ライフサイエンスコーパス: cell expansion

1 ngation growth of shoot tissues by promoting cell expansion.

2 at may provide a dynamic module for altering cell expansion.

3 ctively drive and specify the extent of stem-cell expansion.

4 great impact on cell wall properties during cell expansion.

5 buted primarily to inhibition of mesenchymal cell expansion.

6 capable of inducing a significant human beta-cell expansion.

7 d actin nucleation and assembly during plant cell expansion.

8 ortant role of IL-18 in driving gammadelta T cell expansion.

9 r autophagy in directly limiting mucosal TH2 cell expansion.

10 is ESP mutants, it cannot rescue anisotropic cell expansion.

11 edundant roles supporting pulmonary CD8(+) T cell expansion.

12 loss of T-cell surveillance, led to fatal B-cell expansion.

13 ting T cell homeostasis and supporting T reg cell expansion.

14 It is unknown whether LPS mediates ductular cell expansion.

15 protective environment, enabling rapid stem cell expansion.

16 maintained from precursor through peak of T-cell expansion.

17 oliferation and postponing the transition to cell expansion.

18 usly related to the magnitude of NKG2C(+) NK cell expansion.

19 nvironmental cues, such as light, to promote cell expansion.

20 agnitude of virus-specific effector CD8(+) T cell expansion.

21 ate the transition between cell division and cell expansion.

22 nts regulatory T-cell and IL-10-expressing T-cell expansion.

23 ledons unfurling, during the period of rapid cell expansion.

24 ed bone loss in vivo is associated with Th17 cell expansion.

25 an in vivo model of squamous cancer-stromal cell expansion.

26 ves of cell division, followed by a phase of cell expansion.

27 g ratio and further encourages oligoclonal T-cell expansion.

28 lasma membrane (PM) H(+)-ATPases and promote cell expansion.

29 mmunocompromised mice to mimic ART-induced T-cell expansion.

30 ring scaffolds, and even substrates for stem cell expansion.

31 division and cell merging that are shaped by cell expansion.

32 subsequent phases of cell proliferation and cell expansion.

33 bryo morphology are a consequence of lack of cell expansion.

34 to deliver material for wall remodelling and cell expansion.

35 ht to attenuate autoreactivity by limiting T cell expansion.

36 latory molecules are implicated in driving T cell expansion.

37 erent stages of development, likely limiting cell expansion.

38 s provide additional insight into human beta-cell expansion.

39 portance for temporal and spatial control of cell expansion.

40 ementary processes: biomass biosynthesis and cell expansion.

41 , but also plays a direct role in regulating cell expansion.

42 shape and are unstable at the time scales of cell expansion.

43 ting this molecule as a trigger for CD4(+) T cell expansion.

44 at this MPK cascade affects auxin-influenced cell expansion.

45 PRMT5 is an important modulator of CD4(+) T cell expansion.

46 microtubule organization during anisotropic cell expansion.

47 o the emerging description of auxin-mediated cell expansion.

48 d by a combination of cell proliferation and cell expansion.

49 ility of these regulatory ILCs to suppress T cell expansion.

50 y of biomass, while its extensibility limits cell expansion.

51 was the most effective in reducing leukemic cell expansion.

52 ream of MPK1 in influencing auxin-responsive cell expansion.

53 beta-cell FoxM1 pathway and suppresses beta-cell expansion.

54 d that RHM1 is required to promote epidermal cell expansion.

55 mone that inhibits root growth by repressing cell expansion.

56 eages, indicating earlier or separate clonal cell expansions.

57 postinfection were not required for CD4(+) T cell expansion; 2) DCs that infiltrated the cornea >24 h

58 ells also produced GDM, with inadequate beta-cell expansion accompanied by failure to induce PRLR-dep

59 turn significantly reduced donor effector T cell expansion, activation, and migration into GVHD targ

60 cular mechanisms determining specific target cell expansion after an oncogenic hit.

61 e propionate promoted Sema4a-dependent T reg cell expansion, ameliorating both diseases.

62 tical role for IL-10 in driving mucosal mast cell expansion and activation, suggesting that, in its a

63 ters (GCs) are the primary sites of clonal B cell expansion and affinity maturation, directing the pr

64 of LypW with defects in TIV-induced CD4(+) T-cell expansion and antibody affinity maturation suggests

65 s were treated with amitrole, which inhibits cell expansion and chloroplast function.

66 de novo methylation programs that restrict T cell expansion and clonal diversity during PD-1 blockade

67 ransition from cell division to post-mitotic cell expansion and concomitant petal maturation.

68 Numb thereby restricts mammary stem cell expansion and controls the proliferation and lineag

69 cule STAT3 inhibitor, can block Th2 and Th17 cell expansion and cytokine production to prevent house

70 esponses in vivo as evidenced by increased T cell expansion and decreased tumor growth in Cat2(-/-) m

71 AZ signaling mechanism that coordinates stem cell expansion and differentiation during organ renewal.

72 not dependent on MyD88, as myd88(-/-) LSK(-) cell expansion and differentiation remained unaffected a

73 ll ef, Cyrillic for the rapid induction of B cell expansion and differentiation, Ab secretion, and Th

74 enesis through regulating myeloid progenitor cell expansion and differentiation, foam cell formation

75 role for Nr4a1 in the regulation of CD8(+) T cell expansion and effector function through transcripti

76 py is highly promising but requires robust T-cell expansion and engraftment.

77 ng antigen-loaded dendritic cells improved T cell expansion and favored central memory T cell differe

78 d TCM is an intriguing strategy to enhance T cell expansion and function against pathogens or tumors.

79 In addition, DCAF1 is required for T-cell expansion and function during anti-viral and autoim

80 sequent autocrine stimulation is vital for T cell expansion and function.

81 response of glycolysis to promote effector T cell expansion and function.

82 d-derived suppressor cells (MDSCs) inhibit T-cell expansion and functions by versatile mechanisms suc

83 tic pH regulation, steering the rate of root cell expansion and gravitropic response.

84 sed pH abrogates wall loosening required for cell expansion and growth.

85 SCs prevent proper suppression of effector T-cell expansion and hamper the immune system's ability to

86 vo Treg-cell numbers and dampened effector T-cell expansion and IFN-gamma production.

87 ion correlated with robust germinal center B-cell expansion and increased activated CD4(+) T-cell pop

88 y promoted growth of ENS cell spheres during cell expansion and increased the number of newborn neuro

89 , a surface protein that drives polyclonal B cell expansion and induces cell death in the absence of

90 e inhibits initial endogenous alloreactive T-cell expansion and induces more regulation.

91 results indicate that PGX2 both functions in cell expansion and influences secondary wall formation,

92 at create a supportive stroma for neoplastic cell expansion and invasion.

93 has an important role in hematopoietic stem cell expansion and is commonly deregulated in acute leuk

94 s immune responses by restraining effector T cell expansion and limiting nonspecific damage to the ho

95 f Gli proteins with GANT61 inhibited Gli1(+) cell expansion and myofibroblast differentiation and att

96 Despite overt T-cell expansion and neutrophilia, a reduction in conventi

97 ng on the endogenous IL-7 to enhance donor T cell expansion and persistence after lymphodepleting che

98 ulatory programs, which constrain effector T cell expansion and prevent increasing oligoclonality but

99 e as a paracrine signal that sustains tumour cell expansion and progression, suggesting that apelin i

100 trol distinct biological mechanisms, such as cell expansion and proliferation, will enhance crop yiel

101 munity was associated with improved CD8(+) T cell expansion and reduced tolerization, and it was depe

102 The AM forms through limited cell expansion and requires the recruitment of numerous

103 ice with IL-21 strongly promoted donor CD8 T cell expansion and rescued defective donor anti-host CTL

104 cogenic lesions that facilitate unrestrained cell expansion and resistance to antiproliferative signa

105 les induces fungal antigen-specific CD4(+) T cell expansion and resistance to lethal challenge with m

106 the efficacy of mATG in controlling memory T cell expansion and significantly extends heart allograft

107 plastids would then delay the transition to cell expansion and stimulate cell proliferation.

108 These results suggest that delayed effector cell expansion and stochastic variability in effector ce

109 activation in OL lineage cells, and perturbs cell expansion and survival, blunting the process of CNS

110 following demyelination disturbs OL lineage cell expansion and survival, leading to a delay in the r

111 In terms of NK cell expansion and survival, we now report that Kruppel-

112 ulted in profound defects in IL-7-mediated T cell expansion and survival.

113 egrated to achieve the required magnitude of cell expansion and the appropriate balance of effector/m

114 Conversely, B cell expansion and the development of autoantibodies in

115 ate a novel role for IL-10 in promoting mast cell expansion and the development of IgE-mediated food

116 that constitutively express 4-1BBL promote T cell expansion and tumor eradication while reducing exha

117 hanisms of auxin-mediated rapid promotion of cell expansion and underlying rearrangement of cell wall

118 in the cumulus cells, much increased cumulus cell expansion, and an accelerated severance of cytoplas

119 In plant roots, auxin inhibits cell expansion, and an increase in cellular auxin levels

120 ressive CD4(+) T-cell depletion and CD8(+) T-cell expansion, and CD4(+) T-cell depletion is linked di

121 nt and can involve changes in cell division, cell expansion, and cell fate.

122 nuria, glomerular filtration rate, mesangial cell expansion, and collagen type IV and transforming gr

123 PL activation enhances antitumor function, T-cell expansion, and cytokine production and preserves a

124 1-dependent gene expression, limited CD8(+)T-cell expansion, and greatly reduced proinflammatory cyto

125 contribute to homeostasis, pathogen defense, cell expansion, and growth in plants.

126 in T cells inhibited diabetes development, T-cell expansion, and IFN-gamma production.

127 0 (IL-10) production, a delayed gammadelta T cell expansion, and lower antibody and WNV-specific T ce

128 ng IRF3 also developed lung disease, myeloid cell expansion, and T cell cytopenia.

129 n viral epitope mutation, antigen-specific T-cell expansion, and the repertoire of responding clonoty

130 studies of human samples, including clonal B-cell expansions, and also for following antibody affinit

131 nd both CD4(+) T-cell cytopenia and CD8(+) T-cell expansion are associated with morbidity and mortali

132 of ESP in daughter chromatid separation and cell expansion are conserved between gymnosperms and ang

133 bility that RBK1 effects on auxin-responsive cell expansion are mediated through phosphorylation-depe

134 N UP RNA19 (SAUR19) subfamily, which promote cell expansion, are repressed by SOB3 and light, and are

135 display hypersensitivity in auxin-responsive cell expansion assays, suggesting that this MPK cascade

136 isplays hypersensitivity in auxin-responsive cell expansion assays.

137 ction made a modest contribution to CD4(+) T cell expansion at 3 dpi but did not contribute at 7 dpi;

138 ome species to grow more effectively through cell expansion at cool temperatures.

139 course of infection, also showed no T or NK cell expansion at the time.

140 cumulation of IgG-ICs prior to significant B cell expansion, BAFF secretion, and lupus nephritis.

141 IL-12 is required for CD8(+) T cell expansion but drives effector CD8(+) T cells into a

142 H(+)-ATPases (PM H(+)-ATPases) to facilitate cell expansion by both loosening the cell wall through a

143 suggests that circulating FFAs promote beta cell expansion by direct and indirect mechanisms.

144 nt of caspase activity, indicating that Th17 cell expansion by MC occurred through inflammasome-indep

145 nterleukin-25, which indirectly induces tuft cell expansion by promoting interleukin-13 production by

146 rowth, we found that cellulose synthesis and cell expansion can be uncoupled and are regulated by dif

147 cause blockade of GITR ligand prevented Treg cell expansion caused by Ptpn22 KD.

148 These reserves support cell expansion, chloroplast development and root growth

149 Dnmt3a mutations induced hematopoietic stem cell expansion, cooperated with mutations in the FMS-lik

150 In the IL2DT cohort, NK cell expansion correlated with higher postchemotherapy s

151 Enhanced T-cell expansion correlated with increased expression of s

152 In AH patients, ductular cell expansion correlated with portal hypertension and c

153 Stimulation of endogenous beta-cell expansion could facilitate regeneration in patients

154 gene dose in miR-142(-/-) mice rescues the B-cell expansion defect, suggesting that BAFF-R is a bona

155 In plants, anisotropic cell expansion depends on cortical microtubules that ser

156 view is that the direction of turgor-driven cell expansion depends on the cortical microtubule (CMT)

157 -generation sequencing were used to assess T cell expansion, differentiation, and clonal diversity.

158 CMV- and EBV-related T-cell expansions do not impair naive T-cell numbers or ma

159 dual T1D subjects, consistent with in vivo T cell expansion during disease progression.

160 ls can regulate epithelial KIT(+) progenitor cell expansion during murine salivary gland organogenesi

161 l wall loosening in the embryo to facilitate cell expansion during the accumulation of storage reserv

162 ted that IL-6 is required for uncontrolled T cell expansion during the early stage of disease develop

163 increases survivin and intestinal epithelial cell expansion during therapeutic adaptation in patients

164 ifferentiation to myeloid-derived suppressor cell expansion during tumour progression.

165 tance of balancing stromal versus adipogenic cell expansion during white adipose tissue development,

166 strengthen cell walls, therefore restricting cell expansion, during normal growth and in response to

167 parisons, we propose that dysregulation of T-cell expansion enabled by downregulation of immune negat

168 These data reveal that the spatiotemporal cell expansion events driving this transition are not de

169 undescribed protein, named herein BefA (beta Cell Expansion Factor A), which is sufficient to induce

170 f naive B cells initiated a phase of rapid B-cell expansion followed by a proliferative T-cell respon

171 dited route to vaccine delivery or optimal T cell expansion for adoptive cell transfer.

172 e associated with differential expression of cell-expansion genes.

173 ll polarity, often associated with polarized cell expansion/growth in plants, describes the uneven di

174 th inclusion body myositis, the autoimmune T cell expansion has evolved into a neoplastic-like or ove

175 cognized, most publications on age-related T-cell expansions have focused on dominant target proteins

176 Microtubules influence cell expansion; however, the mechanisms by which environ

177 , MEK1/2 inhibitor treatment up-regulated B1 cell expansion, IgM production, phagocytic receptor expr

178 lanoma, the presence of NAC during ex vivo T-cell expansion improved the persistence of adoptively tr

179 grasses is driven by cell proliferation and cell expansion in a basal growth zone [3].

180 t gammadelta TCR expression and gammadelta T cell expansion in AIM.

181 ys a major role in chromatid disjunction and cell expansion in Arabidopsis thaliana.

182 mediated intestinal stem cell and progenitor cell expansion in CD patients, human cells, and preclini

183 LN resident dendritic cells (DC) to CD4(+) T cell expansion in DLNs and restimulation in corneas is u

184 ic skin transplant and alloantigen-induced T cell expansion in draining lymph node experiments.

185 This inhibition of DC activation and T cell expansion in LNG-treated mice also delayed chlamydi

186 s reveals a minor role of p53 in suppressing cell expansion in lung adenomas.

187 ct4, Sox2, Klf4 and c-Myc (OSKM) followed by cell expansion in media that promote lineage differentia

188 raptor deletion ameliorates the aberrant TFH cell expansion in mice lacking Def6.

189 ll immunity and promoted CD4(+)Foxp3(+) Treg cell expansion in numbers.

190 specific IgE production, and intestinal mast cell expansion in offspring.

191 Consistently, beta-cell expansion in response to a high-fat, high-sucrose (

192 Only monocytes supported gammadelta T cell expansion in response to all three stimuli, whereas

193 ified 28 genes that correlated with CD8(+) T cell expansion in response to an acute EBV infection.

194 ery and stability to adjust plant growth and cell expansion in response to changing environmental con

195 portantly, hpaECMs inhibit human naive CD4 T-cell expansion in response to polyclonal stimuli by indu

196 ting cell wall-loosening enzymes that enable cell expansion in shoots.

197 human cells, and with plasmablast and plasma cell expansion in SLE, consistent with the dependence of

198 leaf movement: ethylene induces longitudinal cell expansion in the abaxial petiole epidermis to induc

199 th of Lactobacilli and triggers T regulatory cell expansion in the gut.

200 but it did at a cellular level with reduced cell expansion in the hypocotyl relative to the wild typ

201 -27 were all required for efficient CD8(+) T cell expansion in the lungs.

202 sure is associated with greater regulatory T cell expansion in the mediastinal lymph nodes.

203 nted HMBPP but failed to induce gammadelta T cell expansion in the presence of ZOL or anti-CD277 mAb.

204 of RNAi transformants indicated reduction of cell expansion in vascular bundles, particularly on thei

205 sing a clinically applicable protocol for NK-cell expansion in vitro and in vivo.

206 e functional in driving Ag-specific CD8(+) T cell expansion in vitro but that this process was defect

207 also provide a novel tool for assessing beta-cell expansion in vitro.

208 gnaling is sufficient to drive transformed B-cell expansion in vivo and identify the JNK pathway as a

209 ollaborates with FLT3-ITD to promote myeloid cell expansion in vivo and that this involves a multitar

210 t viruses but thought to decrease in large T-cell expansions, in particular at older ages.

211 licing and reverts haematopoietic progenitor cell expansion induced by mutant U2AF1 expression.

212 how that Ag and cytokine levels during CD4 T cell expansion influence the proportion of activated cel

213 Gibberellic acid (GA)-mediated cell expansion initiates the seed-to-seedling transition

214 Cell expansion is an essential process in plant morphoge

215 per (TFH) cells, is critical as aberrant TFH cell expansion is associated with autoimmune diseases, s

216 here the interplay between cell division and cell expansion is instrumental.

217 Strictly controlled cell expansion is linked to asymmetric cell division in

218 rehensive understanding of how auxin induces cell expansion is perplexing, because auxin acts in a co

219 We demonstrate that cell expansion is regulated by protein-mediated changes

220 regulation of IL-10-mediated intestinal mast cell expansion is T cell dependent.

221 tical role in germination by enabling embryo cell expansion leading to radicle protrusion, as well as

222 ives an early, unsustained germinal center B-cell expansion, less reduction of T follicular regulator

223 ontrolling hematopoietic stem and progenitor cell expansion, lineage commitment, and maturation have

224 s represent a powerful resource to monitor T cell expansion, localization, and novel engraftment prot

225 Persistent CD8 T-cell expansion, low CD4/CD8 T-cell ratios, and heightene

226 ults regarding whether large, CMV-specific T-cell expansions maintain their function during human agi

227 peripheral markers affected by peripheral T-cell expansion, making it difficult to assess the role o

228 istribution that accompany compensatory beta-cell expansion may be key to developing novel antidiabet

229 ntigen-specific TCM, resulting in enhanced T cell expansion measured during subsequent booster inject

230 on were responsible for most of the CD4(+) T cell expansion measured in the DLNs at 3 and 7 d postinf

231 tes that multiple genetic and spatiotemporal cell expansion mechanisms underlie the seed to seedling

232 e lack of impact of Klhl6 deficiency on GC B cell expansion, mutants could contribute to the oncogeni

233 Cell expansion needs to be carefully regulated to produc

234 G responses by enhancing early Ag-specific B cell expansion, not by altering B cell development.

235 hese results indicate that although in vitro cell expansion of embryonic tooth mesenchymal cells rend

236 on and single filament dynamics during axial cell expansion of living epidermal cells.

237 lability of large numbers of cells, in vitro cell expansion of tooth-inducing cell populations is an

238 tiviral treatment, Vdelta2(neg) gammadelta T cell expansion onset was associated with recovery, where

239 AFF and APRIL did not cause indiscriminate B cell expansion or an increase in total IgG.

240 t compartment, and that signals derived from cell expansion or chloroplasts may regulate REC1.

241 ntrinsic manner without disrupting Ag-driven cell expansion or effector function.

242 tes in vivo in islets, independently of beta-cell expansion or islet blood flow velocity.

243 rocesses during plant development, including cell expansion, organ initiation, and cell separation.

244 ermissive environment favoring leukemic stem cell expansion over normal HSC maintenance, and evidence

245 iated with delayed Vdelta2(neg) gammadelta T cell expansion (P<0.001).

246 R-23a is indispensable for effector CD4(+) T cell expansion, particularly by providing early protecti

247 cation of factors that correlated with CAR-T cell expansion, persistence, and toxicity and facilitate

248 ell numbers typically improve while CD8(+) T-cell expansion persists, and both CD4(+) T-cell cytopeni

249 se, simultaneously delaying the onset of the cell expansion phase.

250 the addition of NAC to current therapeutic T-cell expansion protocols, offering immediate potential t

251 A Vdelta2(neg) gammadelta T cell expansion rate of >0.06% per day predicted the grow

252 infiltration was secondary to reduction of T-cell expansion rather than less trafficking.

253 Here, we find that active surface cell expansion represents the key process coordinating t

254 nversely curbs tumour growth and cancer stem cell expansion, restores chemosensitivity and blocks met

255 the mechanisms of ESP-mediated regulation of cell expansion seem to be lineage-specific.

256 Whereas beta cell expansion seems an obvious therapeutic approach to

257 or role in membrane fusion and contribute to cell expansion, signaling, and polar growth in plants.

258 levation of plasma glucagon levels and alpha-cell expansion similar to wild-type mice.

259 ncogenic activities of phospho-HLXB9 in beta-cell expansion strategies to alleviate beta-cell loss in

260 ly partially modified the spatial pattern of cell expansion, suggesting that the diverse growth polar

261 11c(+) dendritic cells abrogates secondary T cell expansion, suggesting that virus-infected follicula

262 that the STING N153S mutation caused myeloid cell expansion, T cell cytopenia, and dysregulation of i

263 Long-term survivors had more pronounced T-cell expansion than patients with OS <30 months.

264 have a greater requirement for GA to promote cell expansion than the lower embryo axis.

265 ears of age showed smaller effector memory T-cell expansions than those infected between 2 and 6 year

266 in monoclonal B lymphocytosis (MBL, 7%), a B-cell expansion that can evolve to CLL.

267 f CD4(+) T-cell restoration and the CD8(+) T-cell expansion that characterize HIV infection.

268 proteins may be involved in signaling during cell expansion that coordinates proton pumping and cellu

269 V-segment usage, somatic hypermutation and B cell expansion that elucidates the dominance of F-allele

270 ts that elevated IL-15 may also drive CD8+ T cell expansion that is linked to increased morbidity and

271 n of cell-cycle progression and post-mitotic cell expansion that together sculpt organ form.

272 Later on, during cell expansion, the plasmodesmata pore widens and the tw

273 IL4I1 modulates inflammation by regulating T cell expansion, thereby permitting the formation of a fa

274 ells with osteoclasts (OC) can enhance tumor cell expansion through activation of complex signaling t

275 also the potential for pancreatic islet beta-cell expansion through c-MET regulation to ameliorate be

276 uction, together with the inhibition of CK5+ cell expansion through RAR/PR cross talk, may explain th

277 vated effector CD4(+) T cells can boost Treg cell expansion through TNF or IL-2.

278 pDCs and microbial colonization induce T reg cell expansion to protect against severe bronchiolitis a

279 action, VEGFA upregulates Sox2 to drive stem cell expansion, together with miR-452 loss and Slug upre

280 D70 expression in T cells, and CD70 limits T cell expansion via a regulatory T cell-independent mecha

281 LPS-TLR4 pathway role in ductular cell expansion was assessed in human and mouse progenito

282 Reduced CD4(+) T cell expansion was not due to a further block in thymocy

283 DELLA protein RGA, expansin gene EXPA3, and cell expansion was quantified within distinct cell types

284 ditions of impaired TCR signaling, reduced T cell expansion was the limiting factor in antiviral immu

285 sulinomas hold the "genomic recipe" for beta cell expansion, we surveyed 38 human insulinomas to obta

286 , 12, and 24 mo), posttransplant NKG2C(+) NK cell expansions were not observed in every patient with

287 elongated parthenocarpic fruit and increased cell expansion, whereas simultaneous treatment with the

288 Therefore, clofazimine enhances Tcm cell expansion, which in turn provides improved vaccine

289 in-Barr virus (EBV) induce effector memory T-cell expansions, which are variable and potentially depe

290 BMP2 promotes ALDH(+)CD133(+) cell expansion while suppressing the proliferation of AL

291 Exogenous IL-18 enhanced the gammadelta T cell expansion with all three stimuli, remarkably also i

292 ytotoxic, inflammatory cytokine immunity, to cell expansion with diminished cytokine but increased co

293 ungal hyphae, possess a typical tip or polar cell expansion with growth limited to the apical dome.

294 potent stem cells allowed enhanced erythroid cell expansion with preserved differentiation.

295 d to wild-type roots, where auxin suppresses cell expansion within 1 min of treatment.

296 ing factor neutralization inhibited DC and T-cell expansion within pericardial AT, and translated int

297 tatory and inhibitory pathways to coordinate cell expansion within single cells and between cells in

298 teractions of PD-L1 with CD80 augment CD8+ T cell expansion without increasing anergy, exhaustion, or

299 1) Notch2 haploinsufficiency limits NOD MZ B cell expansion without preventing type 1 diabetes, 2) BT

300 erforin-expressing dendritic cells induces T cell expansion, worsening autoimmunity and surprisingly