ライフサイエンスコーパス: terminally differentiated

1 t majority of symbionts has been regarded as terminally differentiated.

2 rapidly than adult cells and quickly became terminally differentiated.

3 sts, withdraw from the cell cycle and become terminally differentiated.

4 tinued proliferation and clonal expansion of terminally differentiated acinar cells in all major sali

5 mia efficiently stimulates the conversion of terminally differentiated acinar cells to beta-like cell

6 demonstrate that binuclear acinar cells are terminally differentiated acinar cells.

7 s of unique transcriptional states to become terminally differentiated acinar, ductal and myoepitheli

8 Conversion of mesenchymal stem cells into terminally differentiated adipocytes progresses sequenti

9 Here, we identified a subset of lincRNAs in terminally differentiated adult human retinal neurons ba

10 ficantly elevated frequencies of circulating terminally differentiated alpha-NAC-specific CD8(+) T ce

11 hils, a leukocyte subset generally viewed as terminally differentiated and catabolic.

12 e mainly naive and CD26(high) T cells appear terminally differentiated and exhausted.

13 had a higher level of TCR signaling and were terminally differentiated and exhausted.

14 Resting CMV-specific CD8 T cells were terminally differentiated and expressed high levels of t

15 3 (-)2B4(+) cells; in turn, these cells were terminally differentiated and highly susceptible to cell

16 chynomene spp. and that these bacteroids are terminally differentiated and polyploid, similar to bact

17 osphohydrolase, down-regulates dNTP pools in terminally differentiated and quiescent cells, thereby i

18 Mature neutrophils are terminally differentiated and short-lived with a high tu

19 n tumours consist of distinct populations of terminally differentiated and stem-like cells.

20 monstrating that this tolerized state is not terminally differentiated and that tolerized DCs can rec

21 In vivo, type I cells are thought to be terminally differentiated and their ability to give rise

22 at mammalian adult cardiomyocytes (ACMs) are terminally-differentiated and are unable to proliferate.

23 t neuronal populations that are postmitotic, terminally differentiated, and non-regenerating, depend

24 ranscriptionally distinct from conventional, terminally differentiated, antigen-induced peripheral bl

25 or the T-box transcription factor T-bet lack terminally differentiated antitumor CD27(low)KLRG1(+) NK

26 The hepatic NKG2C+ population was terminally differentiated, as in the circulation, but de

27 Glioblastoma can originate from terminally differentiated astrocytes and neurons, which

28 tudied multiple myeloma (MM) as a model of a terminally differentiated B cell malignancy that selecti

29 lts from clonal expansion of an Ig-secreting terminally differentiated B cell.

30 Ig secretion by terminally differentiated B cells is an important compon

31 originate from plasma cells (PCs), which are terminally differentiated B cells.

32 marrow are heterogeneous, consisting of (a) terminally differentiated B-1-derived plasma cells expre

33 erials, which is difficult for unculturable, terminally differentiated bacteroids.

34 In contrast, ablation of Foxo1 in terminally differentiated beta-cells did not increase be

35 ossible to deliver safely stem cell-derived, terminally differentiated, biologically and genetically

36 Genome-wide mapping of H4K16ac in terminally differentiated blood cells, along with functi

37 transition from hematopoietic stem cells to terminally differentiated blood cells.

38 at coordinate the final mitotic divisions of terminally differentiated bone marrow (BM) erythroid cel

39 in infarcted hearts and emerged de novo into terminally differentiated cardiac myocytes, smooth muscl

40 unchanged "educated" (CD11b(+)CD27(+)) and "terminally differentiated" (CD11b(+)CD27(-)) NK cell fre

41 production--are specifically associated with terminally differentiated (CD27(-)) allergen-specific CD

42 s thematuration of NK cells from CD27high to terminally differentiated CD27low NK cells, we used Rag-

43 cancer regression and TIL persistence and a terminally differentiated CD39-positive state (CD39(+)CD

44 trophoblast stem cells and distinct types of terminally differentiated CD4(+) T cells.

45 ained significantly increased frequencies of terminally differentiated CD57+KLRG1+ cells in CMV serop

46 rated a greater fall in the concentration of terminally differentiated CD8 effector memory T cells (T

47 Although terminally differentiated CD8 T cells became the predomi

48 ion leads to acute loss of antigen-specific, terminally differentiated CD8 T cells, possibly through

49 at is associated with a relative increase of terminally differentiated CD8 Temra cells protects again

50 vere disease stage had a higher frequency of terminally differentiated CD8(+) T cells than patients a

51 d that an increased proportion of senescent, terminally differentiated CD8(+) T cells would identify

52 ncluding expanded effector and post-effector terminally differentiated CD8(+) T cells.

53 s to the accumulation of more cytotoxic, but terminally differentiated, CD8(+) TEX cells.

54 These results indicate that a terminally differentiated cell type derived from HSCs co

55 Conversion of one terminally differentiated cell type into another (or tra

56 Osteocytes are the terminally differentiated cell type of the osteoblastic

57 nd mouse genomes in embryonic stem cells and terminally differentiated cell types at unprecedented re

58 Progress has also been made in converting terminally differentiated cell types into beta-cells usi

59 mmalian gene expression are established in a terminally differentiated cell.

60 sor effector cells; MPEC) and those that are terminally differentiated cells (short-lived effector ce

61 mechanisms of protection, poor protection by terminally differentiated cells and the importance of T

62 of replicating muscle progenitor cells into terminally differentiated cells and to develop new strat

63 Cell-identity switches, in which terminally differentiated cells are converted into diffe

64 Moreover, terminally differentiated cells can be experimentally pr

65 Deregulation of mitochondrial network in terminally differentiated cells contributes to a broad s

66 As apparently terminally differentiated cells embedded in a mineralize

67 In contrast to quiescent cells, terminally differentiated cells fail to maintain CENP-A

68 method of generating iMS cells from primary terminally differentiated cells has significant scope fo

69 Labeled SP cells give rise to terminally differentiated cells in bone marrow and intes

70 ition from lineage-restricted progenitors to terminally differentiated cells is a central aspect of n

71 of efficient and stable splicing patterns in terminally differentiated cells is critical to maintenan

72 the long-held belief that DNA methylation of terminally differentiated cells is permanent and essenti

73 n proliferating stem or progenitor cells and terminally differentiated cells is unclear.

74 Plasma cells (PCs) are terminally differentiated cells of the B-cell lineage th

75 Podocytes are terminally differentiated cells of the kidney glomerulus

76 portant role in oxidative phosphorylation in terminally differentiated cells such as cardiomyocytes.

77 Glomerular podocytes are highly specialized terminally differentiated cells that act as a filtration

78 f self-renewal and differentiation into more terminally differentiated cells that downregulate Tcf-1

79 Kidney podocytes are highly specialized terminally differentiated cells that form the final barr

80 By converting terminally differentiated cells that harbor even a singl

81 Cardiomyocytes in adult mammalian hearts are terminally differentiated cells that have exited from th

82 Human corneal endothelial cells (HCEnCs) are terminally differentiated cells that have limited regene

83 An alternate approach is to induce terminally differentiated cells to dedifferentiate into

84 eostasis of multicellular organisms requires terminally differentiated cells to preserve their lineag

85 Re-expression of p44/wdr77 caused terminally differentiated cells to re-enter the cell cyc

86 The prospect of changing the plasticity of terminally differentiated cells toward pluripotency has

87 caused reductions in cell numbers only among terminally differentiated cells while proliferation-comp

88 ically considered a homogenous population of terminally differentiated cells with a well-defined and

89 We hypothesize that resident AMs are terminally differentiated cells with low responsiveness

90 H3 from centromeres is a general property of terminally differentiated cells, and the persistence of

91 immune system, were previously thought to be terminally differentiated cells, incapable of altering t

92 to acquire KIRs when maturing from naive to terminally differentiated cells, little information is a

93 te PPARgamma cistrome and show that, even in terminally differentiated cells, PU.1 can remodel the ci

94 Corneal endothelial cells (CECs) are terminally differentiated cells, specialized in regulati

95 Unlike terminally differentiated cells, the impact of epigeneti

96 omyocytes are traditionally considered to be terminally differentiated cells, unable to proliferate.

97 Since not all TAFs are required in terminally differentiated cells, we examined the essenti

98 Parasites completely renovate the terminally differentiated cells, which lack most of the

99 ression loss also resulted in the decline of terminally differentiated cells, which was supplanted by

100 t histone for damaged histones in long-lived terminally differentiated cells.

101 all Hydra stem/progenitor cells, but not in terminally differentiated cells.

102 ding the transposon regulatory gene piwi, in terminally differentiated cells.

103 l differentiation increases from ES cells to terminally differentiated cells.

104 ecific T cells were CD45RO(-)CCR7(-)CD127(-) terminally differentiated cells.

105 intestinal epithelium comprised of villi and terminally differentiated cells.

106 spectrum of cell states, from stem cells to terminally differentiated cells.

107 Podocytes are non-proliferative, terminally differentiated cells.

108 span from early cell morphogenetic events to terminally differentiated cellular functions.

109 alpha5 localizes to the lateral membrane of terminally differentiated colonocytes and that integrin

110 lanted nucleus (ES cell, fetal fibroblast or terminally differentiated cumulus cell) and the recipien

111 e units composed of "dividing" LCs and their terminally differentiated daughter cells.

112 their clonal relationships and characterize terminally differentiated dysfunctional UC CD8(+) T cell

113 nity while other effector cells develop into terminally differentiated effector (TE) cells with limit

114 These data indicate that terminally differentiated effector CD8 T cells acquire e

115 cell subsets along with unique modulation of terminally differentiated effector CD8 T cells by combin

116 but not combination therapy, while activated terminally differentiated effector CD8 T cells expand on

117 fection, an activated CD4(+) T cell produces terminally differentiated effector cells and renews itse

118 s, the Vbeta5(+) subset expressed markers of terminally differentiated effector cells, and their expa

119 ifferentiated CD8 T-cell effector memory and terminally differentiated effector cells.

120 Lower pre-treatment terminally differentiated effector memory (TEMRA) cell f

121 etected and associated with the expansion of terminally differentiated effector memory (TEMRA; CD45RA

122 ild disease along with a strong expansion of terminally differentiated effector memory CD4+T-cells ,

123 Notably, this terminally differentiated effector memory CD8 T cell pop

124 eiling in both subsets an unattended pool of terminally differentiated effector memory cells with pre

125 ustion-/suppression-associated PD1, CD57 and terminally differentiated effector memory cells, with mo

126 ld, which were proliferative and exhibited a terminally differentiated effector memory phenotype.

127 to the expansion of the effector memory and terminally differentiated effector memory subsets.

128 we show that human ALPS DNT have features of terminally differentiated effector memory T cells reexpr

129 daughter cells with a propensity towards the terminally differentiated effector or self-renewing memo

130 ve mTORC1 activation, these cells retained a terminally differentiated effector phenotype and were in

131 nce, most CMV-specific CD8(+) T cells become terminally differentiated effector phenotype CD8(+) T ce

132 l memory T cell, effector memory T cell, and terminally differentiated effector T cell populations to

133 ion, stem-like CD8 T cells give rise to more terminally differentiated, effector-molecule-expressing

134 n the generation of more cytolyticly potent, terminally differentiated effectors that possess limited

135 l subsets-including effector memory (EM) and terminally differentiated EM (TEMRA) CD8(+) T cells-in b

136 profiles in naive, effector memory (EM), and terminally differentiated EM (TEMRA) cells.

137 confined within the effector memory (EM) or terminally differentiated EM CD45RA(+) cell subsets expr

138 Many terminally differentiated endocrine cell types, however,

139 the adult Drosophila posterior midgut, both terminally differentiated enterocyte (EC) and enteroendo

140 em-cell population, but rather indicate that terminally differentiated epithelia reexpress apparent s

141 d cancer stem cells and is also expressed in terminally differentiated epithelial and photoreceptor c

142 Podocytes are terminally differentiated epithelial cells in the kidney

143 Podocytes are terminally differentiated epithelial cells that reside a

144 roid (BFU-E), and increase the production of terminally differentiated erythroid cells.

145 ase Thousand and One Kinase 3 (TAOK3) lacked terminally differentiated ESAM(+) CD4(+) cDC2s in the sp

146 ike CD8 T cell subset that gives rise to the terminally differentiated exhausted CD8 T cells.

147 ir responses highlight the dichotomy between terminally differentiated exhausted T cells that are TCF

148 nds molecular transition from the nascent to terminally differentiated fiber cells in the developing

149 c remodeling facilitate this transition from terminally differentiated gametes to totipotent blastome

150 eted beta cells revealed the collapse of the terminally differentiated gene program, indicated by a l

151 he key cell that prevents albuminuria is the terminally differentiated glomerular podocyte.

152 c YAP1) was mainly detected in luteal cells (terminally differentiated granulosa cells).

153 ll samples, from early T cell progenitors to terminally differentiated helper T cell subsets.

154 onic stem cells (hESCs) from endoderm toward terminally differentiated hepatocytes, thus mimicking th

155 Paneth cells (PCs) are terminally differentiated, highly specialized secretory

156 at the cardiac precursors stage, but not in terminally differentiated hPSC-cardiomyocytes, by transi

157 cell-derived hepatocyte-like cells to their terminally differentiated human counterparts using defin

158 draining lymph nodes became replenished with terminally differentiated human follicular Th cells, pla

159 nvasion, which is crucial for replacement of terminally differentiated hypertrophic chondrocytes by b

160 compartments within conidia, but not within terminally differentiated infection cells, and thus spat

161 d that ventricular endocardial cells are not terminally differentiated; instead, they are angiogenic

162 The daily losses of terminally differentiated intestinal, skin, and blood ce

163 cancer cells that have undergone EMT can be terminally differentiated into adipocytes using the PPAR

164 ymocytes maintained high PLZF expression and terminally differentiated into interleukin 4 (IL-4)-prod

165 lls generated from somatic cells; (2) can be terminally differentiated into mature connective tissue

166 o critically dependent on normal shedding of terminally differentiated keratinocytes, a process terme

167 cells lacking Id2 did not generate a robust terminally differentiated killer cell lectin-like recept

168 as established memory CD8(+) T cells toward terminally differentiated KLRG-1(hi)IL-7Ralpha(lo)GzmB(h

169 tory cytokine IL-12 drives the generation of terminally differentiated KLRG1(+) effector CD8(+) T cel

170 lted from accumulation of greater numbers of terminally differentiated KLRG1(hi) effector CD8 T cell

171 er crystallins and genes highly expressed in terminally differentiated lens fibers.

172 allenging the classic view of neutrophils as terminally differentiated leukocytes destined to die or

173 e myeloid cell lines are, by definition, not terminally differentiated like tissue macrophages.

174 er CD4(+) T cell subsets have been viewed as terminally differentiated lineages with limited flexibil

175 nitors and hence the extent of production of terminally differentiated lineages.

176 tein LL (hnRNPLL) is specifically induced in terminally differentiated lymphocytes, including effecto

177 idence that loss of CD28 cells is typical of terminally differentiated lymphocytes, the aim of this s

178 sion of cell cycle-associated proteins, with terminally differentiated macrophages becoming highly su

179 how HIV-1 achieves efficient replication in terminally differentiated macrophages despite the restri

180 rance and new loop formation are observed in terminally differentiated macrophages, but not TNFalpha-

181 nsduce nondividing cells is key to infecting terminally differentiated macrophages, which can serve a

182 hyltransferase Dnmt3a has high expression in terminally differentiated macrophages; however, its role

183 not only during differentiation but also in terminally differentiated-macrophages and immature dendr

184 In terminally differentiated mammalian auditory hair cells,

185 expression is substantially downregulated in terminally differentiated mast cells as compared with th

186 The adult heart is composed primarily of terminally differentiated, mature cardiomyocytes that ex

187 Reconstitution of effector, central and terminally differentiated memory cell population and inc

188 central memory T cell subsets at onset and 5 terminally differentiated memory T (TEMRA) cell subsets

189 , CD8CD28, CD4CD57PD1, and CD8CD28 end-stage terminally differentiated memory T cells were measured p

190 on of CD8(+)CD28(-) T cells, a population of terminally differentiated memory T cells, is one of the

191 with greater than 35 cells CD8CD28 end-stage terminally differentiated memory T cells/muL rejected, m

192 prisingly DNA replication takes place in the terminally differentiated mother cell as offspring grow.

193 f tissue-restricted genes, a key property of terminally differentiated mTECs.

194 cycling neural progenitor cells but also in terminally differentiated, myelinating oligodendrocytes.

195 view, until now based on in vitro data, that terminally differentiated myeloid cells in vivo are site

196 in HCMV carriers routinely occurs from such terminally differentiated myeloid cells in vivo.

197 onal hematopoiesis and hyperproliferation of terminally differentiated myeloid cells.

198 derived suppressor cells into protumorigenic terminally differentiated myeloid mononuclear cells (TDM

199 nificant downregulation of TFIID subunits in terminally differentiated myocytes, hepatocytes and adip

200 ng skeletal muscle precursors (myoblasts) to terminally-differentiated myocytes is a critical step in

201 the earliest premyogenic progenitor stage to terminally differentiated myofibers, and discuss how thi

202 stemic RNAi approach targeting the nuclei of terminally differentiated myofibers.

203 to complement-mediated injury owing to their terminally differentiated nature.

204 s strongly hindered by their short-lived and terminally differentiated nature.

205 However, terminally differentiated, neuronal SH-SY5Y cells releas

206 ts suggest that telomeres are dispensable in terminally differentiated neurons and provide mechanisti

207 Highly pure (>95%) terminally differentiated neurons derived from pluripote

208 rated acute murine knock-out models of Rb in terminally differentiated neurons in vitro and in vivo.

209 taining the survival and normal functions of terminally differentiated neurons is also crucial for li

210 Neural progenitors and terminally differentiated neurons show distinct redox pr

211 s surprisingly no detectable consequences on terminally differentiated neurons.

212 NB but independently of factors that act in terminally differentiated neurons.

213 igopotent common myeloid progenitor stage to terminally differentiated neutrophils.

214 NK cells, naive T cells, and accumulation of terminally differentiated NK and CD8(+) memory T cells.

215 A slightly increased percentage of terminally differentiated NK cells and functional respon

216 Mature and terminally differentiated NK cells with enhanced effecto

217 ression of inhibitory receptor NKG2A/CD94 on terminally differentiated NK cells.

218 diating antibacterial effector function than terminally differentiated NK cells.

219 larly the CD56(bright) subset, and a lack of terminally differentiated NK cells.

220 Terminally differentiated NKG2C+ cells show KIR expansio

221 In people, expansion of long-lived terminally differentiated NKG2C+ populations occur in th

222 rm (4-day) murine cytomegalovirus infection, terminally differentiated NKs accumulate in the livers o

223 e effects reduced the number and function of terminally differentiated NKT and gammadelta T cells in

224 es in alveolar maturation and can exit their terminally differentiated non-proliferative state.

225 tal Cell, Amulic et al. (2017) show that the terminally differentiated, non-cycling neutrophils repur

226 e HBoV1 genome, and HBoV1 replicates only in terminally differentiated, nondividing cells.

227 Terminally differentiated/nondividing macrophages, which

228 rating de novo cardiomyocyte-like cells from terminally differentiated nonmyocytes in the heart in si

229 ifferent stages of erythropoiesis, including terminally differentiated nucleated RBCs that we term "j

230 biological functions of Olig2 suppressed in terminally differentiated oligodendrocytes?

231 Although their phenotype resembles that of terminally differentiated or exhausted T cells, lack of

232 Inflammation is, however, harmful to terminally differentiated organs, such as the heart and

233 the differentiation of human macrophages to terminally differentiated osteoclasts are dependent on s

234 titative PCR for gene expression analysis in terminally differentiated osteoclasts.

235 r5(+) stem cells are intermingled with their terminally differentiated Paneth cell daughters at crypt

236 activity and were a homogenous population of terminally differentiated Paneth cells.

237 Here we show that despite their terminally differentiated phenotype, human ALPS DNT cell

238 vector-elicited CD8(+) T cells are of a more terminally differentiated phenotype.

239 for Musashi proteins in the morphogenesis of terminally differentiated photoreceptor neurons.

240 r of the transition from progenitor cells to terminally differentiated photoreceptors.

241 not revert back to the parent isotype, and a terminally differentiated plasma cell cannot contribute

242 d a high number of activated CD8(+) T cells, terminally differentiated plasma cells, and activated ep

243 Multiple myeloma (MM), a cancer of terminally differentiated plasma cells, is emblematic of

244 versial, and has gained interest because the terminally differentiated pollen vegetative nurse cell s

245 ssion of the glycoprotein CD101 divides this terminally differentiated population into two subsets.

246 thymus TPA(lo)MHCII(lo) pre-Aire rather than terminally differentiated post-Aire TPA(hi)MHCII(lo) mTE

247 Terminally differentiated post-mitotic cells are general

248 Long-lived cells such as terminally differentiated postmitotic neurons and glia m

249 Additionally, terminally differentiated, postmitotic myofiber nuclei f

250 iminates total cellular miRNA populations in terminally differentiated primary cultures.

251 Vdelta2 T cells presented a terminally differentiated profile, expressed granzyme B

252 the needs for production of their immediate terminally differentiated progeny.

253 rs in the BM and alter the function of their terminally differentiated progeny.

254 Thus, post-mitotic cells, though terminally differentiated, remain plastic to transdiffer

255 define paracellular transport properties of terminally differentiated renal proximal tubule epitheli

256 er dissect the progression from stem cell to terminally differentiated secretory cell.

257 ajor cell fates, CD57(+) CD127(-)-resembling terminally differentiated senescent memory cells and CD1

258 exhibited a skewing of CD8+ T cells toward a terminally differentiated/senescent phenotype.

259 specification of other identity aspects of a terminally differentiated sensory neuron.

260 We demonstrate that terminally differentiated SH-SY5Y cells have neuronal mo

261 These and other properties are analogous to terminally differentiated short-lived CD8(+) T effector

262 oliferation and activated stem cell genes in terminally differentiated somatic cells.

263 monstrate plasticity in the reprogramming of terminally differentiated sperm nuclei and suggest that

264 y in the adult maintains mature DCTs in this terminally differentiated state and prevents renal fibro

265 own about how gene batteries that define the terminally differentiated state of a neuron type are mai

266 Thus, LDB1 maintains the terminally differentiated state of beta cells and is a c

267 reveal a novel mechanism for maintaining the terminally differentiated state of Drosophila photorecep

268 ese cells does not represent conversion to a terminally differentiated state, but rather represents t

269 glycolytic flux drives CD8+ T cells toward a terminally differentiated state, while its inhibition pr

270 eb2 mRNA, which then triggered CTLs to adopt terminally differentiated states.

271 ed a requirement for LDB1 in maintaining the terminally differentiated status of pancreatic beta cell

272 CX3CR1, HAVCR2 (TIM-3), and ZEB2 represents terminally differentiated status with the unique transcr

273 d, the specific accumulation of oocytes, the terminally differentiated stem cell progeny, triggers a

274 oid male gametophyte, the pollen grain, is a terminally differentiated structure whose function ends

275 In the thymus, DOCK8-deficient mice lack a terminally differentiated subset of NK1.1(+) NKT cells e

276 , after: 16.5 +/- 2.3%) and 2) a decrease in terminally differentiated subsets (CD4(+): before: 47.3

277 tissue-resident populations, whereas mature, terminally differentiated subsets mediate immunosurveill

278 in the bladder whereas K20, a marker of the terminally differentiated superficial urothelial cells w

279 erative cytotrophoblast (CTB), precursors to terminally differentiated syncytiotrophoblast (STB) in c

280 T-cell responses in the CD4 compartment and terminally differentiated T cells in the CD8 compartment

281 eline naive T cells and lower percentages of terminally differentiated T cells, compared with nonresp

282 ell response deficiency, a high frequency of terminally differentiated T cells, the presence of monof

283 sistant rejection (CoBRR) is associated with terminally differentiated T cells.

284 ancer efficacy compared with the infusion of terminally differentiated T cells.

285 known properties of highly differentiated or terminally differentiated T cells.

286 content and synthesis in MPEC compared with terminally differentiated Teff.

287 of CD4 effector memory T cells (TEM) and CD8 terminally differentiated TEM (TEMRA), with greater CD4

288 nfirmed an acute and persistent depletion of terminally differentiated TEMRA and cytomegalovirus-spec

289 otection to Mtb rechallenge when compared to terminally differentiated Th1 cells that reside preferen

290 PA:LFn-GAL4:ASO transfection of non- or terminally-differentiated THP-1 cells and Vero cells res

291 subset of RD-histone genes are expressed in terminally differentiated tissues as polyadenylated mRNA

292 ting for myelination studies, or they can be terminally differentiated to myelin basic protein-positi

293 udy, we show that Klrg1(+) Tregs represent a terminally differentiated Treg subset derived from Klrg1

294 vo progression from p63(+) CTB stem cells to terminally differentiated trophoblast subtypes.

295 ity is caused by an accumulation of the most terminally differentiated type of chondrocytes that prod

296 In galegoid plants, the endosymbionts are terminally differentiated, uncultivable polyploid cells,

297 In the bladder the luminal surface of terminally differentiated urothelial umbrella cells is a

298 Although initially viewed as terminally differentiated, we now recognize that Th cell

299 postnatal cochlea, the sensory epithelium is terminally differentiated, whereas tympanic border cells

300 n be similarly reprogrammed and subsequently terminally differentiated with abrogation of tumorigenic