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1 cyte activation, which is the first stage of embryo development.
2 that drive egg activation and initiate early embryo development.
3 9me3 demethylase Kdm4d greatly improves SCNT embryo development.
4 d specifically in the suspensor during early embryo development.
5 -dimensional (2D) to 3D growth occurs during embryo development.
6 quired for fertilization and preimplantation embryo development.
7 ter anthesis, during fertilization and early embryo development.
8 oth of which are a consequence of defects in embryo development.
9 24 TFs across five stages of D. melanogaster embryo development.
10 er to uncover cooperativity among TFs during embryo development.
11 rkably little is known about its role during embryo development.
12 ment TMTC3 rescue of gastrulation in Xenopus embryo development.
13 paradigm of signaling pathway integration in embryo development.
14 in vein connectivity appear early in mutant embryo development.
15 s of previous difficult to access aspects of embryo development.
16 log of LEC1 is expressed during leaf somatic embryo development.
17 ves as a warehouse to provide metal ions for embryo development.
18 for meiotic progression, fertilization, and embryo development.
19 of maternal-specific H3K9me3 modification in embryo development.
20 LEC1, LEC2, and FUS3 are essential for plant embryo development.
21 which AtHDA7 affects female gametophyte and embryo development.
22 or yolk granules and as a source of heme for embryo development.
23 uidic device that can be used to model human embryo development.
24 re clock-controlled in cell lines and during embryo development.
25 ted to be involved in female gametophyte and embryo development.
26 n TET1 is a key regulator at later stages of embryo development.
27 anges in DNA methylation are observed during embryo development.
28 zation of cyclin A2 mRNA and mammalian early embryo development.
29 ies deemed to be critical during ex-vivo egg embryo development.
30 K5)-Cre gene construct is expressed in early embryo development.
31 ability of an oocyte to support early cloned embryo development.
32 iogenesis and cardiac formation during mouse embryo development.
33 sed progressively during the first 3 days of embryo development.
34 hows that Asc regulates cell polarity during embryo development.
35 pregnancy events, including preimplantation embryo development.
36 t live cells and in vivo in zebrafish during embryo development.
37 ment, especially in fatty acid synthesis and embryo development.
38 highly dynamic behavior in early Drosophila embryo development.
39 tions at fertilization and to support proper embryo development.
40 the wild type, suggesting a role of OPDA in embryo development.
41 n had a strong negative impact on subsequent embryo development.
42 n early embryogenesis, and eventually arrest embryo development.
43 ble for expression in the radicle tip during embryo development.
44 s an important role during wound healing and embryo development.
45 ality owing to failure in both endosperm and embryo development.
46 is quite shallow, which is typical of type I embryo development.
47 medicine, or as a model to understand human embryo development.
48 a defect in this process might be fatal for embryo development.
49 n oil content per seed and in disruptions of embryo development.
50 ROTEIN30 is involved in promotion of somatic embryo development.
51 ization, chalazal endosperm enlargement, and embryo development.
52 ms unlikely to explain Arf regulation during embryo development.
53 ecifically within the suspensor during early embryo development.
54 early pregnancy during nascent placental and embryo development.
55 NSM) from the endomesoderm during sea urchin embryo development.
56 of PKA localisation during oocyte and early embryo development.
57 of regulated granules form during oocyte and embryo development.
58 displaying pleiotropic defects in pollen and embryo development.
59 rgence of shape and function: the pillars of embryo development.
60 A localisation occur during oocyte and early embryo development.
61 ion reveals novel RUB-dependent processes in embryo development.
62 2 must be above a threshold level for proper embryo development.
63 oscillations in mammalian eggs that activate embryo development.
64 ng radiation (IR) with no apparent effect on embryo development.
65 yonic lethal, with arrest occurring early in embryo development.
66 re the developmental plasticity of mammalian embryo development.
67 , indicating an essential role for AtOPT3 in embryo development.
68 educed fertility due to defective anther and embryo development.
69 ly, accelerate post-MBT cell cycle speed and embryo development.
70 ng that this molecule is required for normal embryo development.
71 te to the programming of gene expression and embryo development.
72 abnormal pattern formation at all stages of embryo development.
73 s (Arabidopsis thaliana): those defective in embryo development.
74 TP for mammalian oocyte maturation and early embryo development.
75 1 is needed for timely mouse preimplantation embryo development.
76 cells to form following syncytial Drosophila embryo development.
77 xidative pentose phosphate pathway (OPPP) in embryo development.
78 d high-altitude adaptations by regulation of embryo development.
79 eate resilience in the auxin response during embryo development.
80 s, likely via the YDA-MKK4/5 cascade, during embryo development.
81 LIKE KINASE (SERK) genes results in aberrant embryo development.
82 e analysed the role of macroH2A during early embryo development.
83 important for the paternal control of early embryo development.
84 rian follicular fluid (FF) and are linked to embryo development.
85 from heterozygous parents were defective in embryo development.
86 or (AP) axis is a crucial step during animal embryo development.
87 le for SCY2 in chloroplast biogenesis beyond embryo development.
88 al to probe its enantioselective toxicity in embryo development.
89 s) can disrupt endocrine function and impair embryo development.
90 r in the pattern and timing of endosperm and embryo development.
91 ndicating that CRF function is essential for embryo development.
92 tioning in maintaining genomic stability and embryo development.
93 hat does not compromise oocyte maturation or embryo development.
94 various markers, including ATP contents and embryo development.
95 trusion into the polar bodies for successful embryo development.
96 genome activation and is essential for early embryo development.
97 play an essential role in the initiation of embryo development.
98 ocalizes in the cytosol and is essential for embryo development.
99 background level with the progression of the embryo development.
100 ity to induce oocyte activation and initiate embryo development.
101 e-dependent transcription regulation, during embryo-development.
102 ial-to-mesenchymal transitions (EMTs) during embryo development; a process reactivated during cancer
104 morphology, to identify the condition of an embryo development after fertilization in vitro (IVF), b
105 expressed in seeds, where it regulates both embryo development and accumulation of storage compounds
106 TSPO was found necessary for preimplantation embryo development and ACTH-stimulated steroid biosynthe
107 8 copies of the histone gene unit supported embryo development and adult viability, whereas flies wi
108 formation are observed in early stage human embryo development and are associated with pluripotency
110 tes that TEs are highly transcribed in early embryo development and contribute to distinct biological
111 rst nine divisions of Caenorhabditis elegans embryo development and demonstrate that chiral counter-r
113 T-10 also promotes vulva, somatic gonad, and embryo development and ensures meiotic development of th
114 nt CPSF components have been associated with embryo development and flowering time controls, both of
115 UL7 mediates an essential function for mouse embryo development and has been linked with cell transfo
116 currently known about human pre-implantation embryo development and highlight how further studies of
119 mutant revealed that CLPS3 was essential for embryo development and important for female gametophyte
120 ey findings on the roles of SAGA and ATAC in embryo development and in cancer to better understand th
122 tewater and river water composition affected embryo development and led to the alteration of steroido
123 naling is critical to normal preimplantation embryo development and migration of trophoblast stem cel
124 skeletal myoblasts and cardiac tissue during embryo development and muscle cell differentiation, whic
128 F2; an endometrial cytokine known to improve embryo development and pregnancy establishment) between
131 Knockdown of the sulfur dioxygenase impaired embryo development and produced phenotypes of starvation
132 nstrate that AESP plays an essential role in embryo development and provide direct evidence that AESP
133 the channel function delays pre-implantation embryo development and reduces progression to the blasto
134 lin signaling plays an important role during embryo development and regulates angiogenesis, cardiovas
135 a crucial role of Brpf1 in controlling mouse embryo development and regulating cellular and gene expr
137 s in the presence of sucrose restores normal embryo development and seed viability, suggesting that t
139 and JA-deficient mutant spr2 was delayed in embryo development and showed an increased programmed ce
142 ctive demethylation of H3K27me3 during early embryo development and that this mark plays an important
144 sults reveal a role for NGF in early chicken embryo development and, in particular, in the regulation
145 s in the transfer cell layer, retardation of embryo development, and a considerable reduction of star
146 it plays an important role in seed dormancy, embryo development, and adaptation to environmental stre
147 ise during germ cell and/or pre-implantation embryo development, and are a major cause of spontaneous
149 c example of this is perturbation of midline embryo development, and disruption of Hedgehog (Hh) sign
150 three groups (early embryo development, late embryo development, and embryonic root apical meristem l
152 /-) seeds were nonviable, displayed aberrant embryo development, and had >80% reduced oil content ver
155 h calcium regulators are essential for early embryo development, and that knockdown of PmTPCs leads t
163 prove understanding of the genes involved in embryo development, at least one third of which have bee
164 We propose that GPT1 is necessary for early embryo development because it catalyses import into plas
166 ght be the functions of NGF in early chicken embryo development, before its well-established actions
167 are expressed at very early stages of avian embryo development, before the nervous system is formed.
168 dually, with the initial steps of zygote and embryo development being primarily maternally controlled
169 ly provides nutrient supplies for subsequent embryo development but also enforces a space limitation,
170 f aneuploid cells, may paradoxically promote embryo development but contribute to the high rate of sp
171 CTF7 are critical for female gametophyte and embryo development but not for the establishment of mito
172 is a multinucleated syncytium essential for embryo development, but the molecular mechanisms underly
174 of Ca(2+)-induced egg activation events and embryo development by microinjecting a cRNA that encodes
175 fic phospholipase C zeta (PLCzeta) activates embryo development by triggering intracellular Ca(2+) os
177 sed H2O2 generation followed by a failure in embryo development caused by a reduced resistance to wat
178 an important epigenetic marker during early embryo development, cellular differentiation, and cancer
182 erase-like protein Dnmt3l, which, during the embryo development, cooperates with Dnmt3a and Dnmt3b to
183 uble mutant combinations reported to disrupt embryo development; emphasize the importance of followin
184 velopment that are accompanied by a delay in embryo development followed by embryo arrest by early he
186 c subunit has been shown to be essential for embryo development, genetic data regarding the accessory
189 However, the role of endothelial Pak in embryo development has not been reported, and currently,
190 igenetic contributions of sperm chromatin to embryo development have been considered highly limited.
191 ns of oocyte gene expression with successful embryo development have been hampered by the lack of rel
192 uitable for the study of human germ cell and embryo development have been limited until recently.
193 or other factors individually may not affect embryo development, however, they may do so collectively
194 mature human sperm, genes of importance for embryo development (i.e., transcription factors) lack DN
195 ochondrial matrix and is essential for early embryo development in Arabidopsis (Arabidopsis thaliana)
196 versity of chloroplast proteins required for embryo development in Arabidopsis (Arabidopsis thaliana)
198 y a major role in axial morphogenesis during embryo development in both vertebrates and invertebrates
199 the stress treatments used to induce haploid embryo development in culture impinge on this HDAC-depen
200 s thaliana, which is recalcitrant to haploid embryo development in culture, also forms embryogenic ce
205 ctively, our data suggest that PLAG1 affects embryo development in mice and humans through a conserve
206 We investigate patterns of endosperm and embryo development in Mimulus guttatus and the closely r
207 signal ([Ca2+]i) underlies the initiation of embryo development in most species studied to date.
210 rthologs of AGL15 is able to enhance somatic embryo development in other species, thereby facilitatin
213 e formation of sulfonated amino acids during embryo development in the egg at no cost of reduced sulf
214 also essential for both male gametophyte and embryo development in the model plant Arabidopsis thalia
215 small RNA classes through gametogenesis and embryo development in the parasitic nematode Ascaris suu
216 enes varied in expression throughout somatic embryo development in this study, no statistically signi
219 ype was associated with the delayed/arrested embryo development, in most cases, at the heart stage.
220 been applied to various mutants disrupted in embryo development including gnom (gn), acetyl-CoA carbo
221 e treatment partially improved cohesinopathy embryo development including the formation of craniofaci
224 which is the first step in the initiation of embryo development, involves both completion of meiosis
225 ave demonstrated that mouse pre-implantation embryo development is a process of progressive cell fate
228 s indicate that success and failure in human embryo development is largely determined before EGA.
230 ytes are released and fertilized, subsequent embryo development is retarded, and the embryos potentia
231 e or V-ATPase had no obvious effect on plant embryo development, knocking out both resulted in severe
232 ns and grouped them into three groups (early embryo development, late embryo development, and embryon
233 isual phenotypes, but eda9 displayed delayed embryo development, leading to aborted embryos that coul
235 xpression of genes involved in gynoecium and embryo development, lipid metabolism, auxin transport, a
236 ection mechanisms that act downstream of the embryo development master regulators LEAFY COTYLEDON 1 a
237 nt concentrations in culture medium on mouse embryo development, metabolism, and quality as a possibl
240 erm is an absorptive structure that supports embryo development or seedling germination in angiosperm
241 priate "anandamide tone" required for normal embryo development, oviductal transport, implantation, a
242 o P. pacificus adults, the pheromone arrests embryo development, paralyzes J2 larva, and inhibits exi
243 te of aging in birds also was related to the embryo development period, birds grow several times more
244 seed viability, suggesting that the seed and embryo development phenotypes are a result of a maternal
245 OPDA or an OPDA-related compound for proper embryo development possibly by regulating carbohydrate s
246 e rhesus oocytes, leading to preimplantation embryo development, pregnancy, and the birth of a health
247 Although cyclin B1 (CCNB1) is required for embryo development, previous studies concluded that CCNB
249 severe seed defects, which include retarded embryo development, reduced seed weight, and reduced sta
250 at auxin-dependent cell specification during embryo development requires balanced auxin transport inv
252 ABI3 promoter to drive the TPS1 cDNA during embryo development, resulting in rescue of the embryo-le
254 le mutant aborted during the early stages of embryo development showing that these two proteins share
255 ds to defective placentation and compromised embryo development, similar to that resulting from neutr
256 d dynamic roles in many processes, including embryo development, stem cell fate determination, tricho
257 s combined with the effect of gct and cct on embryo development suggests that MED13 and MED12 regulat
259 We report studies of preimplantation human embryo development that correlate time-lapse image analy
260 on DNA methylation heritability during early embryo development that extend beyond conventional impri
261 some aspects of egg fertilization and early embryo development that lead to transcriptional activati
262 on the impact of obe mutations on aspects of embryo development, the effect of such mutations on a br
265 e embryo sac and delay in the progression of embryo development, thereby bringing the seed set down i
266 us effects on the central nervous system and embryo development, these data suggest that superphysiol
269 al in many areas of biology, including early embryo development, tissue homeostasis and tumour growth
270 9(Arf), is activated by Tgfbeta during mouse embryo development to better understand how this importa
271 se 1-phosphate, on oocyte quality as well as embryo development to elucidate the mechanism through wh
273 ment in fertilization outcome and subsequent embryo development to mitochondrial DNA deficient oocyte
274 HPAT3 and HPAT5 function in preimplantation embryo development to modulate the acquisition of plurip
275 eveal a novel function of PADI1 during early embryo development transitions by catalyzing histone tai
277 (DM) adversely affects oocyte maturation and embryo development via mechanisms that are yet unclear.
278 ides insight into the molecular mechanism of embryo development via MIR160a-regulated ARFs, but also
279 Consistent with this observation, early embryo development was also arrested at the 4-cell stage
282 ene family that regulates shoot, flower, and embryo development, was implicated in nitrate signaling
283 f maternally deposited DOT1L is required for embryo development, we carried out a conditional Dot1l k
284 milarities between angiosperm and gymnosperm embryo development, we examined our EST collection for p
285 finitive role of TSPO in steroidogenesis and embryo development, we generated global TSPO null (Tspo(
289 abortion at the end of the globular stage of embryo development, when proplastids in normal embryos d
291 theory as a prelude to its applicability in embryo development where spatial gradients of morphogens
292 effects on both oocyte maturation and early embryo development, which in turn can have lifelong cons
293 ted genes CDKN1C and PHLDA2 are critical for embryo development, which suggests that these genes can
294 Knocking out of CEK4 resulted in defective embryo development, which was complemented by transforma
295 rnal stores of Filia impairs preimplantation embryo development with a high incidence of aneuploidy t
296 cannabinol] levels constrain preimplantation embryo development with aberrant expression of Cdx2, Nan
297 for nonautonomous functions in endosperm and embryo development with genetically nonconcordant seeds
299 Chloroplast translation is also required for embryo development, with genes encoding chloroplast ribo