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1 even translocation (TET)2 regulates CD8(+) T cell differentiation.
2 dritic cell/inflammatory dendritic epidermal cell differentiation.
3 agic degradation of Id proteins can regulate cell differentiation.
4 differentiation genes during embryonic stem cell differentiation.
5 lly shape dynamic enhancer landscapes during cell differentiation.
6 ells to populate the liver and promote blood cell differentiation.
7 ated suppression of RORgammat to enable TH17 cell differentiation.
8 cell expansion and favored central memory T cell differentiation.
9 ctors serve a pioneering function during Tr1 cell differentiation.
10 Here we address the role of Fra-2 in B cell differentiation.
11 anscript regulatory patterns that govern the cell differentiation.
12 activate new transcriptional programs during cell differentiation.
13 ction of NEUROG3 and initiation of endocrine cell differentiation.
14 anscription factors regulate CD4(+) T helper cell differentiation.
15 leading to myelomonocytic and monocytic AML cell differentiation.
16 f early pregnancy and promotes normal breast cell differentiation.
17 h previously unappreciated roles in CD8(+) T cell differentiation.
18 tion stage, suggesting inhibition of mammary cell differentiation.
19 T cell enhancer landscape and affecting Treg cell differentiation.
20 and defects of thymic epithelial progenitor cell differentiation.
21 natural killer T cell (NKT) and gammadelta T-cell differentiation.
22 or 2 (Runx2) as a novel regulator for goblet cell differentiation.
23 activation of Smad2, therefore limiting Th17 cell differentiation.
24 ular helper T (TFH) cells support terminal B-cell differentiation.
25 aintained by MGP, are essential in pulmonary cell differentiation.
26 ants, which affects growth, development, and cell differentiation.
27 ange dynamically as cells progress through T cell differentiation.
28 32 is preferentially upregulated during Th17 cell differentiation.
29 age-specific gene expression programs during cell differentiation.
30 g gene expression at different stages of the cell differentiation.
31 sion by the E2 domains impaired primary lens cell differentiation.
32 scription factors likely controlling Sertoli cell differentiation.
33 activity is required for mouse and human Tr1 cell differentiation.
34 on factors RORgammat and Foxp3 promoted Treg cell differentiation.
35 nstrated a critical role for Cdc42 in plasma cell differentiation.
36 switch recombination and memory B and plasma cell differentiation.
37 production, cell identity gene induction and cell differentiation.
38 phagy selectively represses T helper 9 (TH9) cell differentiation.
39 ternal intestinal bacteria that promote TH17 cell differentiation.
40 co-regulate during mouse T helper 17 (Th17) cell differentiation.
41 e cell cycle is required to allow epithelial cell differentiation.
42 evelopmental defects at multiple stages of B cell differentiation.
43 at Etv5 is a critical CIC target gene in TFH cell differentiation.
44 cell-cycle exit, thereby allowing epithelial cell differentiation.
45 d critical role for miR-18a in limiting Th17 cell differentiation.
46 TNFAIP3 expression in DCs controls TH2/TH17 cell differentiation.
47 arrest complex, to transcripts for male germ cell differentiation.
48 and cell migration but did not prevent fiber cell differentiation.
49 oding TAZ or activation of TAZ directed TH17 cell differentiation.
50 patients with CVID as a central pathway in B-cell differentiation.
51 ell lines showed greater variability in beta-cell differentiation.
52 CD4(+) T cells are potentiated in Th17/Treg cell differentiation.
53 ically, inducing chromatin decondensation or cell differentiation.
54 PML is a tumour suppressor and regulator of cell differentiation.
55 on, but it is inadequate for functional beta cell differentiation.
56 t embryonic stem (ES) cells and regulates ES cell differentiation.
57 e-negative progenitors displayed impaired NK-cell differentiation.
58 rolling the spatio-temporal dynamics of stem cell differentiation.
59 transcription factor that promotes ependymal cell differentiation.
60 r ZNF148 plays a direct role in human muscle cell differentiation.
61 FII expression is required for proper muscle cell differentiation.
62 s rescues the defects of BCR signaling and B cell differentiation.
63 nd upregulated transcripts were enriched for cell differentiation.
64 of new TFs to DNA and significantly blocked cell differentiation.
65 A processing and splicing factors to drive T cell differentiation.
66 nd a transcription program associated with T cell differentiation.
67 ure and controlling cell behavior, including cell differentiation.
68 cent RNA levels and perturbed embryonic stem cell differentiation.
69 cation cycle is tightly linked to epithelial cell differentiation.
71 rgeted drug and gene delivery, directed stem cell differentiation, accelerated tissue formation, effe
74 lays a critical role in pancreatic endocrine cell differentiation, although regulation of Ngn3 protei
75 tly compensate for loss of Btk activity in B cell differentiation, although the underlying mechanism
76 relationship between hippocampal progenitor cell differentiation and adult hippocampal volume, using
77 rabidopsis thaliana) is required to maintain cell differentiation and allow developmental phase trans
78 in human myeloid leukemia cell lines induces cell differentiation and apoptosis and delays leukemia p
82 included in vitro follicular helper T (TFH) cell differentiation and cTFH/naive B-cell cocultures.
86 ficiency and autoimmunity with impaired TH17 cell differentiation and exaggerated responsiveness to t
90 s provide a robust tool for studying human T cell differentiation and for the future development of s
91 neuronal and endocrine cells is critical for cell differentiation and function and requires guanine n
94 currently considered major forces that drive cell differentiation and genome evolution in general, an
95 lex, is one of multiple regulators driving B cell differentiation and germinal center (GC) formation
96 ever, the molecular signals that control TRM cell differentiation and homeostasis are not fully under
98 schemic muscle myopathy and muscle precursor cell differentiation and improved muscle regeneration in
99 d microglia significantly inhibited Th1/Th17 cell differentiation and increased the number of IL-10(+
102 cells (DCs) is crucial for both TH2 and TH17 cell differentiation and is mediated through nuclear fac
103 r transcriptome switch that controls myeloid cell differentiation and maturation and that malfunction
110 affecting normal cellular processes such as cell differentiation and pathological conditions such as
111 gested that histone Khib is involved in male cell differentiation and plays a critical role in the re
112 stages of tooth development and later during cell differentiation and production of hard tissues.
113 o committed monocyte/macrophage or dendritic cell differentiation and provide the first example of a
114 tri, openendo) mice displayed defective beta cell differentiation and recapitulated the Nkx2.2(KO) ph
115 cell area at birth due to impaired endocrine cell differentiation and reduced prenatal proliferation.
119 multiple signaling pathways underlying taste cell differentiation and taste stem/progenitor cell prol
120 e Zc3h12a gene) regulates IL-5-producing TH2 cell differentiation and TH2-mediated inflammation.
123 ature defects in mTEC-dependent regulatory T-cell differentiation and thymocyte maturation, which pro
124 s act through a mechanism of impaired muscle cell differentiation and tissue formation during fetal h
126 cal mechanism by which TGFbeta controls TH17 cell differentiation and uncovers the SKI-SMAD4 axis as
127 ecules involved in oligodendrocyte precursor cell differentiation and validated CCL19 as a target to
129 r Thpok is required for intrathymic CD4(+) T cell differentiation and, together with its homolog LRF,
130 tion of EZH2 is a prerequisite for satellite cells differentiation and identify PJA1 as a new player
133 th pathways involved in inflammation, acinar cell differentiation, and cell junctions being specifica
134 7 as a KLF4 antagonist in corneal epithelial cell differentiation, and explains how two SNPs may cont
135 minantly neuronal and oligodendrocytic donor cell differentiation, and functional locomotor improveme
136 R pathway is a key driver of murine CD4(+) T cell differentiation, and induction of regulatory T (Tre
137 summary, Foxc1 regulates sweat duct luminal cell differentiation, and mutant mice mimic miliaria and
138 We further characterised cell cycle exit, cell differentiation, and PCP establishment in the utric
139 ts regulation of ADORA2B expression on AAMs, cell differentiation, and production of profibrotic medi
140 ontrols the germinal center reaction, plasma cell differentiation, and specific Ab production in resp
141 o nucleosomal regulation of transcription, T cell differentiation, and the inflammatory response and
143 lity, consistent with failed primordial germ cell differentiation as an initiating step in oncogenesi
144 ion and that this led to biased helper CD4 T cell differentiation as well as impaired antibody respon
145 en Hedgehog-induced, promote epithelial stem cell differentiation as well as self-renewal, thus speci
146 tic infection-inducing effects of epithelial cell differentiation, as well as 12-O-tetradecanoylphorb
147 ze this phenotype, we used in vitro CD4(+) T cell-differentiation assays and show that NLRX1-deficien
148 am of Fgf signaling to not only inhibit hair cell differentiation but also to induce and maintain sta
149 mice have normal Th1, Th2, and regulatory T cell differentiation but show defective Th17 differentia
150 icing of U12-type introns functions in human cell differentiation, but it is not known whether this c
151 omatin protein 1gamma [HP1gamma]) stimulates cell differentiation, but its mechanism is unknown.
152 oimmunity because a possible modulation of B cell differentiation by basophils could point to new the
153 nctures of B lineage maturation and effector cell differentiation by controlling B cell activation.
155 tment in ovariectomized mice suppressed Th17 cell differentiation by inhibiting transcription factor
158 levels decrease markedly with completion of cell differentiation, corresponding with an increase in
159 ietic stem/progenitor cells (HSPCs) promotes cell differentiation, coupled with reduced cell prolifer
160 ocyte, B-lymphocyte, and natural killer (NK)-cell differentiation defect in interleukin-2 gamma-chain
161 a new mechanism that controls intrahepatic T-cell differentiation during atherosclerosis development
163 fundamental role in somatic and reproductive cell differentiation during early anther development in
165 se characterized by profound changes in stem cell differentiation, epithelial cell phenotypes and fib
169 nstrates that Treg cells are important for B-cell differentiation from HSCs by maintaining immunologi
170 ed role for the minor spliceosome to promote cell differentiation from stem cells to terminal fates.
171 t require peripheral activation for effector cell differentiation, gammadelta T cells instead can be
173 exogenous TH precociously activates the beta-cell differentiation genes pax6b and mnx1 while downregu
175 While metabolic reprogramming during Treg cell differentiation has been extensively studied, the b
176 he involvement of reticulocalbin-2 (RCN2) in cell differentiation has been reported, its function in
179 ution of DNA replication and mitosis in stem cell differentiation has not been extensively studied.
180 but post-transcriptional regulation of Th17 cell differentiation has remained less well characterize
181 ription factors that are essential for islet cell differentiation have been well characterized; howev
182 cell and B-cell cocultures, they inhibited B-cell differentiation, impeded immunoglobulin secretions,
186 CD-mediated inhibition of mammary epithelial cell differentiation in a three-dimensional cell culture
188 nockdown of Etv5 suppresses the enhanced TFH cell differentiation in Cic-deficient CD4(+) T cells, su
189 mplications and a skewed follicular helper T-cell differentiation in defined monogenic immunodeficien
192 sed method can rapidly and accurately detect cell differentiation in live cells and label-free manner
194 der subconfluent conditions, or induction of cell differentiation in primary cultures upregulated the
195 to exploit the information of the lineage of cell differentiation in terms of correlation structure b
196 e expressed during all stages of neural stem cell differentiation in the dentate gyrus, with higher e
198 re, examined cytokine signaling and CD4(+) T cell differentiation in these cohorts to characterize co
199 -related orphan receptor (ROR)gammat(+) Th17 cell differentiation in vitro and increased the number o
200 icular helper cells, TPH cells induce plasma cell differentiation in vitro through IL-21 secretion an
201 eral alternating events of cell division and cell differentiation in which exponential and stationary
202 es blastema accumulation, it does not rescue cell differentiation, indicating that macrophages play a
204 catabolism and energy homeostasis as well as cell differentiation, inflammation, and metabolism.
205 inhibition significantly reduced Wt1 lineage cell differentiation into adipocytes after myocardial in
207 mechanisms underlying human pluripotent stem cell differentiation into late primordial germ cells, me
208 78 is up-regulated during hematopoietic stem cell differentiation into mature megakaryocytes (Mks).
210 ug treatment caused a striking bias of CD4 T cell differentiation into Th1 cells and substantially im
212 Studying transcript regulatory patterns in cell differentiation is critical in understanding its co
213 ht how tight quantitative control of hepatic cell differentiation is exerted through specific gene re
217 ulator of mammary alveologenesis and luminal cell differentiation, is markedly reduced in mammary epi
218 ar differentiation states and reconstructing cell differentiation lineages in scRNA-seq analysis.
219 tes based on single cell entropy and predict cell differentiation lineages via the construction of en
222 the Nodal-Pitx2 pathway controls lateralized cell differentiation, migration, and other aspects of ce
223 nt has been implicated as a key regulator of cell differentiation, migration, and proliferation.
225 us CCL19 abolished oligodendrocyte precursor cell differentiation observed in patients with high remy
226 ated by 6.4-fold during IL-13-induced goblet cell differentiation of human bronchial epithelial cells
227 es TGF-beta/Smad3 signaling in smooth muscle cell differentiation of mesenchymal progenitor cells.
230 and WT mice showed that gene sets related to cell differentiation, particularly astrocyte lineage gen
233 Knockdown of RIMA causes delayed onset of cell differentiation, phenocopying the effects of IYO kn
235 provide key insights into poorly understood cell differentiation processes of considerable physiolog
238 role for these events in modifying normal B-cell differentiation programs and impeding germinal cent
240 inhibitor p27, which are essential for mast cell differentiation, proliferation, and cytokine produc
241 ing embryogenesis and in adulthood including cell differentiation, proliferation, and death in variou
244 sion of TFH cell motility, alteration of TFH cell differentiation, reduced TFH abundance and suppress
245 he role of miR-31 is restricted to human TFH cell differentiation, reflecting a species specificity o
246 oth constitutively expressed during CD8(+) T cell differentiation, regulated the formation of termina
251 hat Hsp90 or BRAF inhibitor-induced melanoma cell differentiation resulted in an upregulation of tyro
252 ell differentiation, with a leaky block in T-cell differentiation resulting in an oligoclonal T-cell
253 ke factor (SPDEF), a known factor for goblet cell differentiation, resulting in an activation of SPDE
255 the mechanisms/pathways involved in leukemic cell differentiation revealed that binding of S100A9 to
256 l role of TH during terminal human erythroid cell differentiation; specific depletion of TH from the
257 t study, we outline the role of Dll4 in Treg cell differentiation, stability, and function in RSV inf
258 tes is thought to involve a compromised beta cell differentiation state, but the mechanisms underlyin
259 ritically important molecules required for T cell differentiation, such as JAK2 and IL12RB2, are regu
260 opmental genes involved in the photoreceptor cell differentiation suggest that a role of both protein
261 l biogenesis pathway, which might underlie a cell differentiation switch in yeast mating response.
262 man endometrial epithelial tissue, including cell differentiation, the presence of junctional complex
263 m and repress Il4 expression to modulate Th9 cell differentiation, thereby implicating IRF8 as a pote
264 blishing Runx3 as a central regulator of TRM cell differentiation, these results provide insight into
265 AIP3-deficient DCs induced HDM-specific TH17 cell differentiation through increased expression of the
267 rein, we provide an updated perspective on T cell differentiation through the lens of recent advances
268 s all-trans-retinoic acid (ATRA)-induced AML cell differentiation, through regulating expression of t
269 uppressive state to cancer by promoting Treg cell differentiation, thus offering a potential therapeu
270 s (TBs) can be used to guide reseeded dental cell differentiation to form whole bioengineered teeth,
272 ZIKV infection was characterized by a CD4 T cell differentiation toward effector cells and by a lowe
273 arget X-box-binding protein 1 (XBP1) drive B-cell differentiation toward plasma cells and have been s
274 ion states of single cells and reconstructed cell differentiation trajectories that have been previou
276 ks were enriched near genes that function in cell differentiation, tRNA modification, nuclease activi
277 dynamics of early mouse embryonic stem (mES) cell differentiation, uncovering discrete transitions ac
279 tivating signals influence the outcome of Th cell differentiation via differential regulation of matu
280 and deacetylation of the Rorc locus and TH17 cell differentiation via SMAD4: ectopic SKI expression i
283 a, IL-6, and IL-23, whereas HDM-specific TH2 cell differentiation was hampered by increased IL-12 and
284 the cytokine that is important for B- and T-cell differentiation was knocked into its respective mou
286 and found that PRDM1, a master regulator in cell differentiation, was significantly upregulated.
288 e out the spatiotemporal regulation of islet cell differentiation, we used a Neurog3-Cre allele to ab
289 Pro-B cell proliferation and small pre-B cell differentiation were fully rescued by expression of
290 PR1 was progressively downregulated during T cell differentiation whereas S1PR2 expression remained s
291 TAZ or overexpression of TEAD1 induced Treg cell differentiation, whereas expression of a transgene
292 vo analyses revealed that S100A9 induces AML cell differentiation, whereas S100A8 prevents differenti
293 cer of FKBP-DD, does not interfere with stem cell differentiation, whereas tamoxifen has significant
294 for ILC2 activation that contributes to TH2 cell differentiation, which is associated with IRF4 and
295 latory mechanism through induction of itBreg cell differentiation, which takes place in palatine tons
296 r (IRF)-8, which promotes monocyte/dendritic cell differentiation while limiting granulocyte developm
297 specifically inhibited mouse and human Th17 cell differentiation while promoting the generation of F
298 ndrome, is known to affect neural progenitor cell differentiation, while haploinsufficiency of DYRK1A
299 inhibited the house dust mite-induced goblet cell differentiation with a 75% reduction in mucus overp
300 ) mice present with a complete blockade of B-cell differentiation, with a leaky block in T-cell diffe
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