ライフサイエンスコーパス: mature @ cell

1 1, adaptive immunity, alphabeta T cells, and mature B cells.

2 repertoire, and antigen-driven selection of mature B cells.

3 through editing toward lambda light chain in mature B cells.

4 ytic leukaemia (CLL) is a clonal disorder of mature B cells.

5 blocks by expressing bnAbs conditionally in mature B cells.

6 previously described, a 2-fold reduction in mature B cells.

7 hrough Nod1 promotes competitive survival of mature B cells.

8 ment, enabling the expression of VRC26UCA in mature B cells.

9 role for Fbw7 in the survival and fitness of mature B cells.

10 sential regulator of cellular homeostasis in mature B cells.

11 block at the pro-B cell stage and a lack of mature B cells.

12 V-2) strain has the unique ability to infect mature T cells.

13 evealed an intrinsic proliferative defect of mature T cells.

14 eration of a large number of double negative mature T cells.

15 ays a significant role in the homeostasis of mature T cells.

16 ng the specific impact of Notch signaling in mature T cells.

17 stem and progenitor cells (HSPCs) through to mature T cells.

18 h positive and negative selections to become mature T cells.

19 identity and shape the proper generation of mature T cells.

20 red for PT progenitors to differentiate into mature PT cells.

21 necessary for the generation of functionally mature LTi cells.

22 ss central to stimulus-secretion coupling in mature beta cells.

23 this is partially compensated for by longer mature root cells.

24 odulates the differentiation and function of mature blood cells.

25 cell lineage and the effect ceases as cells mature to EE cells.

26 f HSCs, but there were no obvious defects in mature immune cells.

27 o transiently upregulated by high glucose in mature IDG-SW3 cells.

28 in a shift from luminal progenitor cells to mature luminal cells.

29 lveolar epithelial cells and morphologically mature type II cells.

30 eding, migrate into the gonad primordia, and mature into germ cells.

31 tightly regulated process that generates all mature red blood cells.

32 s to ECFCs and can also trigger sprouting of mature endothelial cells.

33 second strain of EBV, EBV type 2, to infect mature peripheral T cells.

34 the cellular protein CD21 to gain entry into mature peripheral T cells.

35 aintenance of the transducing stereocilia in mature cochlear hair cells.

36 ption of how to phenotypically characterize, mature, and freeze the cells.

37 old KO BM are differentiating cells that can mature into functional B cells.

38 structure of the transducing stereocilia in mature mouse cochlear hair cells.

39 B2, significantly enhances the production of mature enucleated red blood cells.

40 rs cannot produce multiple basal bodies, and mature into single ciliated cells.

41 ical NF-kappaB signaling was impaired in all mature naive CVID-derived B cells.

42 med electron tomography (ET) of immature and mature Ty3 particles within cells.

43 uited to germinal centers, and they affinity matured, and formed memory B cells.

44 well as the caspase-1-mediated generation of mature IL-1beta secreted from cells.

45 ion deficits along with dramatic decrease in mature oligodendrocytes and their progenitor cells.

46 ow that deletion of Stim1 and Stim2 genes in mature Treg cells abolishes Ca(2+) signaling and prevent

47 identical grafts, containing high numbers of mature NK cells, according to PT-Cy-based protocols in 2

48 Thus, incorporating affinity-matured ligands for NK cell-activating receptors might r

49 y control Ca2+ fluxes that are essential for mature T-cell activation and differentiation and protect

50 Thus, Pdap1 protects mature B cells against chronic ISR activation and ensure

51 Mature blood cells all derived from a pool of rare long-

52 Mature granule cells also contributed to functional moss

53 exhibit a transcriptional profile similar to mature alpha cells and although they produce proinsulin

54 We reveal novel sub-types of immature and mature gammadelta T cells and identify an unp

55 ng IgG mu heavy chain-null mice deficient in mature B cells and by IgG transfer.

56 s in mice leads to the prolonged survival of mature B cells and expanded B cell compartments in secon

57 e responsible for the lifelong production of mature blood cells and are the rational target for clini

58 mal promoters are densely methylated in less mature CD56(bright) NK cells and are progressively demet

59 rst example of phenotypic continuity between mature CLL cells and their progenitors in the bone marro

60 Circulating mature endothelial cells and circulating endothelial pro

61 s, NSG-SGM3 mice supported the population of mature human tissue-resident mast cells and basophils.

62 Transcriptional profiling of normal ER(+) mature luminal mammary epithelial cells and ER(+) breast

63 characterized by the excessive production of mature myeloid cells and arise from the acquisition of s

64 ate that group 1 ILCs consist of circulating mature natural killer (NK) cells and tissue-resident ILC

65 showed myeloid hyperplasia with predominant mature neutrophils, and decreased progenitor cells and l

66 a stochastic process exclusive to subsets of mature NK cells and CD8(+) T cells.

67 xtranodal lymphoid neoplasms that arise from mature postthymic T cells and localize to the skin.

68 Remarkably, CLas was present in both mature sieve element cells and nucleated nonsieve elemen

69 expressing ThPOK compared with wild-type CD4 mature T cells and compromising cytotoxic program, faile

70 esulting in the continued presence of CD8(+) mature T cells and the generation of a large number of d

71 they undergo development from precursors to mature, circulating cells and how our understanding of t

72 1 (a gene-expression pattern associated with mature follicular B cells) and also attained increased c

73 Mature erythrocytes, immature erythroid cells, and phago

74 As Gdf11 is expressed by mature hematopoietic cells, and erythroid precursor cell

75 A/C helps distinguish normal from neoplastic mature T cells, and VAMP-7 recapitulates light-cytometri

76 d levels of 36 blood cell traits (platelets, mature/immature red cells, and myeloid/lymphoid/compound

77 In normal adult mice, most mature B cells are enriched for Nod1 up-regulated cells,

78 In response to T cell-dependent antigens, mature B cells are stimulated to form germinal centers (

79 Mature double negative (DN) T cells are a population of

80 Whereas these mature effector cells are extensively studied, the diffe

81 d IFN-gamma led to a significant increase in mature CD27(-) CD11b(+) NK cells as well as a significan

82 ts suggest that motoneuron properties do not mature by cell autonomous mechanisms alone, but also dep

83 The exchange of mature B cells between blood and bone marrow is sensitiv

84 autophagosomes containing synaptic material mature in the cell body.

85 ghtly regulated in thymocytes, as well as in mature T cells both at steady state and upon stimulation

86 en implicated in inhibiting BCR signaling in mature B cells but promoting pre-BCR signaling during ea

87 This intermediate gives rise to mature-like cardiomyocytes in control cells but, mutant

88 and its ligand IL-33 are known regulators of mature myeloid cells, but their roles in AML are not kno

89 s from multipotent CPCs to intermediates and mature cardiac cells by population and single-cell RNA-s

90 s the differentiation of PT progenitors into mature PT cells by regulating the expression of genes as

91 Phenotypic analysis indicated a mature state of DN B cells by low CD5, CD10, and CD38 ex

92 al immature thymocytes to differentiate into mature T cells by binding to peptide-MHC ligands togethe

93 equirements for the generation of terminally mature functional innate effector cells can be elucidate

94 established differentiation therapies, some mature leukemia cells can de-differentiate and reacquire

95 D28 signaling results in the accumulation of mature, peripheral TRA-specific T cells capable of media

96 56(bright) NK cells and is confined to fully mature NK cells characterized by the NKG2A(-)KIR(+)CD57(

97 Mature B cells coexpress both IgM and IgD B-cell antigen

98 for selection of B cells into the follicular mature versus marginal zone B cell compartment.

99 In mature Treg cells, continued expression of FOXP3 maintai

100 ciated Ifng promoter demethylation, the less mature phenotype of Tyk2(-/-) NK cells correlated with a

101 Es are functionally distinct from their more mature but still naive T cell counterparts, because they

102 variant transcription factor 2 (ETV2)(3) in mature human endothelial cells cultured in a serum-free

103 ls, providing insights toward vaccination of mature B cell-deficient individuals and implications in

104 ctile waves and their synchronization within maturing, unlabeled induced pluripotent stem cell-derive

105 a robust means for expansion of functionally mature stem cell-derived astrocytes for preclinical inve

106 Mice with specific deletion of Ikaros in mature B cells developed systemic autoimmunity.

107 tional, as judged by its capacity to support mature T cell development in vivo after transplantation

108 Mature B2 cells differentiated into bona fide B1 cells u

109 ed glycolysis pathway, which is required for mature AT1 cell differentiation.

110 y modifying the immunoglobulin (Ig) genes of mature B cells directly using genome editing technologie

111 cell depletion in mice, that a population of mature B cells distinguishable by IgD(low/-) expression

112 Mature B cells diversify their antibody genes by class s

113 ymphocytic leukemia (CLL) is a malignancy of mature B cells driven by B-cell receptor (BCR) signaling

114 istics arise from their differentiation into mature effector cells during thymic development.

115 sion, the accumulation of gamma-tubulin-2 in mature neurons and neuroblastoma cells during oxidative

116 T cell population that seeds development of mature Tex cells early during chronic infection.

117 We show that in mature zebrafish hair cells, evoked presynaptic-Ca(2+) i

118 y little is known on the mechanisms by which mature endothelial cells exit from a quiescent state and

119 We find expression of viral receptor ACE2 in mature choroid plexus cells expressing abundant lipoprot

120 Mature naive B cells expressing BCRs of the IgM and IgD

121 eceptor-deficient mice, the thymus generates mature T cells expressing MHC-independent TCRs that reco

122 on as a result of decreased competition with mature granule cells for synaptic inputs.

123 lt-born DG granule cells, which compete with mature granule cells for synaptic integration.

124 ), as well as strategies to characterize and mature the cells for further analysis.

125 of peripheral B cell tolerance that restrain mature B cells from mounting inappropriate responses to

126 tantial advances have been made in producing mature beta-cells from human pluripotent stem cells that

127 Tregs continuously constraining one-third of mature CD4(+)Foxp3(-) cells from converting to pathogeni

128 Even though Plerixafor liberates HSPCs and mature immune cells from bone marrow, competitive repopu

129 fficient platform for generating functional, mature T cells from human PSCs.

130 -like macrophages increase the production of mature, enucleated erythroid cells from umbilical cord b

131 dults, implying continued essential roles in mature endocrine cell function.

132 ling, pericytes upregulate genes involved in mature pericyte cell function, together with a remarkabl

133 y diphtheria toxin-based ablation of >50% of mature DG granule cells (GCs) or by prolonged brain-spec

134 characterized events is the acquisition of a mature T-cell gene expression program characterized by t

135 In mature Th17 cells, GSK-J4 induces an altered transcripti

136 ad entered a new phase of proliferation, and mature MTB cells had begun to move from the main body of

137 However, differentiation of human PSCs into mature, conventional T cells has been challenging with e

138 Notably, mature taste cells have life spans of only 5-20 days and

139 rlying the high-level expression of GATA1 in maturing erythroid cells have been studied extensively,

140 Mature mammalian cochlear hair cells (HCs) do not sponta

141 Mature hepatocyte-like cells (HLCs) derived from human i

142 s, as we have defined a function for CD21 on mature peripheral T cells, i.e., as a receptor for EBV.

143 n-binding protein 1 (LDB1) serve to maintain mature adult beta cell identity, revealing clues as to h

144 nd Cd11c mRNA levels, and the frequencies of mature dendritic cells, IFNgamma-, and IL-17- producing

145 IgD(dim)IgM(dim)CD21(neg)) at the expense of mature B cells (IgD(+)IgM(+)CD21(+)).

146 In the mature mammalian cochlea, inner hair cells (IHCs) are ma

147 Inducible ablation of LDB1 in mature beta cells impaired insulin secretion and glucose

148 ng is absolutely required for development of mature B cells in mice.

149 nses to BCR cross-linking and the absence of mature B cells in the bone marrow.

150 Mature B cells in the periphery are also reduced and cha

151 etion of Spi1 and Spib resulted in a lack of mature B cells in the spleen and a block in B cell devel

152 docrine progenitors, and differentiating and mature beta cells in vivo Pdx1(DeltaAREAII/-) mice exhib

153 haracterized by the expansion of monoclonal, mature CD5(+)CD23(+) B cells in the peripheral blood, se

154 uman embryonic stem cells, the generation of mature functional beta cells in vitro has remained elusi

155 oxetine, increases D1 receptor expression in mature granule cells in the dentate gyrus.

156 ment of CMML and JMML disease-initiating and mature leukemic cells in vivo, allowing creation of gene

157 e and increase differentiation and output of mature myeloid cells in response to stress stimuli to pr

158 d autoreactive new emigrant/transitional and mature naive B cells in NMOSD patients compared to healt

159 Myom2-RFP(+) PSC-CMs exhibited more mature phenotypes than RFP(-) cells in morphology, funct

160 lithium can trigger transdifferentiation of mature principal cells to intercalated cells in adult ki

161 Fate tracing revealed mature principal cells in the inner stripe of the outer

162 severely immunodeficient with an absence of mature T, B, and NK cells in the immune system.

163 ers (HLCs) resemble the glycan features of a mature tissue rather than cells in culture.

164 LK could restore progenitor-like features in mature CD30+ peripheral CD4+ T cells, in keeping with a

165 Mature human B cells infected by Epstein-Barr virus (EBV

166 Inf-cDC2s matured in response to cell-intrinsic Toll-like receptor

167 Mature induced pluripotent stem cell (iPSC)-derived cort

168 n to be affected in schizophrenia (SCZ) when matured-from induced pluripotent stem cells (iPSCs) deri

169 ring embryogenesis, but the role of Notch in mature beta cells is unclear.

170 (CH) arises when a substantial proportion of mature blood cells is derived from a single dominant hem

171 Tightly regulated production of mature blood cells is essential for health and survival

172 Adoptive transfer of mature NK cells is sufficient to delay both T-lymphoma g

173 The mature surface of live cells is characterized by a lands

174 alphabeta T cell antigen receptors (TCRs) on mature T cells is selected in the thymus where it is ren

175 lphabeta T cell receptor (TCR) repertoire on mature T cells is selected in the thymus, but the basis

176 f ageing, whereas the function of individual mature thymic epithelial cells is compromised only modes

177 s to the sensitivity of B cell precursors as mature B cells largely tolerated their loss.

178 its dependence on POM121, and a reduction of mature NPCs in Torsin-deficient cells lead us to conclud

179 f4a with Osr2Cre led to the complete loss of mature PT cells, lethal to the Hnf4a mutant mice.

180 acquires frequent inactivating mutations in mature B cell malignancies, especially in the MYD88(L265

181 lymphoma (PTCL) is a heterogeneous group of mature T-cell malignancies; approximately one-third of c

182 allosum and external capsule, and decline of mature oligodendrocytes and oligodendrocyte precursor ce

183 rogenitor cells, and a subset of these cells mature into mesangial cells (MCs) that continue to expre

184 Mature dendritic cell (mDC) vaccination with tumor-encod

185 ervical cancer micromilieu and found CD83(+) mature dendritic cells (mDC) coexpressing IL23 in the st

186 s in 8% of cases the translocation occurs in mature B cells mediated by activation-induced cytidine d

187 puts, abGCs exert monosynaptic inhibition of mature granule cells (mGCs) through group II metabotropi

188 Indeed, mature peritoneal cavity B-1a cells migrated to BM in a

189 K3 kinase inhibition can greatly enhance the mature character of NK cells most desired for effective

190 Mantle cell lymphoma (MCL) is a mature B-cell neoplasm initially driven by CCND1 rearran

191 Hairy cell leukemia (HCL) is a chronic mature B-cell neoplasm with unique clinicopathologic fea

192 Anaplastic large cell lymphoma (ALCL) is a mature T cell neoplasm that often expresses the CD4+ T c

193 l prolymphocytic leukemia (T-PLL) is a rare, mature T-cell neoplasm with a heterogeneous clinical cou

194 Mature B-cell neoplasms are the fifth most common neopla

195 c miRNA whose expression is lost in numerous mature B-cell neoplasms.

196 assessed the role of the E3 ligase FBXW7 in mature B-cell neoplasms.

197 as improved survival rates for children with mature B-cell non-Hodgkin lymphoma (NHL); however, assoc

198 younger than 18 years of age with high-risk, mature B-cell non-Hodgkin's lymphoma (stage III with an

199 and adolescents with high-grade, high-risk, mature B-cell non-Hodgkin's lymphoma and was associated

200 cacy and safety in children with high-grade, mature B-cell non-Hodgkin's lymphoma are limited.

201 S similarly showed reduced myelin thickness, mature oligodendrocyte cell numbers and mRNA levels of m

202 in myelination, and mutant mice had reduced mature oligodendrocyte cell numbers, reduced myelin thic

203 em cells (HSCs) in the bone marrow (BM) form mature blood cells of all lineages through expansion of

204 e click chemistry to fluorescently label the mature PG in whole bacterial cells of Bacillus subtilis.

205 nditions of nutrient starvation and that the mature Red Blood Cells of some RTT patients retain mitoc

206 ansmission under physiological conditions at mature synapses made by Purkinje cells onto neurons in t

207 sence of GW and inflammatory signals, either mature dendritic cells or IL12, also demonstrated enhanc

208 d innate immunity, induced via modulation of mature myeloid cells or their bone marrow progenitors, m

209 (>18 years) with newly diagnosed, untreated mature T-cell or NK lymphomas (WHO 2001 or 2008 classifi

210 In total, 1695 patients with mature T-cell or NK lymphomas were enrolled between Oct

211 trans-Golgi network and are not retained in mature DCVs in the cell periphery.

212 Patients in MMR and MR(4.5) had a more mature, cytolytic CD57(+)CD62L(-) NK cell phenotype, con

213 tocompatibility complex class II (MHC)-II(+) mature antigen-presenting cell population kinetics durin

214 FOB cells are the dominant mature B cell population in the secondary lymphoid organ

215 f T cells in the maintenance/survival of the mature naive peripheral B cell population.

216 of PRMT5 and PRMT5 is vital to support both mature and immature GBM tumour cell populations.

217 gase Fbw7 is required for the maintenance of mature B cell populations in mice.

218 s are culled by immunological tolerance from mature B-cell populations.

219 y detected by measuring the precursor or the mature cytokine of bulk cell populations by techniques s

220 tially infected neural progenitor cells over mature neurons, reduced both cell populations, and cause

221 these findings, viral glycoproteins fail to mature in SPCA1-deficient cells preventing viral spread,

222 and uncover a thymus-independent pathway for mature T cell production in the bone marrow.

223 ry (EM) CD4(+) T cells, while naive and less mature memory cells prove to be more resistant.

224 Therefore, maturing Bienertia chlorenchyma cells provide a unique o

225 associated with patient outcome, and a high mature neutrophil/T-cell ratio resulted in inferior prog

226 The mature red blood cell (RBC) lacks a nucleus and organell

227 t islets are thought to contain functionally mature beta cells, recent analyses of transgenic rodent

228 ferentiating B cells can directly generate a mature B cell receptor (BCR) and bypass the requirement

229 the recovery of bone marrow cellularity and mature blood cell recovery at 21-30 days post-irradiatio

230 A subset of mature NKT cells remain thymic resident, but their activ

231 Regeneration of mature mammalian inner ear hair cells remains to be a ch

232 velopment of Treg cells, but its function in mature Treg cells remains unclear.

233 ly tolerated or positively selected into the mature B cell repertoire as well as at what stage, to wh

234 itive selection by endogenous Ags shapes the mature B cell repertoire.

235 (and may even be actively selected into) the mature B cell repertoire.

236 n early life determines the clonality of the mature B-1 B cell repertoire and ensuing antibody respon

237 The mature naive B cell repertoire consists of three well-de

238 Mature mammalian auditory hair cells require transmembra

239 early hematopoietic progenitors and splenic mature B cells, respectively.

240 ther factors appear to influence the fate of mature B cells responding to antigen in vivo.

241 ltiple inhibitors that blocked production of mature glucagon from proglucagon, beta-cells retained th

242 Notably, A2AR-deficient, terminally mature NK cells retained proliferative capacity and exhi

243 moxifen-inducible genetic lineage tracing of mature adipocytes and single-cell RNA sequencing reveale

244 ere, we profiled >25,000 differentiating and mature mouse neutrophils using single-cell RNA sequencin

245 olecular brake on plasticity and maintaining mature PV+ cell signaling.

246 f miRNAs in RPE cells, we used two different mature RPE cell-specific Cre recombinase drivers to inac

247 and partial deletion at the transitional to mature B cell stage, but become Env(-) upon receptor edi

248 After ablation of mature NK cells, starting from day 15 after HSCT and fav

249 signaling via Hes1 regulates maintenance of mature renal epithelial cell states.

250 In developing and mature sensory hair cells, stereocilia are connected to

251 Marginal zone B cells (MZB) are a mature B cell subset that rapidly respond to blood-borne

252 differentiation were consistently present in mature myeloid cells such as neutrophils and monocytes a

253 ion of the CAR-28/zeta led to elimination of mature CAR(+) T and B cells, suggesting that the CAR-med

254 erates has been puzzling and its function in mature T cells suggests promoting rather than repressing

255 , causing a torsional stress that breaks the mature F-pilus at the cell surface.

256 s and introduced 24 new residues forming the mature protein, alpha1(Lys374Serfs)*(25) Cell surface ex

257 -1, CD34, VE-Cadherin, FLK1, and TIE2 lacked mature arterial, venal, and lymphatic cell-surface marke

258 ally, we show wild-type Tcrb alleles produce mature alphabeta T cells that express upstream Vbeta pep

259 crucial survival factor for transitional and mature B cells that acts as rheostat for the maturation

260 low level (BD(L)) are a novel population of mature B cells that emerge in the spleen from the transi

261 d thymic Treg [tTreg] cells) or derived from mature conventional CD4(+) T cells that underwent TGF-be

262 into computational models of developing and mature cortical pyramidal cells that express NaV1.2.

263 During infection, dendritic cells (DC) mature into antigen-presenting cells that activate T cel

264 hey undergo an additional maturation step to mature naive T cells that circulate through secondary ly

265 ctory from primitive progenitor-like to more mature neuronal-like cells, the relative proportions of

266 cursor to immature memory and finally from immature to mature memory cells, the latest being a no-ret

267 microbial products in promoting survival of mature B cells through up-regulated Nod1, providing a po

268 Both fusion proteins matured monocyte-derived dendritic cells through TLR5.

269 karos expression was deleted specifically in mature T cells, thus avoiding defects observed in germli

270 lative contribution of adult-born (abGC) and mature (mGC) granule cells to epileptiform network event

271 GR deficiency results in impaired homing of mature B cells to bone marrow, whereas migration to othe

272 oral immunity is dependent on the ability of mature B cells to undergo antibody gene diversification

273 ity of its differentiation intermediates and mature effector cells to expand upon demand, thereby pro

274 m human stem cells allow differentiating and mature human retinal cells to be studied in unprecedente

275 myeloid-biased hematopoietic stem cells and mature myeloid cells to levels in young animals, but lym

276 -activation is sufficient to reprogram fully mature supporting cells to proliferate and regenerate ha

277 esent at the tips of the tall stereocilia in mature hair cells, together with PCDH15 isoforms CD1 and

278 tic-myeloid origin and distinguish them from mature lymphatic endothelial cells, tumor-infiltrating l

279 xpression of the IgM and IgD BCR isotypes on mature naive follicular B cells tunes responsiveness to

280 pend on their capacity to differentiate into mature and functional cell types after transplantation.

281 intercalated cell program from turning on in mature Aqp2(+) cell types.

282 lls can differentiate in culture to generate mature basal and luminal cell types, including ER+ cells

283 Homogeneous populations of mature differentiated primary cell types can display var

284 vitro with evidence of differentiation into mature epithelial cell types found in native human airwa

285 These functionally mature HILOs contain endocrine-like cell types that, upo

286 Using human brain organoids comprised of mature neural cell types as a three-dimensional tissue s

287 stem cell activity or interconversion among mature resident cell types (transdifferentiation).

288 differentiation of immature blast cells into mature, functional cell types and lineages of the immune

289 y exercise, and permanently marked activated mature hippocampal dentate granule cells using condition

290 , an assay based on the examination of early mature B (eBm5) cells was able to discriminate OIS patie

291 atients, the CD19(+)CD24(int)CD38(int) naive mature B cells were high in CHC-HCC patients with good p

292 tion profile of bone marrow populations, and mature IgD+ B cells were enriched in sialylated bone mar

293 that plasmablast, plasma, transitional, and mature naive B cells were resistant to VACV infection, w

294 Here we found that mature T(reg) cells were generated through two distinct

295 Lastly, we found affinity-matured polyreactive B cells were typically derived from

296 ile other B subsets, including transitional, mature naive, memory, and plasma cells, were highly susc

297 ss II(+)NK1.1(+) population as precursors to mature NK (pre-mNK) cells, which also expressed high lev

298 Mature and terminally differentiated NK cells with enhan

299 tor dominant negative mastermind-like within mature T cells with C. neoformans Inhibition of T cell-r

300 Functionally matured NK cells with high expression of CX3CR1, HAVCR2