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1 otent stem cells in somatic tissues (somatic gametogenesis).
2 t of secondary sex characteristics (SSC) and gametogenesis.
3 meiosis, the key developmental programme of gametogenesis.
4 -mediated testosterone metabolism to disrupt gametogenesis.
5 ed fertility attributable to a hampered male gametogenesis.
6 trol of zygote formation, recombination, and gametogenesis.
7 narily conserved function for this enzyme in gametogenesis.
8 a critical role in transposon silencing and gametogenesis.
9 lays a significant role specifically in male gametogenesis.
10 catalyzes this modification, is required for gametogenesis.
11 ess diverse aspects of stem cell biology and gametogenesis.
12 g yeast resetting of life span occurs during gametogenesis.
13 eginning at the late pachytene stage of male gametogenesis.
14 on of PS+ vs. PS- genomes takes place during gametogenesis.
15 a screen to uncover genes that control mouse gametogenesis.
16 rst mitotic division in both male and female gametogenesis.
17 tative cells and the different cell types of gametogenesis.
18 nd changes in developmental programs such as gametogenesis.
19 ne in the gametophyte at different stages of gametogenesis.
20 ed brood sizes and low penetrance defects in gametogenesis.
21 d and then specialized to function in animal gametogenesis.
22 uld not be generated due to a defect in male gametogenesis.
23 evelopment and are irreversibly committed to gametogenesis.
24 ion of coding and non-coding RNAs needed for gametogenesis.
25 ike genes to serve paralog-specific roles in gametogenesis.
26 es in transposon silencing and regulation of gametogenesis.
27 ing defect) but were sterile with defects in gametogenesis.
28 e PfGCbeta gene had no significant effect on gametogenesis.
29 have been driven by the specialized needs of gametogenesis.
30 led to a severely reduced ability to undergo gametogenesis.
31 ressing how many cell divisions occur before gametogenesis.
32 d in the MT(+) locus, is operant during plus gametogenesis.
33 o regulate multiple steps in male and female gametogenesis.
34 sterility of Miwi mutants suggest a role in gametogenesis.
35 ons (ICRs) that are differentially marked in gametogenesis.
36 ar differentiation for germline cells during gametogenesis.
37 NMD and display defects in embryogenesis and gametogenesis.
38 -specific RNA-binding proteins essential for gametogenesis.
39 for sex-specific de novo methylation during gametogenesis.
40 so infertile and exhibit a primary defect in gametogenesis.
41 a methylation imprint acquired during female gametogenesis.
42 tant reduction in germline proliferation and gametogenesis.
43 rerequisites for cell fate determination and gametogenesis.
44 gonadal cells to promote steroidogenesis and gametogenesis.
45 ntestinal tract motility, melanogenesis, and gametogenesis.
46 wing examination of the function of BRCA2 in gametogenesis.
47 rmline epigenetic modification and mammalian gametogenesis.
48 ation specifically affects post-meiotic male gametogenesis.
49 n to optimize gamete quality through somatic gametogenesis.
50 elopment and male testis differentiation and gametogenesis.
51 parental chromosomes during male and female gametogenesis.
52 ol region (ICR) is differentially set during gametogenesis.
53 rom the surrounding somatic cells throughout gametogenesis.
54 ow parental imprinting is established during gametogenesis.
55 eiotic chromosome morphogenesis and complete gametogenesis.
56 ocated to the nucleus at a specific stage of gametogenesis.
57 and tissue-specific target genes during male gametogenesis.
58 (Nesp and Gnasxl) is not established during gametogenesis.
59 g limb development, hair growth, hearing and gametogenesis.
60 e COII(G177S) might specifically impair male gametogenesis.
61 for normal haematopoiesis, melanogenesis and gametogenesis.
62 ctions in hemato- poiesis, melanogenesis and gametogenesis.
63 nterstitial cells during asexual budding and gametogenesis.
64 ion and terminal differentiation during male gametogenesis.
65 lates gene expression during development and gametogenesis.
66 f a specialized cell type, a process akin to gametogenesis.
67 n lineage differentiation and on the path to gametogenesis.
68 ssion during early embryonic development and gametogenesis.
69 ing of parental imprints in 15q11-q13 during gametogenesis.
70 s suggesting unique roles for these genes in gametogenesis.
71 ution of the germline is required for normal gametogenesis.
72 des many of the differentiative processes of gametogenesis.
73 and cell wall synthesis during budding yeast gametogenesis.
74 ractory mosquito genotypes to block parasite gametogenesis.
75 the Morc gene acts specifically during male gametogenesis.
76 re mother cells, which were able to initiate gametogenesis.
77 tiating the switch from vegetative growth to gametogenesis.
78 velopmental control of these factors in male gametogenesis.
79 and functions including steroidogenesis and gametogenesis.
80 key cell-cycle transitions during Plasmodium gametogenesis.
81 ay in epigenetic regulation during mammalian gametogenesis.
82 reening for environmental agents that affect gametogenesis.
83 anscriptionally active TEs for RdDM prior to gametogenesis.
84 ecific translational control is required for gametogenesis.
85 regates to function as central regulators of gametogenesis.
86 cells adopt equal size cell divisions during gametogenesis.
87 als that FBL17 function is not restricted to gametogenesis.
88 ant roles in developmental processes such as gametogenesis.
89 to activate DNA-methylated promoters during gametogenesis.
90 fect was caused primarily by exposure during gametogenesis.
91 or all of PGC specification, development, or gametogenesis.
92 state from fetal stages through meiosis and gametogenesis.
93 espread methylation events that occur during gametogenesis.
94 ction in genes regulating pollen development/gametogenesis.
95 late stages of sexual development, including gametogenesis.
96 entral to initiating the meiotic program and gametogenesis.
97 cifies meiotic recombination hotspots during gametogenesis.
98 evelopment and single nurse cells supporting gametogenesis.
99 ected to high and low pCO2 conditions during gametogenesis.
100 e and female sterility because of defects in gametogenesis.
101 but also to protect genome integrity during gametogenesis.
103 rolled by blue and red light at the steps of gametogenesis along with its restoration and germination
104 n of epigenetic modifications imposed during gametogenesis and additional modifications imposed after
105 of GnRH neurons at puberty onset, leading to gametogenesis and an increase in gonadal steroid hormone
107 ylation patterns that are established during gametogenesis and are required for the allele-specific e
108 egions that are differentially marked during gametogenesis and can act over hundreds of kilobases to
110 ites for methylation at particular stages of gametogenesis and early development), studies of DNA met
112 ights into which genes are required for both gametogenesis and embryo development and might therefore
113 ed known and novel small RNA classes through gametogenesis and embryo development in the parasitic ne
114 ndicate that OGT activity is required during gametogenesis and embryogenesis with lethality occurring
115 are evident in mammals, particularly during gametogenesis and embryogenesis, but little information
122 genetic programming events take place during gametogenesis and fetal development and are thought to h
123 S+ genomes is specifically suppressed during gametogenesis and germination of zygospores, a phenomeno
127 a transcriptional cascade programming yeast gametogenesis and may also be a target of meiotic checkp
131 ys, in part mimicking those occurring during gametogenesis and normal human development, as evidenced
132 rt studies on MID expression patterns during gametogenesis and on a second gene unique to the MT(-) l
133 rns at imprinted loci are established during gametogenesis and post fertilization and their alteratio
136 lar mechanisms underlying sex determination, gametogenesis and reproductive physiology for most paras
137 mutants displayed unusual phenotypes during gametogenesis and resembled mutants in mitochondrial tra
142 ty at the chromatin interface and may impact gametogenesis and some developmental aspects of fragile
143 d gametocytogenesis in erythrocytes, nor for gametogenesis and sporogony in the mosquito vector.
144 G3 is a crucial cohesin subunit in mammalian gametogenesis and supporting our proposal that STAG3 is
145 ic modifications that are established during gametogenesis and that are maintained throughout somatic
146 g-specific activities that are essential for gametogenesis and that regulation of subcellular Dalpha1
147 nto fundamental processes of male and female gametogenesis and the earliest phases of embryonic life
148 ernal conditions impact the offspring during gametogenesis and through fetal/early-postnatal life, th
150 d changes in osmoregulation, locomotion, and gametogenesis, and (b) compare the resultant profiles wi
151 (H4S1ph) is evolutionarily conserved during gametogenesis, and contributes to post-meiotic nuclear c
152 pment, including proliferation, meiosis, and gametogenesis, and ensures a robust response to RNA inte
153 f dicentric chromatids is synthesized during gametogenesis, and kinetochore protein dephosphorylation
154 s, plays an essential role in hematopoiesis, gametogenesis, and melanogenesis during both embryonic a
157 y essential roles in stem cell self-renewal, gametogenesis, and RNA interference in diverse organisms
158 Flagellar CrPKD2 increased fourfold during gametogenesis, and several CrPKD2 RNA interference strai
159 gue (Mvh), a gene that is essential for male gametogenesis, and show that Dazl stimulates translation
160 cal cellular processes including phototaxis, gametogenesis, and the biogenesis of the photosynthetic
161 blished in male and female germ cells during gametogenesis, and the de novo DNA methyltransferase DNM
162 De novo mutations (DNMs) originating in gametogenesis are an important source of genetic variati
164 ession at specific stages during meiosis and gametogenesis, as compared to vegetative growth and star
165 vitro model system for studies of mammalian gametogenesis, as well as for the development of new str
168 evels in February and July-August but during gametogenesis (August to January) and spawning (March to
169 ylation in this region is established during gametogenesis, being present in oocytes and absent in sp
170 1 is not necessary for microsporogenesis and gametogenesis but is essential for pollen germination.
171 A, kynurenic acid (C10H6NO3), also activated gametogenesis but only at higher concentrations and with
172 The two mutations do not affect embryonic gametogenesis but the KitY719F mutation blocks spermatog
174 ion and terminal differentiation during male gametogenesis by regulating chromatin conformation in pr
175 gen starvation and (ii) the role of Yvh1p in gametogenesis can be genetically distinguished from its
176 firm evidence that meiosis, the hallmark of gametogenesis, can be faithfully replicated outside of t
178 lyadenylation-regulated translation, such as gametogenesis, cell cycle progression, and synaptic plas
179 kinesis, transcription regulation, mammalian gametogenesis, centrosome duplication, and suppression o
180 mental transition that enables the resultant gametogenesis-competent cells to respond to feminizing o
181 t the Tmem48 mutation is responsible for the gametogenesis defects and skeletal malformations in the
184 in mammals, is established and reset during gametogenesis; defects in this process in the parent can
185 shment of patterns of DNA methylation during gametogenesis depends in part on DNMT3L, an enzymaticall
187 or a variety of biological processes such as gametogenesis, developmental transitions, and sex determ
189 -interacting RNAs (piRNAs) are essential for gametogenesis, embryogenesis, and stem cell maintenance
191 ription factor essential for later stages of gametogenesis extends the replicative life span of aged
192 atm; and 6.7, pCO2 18480 microatm) on oyster gametogenesis, fertilization, and early larval developme
194 Meiotic recombination is a critical step in gametogenesis for many organisms, enabling the creation
195 it 3, was disrupted in Arabidopsis thaliana, gametogenesis frequently failed due to defects in cell d
198 control of the developmental program of male gametogenesis, function to direct cell type- and stage-s
200 , spermatogenesis, testicular determination, gametogenesis, gonad differentiation, and possibly sex d
202 cue experiments suggest that male and female gametogenesis have distinct requirements for importin al
204 thylation on the parental H19 alleles during gametogenesis implies that the two unmethylated alleles
205 s an important role in meiosis induction and gametogenesis in adult medaka but contrary to common exp
208 l number of genes whose elimination disrupts gametogenesis in both sexes after the major events of me
214 rtant for germline stem cell maintenance and gametogenesis in males, whereas ectopic expression in fe
220 quality can explain the stability of somatic gametogenesis in plants and basal metazoans, the evoluti
221 he fundamental mechanisms that regulate male gametogenesis in plants and demonstrate that their sensi
222 /26S proteasome system is important for male gametogenesis in plants and suggest that deubiquitinatio
223 different form of cytokinesis occurs during gametogenesis in Saccharomyces cerevisiae, in which four
224 vation that eIF4E levels are elevated during gametogenesis in several organisms suggests that eIF4E m
226 Finally, reduced fertility and irregular gametogenesis in the Arabidopsis SWR1 mutants indicate a
227 tyrosine kinase (RTK) genes expressed during gametogenesis in the cnidarian Hydra vulgaris, we isolat
235 Thus, our results show that investigation of gametogenesis in yeast provides novel insights into chro
246 spermatocytes, we found that male and female gametogenesis is severely disrupted in Atm-deficient mic
248 n priming, which may be downregulated during gametogenesis, is indispensable for robust maintenance o
249 , expression of IME1, the central inducer of gametogenesis, is inhibited in cis by transcription of t
252 AF-like gene (At5g26290) exhibiting aberrant gametogenesis led us to investigate the developmental ro
253 ty of invertebrates in the initial stages of gametogenesis, male and female germ cells develop in ful
254 expansion and vegetative segregation during gametogenesis may be effective in reducing genetic varia
255 osaicism together with sexual differences in gametogenesis might explain a considerable fraction of u
257 Reduction of the genetic information before gametogenesis occurs in meiosis, when cross-overs (COs)
266 ng Mrp4(-/-) mice had significantly impaired gametogenesis, reduced testicular testosterone, and disr
267 rimordial germ cells is robust, but terminal gametogenesis remains inefficient and doubts about gamet
268 puts influence early meiotic progression and gametogenesis remains poorly understood in metazoans.
272 ic marks imposed on the X chromosomes during gametogenesis, responsible for normal imprinted X inacti
273 ur model suggests that sexual dimorphisms in gametogenesis result in a greater proportion of somatica
274 ethylation marks are erased and reset during gametogenesis, resulting in paternal or maternal imprint
275 d that Ndt80 functions at pachytene of yeast gametogenesis (sporulation) to activate transcription of
277 for its function in germline specification, gametogenesis, stem cell maintenance, transposon silenci
278 n, epigenetic information established during gametogenesis, such as gametic imprints, cannot be resto
280 ologs may perform conserved functions during gametogenesis, that in C. elegans certain aspects of ooc
281 ons affect hematopoiesis, melanogenesis, and gametogenesis, the Ph mutation affects melanogenesis and
282 these ranged from defects in early stages of gametogenesis to later defects affecting pollen germinat
283 ents processes that normally function during gametogenesis to prepare the gamete genomes to support d
284 stigation of chromatin reorganization during gametogenesis, using the model eukaryote Saccharomyces c
285 e intra-species, intra-individual, and intra-gametogenesis variations in the meiotic program, A. rhod
289 and how chromatin regulates AGSC biology and gametogenesis, we derived stage-specific high-resolution
290 h the known requirements of JAK signaling in gametogenesis, we find that mutants of upd3 show an age-
291 cause defects in germ cell proliferation or gametogenesis, we identified sets of genes with germline
292 xpressed and play a crucial role during male gametogenesis, whereas endo-siRNAs are essential for ooc
293 usion-bridge cycles possibly occurred during gametogenesis, which led to further chromosomal rearrang
294 ivated a subset of control genes involved in gametogenesis while down-regulating protein biosynthesis
297 rease in the number of cell divisions before gametogenesis, with a concomitant increase in mutations
298 the sporophyte and gametophyte affect female gametogenesis, with different developmental outcomes det
299 ermline stem cell proliferation, meiosis and gametogenesis, yet how these key transitions are coordin
300 cluding stem cell proliferation, meiosis and gametogenesis, yet the nature of these fundamental signa
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