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1 actor network for fine-tuning the osteoblast differentiation program.
2 d promotes a predetermined erythroid-lineage differentiation program.
3 rneuron neurogenesis is a key step in the RC differentiation program.
4 ermines the availability of E boxes for each differentiation program.
5 1 and PPARg were critical to the ATRAinduced differentiation program.
6 n activator during GATA-1-directed erythroid differentiation program.
7 l regulators of the hypertrophic chondrocyte differentiation program.
8 et, transcription factors that drive the Th1 differentiation program.
9 e-TCR results in induction of the gammadelta differentiation program.
10 tor T-bet, a critical regulator of the T(H)1 differentiation program.
11 rs by the thymic stroma initiates the T-cell differentiation program.
12 th full expression delayed until late in the differentiation program.
13 ion of a short wavelength-sensitive (S) cone differentiation program.
14 entiation, acting as nodal regulators of the differentiation program.
15 lopment, no single gene regulated the entire differentiation program.
16 ression to act in concert with smooth muscle differentiation program.
17 n cells both before and after initiating the differentiation program.
18  but only when administered early during the differentiation program.
19 x1 activity and for inhibition of the T(H)17 differentiation program.
20 that directly regulates a cell-type-specific differentiation program.
21 s but not for the maintenance of the retinal differentiation program.
22 coding important components of the epidermal differentiation program.
23 ant with the reexpression of the chondrocyte differentiation program.
24 e epidermal keratinocyte (KC) granular layer differentiation program.
25 on, suggestive of an accelerated chondrocyte differentiation program.
26 ogical changes of cell fusion as part of the differentiation program.
27 oxp3 and thus establishing an unopposed Th17 differentiation program.
28 revent inappropriate expression of the shaft differentiation program.
29 transition) it accelerated the memory T-cell differentiation program.
30 es and undergo a sophisticated morphological differentiation program.
31 from the same precursor and follow a related differentiation program.
32  cascade linking asymmetric division to this differentiation program.
33  keratinocyte progression through a terminal differentiation program.
34 ectopic activation of the foregut/esophageal differentiation program.
35 additional cytokines also play a role in the differentiation program.
36  progenitors to orchestrate the complex hair differentiation program.
37 C that have not yet completed their terminal differentiation program.
38 n block of the swarmer-to-stalked cell polar differentiation program.
39 al, and proteins that regulate the epidermal differentiation program.
40 mmune response and induces an optimal memory differentiation program.
41 o showed profound alterations in the corneal differentiation program.
42  for Ezh2 in repression of the smooth muscle differentiation program.
43 ed expression in cells that begin the acinar differentiation program.
44  is regulated in concert with the epithelial differentiation program.
45 ylation and Th2 LCR activation in the type 2 differentiation program.
46 ation of some aspects of the lens fiber cell differentiation program.
47 o prevent skewing of the conventional B cell differentiation program.
48  of neuronal development are integrated as a differentiation program.
49 ycle progression and initiating the myogenic differentiation program.
50 e stromal cultures, it markedly advanced the differentiation program.
51  inhibitor disrupts subsequent events in the differentiation program.
52 iac cell cycle and the timing of the cardiac differentiation program.
53 hat their expression is part of the terminal differentiation program.
54 otential inversely related to the stratified differentiation program.
55  self-renewing population and diminishes the differentiation program.
56 predict whether they induce a competent Th17-differentiation program.
57 ession of this protein inhibits the myoblast differentiation program.
58 uggesting that these represent a coordinated differentiation program.
59 s, to implement the growth plate chondrocyte differentiation program.
60 RA activates a RARalpha-dependent epithelial differentiation program.
61 Pax7 cleavage and initiation of the myogenic differentiation program.
62  self-renewal program and an increase in the differentiation program.
63 antagonists also showed an impaired terminal differentiation program.
64 ctivation of the insulin-producing beta-cell differentiation program.
65 pressed genes as a novel part of the overall differentiation program.
66 sible for the initiation of the crystal cell differentiation program.
67 intermediate step in the prostate epithelial differentiation program.
68 , where lens epithelial cells initiate their differentiation program.
69 T cells by regulating commitment to the Th17 differentiation program.
70 ch enabled the induction of a monocytic cell differentiation program.
71 otal regulators of several lineage-selective differentiation programs.
72 K27ac signatures, which identify remnants of differentiation programs.
73 n shown to alter gene expression profile and differentiation programs.
74 equestering SWI/SNF to prevent activation of differentiation programs.
75 hange was derepression of cell-type-specific differentiation programs.
76 ese two subsets of NKT cells undergo similar differentiation programs.
77  their capacity to divide and initiate their differentiation programs.
78  state of self-renewal into lineage-specific differentiation programs.
79 issue-specific gene expression in individual differentiation programs.
80 rived organoids through sequential rounds of differentiation programs.
81 nvironmental signals induce diverse cellular differentiation programs.
82 cycle that orchestrate the cell division and differentiation programs.
83 cific alternative splicing critical for cell differentiation programs.
84 n the transcriptional regulation of cellular differentiation programs.
85 al regulation of skeletal and cardiac muscle differentiation programs.
86 complex may determine the onset of erythroid differentiation programs.
87  the role of Akt signaling in the pancreatic differentiation programs.
88 s that do not appropriately execute cellular differentiation programs.
89 d -sensitive tumors within distinct stemness/differentiation programs.
90 lineage-restricted progeny to execute normal differentiation programs.
91 NA methylation in blocking tumor-suppressive differentiation programs.
92 ression as response to metabolic changes and differentiation programs.
93 liferate fully and complete their respective differentiation programs.
94 cell types become polyploid as part of their differentiation programs.
95 tiple, pre-existing neural plate border cell differentiation programs.
96 tion imprints unique and long lasting T-cell differentiation programs.
97 her by the Ras(V12) oncoprotein or by failed differentiation programs.
98 o track donor CD8 T cells, we found that the differentiation programs acquired by CD8 T cells after b
99 ial to partially or fully revert to a memory differentiation program after transfer to infection-free
100 d here, MSC-derived chondrocytes underwent a differentiation program analogous to that observed durin
101 ich these tumors arise, restore the myogenic differentiation program and block the tumorigenic phenot
102  a delay in the activation of a pan-neuronal differentiation program and cell cycle exit of ventral n
103 ained and secretory cells execute a terminal differentiation program and convert into ciliated cells.
104 immunization with parasites undergo a unique differentiation program and have enhanced expression of
105 turation is an integral part of the red cell differentiation program and illustrates specific mechani
106 g during development abrogated the lymphatic differentiation program and rescued the lymphatic phenot
107 le germ line stem cells undergo a multi-step differentiation program and sequentially become spermato
108  for Myocd in repressing the skeletal muscle differentiation program and suggest that this transcript
109 t alters the normal prostate epithelial cell differentiation program and that through this cellular p
110 ck in both the swarmer-to-stalked cell polar differentiation program and the initiation of DNA replic
111  modularity among the features of a neuronal differentiation program and their coordination by Prd an
112 toplasmic transport, may disrupt normal cell differentiation programs and accelerate the cancer proce
113  of expression of key genes required for the differentiation programs and chromatin reorganization th
114  central bona fide components of neuronal TF-differentiation programs and establish the importance of
115  for these events in modifying normal B-cell differentiation programs and impeding germinal center ex
116 r understand the role of Itk signaling in TH differentiation programs and in the development and mole
117   How a particular cell size is specified by differentiation programs and physiology remains one of t
118                   The regulatory networks of differentiation programs and the molecular mechanisms of
119 life cycle strictly adheres to the host cell differentiation program, and as such, native HPV virions
120 ) is a master regulator of developmental and differentiation programs, and CBF alterations are freque
121 motes beta-cell while suppressing delta-cell differentiation programs, and is crucial for postnatal b
122 one (PZ) from stem cell descendants in which differentiation programs are activated.
123 ferentiation but also by suppressing non-RGC differentiation programs as a safeguard mechanism.
124                              Tissue-specific differentiation programs become dysregulated during canc
125 ient to induce CD8 T cells to complete their differentiation program, become effector T cells, and su
126 nd on Bcl11b, while initiation of the T-cell differentiation program begins earlier with the inductio
127 target genes as immature thymocytes initiate differentiation programs, biochemically linking MAPK sig
128 ain their capacity to execute the follicular differentiation program but fail to maintain it owing to
129 ing that TopIIbeta is not required for early differentiation programming but is specifically required
130 in-containing 16 (PRDM16) drives a brown fat differentiation program, but the mechanisms by which PRD
131 tcompete the execution of a neuropeptidergic differentiation program by direct interaction with the U
132 -dependent activation of Ngn-3 initiates the differentiation program by inducing microRNA (miR)-7 exp
133 entral progenitors from a serotonergic to V3 differentiation program by repressing Ascl1 in spinal p3
134 en subpopulations spanning the entire B cell differentiation program by whole-genome bisulfite sequen
135 cumulation of malignant blasts with impaired differentiation programs caused by recurrent mutations,
136 ssor pathways to initiate cycle arrest and a differentiation program characteristic of senescent cell
137  cognate iNKT cell help resulted in a B cell differentiation program characterized by extrafollicular
138            Whether there exists an intrinsic differentiation program common to all EBs is unknown.
139 velopmental clock characteristic of an early differentiation program common to all EBs, further estab
140  immunotherapy can be influenced by opposing differentiation programs conferred by IL-2 and IL-21, a
141 epigenetic modulation of the oligodendrocyte differentiation program contributes to the age-dependent
142 epigenetic modulation of the oligodendrocyte differentiation program contributes to the age-dependent
143 nd oncogenic plasticity via a switch between differentiation programs controlled by SOX2 and SOX9, th
144                 In red cell development, the differentiation program directed by the transcriptional
145 ere highly functional and underwent a memory differentiation program distinct from that described for
146 nalyzed seemed to undergo an effector memory differentiation program distinct from that of CD4(+) T c
147 e zebrafish jawbone thus employs a cartilage differentiation program distinct from that seen during d
148 lls are unfit to undergo the conventional GC differentiation program due to impaired B cell receptor
149  has a key role in restricting the airway SM differentiation program during airway formation.
150 s essential for cells to initiate a terminal differentiation program during development, but what con
151                               Thus, the Tc17 differentiation program during GVHD culminates in a high
152 mesenchymal transition (EMT) is an essential differentiation program during tissue morphogenesis and
153   Competence for genetic transformation is a differentiation program during which exogenous DNA is im
154 at regulates hematopoietic transcription and differentiation programs during hematopoiesis and leukem
155 le to support the advancement of the stromal differentiation program even in the absence ovarian E in
156 catenin signaling, thereby shifting the skin differentiation program from forming hair follicles to s
157 t cells either propagate or undergo a unique differentiation program: fusion into an overlying syncyt
158 dicate that diversification of an epithelial differentiation program has allowed at least two develop
159 es telomere gene-silencing features [6-8] to differentiation programs has yet to be elucidated.
160                   The regulatory networks of differentiation programs have been partly characterized;
161 igration and initiation of the smooth muscle differentiation program, however, it is essential for re
162 NAs) have the potential to regulate cellular differentiation programs; however, miRNA deficiency in p
163 s and demonstrate that these MF-SCs retain a differentiation program identical to that of normal hema
164 ncy activated cytolytic and T helper 1 (Th1) differentiation program in a cell-intrinsic T cell recep
165  that DEK overexpression disrupts the normal differentiation program in a manner that is independent
166 selectively establishing a specific terminal differentiation program in a stepwise fashion.
167             EC initiate a smooth muscle cell differentiation program in adjacent ASC and propagate th
168 pears to reawaken an endocrine developmental differentiation program in adult pancreatic ductal cells
169 e cells results from activation of a myeloid differentiation program in bone marrow (BM) by a novel m
170 ing that the receptor initiates the invasive differentiation program in distal regions of the develop
171 n to multiple functions during the erythroid differentiation program in human and mouse.
172 ed MKK6-p38MAPK cascade activates a monocyte differentiation program in human granulocyte colony-stim
173 ch survival results from a skewed macrophage differentiation program in p47(phox-/-) mice that favors
174 generated Th17 cells poorly maintained their differentiation program in vitro and could be reprogramm
175  for the normal progression of the adipocyte differentiation program in vitro.
176 s necessary for each step of the muscle cell differentiation program in vitro.
177 s (SMCs) from contractile to chondro-osseous differentiation programmed in response to increases in P
178 o-oncogene TLX1/HOX11 inhibits hematopoietic differentiation programs in a number of murine model sys
179 ire the precise execution of carefully timed differentiation programs in both T and B cell compartmen
180 s substantial reorganization of the terminal differentiation programs in hair follicle keratinocytes.
181 athogens and how they each instruct specific differentiation programs in responding CD4 T cells.
182 cell cytolytic activity and modulates T cell differentiation programs in response to antigen, promoti
183 ability to regulate developmental growth and differentiation programs in several transformed neural p
184 resulting in diversification of motor neuron differentiation programs in specific motor neuron subtyp
185 ors that drive neuron type-specific terminal differentiation programs in the developing nervous syste
186       TET1 regulates numerous genes defining differentiation programs in the epiblast and extraembryo
187 into combinatorial codes that drive terminal differentiation programs in the nervous system and revea
188                                     Terminal differentiation programs in the nervous system are encod
189  Arx, and Pax4, revealed the authenticity of differentiation programs in vitro.
190 oprotein Ski dramatically affects growth and differentiation programs, in some cases leading to malig
191 mablasts are potent inducers of the Tfh cell-differentiation program, including the expression of the
192 F1A as a pivotal element in the granulocytic differentiation program induced by ATRA in APL.
193 mall intestinal stem cells enter the gastric differentiation program instead of producing intestinal
194 echanism by which to direct the chondrogenic differentiation program into either permanent articular-
195 stood normal and pathologic stressors on the differentiation program is also presented.
196          These findings demonstrate that the differentiation program is genetically determined by E b
197  In sum, our results suggest that an altered differentiation program is induced following early and s
198                  The mechanisms by which the differentiation program is initiated after cell cycle ar
199 , in response to ST infection, a Paneth cell differentiation program is initiated that leads to an ex
200                          The pre-TCR-induced differentiation program is orchestrated by a network of
201 loid differentiation while also blocking the differentiation program is presented.
202                                 Much of this differentiation program is recapitulated when M. tubercu
203                 Here we show that the muscle differentiation program is repressed by hypoxia in vitro
204 fication, but how they interact to drive the differentiation program is unknown.
205  suggest that loss of both active and latent differentiation programs is required for tumors to reach
206          One of the key features of cellular differentiation programs is stability.
207  pomalidomide induced a fetal-like erythroid differentiation program, leading to a reversion of gamma
208  of HSCs can be distinguished based on their differentiation programs: lymphoid biased, balanced, and
209  somatic and germinal cell proliferation and differentiation programs must be executed in flowers.
210 n, lineage allocation, and implementation of differentiation programs need to be tightly coordinated
211 l progenitor cell proliferation and neuronal differentiation programs observed in vivo remains unclea
212 ty of a battery of genes that constitute the differentiation program of a postmitotic cell type.
213 ing strategy, notably its involvement in the differentiation program of a social amoeba.
214 ene expression for establishing the terminal differentiation program of B cells.
215 ogate whether tissue inflammation alters the differentiation program of basal cells, we conducted lin
216 tween mitochondrial lipid metabolism and the differentiation program of breast cancer cells, thereby
217 e first time that bile inhibits the squamous differentiation program of esophageal epithelial cells.
218 eterminant of the lineage fate and multistep differentiation program of growth plate chondrocytes and
219 ay, we tested the effects of 20(OH)D3 on the differentiation program of keratinocytes and on the expr
220  development by altering the terminal B-cell differentiation program of MCL and provide perspectives
221 ssion underlies the epigenetically inherited differentiation program of most immune cells.
222 tric divisions are connected to the terminal differentiation program of neuronal subtypes is poorly u
223 es, but evidence for miRNAs that control the differentiation program of specific neural cell types ha
224 iptional regulatory networks that govern the differentiation program of Th17 cells, and focus on how
225 d ASEL and ASER, are disrupted such that the differentiation program of the ASER neuron is derepresse
226 as a terminal selector to drive the terminal differentiation program of the cholinergic AIY interneur
227  temporally compressed cell divisions in the differentiation program of the erythroid lineage in the
228 opagation potentially through abrogating the differentiation program of the infected epithelium.
229  to PanIN formation by abrogating the normal differentiation program of tumor-initiating cells.
230 e show that ttx-3 also controls the terminal differentiation program of two additional, distinct neur
231 ene expression in the thymus reflects normal differentiation programs of epithelia.
232 munoregulatory capacity while repressing the differentiation programs of multiple effector lineages i
233 rns of p63 and keratin expression reflecting differentiation programs of other epithelial tissues pro
234 ater on, in selectively controlling terminal differentiation programs of specific neuron types, but n
235          This may reflect differences in the differentiation programs of these tissues.
236   However, the role of the Th1 CD4(+) T cell differentiation program on the ability to control parasi
237 ponsible for executing one branch of the SGN differentiation program orchestrated by the Gata3 transc
238 n integral part of the intestinal epithelial differentiation program, perhaps serving to release cell
239 exhibited a striking arrest in the epidermal differentiation program, perishing within 2 weeks of bir
240 drocytes progress through a well coordinated differentiation program regulated by multiple extracellu
241 tworks underlying lineage fate decisions and differentiation programs remain poorly understood.
242 osis, but the stimulus for and importance of differentiation programs remain unknown.
243                                         Cell differentiation programs require dynamic regulation of g
244                                              Differentiation programs require strict spatial and temp
245 rigger the process of maturation, a terminal differentiation program required to initiate T-lymphocyt
246 larval development where it directs cellular differentiation programs required for adult fates.
247                           Regulation of cell differentiation programs requires complex interactions b
248                               Maintenance of differentiation programs requires stability, when approp
249                                         This differentiation program resembled the embryological deve
250 e oncogene E2F-1 blocks the myeloid terminal differentiation program, resulting in proliferation of i
251 pool, but it is also critical to control the differentiation program shutting off the c-Myc gene in l
252 and two alleles permitted the execution of a differentiation program similar to that found with all f
253 limited degree of donor cell chimerism and a differentiation program skewed toward myeloid lineages.
254 mal survival predictor, a model based on ESC/differentiation programs stratified patient outcomes in
255                                              Differentiation programs such as meiosis depend on exten
256 in the response were imprinted with a unique differentiation program, such that their magnitude of pr
257 suggest that in addition to lineage-specific differentiation programs, T and B lymphocytes use a comm
258                Studies of stem cells and the differentiation program termed the epithelial-mesenchyma
259 m promotes B-ALL self-renewal by impairing a differentiation program that can be re-engaged despite t
260                     Senescence is a terminal differentiation program that halts the growth of damaged
261 l receptor signaling, these cells initiate a differentiation program that includes complex changes in
262 +) cells could be generated through a unique differentiation program that involved two phases: a pre-
263                     We show that the type of differentiation program that is controlled by ttx-3 in d
264 ter than 2 weeks of age undergo a structural differentiation program that is different from that of c
265 enin, responding cells switch on an alveolar differentiation program that is indistinguishable from t
266 , this organ arises as a result of a complex differentiation program that is initiated by exogenous s
267  granulocytes and macrophages via a distinct differentiation program that is tightly controlled by my
268 mal transition (EMT), which is a cellular de-differentiation program that promotes invasion and metas
269 t a long-lived granuloma-resident macrophage differentiation program that regulates granulomatous tis
270 actors cause perturbations in the blood cell differentiation program that result in various types of
271 lopment depends on the accurate execution of differentiation programs that allow pluripotent stem cel
272 ing environment, signaling networks activate differentiation programs that promote their individual o
273  established paradigm for analysing the cell differentiation programs that underpin the production of
274 a, iris and ciliary body had initiated their differentiation programs thereby precluding analysis of
275 ome and concomitantly suppresses interneuron differentiation programs, thereby serving as a potent an
276 cal role for eRNAs in regulation of myogenic differentiation program through increasing chromatin acc
277 enitor cells exit the cell cycle and execute differentiation programs through extensive genetic repro
278   Thus, NEMO governs survival and osteoclast differentiation programs through serial regulation of mu
279 d a defined, serum-free and low cell-density differentiation program to generate endothelial and hema
280       In utero, iPS-derived chimera executed differentiation programs to construct normal heart paren
281 otic cell cycles coordinated with growth and differentiation programs to generate functional sperm.
282 on to maintain a balance of self-renewal and differentiation programs to sustain tissue homeostasis t
283  and directs UNC-86 to induce an alternative differentiation program toward a glutamatergic neuronal
284        Exposure of BCs to EGF shifted the BC differentiation program toward the squamous and epitheli
285 tem cells: they initiate but do not complete differentiation programs toward memory cells.
286 s enabling proper activation of the neuronal differentiation program under neurogenic cue.
287 cated that disrupted expression of epidermal differentiation programs under the control of ZNF750 and
288 ignaling is a major early inducer of the Tfh differentiation program unexpectedly mediated by both ST
289 er Th17 conditions, suggesting that the Th17 differentiation program was initiated normally.
290 es of the meiotic chromosome segregation and differentiation program were identified.
291 ext to healthy hepatocytes but begin biliary differentiation program when co-cultured with injured he
292 sorptive enterocytes by repressing secretory differentiation programs, whereas low Notch permits secr
293 iate rapid monocyte mobilization and dictate differentiation programs whereby these cells give rise t
294 otential and globally repressing undesirable differentiation programs while selectively establishing
295  T-bet cooperate to switch on a terminal CTL differentiation program, while simultaneously repressing
296 182 as a regulator of apoptosis, growth, and differentiation programs whose expression level is corre
297 genitors were shown to possess an autonomous differentiation program with a capacity to complete term
298 is characterized by persistent underlying de-differentiation program with complex etiology.
299 is tightly linked to the epithelial terminal differentiation program, with the virion-producing phase
300 e integrated to collectively induce distinct differentiation programs within Ag-specific CD8(+) T cel

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