ライフサイエンスコーパス: cell-specific

1 ross the Orthopneumovirus genus and not host-cell specific.

2 Cell-specific (13) C uptake was influenced by temperatur

3 We found that cell-specific (13) C uptake was similar for both groups

4 Using computer simulations, we generate cell-specific 3D chromosomal structures and compare them

5 T cell specific ablation of IL-1R1 decreased tumor-elicite

6 genetic, pharmacologic, RNAscope assay, and cell-specific ablation methods, we dissected a neural ci

7 T cell-specific ablation of CD83 expression resulted in ag

8 T cell-specific ablation of Dot1L resulted in loss of naiv

9 erate with IL-25 to activate ILC2s, and tuft-cell-specific ablation of leukotriene synthesis attenuat

10 Here we report that T(reg) cell-specific ablation of mitochondrial respiratory chai

11 Rgamma reprogramming is altered in mice with cell-specific ablation of the dopamine D2 receptor (D2R)

12 T reg cell-specific ablation of the Rag family small GTPases R

13 nsition driver transcription factors in stem cell-specific accessible regions that become repressed i

14 or of cytokinesis 2 (DOCK2), a hematopoietic cell-specific actin effector protein, has been implicate

15 cs of the channelrhodopsin-2 (ChR2) used for cell-specific activation are too slow to follow the high

16 aptic plasticity is associated with parallel cell-specific activity of MMP-2 and MMP-9.

17 The T cell-specific adaptor protein (TSAd), encoded by the SH2

18 Upon T cell-specific alpha-CD3, alpha-CD28 stimulation, MAIT ce

19 n vitro, with particular impact on a Schwann cell-specific alternative promoter.

20 ation, and regulation apparently arises from cell-specific alternative splice variants of the single

21 Cell-specific alternative splicing modulates myriad cell

22 r studies define the molecular mechanisms of cell-specific alternative splicing of a functionally val

23 In sensory neurons, cell-specific alternative splicing of the presynaptic Ca

24 Moreover, the finding that proximal tubule cell-specific amphiregulin knockout mice were protected

25 Tissue- or cell-specific analysis of gene expression has potential

26 er, these data confirm that M2 function is B cell-specific and demonstrate that M2 primarily function

27 T have prompted identification of other more cell-specific and functionally relevant biomarkers.

28 Using cell-specific and genetically targeted approaches we hav

29 Relative to females, males had reduced B cell-specific and NK cell-specific transcripts and an in

30 These results imply cell-specific and pathway-specific effects of GCs, and a

31 ed Ag presentation to CD8 T cells, revealing cell-specific and temporal features involved in the gene

32 LXRalphabeta's functions are cell specific, and the resulting phenotypes are mutually

33 an gain power as fine-mapping resolution and cell-specific annotations become richer.

34 In this Review, we use a layer-specific and cell-specific approach to integrate physiological accoun

35 Using in vivo cell-specific approaches, we observed that loss of LXR f

36 rting cell lineage and becomes pre-granulosa cell-specific as the gonads differentiate.

37 hagy to T-cell allo-immunity, we generated T-cell-specific Atg5 knock-out mice.

38 r, an animal model that could recapitulate T cell-specific autoimmune responses by initiating and sus

39 We show that germ cell-specific BAF knockdown causes phenotypes that mirro

40 In endothelial cell-specific Bmpr2-knockout mice unable to stabilize p5

41 Cell specific CB1 deletion in dorsal telencephalic gluta

42 nk conditioning, and both global and granule-cell-specific CB1KOs display normal cerebellum-dependent

43 Finally, cerebellar granule-cell-specific CB1KOs exhibit normal eyeblink conditionin

44 ng macrophage-specific (CD14) but not CD4+ T cell-specific (CD3) antibodies, suggesting that M-tropic

45 Assessment of beta cell-specific CD8(+) T cell anatomical distribution and

46 ovide new insight into the longevity of beta cell-specific CD8(+) T cell responses and document the u

47 The pool of beta cell-specific CD8(+) T cells in type 1 diabetes (T1D) su

48 ell 'multipotency index' and found that beta cell-specific CD8(+) T cells retained a stem-like epigen

49 iated epigenetic programs in individual beta cell-specific CD8(+) T cells.

50 pment with submission of 10,932 novel tissue/cell specific CDS to the NCBI database for this importan

51 elatively little is known about accompanying cell-specific changes in gene expression.

52 SATB1 is an important T-cell specific chromatin organizer in cutaneous T-cell ly

53 transcription factor Foxp3 establishes Treg-cell-specific chromatin architecture indirectly, mostly

54 Integration of cell-specific chromatin data with a bulk tissue study of

55 ms of Raf activation, and point to targeting cell-specific, chromatin-accessible, and parallel (or re

56 Pathway- and cell-specific circuit control was also facilitated by en

57 The epithelial cell-specific clathrin adaptor protein (AP)-1B has a wel

58 Here we show that OCA-B, a B cell-specific coactivator essential for germinal center

59 utational framework, can be used to discover cell-specific cofactors, screen for synthetic cooperativ

60 e-body miR-155 knockout mice and endothelial cell-specific conditional miR-155 (VEC-Cre-miR-155 or VE

61 Herein, two different strains of cell-specific conditionally deficient mice were used to

62 ype specificity, preventing investigation of cell-specific contributions of protein synthesis.

63 ated that a promoter variant is causal for T cell-specific control of HLA-DQB1 expression.

64 Bmp1 and Tll1 genes in mice using a Schwann-cell-specific Cre causes ectopic clustering of nodal pro

65 Finally, using a cell-specific CRISPR-Cas9 approach, we demonstrate that

66 d flow-induced vasodilatation in endothelial cell-specific CSE knockout mice and in a small collectiv

67 B cell-specific cullin 3-deficient mice show reduced devel

68 NK cell-specific deletion of Adrb2 resulted in impaired NK

69 ulin into knockout mice with proximal tubule cell-specific deletion of amphiregulin's releasing enzym

70 Upon cell-specific deletion of C/EBPbeta in CD11c(+)MHCII(hi)

71 n sharp contrast, mice harboring endothelial cell-specific deletion of IDO show an improvement of car

72 reover, bone marrow chimeric mice with CD4 T cell-specific deletion of IL-10 increased PF4/heparin-sp

73 TCR activation, as mice engineered with a T cell-specific deletion of IRAP fail to develop efficient

74 this study, we define the consequences of B cell-specific deletion of PIK3IP1.

75 Cell-specific deletion of Plk1 in embryonic myoblasts le

76 Hematopoietic cell-specific deletion of PTN suppressed CML development

77 ed intestinal tissues from mice with myeloid cell-specific deletion of PTPN2 (Ptpn2-LysMCre mice) and

78 We found that B cell-specific deletion of Ship2, but not of its close ho

79 Using a mouse model with inducible beta-cell-specific deletion of the Akt1 gene (betaA1KO mice),

80 Myeloid cell-specific deletion of the neutrophil cytosolic facto

81 is independent of T-cell exhaustion, using B-cell-specific deletion of the transcription factor IRF4

82 ssing a point mutant thereof, or mice with T cell-specific deletion of the transcription factor RUNX1

83 Here, we report that B cell-specific deletion of the X-linked gene, Cosmc, and

84 Cell-specific deletion reveals a requirement for GATA6 i

85 stand their biology, but also may permit the cell-specific delivery of small molecules to improve the

86 idazolate frameworks (ZIFs) for targeted and cell-specific delivery of this genome editing machinery.

87 a1 integrin-blocking antibody or endothelial cell-specific depletion of beta1 integrin attenuated FMD

88 excitatory-inhibitory balance is dynamic and cell specific, determined by distinct plasticity rules a

89 We map the cell-specific differential expression of prognostically

90 nd validated Gal4-UAS based CRISPR tools for cell-specific disruption of key molecular clock componen

91 ows efficient analysis of aged and cancerous cell-specific DNA methylation patterns for diagnostic an

92 These data provide insight into cell specific effects of PRKN mutations, in particular i

93 oid action and emphasize the multifactorial, cell-specific effects of these drugs, with potential imp

94 sues, it is needed to design sgRNA with high cell-specific efficacy and specificity.

95 ow transplantation, and in mice with myeloid cell-specific EGFR deficiency.

96 We validated pacemaker cell-specific elements in the SHOX2 and TBX3 loci.

97 , using eFOV-microendoscopes we demonstrated cell-specific encoding of behavioral state-dependent inf

98 to open chromatin, and classify sets of stem cell-specific, endoderm-specific, and shared accessibili

99 with only 100% lithium excess can deliver a cell specific energy of >300 W h kg(-1) with a Coulombic

100 alyses showed that these five loci contained cell-specific enhancers that differed between normal lum

101 pecific phospholipase C gamma 2 (PLCG2), a B cell-specific enzyme that stimulates intracellular Ca(2+

102 by characterizing the intestinal epithelial cell-specific EP4 knockout (EP4 cKO) mice.

103 essential regulatory elements for driving M-cell-specific expression in rice leaves.

104 from three C(4) grass species could drive M-cell-specific expression of a reporter gene in rice.

105 Hair cell-specific expression of the known HSP70 receptor TLR

106 tion and may have implications for tissue or cell-specific expression of the virus.

107 Transgenic, hair cell-specific expression of Tmc2b-mEGFP rescues the beha

108 ns in individual samples and estimate tissue/cell-specific expression profiles.

109 pstream element(s) is required for driving M-cell-specific expression.

110 e colon is mediated by multiple enzymes with cell-specific expression.

111 etween cell types, implying the influence of cell-specific factors in dictating turnover rate.

112 uitin ligase complex can recruit endothelial cell-specific factors, AGO2 (associated with angiogenesi

113 Integration of cell-specific fate mapping, single-cell genomics, and hu

114 odds ratio (OR) = 58, P = 1 x 10(-75)) from cell-specific features, including chromatin conformation

115 (b) a cell-specific methanogenic activity to cell-specific fermentation activity ratio of >1000.

116 ) mice and in SIP cells from mice expressing cell-specific fluorescent reporters purified by fluoresc

117 tline an immunotherapy in which endogenous T cells specific for a noncancer antigen are retargeted to

118 We show how the same approach of CAR T cells specific for CD30 (CD30.CAR-Ts) can be used to tre

119 Similarly, a fraction of naive human B cells specific for clinically-relevant Ags derived from

120 he presence of a broad repertoire of naive T cells specific for cryptic H1-HA peptides and demonstrat

121 tegies are not effective in the absence of T cells specific for displayed tumor antigens.

122 s a common feature of populations of naive B cells specific for foreign Ags and a moderate level of c

123 Using G9Calpha(-/-)CD8(+) T cells specific for proinsulin, we studied the mechanisms

124 hese results show that self-HLA-restricted T cells specific for self-antigens such as MiHA in MiHApos

125 tionality throughout latency, while CD8(+) T cells specific for subdominant epitopes undergo function

126 ctively expand both low- and high-affinity B cells specific for the antigenic bait during immunizatio

127 ntially the result of cross-recognition by T cells specific for the common cold coronaviruses.

128 ss-recognition of the novel coronavirus by T cells specific for the common cold coronaviruses.METHODS

129 In vitro expansion studies suggested that T cells specific for the HCoV-NL63 spike protein in this i

130 against the parasite is mediated by CD8(+) T cells specific for the immunodominant CSP-derived epitop

131 In the C57BL/6 mouse, CD8(+) T cells specific for the immunodominant epitope from glyco

132 cle, we explore the contribution of CD8(+) T cells specific for the major antigenic epitope for HSV-1

133 We isolated B cells specific for the SARS-CoV-2 envelope glycoprotein

134 ptide pools.CONCLUSIONHDs have circulating T cells specific for the spike proteins of HCoV-NL63, HCoV

135 interferon gamma (IFN-gamma)-producing CD4 T cells specific for VZV glycoprotein E and all other stru

136 ain-Containing Protein (FCHSD2) has a cancer-cell specific function in regulating CME in non-small-ce

137 plication, suggesting that Alms1a has a stem-cell-specific function in centrosome duplication.

138 n controversial, owing to differences in the cell-specific functions of AhR and the different activat

139 evidence to suggest that some expansins have cell-specific functions, in root hair and pollen tube de

140 beta-cell-specific Furin knockout (betaFurKO) mice are glucos

141 cretion response of islets from HFD-fed beta cell-specific Galpha(z)-null mice is significantly impro

142 ed diabetes is beta-cell autonomous, as beta cell-specific Galpha(z)-null mice phenocopy the full-bod

143 ture was aligned to differential patterns of cell-specific gene expression in the fetal cortex.

144 Activation of beta-catenin-driven and stem cell-specific gene expression in the presence of Apc (Mi

145 d assess variability in cell composition and cell-specific gene expression in the skin of patients wi

146 ate and performed a computational search for cell-specific gene expression patterns.

147 ealth of information about the mechanisms of cell-specific gene expression, chromosome dynamics, prot

148 tical player in the regulation of tissue and cell-specific gene expression.

149 m multiplex families to identify significant cell-specific gene network alterations in SCZ, these stu

150 hts into relevance of noncoding variants for cell-specific gene regulation and for disease associatio

151 DNA binding of MEF2A and into its role in B cell-specific gene regulation.

152 dimensional organization of DNA to establish cell-specific gene-expression programs.

153 sociated genes as well as activation of hair cell-specific genes required for normal functional matur

154 nor zygotic genome activation (ZGA) genes (2-cell-specific genes) in pluripotent and differentiated c

155 itecture, and perturbs transcription of hair cells specific genes during zebrafish development.

156 Using cell-specific genetic tracing with an Ascl1(CreERT2) mou

157 Cis-regulomes underlying immune-cell-specific genomic states have been extensively analy

158 Here, we identify the germ cell specific Golgi glycoprotein MGAT4D as a protector o

159 e model for crescentic GN, in mice lacking T cell-specific IL-6Ra.

160 ng approach and expands the possibilities of cell-specific imaging and pharmacology.

161 ntification of gp120 glycopeptide-induced, T cell-specific immune responses offers a foundation for d

162 This CTLA-4-dependent inhibition was Tfh cell specific in that CTLA-4 expression by Tfh cells was

163 Using cell-specific inducible genetics, we find that a Wnt4-Rh

164 approach by first generating mice with beta-cell-specific inducible overexpression of Bmal1 (core ci

165 ating that the adopted technique can provide cell-specific information and knowledge, closely linked

166 Purkinje cell-specific inhibition of protein kinase C decreased a

167 The mechanisms governing cell-specific injury in AMR remain unclear.

168 Surprisingly, B cell-specific IRF-1 deficiency attenuated the establishm

169 Further, we found that B cell-specific IRF-1 deficiency led to reduced levels of

170 Moreover, the expression of stromal cell-specific ISLR and ETS1 significantly increased in i

171 irway cultures establish NEK10 as a ciliated-cell-specific kinase whose activity regulates the motile

172 Mice with germ cell-specific Klotho (gcKL) deficiency neither had a cha

173 Global or endothelial-cell-specific knockdown of tmem33 impairs multiple downs

174 al shRNA and conditional mutation to produce cell-specific knockdown or deletion of a key NMDAR subun

175 urther analysis of GABA subtypes showed that cell-specific knockdown or deletion of GluN2B in Sst int

176 Mice with a Purkinje-cell-specific knockout (KO) of the calcium-activated K+

177 ase was absent from PIs from NOX4-null, beta-cell-specific knockout mice (NOX4betaKO) (though not fro

178 es, as well as the elaborate conditional and cell-specific knockout mouse studies that brought the ro

179 In this study, we show that mice with B cell-specific knockout of caspase-9 had decreases in GC

180 GC B cells and Ab production in mice with B cell-specific knockout of caspase-9.

181 e generated a mouse model with hematopoietic cell-specific knockout of Hopx (Hopx(-/-)).

182 Cell-specific knockout of KLF4 in pericytes fully replic

183 the SSRI, fluoxetine, are abolished by mossy cell-specific knockout of p11 or Smarca3 or by an inhibi

184 s and showed that its elimination in myeloid cell-specific L13a knockout mice (L13a KO) increased ath

185 tic manipulation of cells, intracellular and cell-specific labeling has become possible.

186 racterizing and evaluating methodologies for cell-specific labeling of biomolecules.

187 s a growing interest in molecular imaging of cell-specific lineage markers of the immune system using

188 (2020) show by cell-specific lipidomics that Trem2 deficiency leads to

189 very and functional elucidation of a human B cell-specific lncRNA with high levels of expression in t

190 accompanied by a male-specific decline in B-cell specific loci.

191 In vivo, granulosa cell-specific loss of Lats1/2 caused the ovarian parench

192 eoplastic changes associated with epithelial cell-specific loss of Trp53.

193 express the cortactin homolog hematopoietic cell-specific lyn substrate-1.

194 Using mouse genetic tools for cell-specific manipulation, we discovered excitatory neu

195 isolate and genetically manipulate PSCs in a cell specific manner.

196 o and alter the transcriptional program in a cell-specific manner in a mouse model of synpolydactyly.

197 e models targeting either whole ERalpha in a cell-specific manner or ERalpha subfunctions (membrane/e

198 etic protein can stimulate regeneration in a cell-specific manner, but also provide a blueprint of ho

199 nels and receptors occurs in a concerted and cell-specific manner, resulting in the appearance of bra

200 eraction between opioids and pheromones in a cell-specific manner.

201 its cellular and exosomal localization in a cell-specific manner.

202 ther herpesviruses to reinforce latency in a cell-specific manner.

203 debCAM) that can automatically detect tissue/cell-specific markers, determine the number of constitue

204 Using cell-specific markers, we demonstrate that pericytes rat

205 n neurons and astrocytes further highlighted cell-specific mechanisms to counteract redox imbalance.

206 established as an inducible and mesenchymal cell-specific mediator of disease progression in cancer

207 We discovered novel malignant-cell-specific metabolic vulnerabilities targetable by sm

208 gulates microglia polarization, we highlight cell-specific metabolome reprogramming as a promising no

209 fermentation ratio higher than 0.6 and (b) a cell-specific methanogenic activity to cell-specific fer

210 We examined the effect of cancer cell-specific MHCII (csMHCII) expression in lung adenoca

211 r distribution in wild-type and intercalated cell-specific mineralocorticoid receptor knockout mice.

212 tion of target sequences for skeletal muscle cell-specific miR-206.

213 er new database feature is the prediction of cell-specific miRNA targets.

214 Altogether, these data indicate that T cell-specific miRNAs play pivotal roles in regulating li

215 -suppressive role of KDM6A deficiency with a cell-specific molecular mechanism that underlies PDAC su

216 type natriuretic peptide], ESM [endothelial cell-specific molecule]-1, cathepsin L1, osteopontin, an

217 We used cell-specific monoclonal antibodies to eliminate neutrop

218 , we identified a mechanism whereby opposing cell-specific motogenic functions of a multifunctional i

219 this, we first tested three inducible mural cell-specific mouse lines using a sensitive Ai14 reporte

220 We observed that some cell-specific mRNAs accumulate non-homogenously within c

221 e of an interaction network and/or selecting cell-specific networks has a limited effect on accuracy.

222 Our results advance our understanding of how cell-specific neurobiological gradients produce a hierar

223 Recording cell-specific neuronal activity while monitoring behavio

224 Myeloid-cell-specific Nlrp12-deficient mice display a heightened

225 Here we show that T cell-specific Notch deficiency in mice prevented house d

226 Although the endothelial cell-specific NRP1 knockout mice did not exhibit any sig

227 Smooth muscle cell-specific overexpression of Smad7 completely suppres

228 The VAM method computes cell-specific pathway scores to transform a cell-by-gene

229 udy common herpesvirus assembly pathways and cell-specific pathways for membrane reorganization.IMPOR

230 revious screens, we succeeded in finding new cell-specific patterns, which we validated by in situ an

231 in meiosis by generating the first male germ cell-specific Phb-cKO mouse.

232 The MAIT cell-specific phenotype did not extend to other innate l

233 gene is upstream of the gene encoding the B cell-specific phospholipase C gamma 2 (PLCG2), a B cell-

234 We are just beginning to unravel the cell-specific, physiological roles served by BK channels

235 ometry to assess changes in BNST plasticity, cell-specific physiology, and cellular activity profiles

236 However, T cell-specific PKM2 deletion impairs Th17 cell differenti

237 endow excitatory circuits with pathway- and cell-specific plasticity.

238 (DT) receptor was expressed behind the hair-cell specific Pou4f3 promoter.

239 The scRNA-seq, comprehensive, cell-specific profiles provide a valuable resource for e

240 dulthood, with greater impact on the Schwann cell-specific promoter.

241 , 2020) reveal an essential function of germ cell-specific protein GCNA in the genome maintenance of

242 HMCES (5hmC binding, embryonic stem cell-specific-protein), originally identified as a prote

243 ction of viral load, while transcripts for B cell-specific proteins and neutrophil chemokines were el

244 anatomy-based approach, as the identities of cell-specific PSC molecular markers have remained elusiv

245 T-cell-specific PTPN2 deficiency prevented tumours forming

246 morphological changes were assessed in mural cell-specific R26-mTmG reporter mice, in which low doses

247 When sample preparation is accounted for, cell-specific rates increase and are more consistent wit

248 receptor X2 (MRGPRX2) is regarded as a mast cell-specific receptor mediating non-IgE-dependent activ

249 Cell-specific receptor Notch3 signaling independently or

250 Cell-specific recruitment of co-regulatory complexes by

251 geted imaging mass spectrometry demonstrates cell-specific reduction of phospholipids containing 22:6

252 cell context-dependent effect resulted from cell-specific regulation of extracellular signal-regulat

253 Primary endothelial cell-specific regulation of hypoxia-inducible factor (HI

254 ecific transcriptional regulators and infers cell-specific regulation of protein-coding genes, long i

255 of neuron-specific genes, that ASEs provide cell-specific regulatory information with evidence for c

256 s accompanied by the appearance of quiescent cell-specific repressors and rewiring of the interaction

257 ents demonstrate the in vivo sequelae of the cell-specific requirements for the functions of AK2 and

258 y AD, but suction blistering was superior in cell-specific resolution for high-abundance transcripts

259 al smoking response networks and hundreds of cell-specific response genes, redefining the penetrance

260 single-cell omics approaches to characterize cell-specific responses to drugs or environmental stimul

261 tes, connect these into lineages, and define cell-specific responses to smoking.

262 o promoted Cd40 mRNA association with Muller cell-specific ribosomes isolated from the retina of Ribo

263 ngle-cell RNA sequencing in combination with cell-specific Ribotag RNA profiling, assay for transposa

264 lations, making it ideal for high-resolution cell-specific RNA labeling.

265 However, the cell-specific role of BRD4 in adult cardiomyocytes remai

266 CD8+ effector, CD4+ memory, and regulatory T-cell-specific signatures.

267 We also created a beta cell-specific SMAD7-overexpressing mouse line by crossin

268 t mediator and contributor in heroin-induced cell-specific synaptic plasticity.

269 as, however, been limited due to the lack of cell-specific targeting methods in brain tissue or livin

270 is biomimetic approach to match the needs of cell-specific targeting, which is unquestionably the mos

271 milar in severity to that triggered by T reg cell-specific TCR deficiency.

272 rly on scRNA-seq data and progress on single cell-specific techniques has been limited.

273 A cascade of three cell-specific TFs and two RBPs are combinatorially requi

274 These changes were modeled by Treg cell-specific Tgfb1 monoallelic inactivation, which indu

275 very promises benefits in the form of single-cell-specific therapeutic and diagnostic capabilities.

276 Thus, B cell-specific Tlr9 deficiency unlinked disease from auto

277 Critically, B cell-specific Tlr9 overexpression resulted in ameliorate

278 e, SLIT enhanced proportions of regulatory T cells specific to RGP.

279 cy of antiviral effector memory CD4(+) T(EM) cells specific to two immunodominant epitopes derived fr

280 splenic B cells purified from young adult B cell-specific Traf3 (-/-) and littermate control mice.

281 IRF8 is an immune-cell specific transcription factor and its expression is

282 wever, the expression of Foxp3, regulatory T cell-specific transcription factor, was enhanced in the

283 lity that RNAPII pool size generally affects cell-specific transcription programs in genome instabili

284 ted as likely candidates for sustaining germ cell-specific transcription programs throughout the peri

285 Asymmetric division also triggers cell-specific transcription, which initiates septal pept

286 tructure and function as well as genetic and cell-specific transcriptional data.

287 nterpreters of the epigenome that facilitate cell-specific transcriptional programs and are therapeut

288 Transcription factor footprinting implicates cell-specific transcriptional regulators and infers cell

289 ouse strains enabled inference of common and cell-specific transcriptional regulators.

290 aenorhabditis elegans early embryos generate cell-specific transcriptomes despite lacking active tran

291 such as patch-clamping and live imaging, and cell-specific transcriptomic analyses.

292 Using paired, cell-specific transcriptomic data and causal inference t

293 es, males had reduced B cell-specific and NK cell-specific transcripts and an increase in inhibitors

294 , we uncover new sets of female gametophytic cell-specific transcripts with predicted biological role

295 Our findings provide evidence for a cell-specific translation program during consolidation o

296 st marker genes TRAP, Cathepsin K, dendritic cell-specific transmembrane protein (DCSTAMP), nuclear f

297 notypes are recapitulated in intestinal stem cell-specific Tsc1 knockout mice.

298 nt cell lines on a global scale, but notable cell-specific variations emerge in the detailed spatial

299 We generated Paneth cell-specific VDR knockout (VDR(DeltaPC)) mice to invest

300 Region- and endothelial cell-specific whole transcriptomic analyses revealed mol