コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 hancer-mediated transcription attenuation in cell fate determination.
2 provides a prototypic example of collective cell fate determination.
3 to which endogenous secretion contributed to cell fate determination.
4 for Nup210 in gene expression regulation and cell fate determination.
5 l regulatory network that guides progressive cell fate determination.
6 al role in controlling embryonic neural stem cell fate determination.
7 gulatory T cells (T(reg) cells) and controls cell fate determination.
8 nes are involved in embryonic patterning and cell fate determination.
9 cycle to allow ample time for DNA repair and cell fate determination.
10 ors are cell surface molecules essential for cell fate determination.
11 , tumor suppression, and monocyte/macrophage cell fate determination.
12 provides new insights into the mechanisms of cell fate determination.
13 tin with proper heterochromatin assembly and cell fate determination.
14 in cells, leads to a complete loss of proper cell fate determination.
15 nected to cell signaling, cell survival, and cell fate determination.
16 aste cell proliferation, differentiation and cell fate determination.
17 sicle initiates morphogenesis and prosensory cell fate determination.
18 ng a reciprocal negative regulation of CD4 T cell fate determination.
19 ished mechanisms of early neural and retinal cell fate determination.
20 determination cascade involved in embryonic cell fate determination.
21 al progenitor cells is required for neuronal cell fate determination.
22 the proteomic dynamics during the process of cell fate determination.
23 ave been shown to play a significant role in cell fate determination.
24 the timing of precursor differentiation and cell fate determination.
25 l-basal cell polarity to Notch signaling and cell fate determination.
26 role for Ctr1 during amphibian and mammalian cell fate determination.
27 emodeling and unravel the complexity of stem cell fate determination.
28 ifferent, but overlapping aspects of retinal cell fate determination.
29 ulation of epigenetic information influences cell fate determination.
30 tes this act to control cleavage pattern and cell fate determination.
31 for Notch signaling, a pathway critical for cell fate determination.
32 esting an important role of phytohormones in cell fate determination.
33 for delineating early steps in photoreceptor cell fate determination.
34 om FGF signaling to balance self-renewal and cell fate determination.
35 through meiosis, cytoskeletal regulation and cell fate determination.
36 resolution of mixed lineage patterns during cell fate determination.
37 egulatory molecules that orchestrate B and T cell fate determination.
38 s that couple metabolism to pluripotency and cell fate determination.
39 ession in HPC play a key role in promoting B cell fate determination.
40 on by chromatin remodeling factors underlies cell fate determination.
41 for the native signaling process in neuronal cell fate determination.
42 essor complex Mi-2/NuRD, for BCL-6-dependent cell fate determination.
43 on did not affect neural induction or neural cell fate determination.
44 ogenitor cells could play important roles in cell fate determination.
45 upts pigmentation, somitogenesis and retinal cell fate determination.
46 and p17Xic3 have an activity that influences cell fate determination.
47 ritical to transcriptional reprogramming and cell fate determination.
48 for cytokine signaling in the process of TH cell fate determination.
49 s a key player in both eye specification and cell fate determination.
50 DNA replication, cell cycle progression, and cell fate determination.
51 rupt Notch processing, thus interfering with cell fate determination.
52 involved in development of cell polarity and cell fate determination.
53 shment of EpiLCs, the epigenome is reset for cell fate determination.
54 3K9me3 is reorganized during development and cell fate determination.
55 in cell proliferation, differentiation, and cell fate determination.
56 f signal transduction in cells are vital for cell fate determination.
57 f the Shh morphogen gradient and influencing cell fate determination.
58 ole in epigenetic control of SE activity for cell fate determination.
59 ory network (GRN), corresponding to specific cell fate determination.
60 r, gene expression, chromatin structure, and cell fate determination.
61 and cadherins required for NC migration and cell fate determination.
62 ave emerged as important factors influencing cell fate determination.
63 ctor, Nkx2.1, for lung epithelial progenitor cell fate determination.
64 layers to regulate embryonic development and cell fate determination.
65 ed with embryonic stem cell self-renewal and cell fate determination.
66 maintaining immune homeostasis by regulating cell fate determination.
67 t connects DNA damage signaling to SirT1 and cell fate determination.
68 on is a classical embryologic model to study cell fate determination.
69 , chromosome copy number could contribute to cell-fate determination.
70 ivation of gene expression during vertebrate cell-fate determination.
71 lated by ADAM10 is critical to hematopoietic cell-fate determination.
72 tat4 to achieve complete IL-12-dependent Th1 cell-fate determination.
73 te neuroblast formation, cell-cycle exit and cell-fate determination.
74 family involved in chromatin remodeling and cell-fate determination.
75 both the A and B classes of genes in vulval cell-fate determination.
76 vation of quiescent cells and/or a switch in cell-fate determination.
77 ll protrusion, migration, proliferation, and cell-fate determination.
78 on of translation is an important feature of cell-fate determination.
79 to explore the functional role of Jagged in cell-fate determination.
80 anisms modelling lineage differentiation and cell-fate determination.
81 Consistent with the role Hh homologs play in cell fate determination, aberrant Hh signaling results i
82 signaling activation and cause a gradient of cell fate determination along the direction of flow.
83 cts of misexpressing NeuroD genes on retinal cell fate determination also suggested shared and diverg
86 ll form the basis for understanding not only cell fate determination and cellular homeostasis in the
87 olecular genetic mechanisms of hematopoietic cell fate determination and commitment within Drosophila
88 TGFbeta signaling in the earliest stages of cell fate determination and demonstrate an interconnecti
89 of various adult stem cells, but its role in cell fate determination and differentiation during liver
90 ortant roles in development, particularly in cell fate determination and differentiation, in addition
94 e most critical genes acting in the steps of cell fate determination and early differentiation of var
95 es for Wnt/beta-catenin signaling in granule cell fate determination and for Wnt/PCP signaling in con
101 ing cascade plays a crucial role in myogenic cell fate determination and lineage progression during t
102 wn to modulate developmental events, such as cell fate determination and maintenance in many species,
103 volutionarily conserved process critical for cell fate determination and maintenance of gene expressi
105 conserved across metazoans, including neural cell fate determination and migration, axon guidance, sy
107 requires coordination of cell proliferation, cell fate determination and morphogenetic movements.
108 gions associated with key factors central to cell fate determination and neural tube patterning.
111 dentified HLH protein GCIP/CCNDBP1 modulates cell fate determination and plays a role in hepatocyte g
112 ssential players in development by acting on cell fate determination and progression towards cell dif
113 ns play critical roles during development in cell fate determination and proliferation, but few studi
114 criptional dominance' model of photoreceptor cell fate determination and provide insights into the pa
115 beta-catenin and are critically involved in cell fate determination and stem/progenitor self-renewal
116 hlight the importance of metabolic cues in T cell fate determination and suggest that metabolic modul
117 es a synthetic biology framework to approach cell fate determination and suggests a landscape-based e
118 s the sex determination signal TRA-1 and the cell fate determination and survival signal UNC-86 to co
120 d fibroblastic cell-cell interactions affect cell fate determination and the organization of skeletal
121 ipheral taste system: embryonic chemosensory cell fate determination and the specification of lingual
123 events during animal development, regulating cell fate determination and tissue growth in a variety o
124 enabled us to identify key genes involved in cell fate determination and to obtain new insights about
125 y has essential roles in cell proliferation, cell fate determination and tumorigenesis by regulating
126 ly dividing cell population just upstream of cell fate determination and updates previous models of s
127 onsider our current understanding of cardiac cell-fate determination and cardiogenesis--largely deriv
129 damentally changed our view on developmental cell-fate determination and led to a cascade of technolo
130 for ERECTA-mediated signaling in growth and cell-fate determination and reveal a role for ERECTA-LIK
131 gehog (Shh) signaling is crucial for growth, cell fate determination, and axonal guidance in the deve
132 target transcription factors that influence cell fate determination, and biological functions of miR
133 identify a novel role for pocket proteins in cell fate determination, and establish a unique cell lin
135 of the WNT7A-PAX6 axis in corneal epithelial cell fate determination, and point to a new strategy for
137 ritical to ensure proper lineage commitment, cell fate determination, and ultimately, organogenesis.
138 al key transcription factors that regulate T cell fate determination are methylated on arginine.
140 ring development, extracellular cues guiding cell fate determination are provided by morphogens.
141 dicates that several aspects of R7 versus R8 cell fate determination are regulated by the transcripti
143 signaling has been described in neuro/glial cell fate determination as well as in modulating neuroge
144 NOTCH receptors have been implicated in cell fate determination, as well as maintenance and diff
146 the signalling pathways that are involved in cell fate determination at the border of the neural plat
148 echanisms that underlie proneural induction, cell fate determination, axonal targeting, dendritic bra
149 ro-RNAs (miRNAs) are important in regulating cell fate determination because many of their target mRN
150 ell-type specific genes provide evidence for cell fate determination beginning in some cells much ear
152 e and cellular metabolism both contribute to cell fate determination, but their interplay remains poo
155 date, the mechanisms underlying multipotent cell fate determination by retinal progenitors remain po
156 g efforts to link copy number variation with cell fate determination by viruses, dynamics of syntheti
157 to demonstrate that stochastic and permanent cell fate determination can be achieved through initiali
159 roblast 5-6 by simultaneously activating two cell fate determination cascades and a sub-temporal regu
160 Wnt signaling is a major pathway regulating cell fate determination, cell proliferation and cell mov
161 upporting a model of a stochastic process of cell fate determination coupled with dynamic patterns of
162 lates multiple cellular processes, including cell fate determination, development, differentiation, p
163 ent consists of several processes, including cell fate determination, differentiation, and maturation
164 of genes involved in cell cycle progression, cell fate determination, DNA damage repair, and apoptosi
165 ulation, the importance of cic in regulating cell-fate determination downstream of Ras appears to var
166 e the relationship between PCP signaling and cell fate determination during asymmetric division of ne
169 ption factors regulate tissue patterning and cell fate determination during development; however, exp
172 ptional factors that play essential roles in cell fate determination during early embryogenesis and o
174 e Notch signal transduction pathway controls cell fate determination during metazoan development.
175 he Dictyostelium homologue of GSK3 (gskA) in cell fate determination during morphogenesis of the frui
176 damage signaling have all been implicated in cell fate determination during neurogenesis, our finding
177 igand for the EMS1 receptor kinase to signal cell fate determination during plant sexual reproduction
180 The Hedgehog (Hh) pathway is required for cell-fate determination during the embryonic life, as we
181 mb and Numbl in the control of myoepithelial cell fate determination, epithelial identity, and lactog
182 The mechanisms that specify photoreceptor cell-fate determination, especially as regards to short-
183 n modifications, but their specific roles in cell fate determination events are poorly understood.
188 ta identify a pathway by which an endogenous cell-fate determination factor blocks oncogene-dependent
190 l whereby Lim1 lies downstream of horizontal cell fate determination factors and functions cell auton
191 g takes advantage of this knowledge and uses cell fate determination factors to convert one lineage i
194 mbers of the let-7 miRNA family control many cell-fate determination genes to influence pluripotency,
196 OR) plays a crucial role in the control of T cell fate determination; however, the precise regulatory
197 nobiotic metabolism, cell cycle progression, cell fate determination, immune function, and inflammato
198 s establish that PBX1 regulates adult neural cell fate determination in a manner beyond that of its h
199 hat p16Xic2 and p17Xic3 might be involved in cell fate determination in a tissue-specific manner by c
200 ch signaling makes critical contributions to cell fate determination in all metazoan organisms, yet r
203 ggests a previously undescribed mechanism of cell fate determination in at least a subset of retinal
204 other EJC components apparently function in cell fate determination in developing male gametophytes
205 on as early events in a program of secretory cell fate determination in developing murine airways.
208 he latter have been implicated in regulating cell fate determination in invertebrates and vertebrates
210 signaling proteins is a master regulator of cell fate determination in metazoans, contributing to bo
211 eless, and sine oculis (so) genes, regulates cell fate determination in metazoans, with dac serving a
220 and intrinsic competence act in concert for cell fate determination in the developing vertebrate ret
221 e interested in the mechanisms that underlie cell fate determination in the endosporic male gametophy
222 he silent mating-type region is critical for cell fate determination in the form of mating-type switc
224 his study, we examined the cell lineages and cell fate determination in the heart by using various ce
225 on cycle 7 (Cdc7) has been shown to regulate cell fate determination in the initial phase of transfor
226 plate, in that it plays an essential role in cell fate determination in the lateral CNS and also, lat
229 understanding of the molecular mechanisms of cell fate determination in the nervous system requires t
231 Dpp activity and DE-cadherin and Rho1 during cell fate determination in the wing, suggesting a broade
232 thematical analysis predicts that stochastic cell fate determination in this case can only be realize
235 fter the first cell division plays a role in cell fate determinations in the early mouse embryo.
236 amily of cell surface receptors important in cell-fate determination in both vertebrates and inverteb
237 not, the mechanisms at play during the first cell-fate determination in mammalian embryos have been d
239 key regulators of development by controlling cell-fate determination in many multicellular organisms.
240 calloped beyond growth to encompass specific cell-fate determination in the context of blood developm
241 nct and common roles for the three miRNAs in cell-fate determination in the inner ear, and these prin
243 ugh LRP6 appeared to be critical for granule cell fate determination, in vivo knockdown of PCP core p
244 are highly conserved proteins that regulate cell fate determination, including those involved in mam
245 ism by which a known physiologic mediator of cell fate determination interfaces with cell cycle contr
247 served signaling pathway and its function in cell fate determination is crucial in embryonic developm
248 widely accepted that the process of retinal cell fate determination is under tight transcriptional c
251 ription factor, and may result from abnormal cell-fate determination, leading to excess S cones at th
254 apability of these melanoma cells to express cell-fate determination molecules, normally expressed du
256 ositive selection results in a change in the cell fate determination of developing iNKT cells, with a
257 ch signaling-mediated lateral inhibition and cell fate determination of external sensory organs.
259 resence of a novel mechanism for controlling cell fate determination of mesenchymal lineages by preve
261 ble, which enables direct study of quadruple cell fate determination on an engineered landscape.
263 enes initially identified for their roles in cell fate determination or signaling during development
264 ivity of Sox2 in promoting proliferation and cell fate determination, our data demonstrate that Sox2
266 tant ellipse, encodes a key component of the cell fate determination pathway involved in Drosophila e
270 ion of genes involved in lineage commitment, cell fate determination, proliferation, and tumorigenesi
271 s are potent morphogens that are involved in cell fate determination, proliferation, apoptosis and ad
272 tion and refinement of these patterns during cell fate determination remain unexplored because of the
273 The data reveal Bcl-3 as a regulator of B cell fate determination, restricting the MZ path and fav
274 inciple for how cells acquire competence for cell fate determination, resulting in the context-depend
275 Ras family GTPases play a pivotal role in cell fate determination, serving as molecular switches t
276 TagA also appears to play a general role in cell fate determination since tagA mutants express a spo
277 ses in eukaryotes, including axis formation, cell fate determination, spindle pole regulation, cell m
278 in CSCs in a variety of cancers and controls cell fate determination, survival, proliferation, and th
281 le for detrusor smooth muscle and urothelial cell fate determination, the mutants have significantly
282 t sequences reflect underlying mechanisms of cell fate determination, they appear to be conserved.
283 ling pathways, suggest that Adam10 regulates cell fate determination through the activation of Notch
284 ch intercellular signaling pathway regulates cell fate determination throughout metazoan evolution, a
285 spindle during cell division is crucial for cell fate determination, tissue organization, and develo
286 ticellular organisms actively regulate their cell fate determination to cope with changing environmen
288 important for diverse processes ranging from cell fate determination to synaptic plasticity; however,
289 nctions by a novel mechanism, independent of cell fate determination, to mediate the decision of neur
290 tion to exhibiting spiral cleavage and early cell fate determination, trochozoans typically undergo i
291 neuromuscular junction formation, and neuron cell fate determination, typically during the pupal stag
293 iptional regulation that coordinates retinal cell fate determination, very little is known about the
296 To further examine the role of Olig2 in NG2 cell fate determination, we used genetic fate mapping of
298 ults suggest that Math1 is critical for both cell fate determination within the intestinal epithelium
299 in disease states with opposing responses in cell fate determination, yet its contribution in pro-sur
300 s crucial for understanding their effects on cell-fate determination, yet it is difficult to obtain t
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。