome analysis of CD8+ T cells specific for a single epitope from Yellow Fever Vi

120 aive B cells was mirrored in a population of cells specific for an Ag to which these individuals were

121 ence of ACPAs in the absence of detectable T cells specific for citrullinated antigens: ACPAs could a

122 y HSV-specific CD8 T cells compared to CD8 T cells specific for control viruses, Epstein-Barr virus (

123 & Microbe, Moguche et al. (2017) show that T cells specific for different immunodominant vaccine anti

124 The phenotype and function of CD8(+) T cells specific for each epitope were compared in HLA-A*0

125 In blood samples from controls, CD4(+) T cells specific for FlaX, A4-fla2, or YidX had a T-helper

126 CD4(+) T cells specific for human CMV (HCMV) are elevated in HIV(

127 We isolated circulating CD4(+) T cells specific for immunoglobulin-derived neoantigens an

128 Importantly, CD4(+) T cells specific for mycobacterial ribosomes accumulate to

129 leukemic effects can be delivered by donor T cells specific for particular minor histocompatibility (

130 Transduced ANS8 CAR T cells specific for the A2 domain proliferated in respons

131 IFN-gamma and IL-17-producing cells specific for the hemagglutinin and nucleocapsid pr

132 y of these mice to expand epitope-specific T cells specific for the model antigen ovalbumin expressed

133 CD4 T cells specific for these HLA class II molecules recogniz

134 1 phenotype; a larger proportion of CD4(+) T cells specific for these proteins in patients with CD ha

135 iven cancers is to elicit cytotoxic CD8(+) T cells specific for virus-derived peptides.

136 Inducible beta-cell-specific FoxM1 deficiency also blocks compensatory

137 s the sole iron exporter in mammals, but its cell-specific function and regulation are still elusive.

138 However, the cell-specific function, downstream mechanisms, or signal

139 4 upstream signalling and instruct dendritic-cell-specific functional DNA methylation changes.

140 embranes, which can bestow nanocarriers with cell-specific functionalities.

141 nhancers are regulatory elements that govern cell-specific functions and harbor disease-associated se

142 uolation along the endosomal system, but the cell-specific functions of PIKfyve in vivo remain unclea

143 enhancers: loci critical for pathologies and cell-specific functions.

144 We previously identified a T cell-specific Gata3 enhancer (Tce1) lying 280 kb downstr

145 ated by retinoic acid gene 8 (Stra8), a germ cell-specific gene activated during meiotic commitment.

146 /E) of lung alveolar epithelial type I (AT1) cell-specific gene aquaporin-5 (Aqp5).

147 mouse is commonly used for conditional hair cell-specific gene deletion/reporter gene activation in

148 cues that tailor the chromatin landscape for cell-specific gene expression programs.

149 riptional regulator that antagonizes T and B cell-specific gene expression programs.

150 Cell-specific gene expression was widely disturbed in in

151 and that loss of GATA6 greatly affects beta-cell-specific gene expression.

152 age differentiation with curated phenotypes, cell-specific gene functions and a multiscale model.

153 s) and associated with highly expressed germ cell-specific genes and histone retention in mature sper

154 In this context, B cell-specific genes and mTOR signaling were associated w

155 ze the transcription factor STAT5 to control cell-specific genes at a larger scale than universal gen

156 sion program is followed by activation of TS cell-specific genes by CAG factors.

157 Widespread expression of donor-cell-specific genes was observed in inappropriate cell t

158 tly regulate the expression of multiple germ cell-specific genes, including Asz1 In addition, conditi

159 ial expression analysis uncovered new immune-cell-specific genes, including novel immunoglobulin-like

160 essary for expression of four embryonic stem cell-specific genes.

161 istinct developmental states, including germ cell-specific genes.

162 Cell-specific genetically encoded photosensitizing prote

163 was attenuated in islets isolated from beta-cell-specific Ghsr knockout MIP-Cre/ERT;Ghsr(f/f) mice.

164 In vivo, T-cell-specific GR deletion in pregnant animals undergoing

165 Using transgenic mouse models for cell-specific HIF expression, we show here that HIF1alph

166 rmones and growth factors, are essential for cell-specific HIF-1 regulation.

167 y, deletion of endothelial (but not myeloid) cell-specific HIF1alpha doubled pulmonary fibrin deposit

168 eration during repair was attenuated in ATII cell-specific HIF1alpha knockout (SftpcCreERT2(+/-);HIF1

169 osylation mutant N69L/S71V had an epithelial cell-specific hyperfusogenic phenotype.

170 The present investigation tested cell-specific immune differences in relationship to the

171 However, data on cell-specific immune effects are largely absent.

172 Organ- and cell-specific immune responses are associated with the o

173 Using beta-cell-specific, inducible PKD1 knockout mice (betaPKD1KO)

174 followed the fates of CCR2(-/-) T cells in T cell-specific inflammatory models.

175 avenous infusion, for studies in either beta-cell specific insulin receptor knock-out (betaIRKO) or c

176 e receptors 1 and 2, dectin 1, and dendritic cell-specific intercellular adhesion molecule 3-grabbing

177 These results establish the utility of cell-specific interventions in the GPe to target functio

178 tin occupancy at sites in the Igh locus is B cell specific, is correlated with histone H4 lysine 20 m

179 a focus on VE-cadherin, a major endothelial cell-specific junctional protein that controls vascular

180 We then paired this recombination with cell-specific knockdown of the netrin-1 receptor DCC to

181 P on beta-cell function by the use of a beta-cell-specific knockout of the ANP receptor with guanylat

182 stinct cellular distribution pattern through cell-specific knockouts.

183 stochemical staining revealed stronger tumor cell-specific labeling for C3 and CFB in invasive cSCCs

184 Cell-specific labeling of RNA can be profiled and imaged

185 In this study, we generated endothelial cell-specific LKB1-knockout (LKB1(endo-/-)) mice by cros

186 Here we show that beta-cell-specific loss of mTORC1 causes diabetes and beta-ce

187 Cell-specific loss of Tsc1 within nestin-expressing cell

188 Cell-specific manipulation of PKC-2 activity revealed th

189 uman CTLA4 gene in a melanocyte and melanoma cell-specific manner.

190 y circumventing the challenge of targeting a cell-specific marker.

191 KO mice had decreased expression of the beta-cell-specific markers pdx1, glut2, mafA, and nkx6.1 and

192 growth parameters by analyzing expression of cell-specific markers revealed that the explant system m

193 odies against OSM, GM-CSF, and hematopoietic cell-specific markers.

194 syndromes of DNA repair deficiency or immune cell-specific maturation or functional defects that sugg

195 By generating a beta-cell-specific Mcl-1 knockout mouse strain (betaMcl-1KO),

196 The AVM also includes cell alignment, cell-specific mechanical properties, cell growth, divisi

197 owever, it is not known whether there are ES cell-specific mechanisms regulating mitotic fidelity.

198 ce lifetime imaging microscopy (FLIM) to map cell-specific metabolic signatures in the kidneys of liv

199 issue samples, highlighting one use of these cell-specific microRNA expression data.

200 Here, we establish the landscape of human cell-specific microRNA expression.

201 miR-223, a myeloid cell-specific microRNA, is one of the most upregulated m

202 ecruitment and pri-miRNA processing to boost cell-specific miRNA production.

203 We find that embryonic stem cell-specific miRNAs mir-93b and mir-427/430/302, as wel

204 Cre, or Cdh5-CreERT2 driver lines to develop cell-specific models of Nox2 perturbation to investigate

205 Furthermore, using cell-specific models, we tailored combination therapies

206 B-cell-specific Moloney murine leukemia virus integration

207 within the SVZ/RMS/OB system resulting in a cell-specific mosaic, suggesting complex EphA4 signaling

208 for targeting HuR domains involved in cancer cell-specific multimerization.

209 One of the latter, BAIAP3, is a secretory cell-specific Munc13-4 paralog of unknown function.

210 Using T cell-specific murine lines genetically altered in expres

211 Abe et al. (2017) identify NLRP14 as a germ-cell-specific negative regulator of DNA sensing that may

212 A novel role for myeloid cell-specific neuropilin 1 in mitigating sepsis.

213 Germ cell-specific, but not Sertoli cell-specific Nhe8 disruption recapitulated the globozoo

214 were monitored in wild-type (WT) and myeloid cell-specific Nrp1 knockout (Nrp1(myel-KO)) mice fed an

215 Here, we reported that myeloid cell-specific Nrp1-deficient mice exhibited enhanced sus

216 o address this problem, we generated myeloid cell-specific Nrp1-knockout (Nrp1(myel-KO)) mice and app

217 -targeted electrophysiological recording and cell-specific optogenetic manipulation in both anestheti

218 in postmitotic cells to precisely coordinate cell-specific output.

219 have demonstrated that, although mice with T cell-specific overexpression of miR-27 harbor dysregulat

220 vivo, vascular smooth muscle cell/mesangial cell-specific overexpression of Nox5 in a mouse model of

221 Accordingly, stem cell-specific oxygen signaling pathways precisely contro

222 ouse colon tissues and intestinal epithelial cell-specific p38gamma knockout (KO) attenuates colitis

223 We review the intestinal mesenchymal cell-specific pathways that regulate these processes, wi

224 Collectively, these findings unveil distinct cell-specific patterns of E-selectin ligand expression a

225 Cell-specific patterns of microRNA expression were used

226 uced with the tamoxifen-inducible, satellite cell-specific Pax7(CreER) system in postnatal satellite

227 ingly extensive range of progenitor and beta-cell-specific Pdx1 functions.

228 Surprisingly, nerves of Schwann cell-specific Pex5 mutant mice were unaltered regarding

229 tion of either Hif1a or Hif2a in endothelial cell-specific Phd2 mutants demonstrated that the develop

230 proteome for normal IE function, providing a cell-specific pool of candidates for novel, important HC

231 e the reads aligned to this gene to estimate cell-specific preferences for splicing, mutation load, o

232 unt for the establishment and maintenance of cell-specific programmes.

233 Cre(ERTM) recombinase regulated by an acinar cell-specific promoter (Ptf1a).

234 ressing S-della under the control of a guard-cell-specific promoter was sufficient to increase stomat

235 overexpressed under the control of the guard-cell-specific promoter, GC1.

236 mmon upregulation of marginal zone B- and B1-cell-specific protein (MZB1), the expression of which id

237 THEMIS, a T cell-specific protein with high expression in CD4(+)CD8(

238 reverse-phase protein arrays, the lymphocyte cell-specific protein-tyrosine kinase (LCK) as aberrantl

239 ve expression and localization of epicardial cell-specific proteins.

240 plications after hearing onset, we show that cell-specific purinergic modulation follows a precise to

241 arly strong prediction performance, with all cell-specific R (2)>0.90 and R M S E<4.00 %.

242 For both strains, cell-specific rates of NO turnover and N2 O production r

243 le (SLAM) family of homotypic haematopoietic cell-specific receptors, we determined that phagocytosis

244 We used chemogenetics to extend D1-/D2-MSN cell specific regulation to cue-reinstated cocaine seeki

245 The sequential cell-specific regulation of autocrine/paracrine and juxt

246 er Cdx2 regulatory elements including a stem-cell specific regulatory sequence and an element that dr

247 different populations, gene expression, and cell-specific regulatory annotation can be effectively i

248 data further indicate that ATAC-seq detects cell-specific regulatory elements for cell types compris

249 t NOTCH1 transactivates MYC via binding to B-cell-specific regulatory elements, thus implicating this

250 We also perform cell-specific rescues, determining DAF-6/patched-related

251 However, to produce cell-specific responses, TGF-beta pathways are heavily r

252 We show that the germ cell-specific RNA-binding protein deleted in azoospermia

253 identify clock-relevant phosphatases, clock-cell-specific RNAi knockdowns ofDrosophilaphosphatases w

254 system, renal, and vascular levels, but the cell-specific role of Nox2 in BP regulation is unknown.

255 These results identify distinct cell-specific roles for Nox2 in BP regulation.

256 with tamoxifen-inducible, pancreatic acinar cell-specific Sec23b deletion.

257 he aptitude to triage stimuli depends on the cells' specific sensitivities to different chemoattracta

258 e the scalability of SeqUnwinder to discover cell-specific sequence features from over one hundred th

259 We investigated cell-specific signaling events underlying the immunosupp

260 IgG4, IgE, and cell-specific signatures are regulated in patients, sugg

261 the simultaneous, temporally controlled, and cell-specific silencing of multiple genes or pathways.

262 To dissect cell-specific Smad3 actions in myocardial infarction, we

263 The effects of cell-specific Smad3 loss on the infarcted heart were stu

264 We found that Treg cell-specific super-enhancers (Treg-SEs), which were ass

265 ltiple complex isoforms, including several B cell-specific surface receptors.

266 B cell-specific survival ligand concentrations were measur

267 We generated beta-cell-specific Syn-1A-KO (Syn-1A-betaKO) mice to mimic be

268 aracterized the pathogenic potential of beta cell-specific T cells, we have limited mechanistic insig

269 t sequence properties of multi-condition and cell-specific TF binding sites after controlling for une

270 To examine this possibility, beta-cell specific TFG knockout mice (betaTFG KO) were genera

271 s has resulted in an unmet clinical need for cell-specific therapy in the treatment of FSGS and other

272 Intercellular MHC transfer was donor-cell specific; thymic DC readily acquired MHC from TEC p

273 ls or re-engineer natural materials to model cell-specific tissue-like 3D modules, which can seamless

274 rrounding normal breast tissue to identify T cells specific to each, as well as their abundance in pe

275 enic mouse system in which TCR-transgenic Th cells specific to hen egg lysozyme (HEL) are adoptively

276 V persistence did not further erode memory T cells specific to LCMV.

277 CD4(+) T cells specific to the HCMV proteins studied were predomi

278 of lymphocytes and proliferation of CD8(+) T cells specific to tumor-associated antigens, resulting i

279 f effector memory CD8(+) T cells (CD8(+) TEM cells) specific to three epitopes derived from the HSV-1

280 animals lacking distinct lung APC subsets or cell-specific Toll-like receptor (TLR) 4 signaling.

281 d myotube formation, we demonstrate that the cell-specific topology of syncytial nuclei is dependent

282 R targeting a peptide of the intracellular B cell-specific transcription factor BOB1 presented in the

283 f numerous genes via the regulation of the B cell-specific transcription factor PAX5.

284 to asymmetric division and activation of the cell-specific transcription factor sigma(F), a hallmark

285 BACH2, a B-cell-specific transcription factor, plays a critical rol

286 ell as indirect in vivo measurements such as cell-specific transcriptional analysis of ABA metabolic

287 quence the 3'-end of each message to build a cell-specific transcriptional landscape.

288 Cell-specific transcriptional profiling revealed that mi

289 latory elements such as enhancers coordinate cell-specific transcriptional programmes by engaging in

290 toolset for cell-type specific profiling of cell-specific transcriptomes derived from complex biolog

291 timize parameters of FCM algorithm for human cell-specific transcriptomic data and identify robust ge

292 Strikingly, B-cell-specific transgenic overexpression of spry2 in mice

293 Dendritic cell-specific transmembrane protein (DC-STAMP) plays a k

294 silonRIbeta is a potential approach for mast cell-specific treatment of allergic diseases.

295 ns, advances in DNA sequencing indicate that cell-specific variants affect a number of phenotypes and

296 dy VDR KO, T cell-specific VDR (T-VDR) KO, B cell-specific VDR (B-VDR) KO, and vitamin D deficient mi

297 Whole-body VDR KO, T cell-specific VDR (T-VDR) KO, B cell-specific VDR (B-VDR

298 Endothelial cell specific Vegfr-2 disruption in newborn mice not onl

299 ed by a large complex bound to DNA by the ES cell-specific zinc-finger protein ZFP809.

300 The wild-type (WT) form of the beta-cell-specific Zn(2+) transporter, ZNT8, is linked to T2D