ライフサイエンスコーパス: delta cell

1 other and with an additional cell type: the delta cell.

2 vely expressed in the somatostatin-secreting delta cell.

3 2 expression and budding are delayed in ccr4 delta cells.

4 pable of increased Ty1 transposition in pmr1 Delta cells.

5 p210 level in Bcr-Abl-transduced SHP-2Delta/Delta cells.

6 ignaling was greatly decreased in SHP-2Delta/Delta cells.

7 endogenous IL-2 RNA degradation in TCR gamma delta cells.

8 in sister kinetochore coorientation in spo13 Delta cells.

9 e cells was missing in all of the above crd1 Delta cells.

10 bud6 delta cells but are proficient in kar9 delta cells.

11 lectively impaired at the bud cortex in bud6 delta cells.

12 in MMS-treated mag1 Delta rad14 Delta rad26 Delta cells.

13 otein exacerbates the defects of sid2-1 sic1 Delta cells.

14 ed for the preanaphase arrest of sid2-1 sic1 Delta cells.

15 ed tubules, similar to the phenotype of dnm1 Delta cells.

16 ions were absent in both nvj1-Delta and vac8-Delta cells.

17 unctioning islets containing alpha, beta and delta cells.

18 ducing beta cells and somatostatin-producing delta cells.

19 er than wild-type in nup188-Delta and nup170-Delta cells.

20 nificantly faster in nup188-Delta and nup170-Delta cells.

21 S-GFP nuclear localization defects of nup188-Delta cells.

22 in the pancreatic islet, especially in islet delta cells.

23 cidergic neurons in midbrain, and pancreatic delta cells.

24 ssed in alpha, beta and PP cells, but not in delta cells.

25 role that is increasingly emerging for gamma delta cells.

26 alpha beta cells, but lack mature TCR gamma delta cells.

27 yruvate kinase activity was elevated in mck1 delta cells.

28 and partially restore actin cables in mdm20 delta cells.

29 ly longer than for rats bearing C6 or C6trkA delta cells.

30 eptors were found predominantly in alpha and delta cells.

31 ne recombination in thymically derived gamma delta cells.

32 ion is a frequent occurrence in thymic gamma delta cells.

33 e opposite, beta cells surrounding alpha and delta cells.

34 atostatin secretion via cognate receptors on delta cells.

35 ed translational efficiency of mRNAs in tit1-Delta cells.

36 ce exposure of the Als3 adhesin on slr1Delta/Delta cells.

37 gene up-regulation, and slow growth of sla1-Delta cells.

38 alpha cells but substantial in OFF alpha and delta cells.

39 otein expression in mouse alpha-, beta-, and delta-cells.

40 alpha-cells, and that Kv2.2 is expressed in delta-cells.

41 ity via gap junction-dependent activation of delta-cells.

42 d almost exclusively in pancreatic beta- and delta-cells.

43 the <10% of beta-cells situated <20 um from delta-cells.

44 identity of human alpha-, beta-, gamma- and delta-cells.

45 eatic polypeptide cells but not to alpha- or delta-cells.

46 nds that limit paracrine signaling from beta/delta-cells.

47 lusive effect by AG-induced SST release from delta-cells.

48 ed of a collection of >500 alpha-, beta- and delta-cells.

49 essed at the mRNA, but not protein, level in delta-cells.

50 asse reprogramming of somatostatin-producing delta-cells.

51 glucagon(+) alpha-cells, and somatostatin(+) delta-cells.

52 ct inhibition via somatostatin released from delta-cells.

53 ucing alpha-cells and somatostatin producing delta-cells.

54 ecretion, and cross regulation of alpha- and delta-cells.

55 high glucose levels due to the inhibition by delta-cells.

56 ects that parallel those found in PLK1(Delta/Delta) cells.

57 ed oxidant-induced cell death in Fra-1(Delta/Delta) cells.

58 ss response, are dysregulated in Lmnb1(Delta/Delta) cells.

59 that this association is lost in Lmnb1(Delta/Delta) cells.

60 mune disease, may be a general one for gamma delta + cells.

61 tions of alpha-cells (5%), beta-cells (92%), delta-cells (1%), and pancreatic polypeptide cells (2%).

62 : 62.9 +/- 3.1% vs. 75.5 +/- 0.9%, P = 0.02; delta-cells: 2.8 +/- 0.5% vs. 4.4 +/- 0.4%, P = 0.05), w

63 f the Fc epsilon RI gamma-chain in TCR-gamma delta cells, a TCR-gamma delta transgenic mouse (G8) has

64 Peripheral TCR gamma delta cells accumulate GFP RNA faster than endogenous IL

65 nhx1 delta cells accumulate late Golgi, prevacuole, and lysos

66 horylation is substantially reduced in SpMYH Delta cells after hydrogen peroxide treatment.

67 The vph1Delta/Delta cells also had abnormal endocytosis and vacuolar m

68 Mice infected with slr1Delta/Delta cells also had an increased brain fungal burden, w

69 CHI-D delta-cells also comprised 10% of cells displaying nucle

70 In OFF Delta cells, AMPAR- and NMDAR-mediated responses could b

71 of age show marked hyperplasia of alpha and delta cells and a relative diminution of beta cells.

72 GAL10 genes is reduced in MMS-treated rad26 Delta cells and also in mag1 Delta rad14 Delta cells, wh

73 ng extracts derived from fir1 Delta and pbp1 Delta cells and from cells lacking the Fir1p interactor,

74 ls were much less invasive than C6 or C6trkA delta cells and had a greater rate of apoptosis.

75 and Spt23p processing is suppressed in rsp5 Delta cells and in wild-type RSP5 cells upon expression

76 PMN occurs normally in apg7-delta cells and is, therefore, not dependent on macroaut

77 Ssb1p stimulates nuclear transport in nup188-Delta cells and NES-containing Ssa1p does not.

78 producing beta cells, somatostatin-producing delta cells and pancreatic polypeptide-producing PP cell

79 al regulator specifically required for islet delta cells and suggest compromised paracrine control as

80 Gamma delta cells and their putative ligands have been linked

81 , the ratios of bulk-sorted beta, alpha, and delta cells and their respective hormone-specific RNA-Se

82 ced in p38gamma/p38delta-deficient (p38gamma/delta(-/-)) cells and tissues without affecting TPL2 mes

83 TCR-alpha/beta+ cells but contain TCR-gamma/delta+ cells and a small population of a unique CD4+, TC

84 Somatostatin (SST) is secreted by islet delta-cells and by extraislet neuroendocrine cells.

85 New molecular abnormalities in delta-cells and marked proliferative increases in other

86 Conversely, optoinhibition of delta-cells and somatostatin secretion reduced rather th

87 tein carboxypeptidase Y is missorted in nhx1 delta cells, and is secreted from the cell.

88 t consisting of two-state alpha-, beta-, and delta-cells, and analyze effects of known chemical inter

89 ls during epithelial infections, since gamma delta + cells are commonly abundant within epithelia.

90 akr1 delta cells are also defective for endocytosis of the al

91 bck2 delta double deletions, cln3 delta ccr4 delta cells are also inviable.

92 Gamma delta cells are attractive candidates for mediators of a

93 ducing beta cells and somatostatin-producing delta cells are drastically reduced, while the numbers o

94 Most delta cells are elongated and have a well-defined cell s

95 heterogeneity among delta cells, where most delta cells are entrained by oscillatory Ca(2+) behavior

96 Delta cells are important paracrine regulators of beta c

97 beta cells and the development of TCR gamma delta cells are partially independent of the T domain.

98 pombe growth is resistant to rapamycin, sla1-Delta cells are sensitive, consistent with deficiency of

99 n-essential for yeast cell growth, but sec28 Delta cells are thermosensitive.

100 8alpha/beta T cells disappear, but TCR-gamma/delta cells are unaffected by the absence of beta2m.

101 rga4 Delta cells are wider in diameter and shorter in length,

102 TCR gamma delta cells, as well as alpha beta TCR-NKT cells, exhibi

103 Paradoxically, optoactivation of delta-cells at 6 mmol/L glucose increased insulin secret

104 eatic alpha-cells and somatostatin-producing delta-cells become insulin-expressing cells after the ab

105 Mutant coatomer from sec28 Delta cells behaves as an unusually large protein comple

106 These contacts are eliminated in bud6 delta cells but are proficient in kar9 delta cells.

107 ressor of the respiratory deficiency of coa2 Delta cells but lacks suppressor activity for two other

108 ps36 enhances the pheromone response in sst2 Delta cells but not in wild type.

109 ted in stimulation of electrical activity in delta-cells but suppression of alpha-cell activity.

110 h pretreatment with hydroxyurea renders tel1-Delta cells (but not wild type) MMS-sensitive, demonstra

111 ta gene rearrangements occur in thymic gamma delta cells, but the frequency of in-frame rearrangement

112 in Schizosaccharomyces pombe tit1+ and tit1-Delta cells by using a beta-galactosidase codon-swap rep

113 r data provides an integrated picture of how delta cells can modulate beta cell activity under physio

114 ic progenitor cells; and (2) donor TCR gamma/delta+ cells can facilitate the alloengraftment of rigor

115 These results show that (1) host TCR gamma/delta+ cells can reject repopulating donor cells, presum

116 elial lymphocytes (IEL), including TCR gamma delta cells, can develop extrathymically.

117 In contrast, akr1 delta cells cannot carry out ligand-mediated endocytosis

118 Provocatively, both the gamma delta cell clones and primary gamma delta cells in vivo

119 In this report, gamma delta cell clones are described that conform strikingly

120 is increased by greater than 5-fold in akr1 delta cells compared with AKR1 cells.

121 e pancreas shows a dramatic loss of beta and delta cells, contrasting a smaller relative loss of alph

122 juveniles display 'somatostatin-to-insulin' delta-cell conversion, involving dedifferentiation, prol

123 Although cac1 delta cells could establish and maintain transcriptional

124 her, our study demonstrated adult alpha- and delta-cells could regenerate, and both self-duplication

125 iferating cell marker Ki67 showed alpha- and delta-cells could replicate, suggesting self-duplication

126 beta-cells (current density 9 pA/pF), 91% of delta-cells (current density 148 pA/pF), and 6% of alpha

127 rough recognition of autoantigens, and gamma delta-cell-deficient mice, unlike mice deficient in alph

128 e synthesize IL-7, suggesting that TCR gamma delta cell development could occur in either site.

129 progenitors and may regulate alpha, beta and delta cell development.

130 ssion in IL-7Ralpha(-/-) mice to drive gamma/delta cell development.

131 coregulator during islet alpha-, beta-, and delta-cell development through Isl1-dependent and potent

132 tely one-third of HO HML alpha MAT alpha hmr delta cells die because they fail to repair the HO endon

133 at Mnx1 promotes beta-cell while suppressing delta-cell differentiation programs, and is crucial for

134 pancreas, we show that Hhex is required for delta-cell differentiation.

135 rotective immunity, while mice lacking gamma delta + cells display exaggerated intestinal damage, app

136 Mid2p colocalizes with septins, and mid2 Delta cells display disorganized, diffuse septin rings a

137 Here, we report that Lmnb1(Delta/Delta) cells displayed striking nuclear rotation, with a

138 trast, we show that thymically derived gamma delta cells do not make detectable rearrangements of the

139 Of particular interest is the role of gamma delta + cells during epithelial infections, since gamma

140 In she1 Delta cells, dynein is activated throughout the cell cyc

141 fects at 11 degrees C and 37 degrees C. rom2 delta cells exhibit morphological defects.

142 ar compartment requires Nhx1p, and that nhx1 delta cells exhibit phenotypes characteristic of the "cl

143 Unlike TCR-alpha beta cells, TCR-gamma delta cells express a distinct member of the zeta family

144 Islet epsilon-cells produce ghrelin and delta-cells express growth hormone secretagogue receptor

145 alpha-cells did not express Glp1r mRNA and delta-cells expressed Glp1r mRNA but not protein.

146 In snf3 delta cells expression of HXT6 is constitutive even when

147 At high osmolarity, spm1 delta cells fail to form colonies.

148 usly developed tumors, and primary Usp3Delta/Delta cells failed to preserve chromosomal integrity.

149 Purification of islet beta-, alpha- and delta-cells followed by transcriptome analysis (RNA-seq)

150 Second, the inhibitory interactions of delta-cells for glucagon and insulin secretion prevent t

151 xpression, because intraepithelial TCR-gamma delta cells from the zeta-deficient mice did not respond

152 methods to highly purify alpha-, beta-, and delta-cells from human fetal and adult pancreata by intr

153 to the fetal pancreas, and implied immature delta-cell function.

154 on and induces ectopic expression of crucial delta cell genes, including somatostatin.

155 ertonic stress or elevated temperature, spm1 delta cells grow as short branched filaments in which th

156 mponents of the ETS was also reduced in crd1 Delta cells grown at elevated temperatures because of re

157 Microarray analyses revealed that mds3 Delta/Delta cells had an expression profile indicative of a hy

158 FLAG-mu cells, MbetaCD treatment of HEK FLAG-delta cells had no effect on acute inhibition or sensiti

159 Fra-1(Delta/Delta) cells had elevated basal levels of antioxidant en

160 ze of ccr4 delta cells, suggesting that ccr4 delta cells have a G(1)-phase cyclin deficiency.

161 eased numbers of T cell receptor (TCR)-gamma/delta cells have been observed in animal models of influ

162 Rapidly aging sip2 Delta cells have higher levels of histone H3 kinase acti

163 for3 Delta cells have normal microtubule dynamics and cortica

164 ast in part because thymically derived gamma delta cells have rarely been studied.

165 These results demonstrate that TCR gamma/delta cells have the capacity to cause acute lethal GVHD

166 Like Oct1(-/-) cells, Lmnb1(Delta/Delta) cells have elevated levels of reactive oxygen spe

167 In TCR gamma delta cells, IL-2-producing cells are a subset of the GF

168 o commit to division, the large size of ccr4 delta cells implies that they may have a size-specific p

169 To define the role of TCR-gamma/delta cells in anti-HSV-1 immunity, TCR-alpha-/- mice tr

170 that contained B cells and monoclonal gamma delta cells in close juxtaposition.

171 lucidate the potential function of TCR gamma/delta cells in GVHD, we have used transgenic (Tg) H-2d m

172 etely removed coupling between beta and most delta cells in HG.

173 cells suggests a specialized role for gamma/delta cells in mucosal immunity.

174 However, a direct role for TCR-gamma/delta cells in protective immunity for pathogenic viral

175 c potential of Bcr-Abl-transduced SHP-2Delta/Delta cells in recipient animals was compromised.

176 Little is known about the role of islet delta cells in regulating blood glucose homeostasis in v

177 Most of the TCR-gamma/delta cells in the iIELs also bear CD8alpha/alpha, and t

178 ng beta cells and the somatostatin-producing delta cells in the islets of Langerhans in the pancreas.

179 sponsible for the selective deficit in gamma/delta cells in these mice, since a high copy TCR-gamma t

180 he gamma delta cell clones and primary gamma delta cells in vivo showed a strong association of the T

181 that non-beta-cells such as alpha-cells and delta-cells in adults can regenerate, and that the regen

182 ular, it has not been resolved whether gamma delta cells, independent of any other T cells, can help

183 a2+]i imaging experiments, optoactivation of delta-cells induced islet-wide beta-cell [Ca2+]i transie

184 ntation (BMT) confirmed that G8 Tg TCR gamma/delta cells infiltrated GVHD target tissues (skin, liver

185 or optoinhibition of somatostatin-releasing delta-cells inhibits and stimulates electrical activity

186 The infusion of G8 Tg (H-2Td) TCR gamma/delta cells into lethally irradiated [900 cGy total body

187 In contrast, injection of TCR gamma/delta+ cells into irradiated (900 cGy TBI) B6.A-TIaa Boy

188 of intracellular levels of arginine in btn1-Delta cells is detrimental and is suggestive that btn1-D

189 The rapid-aging phenotype of sip2 Delta cells is fully rescued by blocking recombination a

190 trate that the ectopic expression of Pax4 in delta cells is sufficient to induce their conversion int

191 The respiratory deficiency of coa2 Delta cells is suppressed either by the presence of a mu

192 c islets; within the islet the percentage of delta-cells is increased, while the percentage of alpha-

193 , and the resulting cold sensitivity of taz1 Delta cells, is suppressed by mutated alleles of Top2 th

194 Giving 5,000 gamma delta+ cells isolated from the hearts of H3 virus-infect

195 BALB/c mice, transient depletion of all TCR-delta(+) cells just before airway challenge resulted in

196 In both models of HSV-1 infection, TCR-gamma/delta cells limited severe HSV-1-induced epithelial lesi

197 the permissive temperature, cdp1-1 and cdp1 delta cells lost chromosomes at a frequencies approximat

198 IL-2 gene expression in transgenic TCR gamma delta cells may be explained by subset-specific IL-2 gen

199 Thus, this study demonstrates that TCR-gamma/delta cells may play an important regulatory role in hum

200 nt deficiency in tRNA nuclear export in sla1-Delta cells may trigger the AAM response, we show that m

201 ce were found to be susceptible to TCR gamma delta+ cell mediated GVHD-induced lethality characterize

202 t organs are responsible for G8 Tg TCR gamma/delta+ cell mediated lethality.

203 observed protection resulted from TCR-gamma/delta cell-mediated arrest of both viral replication and

204 have specifically examined whether TCR gamma/delta+ cells might be capable of eliminating BM-derived

205 When expressed in a ste5 delta cell, mutant Ste5 proteins that are defective in t

206 e of thymic IL-7 in development of TCR gamma delta cells, newborn TCR beta-deficient (TCR beta(-/-))

207 OFF delta cell NMDA receptors were composed of GluN2B subuni

208 nt with its detection in two-thirds of CHI-D delta-cell nuclei, similar to the fetal pancreas, and im

209 Alternatively, in the absence of Arx, delta cell numbers are increased and Nkx2.2 becomes esse

210 Overall PPAR-delta+ cell numbers declined at 1 day post injury (dpi),

211 In addition, we found delta-cell numbers doubled by Day 6 following STZ treatm

212 In vac8-Delta cells, Nvj1p-GFP generally failed to concentrate i

213 e, no development of graft-derived TCR gamma delta cells occurred, indicating that extrathymic IL-7 d

214 In contrast, intraepithelial TCR-gamma delta cells of G8.zeta-/- mice expressed high levels of

215 At permissive temperatures, rom2 delta cells often form elongated buds and fail to form n

216 s growing on glucose and galactose, and snf1 Delta cells on galactose.

217 y factors secreted by neighbouring beta- and delta-cells (paracrine regulation) have been proposed to

218 nes representing distinct alpha-, beta-, and delta-cell phenotypes.

219 s, and recent experiments confirm that gamma delta cells play a significant role in autoimmune diseas

220 The demonstration that TCR-gamma/delta cells play an important protective role in murine

221 e CD4- CD8+ gamma delta+- or CD4- CD8- gamma delta+-cell population.

222 findings support the conclusion that sst1.1 delta-cells possess a pro-beta identity enabling them to

223 Instead, rfc2 Delta cells proceed into mitosis with incompletely repli

224 01), alpha-cell (r = -0.32, P < 0.0001), and delta-cell (r = -0.25, P < 0.0001) areas.

225 at islets lacking endogenous Ucn3 have fewer delta cells, reduced somatostatin content, impaired soma

226 eling techniques, we demonstrated alpha- and delta-cell regeneration involved cell proliferation.

227 These data suggest alpha- and delta-cell regeneration occurred rapidly following a sin

228 ons, while the biological functions of gamma delta + cells remain unclear.

229 However, the vph1Delta/Delta cells remained competent for filamentation induced

230 h are expressed in pancreatic islet beta and delta cells, respectively.

231 These Tg TCR gamma/delta+ cells respond vigorously to target cells that exp

232 t, when receptor synthesis is shut off, akr1 delta cells retain the ability to mate longer than do AK

233 VAC1, and subcellular fractionation of vac1 delta cells revealed a striking change in the fractionat

234 In mks1 Delta cells, RTG target gene expression is constitutive,

235 In sec28 Delta cells shifted to 37 degrees C, wild-type alpha-COP

236 Additionally, rga4 Delta cells show an altered growth pattern similar to th

237 of INO80 complexes from arp5 Delta and arp8 Delta cells shows that protein complexes remain intact b

238 In sir2 Delta cells, silencing at the donor mating-type loci, te

239 vation of beta-cell G(i/o)-GPCRs and NKAs by delta-cell somatostatin secretion slowed Ca(2+) oscillat

240 lls via gap junction-dependent activation of delta-cells/somatostatin secretion.

241 In rad50 delta cells, some DSBs are not repaired until a broken c

242 ncipal role in defining islet beta cell- and delta cell-specific expression of the IAPP gene.

243 co-localized with somatostatin, a pancreatic delta cell-specific hormone.

244 Moreover, this study revealed that delta cells specifically express receptors that receive

245 We suggest that delta-cell SST exerts a tonic inhibitory influence on in

246 sed Sst(-/-) mice to investigate the role of delta-cell SST in the regulation of insulin and glucagon

247 In addition, delta-cell SST is implicated in the nutrient-induced sup

248 However, the specific intraislet function of delta-cell SST remains uncertain.

249 Optical activation or delta-cells stimulate somatostatin secretion.

250 the presence of appropriate beta, alpha, and delta cell subsets.

251 LN2, CLN3, and SWI4 reduces the size of ccr4 delta cells, suggesting that ccr4 delta cells have a G(1

252 , rescues filamentation defects of hir1Delta/Delta cells, suggesting that Hir1 impacts the early phas

253 olar growth similar to that observed in tea1 Delta cells, suggesting that Shk1 and Tea1 may regulate

254 maintain expression of FAS1 in nmt1-451Dino2 Delta cells suggests the existence of another transcript

255 is ring structures, or cycles, of alpha and delta cells surrounding beta cell clusters or the opposi

256 genic mice, only a small proportion of gamma/delta cells survived as long-lived cells; most of these

257 st to TCR transgenic mice, most of the gamma/delta cells surviving in ATx normal mice had a rapid tur

258 -cell analysis revealed that individual cac1 delta cells switch from transcriptionally "off" to trans

259 We find that rtg2 Delta cells take up USA even without the presence of [UR

260 his inhibition is somatostatin released from delta cells that are clustered with beta cells in pancre

261 d gene conversions both in Rad+ and in rad50 delta cells that cannot initiate normal meiotic DSBs.

262 rthritis contain a large proportion of gamma delta cells that proliferate in response to the causativ

263 egulated between T2D and ND alpha, beta, and delta cells that were undetectable in paired whole islet

264 TPA treatment of L epsilon delta, cells that overexpressed the PKC-epsilon delta ch

265 s are transcriptionally close to a subset of delta-cells that we identified in control islets and tha

266 glucose level, beta-cells decreasing it, and delta-cells the precise role of which still needs identi

267 for two E2 activities, i.e., ubc4 delta ubc5 delta cells, the receptor was found to be substantially

268 Since PDX-1 is highly enriched in beta and delta cells, these results suggest that this factor play

269 o constitutive endocytosis exhibited by akr1 delta cells, they are competent to carry out ligand-medi

270 contain a secretory machinery, enabling the delta cell to reach a large number of beta cells within

271 A capacity of gamma delta cells to effect or regulate tissue damage is also

272 has been suggested by the inability of plo1 Delta cells to septate and the prolific septation follow

273 uced binding (P=0.0004) of MiaPaCa-MUC4-NIDO(Delta) cells to the fibulin-2 coated plates compared wit

274 The addition of donor G8 TCR gamma/delta+ cells to TCD donor BM was shown to significantly

275 In pre-diabetes, delta cells undergo morphological changes that may be a

276 us studies, we found that budding yeast swe1 Delta cells undergo premature entry into mitosis, leadin

277 However, tel1-Delta cells, unlike ATM-deficient cells, do not exhibit

278 OFF alpha and delta cells used NMDA receptors for encoding either the

279 riptomes of FACS-purified alpha-, beta-, and delta-cells using bulk RNA-sequencing have facilitated o

280 lp1r expression include pancreatic beta- and delta-cells, vascular smooth muscle, cardiac atrium, gas

281 tivation of the beta-cells propagates to the delta-cells via gap junctions, and the consequential sti

282 on the turnover and lifespan of murine gamma/delta cells was obtained by administering the DNA precur

283 d no effect on AHR, and depletion of all TCR-delta(+) cells was no more effective than depletion of V

284 Activation of the delta-cells was rapid and sensitive to the gap junction

285 e proportion of islets composed of beta- and delta-cells was reduced in the transgenic mice compared

286 e whether such plasticity was also shared by delta cells, we generated and characterized transgenic a

287 In human islets, most beta, alpha, and delta cells were aligned along blood vessels with no par

288 In addition, cac1 delta cells were defective for transcriptional silencing

289 ive alpha cells, and somatostatin-containing delta cells were found scattered throughout the human is

290 Donor- and host-derived TCR gamma delta cells were recovered from thymus grafts, spleen, a

291 te-passage Mre11(ATLD1/ATLD1) Tert(Delta)(/)(Delta) cells were as short as those from Tert(Delta)(/)(

292 Both TCR-alpha-/beta+ and TCR-delta+ cells were found to be capable of producing IL-4;

293 ulin receptors in the somatostatin-secreting delta-cells, when insulin-induced somatostatin secretion

294 considerable functional heterogeneity among delta cells, where most delta cells are entrained by osc

295 d26 Delta cells and also in mag1 Delta rad14 Delta cells, whereas a very severe reduction in transcri

296 CR alpha beta receptor and not the TCR gamma delta cells, which exclusively express CD8 alpha alpha.

297 f endocrine cells, primarily alpha, beta and delta cells, which secrete glucagon, insulin, and somato

298 required for development of thymic TCR gamma delta cells, while peripheral IL-7 was sufficient for de

299 hosphotyrosine accumulates on Cdc28 in cdc55 delta cells whose spindles have been depolymerized, and

300 arrest is maintained in the majority of bub3 Delta cells, yet they die, suggesting that Bub3p is esse