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1 hese de novo mutations occurred during early germ cell development.
2 pecific endosiRNAs present during primordial germ cell development.
3 ptor (Kit) is haplosufficient for primordial germ cell development.
4 essential role for CBP in maintaining normal germ cell development.
5 s RNA-binding proteins play crucial roles in germ cell development.
6 y are evolutionarily conserved regulators of germ cell development.
7 dard for exploring Dazl's roles in embryonic germ cell development.
8 s, whereas hnRNP A1 is down-regulated during germ cell development.
9 n of somatic-cell gene products critical for germ cell development.
10 es in translational-associated events during germ cell development.
11 fic RNA binding proteins may bind to promote germ cell development.
12 RNA helicase activities, and participates in germ cell development.
13 d translational silencing, thereby promoting germ cell development.
14 trate is an early molecular marker of female germ cell development.
15  cellular machinery that may be required for germ cell development.
16 known to undergo dynamic change during mouse germ cell development.
17 eine from E10.5-13.5, as this coincides with germ cell development.
18 ne product in the postmeiotic stages of male germ cell development.
19 ually exclusive manner with CTCF during male germ cell development.
20 sume distinct, yet overlapping, functions in germ cell development.
21 her maternal RNAs, which promotes primordial germ cell development.
22 diatric GCTs arise from a different stage of germ cell development.
23 novel function for a transient cyst stage of germ cell development.
24 rental identity at the H19 locus during male germ cell development.
25 tion for APC/C(Ama1) specifically adapted to germ cell development.
26 s that Nectin-2 functions at a late stage of germ cell development.
27 r the importance of these proteins in normal germ cell development.
28 ot essential for hematopoiesis or primordial germ cell development.
29 stemic and local (i.e., niche) regulation of germ cell development.
30 e stored and translated at specific times of germ cell development.
31 terns at the H19 locus during postnatal male germ cell development.
32 hysiological role of TR2/TR4 heterodimers in germ cell development.
33 r Gli and Gli3 during mitotic stages of male germ cell development.
34 o the reprogramming events that occur during germ cell development.
35 gulated fetal-maternal interactions and male germ cell development.
36 n of a gene, stonewall, that is required for germ cell development.
37 e small non-coding RNAs essential for animal germ cell development.
38 g that piRNA-guided cleavage is critical for germ cell development.
39 cycle machinery components by the program of germ cell development.
40 3Y functions in the earliest stages of human germ cell development.
41 piRNA machinery to mouse mRNAs essential for germ cell development.
42 oncoding RNAs, including genes essential for germ cell development.
43  which has a critical function in mouse male germ cell development.
44 for embryonic development and regulates male germ cell development.
45 ng genes encoding proteins important in male germ cell development.
46 unctions cell non-autonomously in regulating germ cell development.
47 ibute to tools for genetic analysis of human germ cell development.
48 served in teleosts regardless of the type of germ cell development.
49 terns exist on piRNA genes much earlier than germ cell development.
50 at 3p24.3, is required for the regulation of germ cell development.
51 r is established is central to understanding germ cell development.
52 ly conserved RNA helicase involved in animal germ cell development.
53 ferences, in the means by which they control germ cell development.
54 e-specific RNA-binding protein that controls germ cell development.
55 ryonic cell transcription factor 1) in mouse germ cell development.
56  essential for postnatal survival as well as germ cell development.
57  imposed by small noncoding RNAs during male germ cell development.
58 namic, changing size at precise times during germ cell development.
59 ally reprogrammed during early embryonic and germ cell development.
60 lity is common and frequently linked to poor germ cell development.
61 on of germ plasm into pole cells and impairs germ cell development.
62 which have not been implicated previously in germ cell development.
63  the necessary human genetic system to study germ cell development.
64 arians to identify genes required for proper germ cell development.
65 om mitosis to meiosis is a unique feature of germ cell development.
66 en for genes required for discrete stages of germ cell development.
67 e receptor-mediated gene activation and male germ cell development.
68 g occurs: early mouse embryos and primordial germ cell development.
69 nd Nes in two distinct aspects of Drosophila germ cell development.
70  to regulate different aspects of C. elegans germ cell development.
71 Sm protein methylation is a pivotal event in germ-cell development.
72  that has been directly shown to function in germ cell development across diverse species from flies,
73  role for alternative splicing regulation in germ cell development and a central role for Ptbp2 in th
74     Thus, cysts are invariant units of mouse germ cell development and cyst fragmentation provides in
75 e to corroborate that genes influencing male germ cell development and differentiation have emerged a
76 tic germ cells by Sertoli cells is vital for germ cell development and differentiation.
77 sing male-specific impact of RNAi factors on germ cell development and fertility, consistent with tes
78 components of the genetic pathway regulating germ cell development and function are evolutionarily co
79                                              Germ cell development and gametogenesis require genome-w
80 rgo coordinate changes in methylation during germ cell development and give further insights into ger
81 f KIT tyrosine kinase is critical for normal germ cell development and is observed in the majority of
82  knockout (T-AR-/y) mice revealed incomplete germ cell development and lowered serum testosterone lev
83    To identify genes important in regulating germ cell development and mammalian fertility, we perfor
84  understanding of the basic biology of human germ cell development and may provide clinical insights
85 ential gene in the mouse, it is required for germ cell development and meiosis.
86 el biochemical pathway involved in mammalian germ cell development and meiosis.
87  of many aspects of morphogenesis, including germ cell development and neuronal pathfinding.
88 that cytoplasmic Drosophila Rbfox1 regulates germ cell development and represses the translation of m
89 e that FANCB functions at critical stages of germ cell development and reveal a novel function of the
90 indings indicate a potential role for Myc in germ cell development and set the stage for genetic anal
91 ic development of the gonad is essential for germ cell development and sexual reproduction.
92 rm line are those associated with primordial germ cell development and subsequent fetal germline deve
93                           Nos also regulates germ cell development and survival in the ovary.
94  utilize conserved factors to regulate early germ cell development and survival, and that these facto
95                      These results show that germ cell development and TGCT pathogenesis are sensitiv
96 unique set of possibilities for the study of germ cell development and the associated epigenetic phen
97 ion by NRF1 and epigenetic modulation during germ cell development and unequivocally demonstrate a no
98  germline, how this affects other aspects of germ cell development and what studies in Drosophila can
99 t with the absolute requirement for Sin3A in germ cells' development and/or viability.
100 stem for discovering novel genes involved in germ-cell development and malignancy.
101 umber of genes specifically involved in male germ cell development, and deletion of the AZFc region a
102 atic cells of the gonad that is required for germ cell development, and highlight the importance of s
103  that it is essential for Gryllus primordial germ cell development, and is regulated by upstream inpu
104  for silencing transposons during primordial germ cell development, and MIWI-bound piRNAs are require
105 was observed in 4-week-old mutant testes but germ cell development appeared to be normal.
106 tility of male mammals, and abnormalities in germ cell development are apparent in the XXY testis wit
107                             Defects in human germ cell development are common and yet little is known
108    In this review, two major aspects of male germ cell development are discussed: underlying mechanis
109                             Studies of human germ cell development are limited in large part by inacc
110     However, most of the reports on SAGE and germ cell development are limited to descriptive analyse
111 yndrome and control individuals and examined germ cell development as a function of X chromosome comp
112 es, loss of GLP-1 leads to a severe block in germ cell development as early as E17.5.
113 omosome acquired this prominent role in male germ-cell development as it evolved from an ordinary, un
114     This may include a fundamental effect on germ-cell development because PG but not AG cells can di
115                However, Cdk2 is required for germ cell development; both male and female Cdk2(-/-) mi
116 -interacting RNAs (piRNAs) are essential for germ cell development, but analysis of the molecular mec
117  hematopoiesis, melanogenesis and primordial germ cell development, but is critical in spermatogenesi
118 G) play crucial roles in early embryonic and germ cell development by mediating DNA demethylation.
119 itional exposures during critical windows of germ cell development can impact the male germline methy
120 e genes encoding proteins important for male germ cell development, chromosomal segregation and the D
121 utosomal DAZL1 gene, potentially involved in germ cell development, created a unique opportunity to s
122 , multiple genes controlling many aspects of germ-cell development depend on tauCstF-64 for their nor
123 actors that act during the initial stages of germ cell development, differentiation of germ cells in
124 esticular teratomas result from anomalies in germ cell development during embryogenesis.
125  required for anteroposterior patterning and germ cell development during embryogenesis.
126  RNA-binding protein required for primordial germ cell development during later stages of embryogenes
127 nt study, I use a molecular marker to follow germ cell development during P. hawaiensis embryogenesis
128 are critical for BTB function and subsequent germ cell development during spermatogenesis.
129 iniferous epithelium segregates post-meiotic germ cell development from the systemic circulation and
130 e events of meiotic division and postmeiotic germ cell development from the systemic circulation.
131 anding of molecular genetic aspects of human germ cell development has been limited, at least in part
132 ral states and a fuller understanding of how germ cell development has evolved in different arthropod
133        We show here that during normal mouse germ cell development, hnRNP G-T protein is strongly exp
134 ccur during the initial stages of primordial germ cell development; however, all consequences of this
135 redominantly expressed during embryonic male germ cell development; however, it is also expressed in
136 ad, suggesting an unexpected role for Wt1 in germ cell development in addition to a role in the devel
137                                              Germ cell development in C. elegans requires that the X
138 ing RNA and protein, and required for proper germ cell development in C. elegans.
139 ed an ortholog of nanos, a gene required for germ cell development in diverse organisms, from Schmidt
140 ily of RNA binding proteins are required for germ cell development in Drosophila, Xenopus, and Caenor
141 n apoptosis beginning with the first wave of germ cell development in juvenile mice.
142 anisms, including humans and is required for germ cell development in males and/or females.
143 nes of the DAZ family play critical roles in germ cell development in mammals and other animals.
144 nd yet little is known of genes required for germ cell development in men and women.
145 s homologs required for both female and male germ cell development in other organisms; and BOULE, a g
146 ults reveal a conserved function of nanos in germ cell development in planarians and suggest that the
147 and post-transcriptional mechanisms regulate germ cell development in planarians.
148 ment of sexual identity is a crucial step of germ cell development in sexually reproducing organisms.
149 use immunodetection of Vasa protein to study germ cell development in the amphipod crustacean Parhyal
150                       In fact, evaluation of germ cell development in the Arid4a(-/-)Arid4b(+/-) mice
151 with abnormal fusome morphology and arrested germ cell development in the germaria.
152 e nervous system have been shown to regulate germ cell development in the planarian Schmidtea mediter
153 pport the notion that genes governing normal germ cell development in utero are implicated in the dev
154 ression, which is critical for stem-cell and germ-cell development in Drosophila.
155 Bam may regulate somewhat different steps of germ-cell development in oogenesis and spermatogenesis.
156 ms, a few thousand genes may be required for germ cell development including meiosis.
157 ntal evidence that NANOS3 functions in human germ cell development; indeed, NANOS3 is now one of just
158 la melanogaster embryos, we show that normal germ cell development involves extensive programmed cell
159                                              Germ cell development involves major reprogramming of th
160              Yet, our understanding of human germ cell development is poor, at least in part due to t
161                                   Yet, human germ cell development is poorly understood, at least in
162 omatic differentiation, but its role in male germ cell development is unknown.
163                Although a Dazl role in early germ cell development is well established, no function h
164 ecifically in the testis and is required for germ cell development, it is likely that PTCH2 mediates
165 tion provides new insights for understanding germ cell development, neuronal diversity, and transgene
166 polyadenylation-induced translation controls germ cell development, neuronal synaptic plasticity and
167 ether pseudo-tetraploid cells arise early in germ cell development or just prior to meiosis has remai
168 ression of target genes at earlier stages of germ cell development, our results suggest that a simila
169   It plays important roles in epithelial and germ cell development, particularly by repressing c-Myc
170  precise molecular role of these proteins in germ-cell development remains enigmatic; however, they a
171                                       During germ cell development, SUMO-1 was observed at low but de
172                Thus, meiosis and postmeiotic germ cell development take place in the seminiferous epi
173      In addition to its utility for studying germ cell development, this EST collection will be an im
174 activate translationally silent mRNAs during germ cell development through the direct recruitment of
175 ants with defects ranging from problems with germ cell development to abnormal sperm morphology.
176 olog, DAZL (DAZ-like), are required early in germ cell development to maintain initial germ cell popu
177 f detectable RBM expression we see stages of germ cell development up to early meiosis, but not past
178                                   Primordial germ cell development uses programmed cell death to remo
179 viable system to probe the genetics of human germ cell development via use of induced pluripotent ste
180 effects of telomere dysfunction on mammalian germ cell development, we examined the meiotic progressi
181 core PRC2 subunits EED and SUZ12 during male germ cell development, we identified a requirement for P
182   To systematically investigate early murine germ cell development, we lineage marked the progeny of
183         To investigate Ifitm function during germ cell development, we used targeted chromosome engin
184 ade methylation more effectively during male germ cell development, whereas other subfamilies show th
185 opose a de novo DNA methylation model during germ cell development whereby a pattern is established b
186  elucidate the molecular mechanisms of human germ cell development, which has implications not only f
187  provide the first systematic description of germ cell development with molecular markers in a myriap
188 AGE) representing major stages in mouse male germ cell development, with 150,000 sequence tags in eac
189 ome plays an essential role in prefollicular germ cell development within insects such as Drosophila
190 dent on the outcomes of recombination during germ cell development, yet systems to study mammalian ge

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