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1 nstruction of all major organ systems during embryogenesis.
2 rons, similar to neuronal development during embryogenesis.
3 s modulating mRNA stability during zebrafish embryogenesis.
4 s of 3' UTR sequences during early zebrafish embryogenesis.
5 pleiotropic PRC2-independent actions during embryogenesis.
6 y distils the principles thought to underlie embryogenesis.
7 o direct disparate cellular fates throughout embryogenesis.
8 layers from a central core generated during embryogenesis.
9 of human, macaque, and mouse preimplantation embryogenesis.
10 gg by the sperm is the first, vital stage of embryogenesis.
11 ns retinoic acid (RA) plays crucial roles in embryogenesis.
12 d phenotypes can be traced back to defective embryogenesis.
13 ulate and buffer expression variation during embryogenesis.
14 s play a vital yet poorly understood role in embryogenesis.
15 occurs at the 8-cell stage during C. elegans embryogenesis.
16 d loss of the DUB subunits causes defects in embryogenesis.
17 important player in the maternal control of embryogenesis.
18 ence its proper development is essential for embryogenesis.
19 sterile (1) homeotic] and Enok/Br140 during embryogenesis.
20 , and is essential for normal progression of embryogenesis.
21 xpressed SMC5 protein is essential for early embryogenesis.
22 hin the first 2 h of Drosophila melanogaster embryogenesis.
23 l signals to specify germ cells during later embryogenesis.
24 e targeted deletion of Cdc42 occurred during embryogenesis.
25 sses p53, and this function is essential for embryogenesis.
26 cative of arrested seed embryo growth during embryogenesis.
27 e crucial for cell fate determination during embryogenesis.
28 remodeled during mammalian gametogenesis and embryogenesis.
29 gin of hemato-vascular lineages during early embryogenesis.
30 tually nothing has been reported about their embryogenesis.
31 ell dynamics that operate during early human embryogenesis.
32 ic changes in the diverse vertebrates during embryogenesis.
33 vity of origins is largely invariant through embryogenesis.
34 d during early axial patterning in spiralian embryogenesis.
35 nd other mesodermal derivatives arise during embryogenesis.
36 stigating cellular differentiation and human embryogenesis.
37 ycle kinase to slow cell cycles during early embryogenesis.
38 on of blood stem and progenitor cells during embryogenesis.
39 as a basis for comparative studies of plant embryogenesis.
40 th haemoglobin-depleted serum led to aborted embryogenesis.
41 toire and its dynamic usage during zebrafish embryogenesis.
42 sensory and motile functions of cilia during embryogenesis.
43 plays cell-specific regulatory roles during embryogenesis.
44 nd a suite of transcription factors to early embryogenesis.
45 KO) mice were able to form sarcomeres during embryogenesis.
46 oscopy to explore the roles of Pa ESP during embryogenesis.
47 ly from a segment addition zone (SAZ) during embryogenesis.
48 r roles in neuroblast migration during early embryogenesis.
49 sing mutations in FGF receptor (FGFR) during embryogenesis.
50 ion, whereas fewer genes are changing in mid-embryogenesis.
51 ted and fatty acid biosynthetic genes during embryogenesis.
52 tency transcription factor OCT4 during human embryogenesis.
53 e maternally controlled stages of vertebrate embryogenesis.
54 hway generates oocytes capable of supporting embryogenesis.
55 late are micronutrients essential for normal embryogenesis.
56 gene expression and DNA methylation in early embryogenesis.
57 ncestral to arthropods, including short germ embryogenesis.
58 resulted in abnormal cardiac looping during embryogenesis.
59 rosa - actively rupture and withdraw in late embryogenesis.
60 at show polarized expression patterns during embryogenesis.
61 his study are highly relevant to early stage embryogenesis.
62 aematopoietic and cardiac progenitors during embryogenesis.
63 olk sac precursors and seed the liver during embryogenesis.
64 mal heart and vasculature development during embryogenesis.
65 growth are a characteristic feature of early embryogenesis.
66 tion both increased significantly throughout embryogenesis.
67 the assimilation of beta-carotene for proper embryogenesis.
68 ee to which growth occurs concomitantly with embryogenesis.
69 from a failure of neural tube closure during embryogenesis.
70 ophectoderm commitment is regulated in human embryogenesis.
71 ntify transcriptional changes during Odonata embryogenesis.
72 yte differentiation and proliferation during embryogenesis.
73 that Copb2 is essential for early stages of embryogenesis.
74 embryonic stem cells (mESCs) and subsequent embryogenesis.
75 other Arabidopsis peroxins, is essential for embryogenesis.
76 lifelong blood production are created during embryogenesis.
77 re thought to accumulate mostly during human embryogenesis.
78 e Ca(2+) oscillations that normally initiate embryogenesis.
79 ysine 16 (H4K16ac) and is crucial for murine embryogenesis.
80 fusion and skeletal muscle formation during embryogenesis.
81 ally due to de novo, somatic mutation during embryogenesis.
82 f all temporary and definitive organs during embryogenesis.
83 velopmental dispersal, which is critical for embryogenesis.
84 igate how cell position is determined during embryogenesis.
85 note that their expression decreases during embryogenesis.
86 ate," and this state is dampened after early embryogenesis.
87 and mRNA complements throughout T. castaneum embryogenesis.
88 ted with katatrepsis (revolution) during mid-embryogenesis, a 180 degrees rotation of the embryo with
91 amily oligosaccharide (RFO) metabolism, late embryogenesis abundant (LEA) proteins, and photosynthesi
93 NBARC-containing, pathogenesis-related, late embryogenesis abundant, selected transcription factors,
94 tion of stress-inducible genes encoding late-embryogenesis-abundant proteins in transgenic roots was
95 achia in worm tissues leading to blockade of embryogenesis, adult sterility and premature death 18-24
96 so uncover functional redundancy for somatic embryogenesis among other Arabidopsis BBM-like proteins
101 role for BPL-1 in lipid biosynthesis during embryogenesis and demonstrating that dietary fatty acids
102 er cell division is higher during both early embryogenesis and differentiation of primordial germ cel
103 ne, an amino acid essential during mammalian embryogenesis and early development is one of the key ac
105 ASXL3) participate in body patterning during embryogenesis and encode proteins involved in epigenetic
108 ematopoietic stem cells (HSCs) emerge during embryogenesis and give rise to the adult haematopoietic
109 l liver progenitors that seed tissues during embryogenesis and have the ability to repopulate through
111 ault self-organization rules governing early embryogenesis and how they are altered by deterministic
112 ) regulate diverse cellular responses during embryogenesis and in adulthood including cell differenti
113 ues to study mechanobiology in vivo, both in embryogenesis and in disease processes, including cancer
116 closure is an essential stage of Drosophila embryogenesis and is a powerful model system for morphog
118 kinase, MET, which has a pleiotropic role in embryogenesis and modifies a large number of neurodevelo
119 ar alterations in adults exposed only during embryogenesis and morphological alterations in their off
120 anding of coronary artery development during embryogenesis and of how these pathways might be reignit
122 arly into scarce material and to model human embryogenesis and pathophysiological processes are leadi
125 n that EVI and MDS/EVI are not essential for embryogenesis and premetamorphosis in X. tropicalis On t
129 y and governance of the transcriptome during embryogenesis and subsequent developmental processes.
131 with the most conserved phase of vertebrate embryogenesis and suggests an ancient developmental role
132 tic conservation between apogamy and somatic embryogenesis and that such asexual reproduction may be
134 30 parts per billion (ppb) atrazine through embryogenesis and then allowed to mature with no additio
135 cell per cell-doubling event in early human embryogenesis and these are mainly attributable to two k
138 The germ cell lineage is specified early in embryogenesis and undergoes complex developmental progra
142 des gaining insights into species evolution, embryogenesis, and human disease, interspecies blastocys
144 module regulates a subset of genes in early embryogenesis, and loss of the DUB subunits causes defec
146 ore, proper capzb dosage is important during embryogenesis, and regulates both cell behavior and tiss
147 e of neoblasts during Schmidtea mediterranea embryogenesis, and report that neoblasts arise from an a
149 the initial emergence of the medulla during embryogenesis, and the maintenance of the medulla during
150 egarding that many developmental pathways in embryogenesis are dysregulated in cancer, we aim to unra
153 t intercellular differences during mammalian embryogenesis arise in the blastocyst, producing the inn
156 101 vlinc RNA genes likely involved in early embryogenesis based on patterns of their expression and
158 e tumour suppressor p53 is incompatible with embryogenesis, but how p53 is controlled is not fully un
159 anscription factor TWIST is expressed during embryogenesis, but its role in EC responses to shear str
160 Merkel cell-specific deletion of Bdnf during embryogenesis, but not postnatal Bdnf deletion or Ntf3 d
161 lopment, differentiation, proliferation, and embryogenesis, but pathogenesis of many diseases, includ
162 ons and were born among other neurons during embryogenesis, but remained unspecialized until target o
163 tiotemporal gene expression is essential for embryogenesis, but the underlying mechanisms remain unde
164 (hPSCs) recapitulates early aspects of human embryogenesis, but the underlying processes are poorly u
165 l mode wherein germ cells are induced during embryogenesis by cell-cell signaling (induction) or a de
166 ns of FIP200 are sufficient to fully support embryogenesis by maintaining a protective role in TNFalp
167 es are initially specified during Drosophila embryogenesis, by characterizing a cis-regulatory module
170 discontinuous LSECs to continuous ECs during embryogenesis caused liver hypoplasia, fibrosis, and imp
174 We first apply miCLIP to map m(6)A across embryogenesis, characterize its m(6)A 'writer' complex,
175 ow that myomixer expression during zebrafish embryogenesis coincides with myoblast fusion, and geneti
177 of individual MEF2 isoforms in brain during embryogenesis demonstrated that Mef2c loss negatively re
179 mation of limb skeletal muscles during mouse embryogenesis downstream of MET and acts as a potent ind
180 hat signaling of endogenous C5a during mouse embryogenesis drives proliferation of neural progenitor
181 ryonic events are frequently reused later in embryogenesis, during organismal development or in the a
183 t the plasma membrane, is dispensable during embryogenesis, enabling us to define alternative mechani
184 in Caenorhabditis elegans shows that during embryogenesis endodermal cells interact with and regulat
185 the global gene expression involved in plant embryogenesis, especially the early events following fer
190 he effects of maternal and zygotic CTNNB1 on embryogenesis have each been separately assessed, wherea
192 aR1 is also expressed during early mammalian embryogenesis; however, no clearly defined function is a
193 s essential for biological functions such as embryogenesis, immunity, cell renewal, and wound healing
195 Arabidopsis thaliana with known functions in embryogenesis in addition to unique and uncharacterized
197 olutionary hourglass pattern observed during embryogenesis in animals and the developmental process i
202 f five essential TFs over multiple stages of embryogenesis in two distant Drosophila species (with 1.
204 g how and when cells become different during embryogenesis is a goal that is at the forefront of inve
206 tanding the fundamental principles governing embryogenesis is a key goal of developmental biology.
214 Identifying transcriptional changes during embryogenesis is of crucial importance for unravelling e
216 ting this system in Drosophila, we find that embryogenesis is remarkably robust to ectopic Erk signal
218 ically expressed in the pancreas only during embryogenesis, is expressed in islets of diabetic rodent
219 ity, with inhibition of C5a receptors during embryogenesis leading to abnormal brain development and
220 he notion that aberrant p53 signaling during embryogenesis leads to the hematological defects seen la
221 cytes efficiently, whereas deletion later in embryogenesis led to decreased vascular density and lume
224 uripotent stem cells (iPSCs) aims to reenact embryogenesis, maturation and aging of spinal motor neur
227 y, macrophage populations established during embryogenesis, monocyte-derived cells that develop durin
228 t is unclear whether their production during embryogenesis must also be regulated in a temporal fashi
231 cells and specific inhibitors, we show that embryogenesis of ESC- and TSC-derived embryos-ETS-embryo
232 vantages as model systems, the long germband embryogenesis of fruit flies is an evolutionary derived
233 tic analyses demonstrated that the defective embryogenesis of the mpk6 mutant is a maternal effect.
234 h as Onecut2 to inhibit lateral fates during embryogenesis, Pitx3 to promote mDAn development, and Nf
236 development and megasporogenesis, a modified embryogenesis program resulting in seeds with immature e
238 ability in cardiovascular development during embryogenesis, providing insight into the conserved link
239 4 and Avr9, BRI1-ASSOCIATED KINASE 1/SOMATIC EMBRYOGENESIS RECEPTOR KINASE 3 (BAK1/SERK3) associates
240 ociated receptor kinase 1 (BAK1) and somatic embryogenesis receptor kinase 4 (SERK4) redundantly and
243 (ARF ), Leafy cotyledon1 (LEC1) and somatic embryogenesis receptor-like kinase (SERK ) known to be i
245 hic mutant of CPSF100 (esp5) show defects in embryogenesis, reduced seed production or altered root m
249 e max), GmAGL15, are able to promote somatic embryogenesis (SE) in these plants when ectopically expr
250 ages of the life cycle as they contribute to embryogenesis, seed development and germination, cuticle
251 w the crucial functions of KLFs in mammalian embryogenesis, stem cell biology and regeneration, as re
254 en well characterized in cells formed during embryogenesis, such as the neural crest-derived melanocy
255 riptome "inverse hourglass" model for animal embryogenesis, suggesting both plant and animal morpholo
259 le functions have been assigned during later embryogenesis, the role of Gsc in the organizer has rema
260 g conservation of GRN circuitry during early embryogenesis, this study indicates that since the diver
261 provide a multitude of functions, from early embryogenesis through cell differentiation and developme
264 ctive constraint on somatic gene networks in embryogenesis, thus leading to acceleration of an organi
268 cesses ranging from cell differentiation and embryogenesis to cancer metastasis and biomaterial-tissu
269 1), CUC2 and CUC3 regulate each other during embryogenesis to establish the embryonic SAM and to spec
271 expressing progenitors, specified during mid-embryogenesis to produce astroglia and interneurons, swi
272 ganize into specialized tissues during early embryogenesis to supply essential nutrients to all organ
274 suppress axillary meristem formation during embryogenesis, to maintain meristem size, and to precise
275 r spatiotemporal gene expression during rice embryogenesis, to serve as a resource for future functio
278 (DV) and anterior-posterior (AP) axes during embryogenesis, uncertainty exists in the orientation of
279 lone (0.1, 1, and 10 mug/L) during zebrafish embryogenesis using physiological and behavioral end poi
281 critically impacts cell migration and mouse embryogenesis, we demonstrate here that generation of a
283 To further understand the role of H3K79me in embryogenesis, we generated a mouse knockout of Mllt10,
284 ays affected by loss of Tgif function during embryogenesis, we performed transcriptome profiling on w
285 By studying the heart epicardium during embryogenesis, we show that Lb1-null epicardial cells ex
286 with developmental events during rice early embryogenesis, we used microarray analysis coupled with
288 y interference of cat7l RNA during zebrafish embryogenesis were rescued by human CAT7 RNA, enhanced b
289 ied that are expressed in most organs during embryogenesis, where they are believed to play an import
290 in angiosperms are known to promote somatic embryogenesis, which like apogamy produce sporophytes wi
291 he parental genomes during the initiation of embryogenesis, which presumptively derive from divergent
292 quantitatively regulate BBM-mediated somatic embryogenesis, while FUS3 and LEC1 are essential for thi
295 a single novel compound that disrupts early embryogenesis with remarkable stage and species specific
296 muscle fibers over several hours during late embryogenesis, with episodic Ca(2+) signals present in b
297 found that n1-src expression is regulated in embryogenesis, with highest levels detected during the p
298 ing microbial self-organization in biofilms, embryogenesis, wound healing, and cancer metastasis.
299 logical and pathological processes including embryogenesis, wound healing, host immunity, and tumor s
300 vivo live imaging is vital to understanding embryogenesis; yet, tedious sample preparation makes it
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