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1 nd Nes in two distinct aspects of Drosophila germ cell development.
2  to regulate different aspects of C. elegans germ cell development.
3 hese de novo mutations occurred during early germ cell development.
4 ptor (Kit) is haplosufficient for primordial germ cell development.
5 essential role for CBP in maintaining normal germ cell development.
6 pecific endosiRNAs present during primordial germ cell development.
7 e small non-coding RNAs essential for animal germ cell development.
8 y are evolutionarily conserved regulators of germ cell development.
9 dard for exploring Dazl's roles in embryonic germ cell development.
10 s, whereas hnRNP A1 is down-regulated during germ cell development.
11 for embryonic development and regulates male germ cell development.
12 n of somatic-cell gene products critical for germ cell development.
13 es in translational-associated events during germ cell development.
14 fic RNA binding proteins may bind to promote germ cell development.
15 RNA helicase activities, and participates in germ cell development.
16 trate is an early molecular marker of female germ cell development.
17  cellular machinery that may be required for germ cell development.
18 known to undergo dynamic change during mouse germ cell development.
19 ne product in the postmeiotic stages of male germ cell development.
20 ually exclusive manner with CTCF during male germ cell development.
21 sume distinct, yet overlapping, functions in germ cell development.
22 ryonic cell transcription factor 1) in mouse germ cell development.
23 her maternal RNAs, which promotes primordial germ cell development.
24 diatric GCTs arise from a different stage of germ cell development.
25 novel function for a transient cyst stage of germ cell development.
26 rental identity at the H19 locus during male germ cell development.
27 tion for APC/C(Ama1) specifically adapted to germ cell development.
28 s that Nectin-2 functions at a late stage of germ cell development.
29 r the importance of these proteins in normal germ cell development.
30 namic, changing size at precise times during germ cell development.
31 ot essential for hematopoiesis or primordial germ cell development.
32 e stored and translated at specific times of germ cell development.
33 terns at the H19 locus during postnatal male germ cell development.
34 hysiological role of TR2/TR4 heterodimers in germ cell development.
35 r Gli and Gli3 during mitotic stages of male germ cell development.
36 o the reprogramming events that occur during germ cell development.
37 gulated fetal-maternal interactions and male germ cell development.
38 n of a gene, stonewall, that is required for germ cell development.
39 g occurs: early mouse embryos and primordial germ cell development.
40 oaches have shed new insight into human male germ cell development.
41  gene rearrangement in the immune system and germ cell development.
42  the impaired NXT2-NXF activity to disturbed germ cell development.
43 maintenance, and are thought to be linked to germ cell development.
44 n, epigenetic reprogramming and sex-specific germ cell development.
45 minidae-specific LTR5Hs TEENhancers in human germ cell development.
46 matic liquid droplet granules and central to germ cell development.
47 s RNA-binding proteins play crucial roles in germ cell development.
48 on in transposable element regulation during germ cell development.
49 n the regulatory mechanisms underlying fetal germ cell development.
50 chronized, yet highly robust nature of human germ cell development.
51 on and meiosis, which are essential for male germ cell development.
52 ive as well as conserved properties of human germ cell development.
53 me inactivation (MSCI) are critical for male germ cell development.
54 o preserve germline DNA integrity for proper germ cell development.
55 ction already during fetal or first steps of germ cell development.
56 scriptional gene regulation in SSCs and male germ cell development.
57 n remodeling, oxidative stress response, and germ cell development.
58 d translational silencing, thereby promoting germ cell development.
59 eine from E10.5-13.5, as this coincides with germ cell development.
60 stemic and local (i.e., niche) regulation of germ cell development.
61 cytokines, and other biomolecules to support germ cell development.
62 g that piRNA-guided cleavage is critical for germ cell development.
63 cycle machinery components by the program of germ cell development.
64 3Y functions in the earliest stages of human germ cell development.
65 piRNA machinery to mouse mRNAs essential for germ cell development.
66 oncoding RNAs, including genes essential for germ cell development.
67  which has a critical function in mouse male germ cell development.
68 ng genes encoding proteins important in male germ cell development.
69 unctions cell non-autonomously in regulating germ cell development.
70 ibute to tools for genetic analysis of human germ cell development.
71 served in teleosts regardless of the type of germ cell development.
72 terns exist on piRNA genes much earlier than germ cell development.
73 at 3p24.3, is required for the regulation of germ cell development.
74 r is established is central to understanding germ cell development.
75 ly conserved RNA helicase involved in animal germ cell development.
76 ferences, in the means by which they control germ cell development.
77 e-specific RNA-binding protein that controls germ cell development.
78  piRNA pathway to drive piRNA biogenesis and germ cell development.
79  essential for postnatal survival as well as germ cell development.
80  imposed by small noncoding RNAs during male germ cell development.
81 ally reprogrammed during early embryonic and germ cell development.
82 lity is common and frequently linked to poor germ cell development.
83 on of germ plasm into pole cells and impairs germ cell development.
84 which have not been implicated previously in germ cell development.
85  the necessary human genetic system to study germ cell development.
86 arians to identify genes required for proper germ cell development.
87 om mitosis to meiosis is a unique feature of germ cell development.
88 en for genes required for discrete stages of germ cell development.
89 e receptor-mediated gene activation and male germ cell development.
90 Sm protein methylation is a pivotal event in germ-cell development.
91                        During mammalian male germ-cell development, a crucial feature is the repressi
92  that has been directly shown to function in germ cell development across diverse species from flies,
93  role for alternative splicing regulation in germ cell development and a central role for Ptbp2 in th
94 nt in parental chromosomes during primordial germ cell development and after fertilization.
95     Thus, cysts are invariant units of mouse germ cell development and cyst fragmentation provides in
96 e to corroborate that genes influencing male germ cell development and differentiation have emerged a
97 tic germ cells by Sertoli cells is vital for germ cell development and differentiation.
98  is providing new functional perspectives in germ cell development and differentiation.
99  of spermatogenesis, we both precisely stage germ cell development and enrich for rare somatic cell-t
100 sing male-specific impact of RNAi factors on germ cell development and fertility, consistent with tes
101 components of the genetic pathway regulating germ cell development and function are evolutionarily co
102                                              Germ cell development and gametogenesis require genome-w
103 rgo coordinate changes in methylation during germ cell development and give further insights into ger
104 ture targeted mechanistic studies of primate germ cell development and in vitro gametogenesis.
105 f KIT tyrosine kinase is critical for normal germ cell development and is observed in the majority of
106  knockout (T-AR-/y) mice revealed incomplete germ cell development and lowered serum testosterone lev
107    To identify genes important in regulating germ cell development and mammalian fertility, we perfor
108  understanding of the basic biology of human germ cell development and may provide clinical insights
109 ential gene in the mouse, it is required for germ cell development and meiosis.
110 el biochemical pathway involved in mammalian germ cell development and meiosis.
111                   The DDR is required during germ cell development and meiosis.
112  of many aspects of morphogenesis, including germ cell development and neuronal pathfinding.
113 as a multifunctional hub for haematopoiesis, germ cell development and nutritional supply.
114 that cytoplasmic Drosophila Rbfox1 regulates germ cell development and represses the translation of m
115 e that FANCB functions at critical stages of germ cell development and reveal a novel function of the
116 indings indicate a potential role for Myc in germ cell development and set the stage for genetic anal
117 ic development of the gonad is essential for germ cell development and sexual reproduction.
118 rm line are those associated with primordial germ cell development and subsequent fetal germline deve
119                           Nos also regulates germ cell development and survival in the ovary.
120  utilize conserved factors to regulate early germ cell development and survival, and that these facto
121                      These results show that germ cell development and TGCT pathogenesis are sensitiv
122 unique set of possibilities for the study of germ cell development and the associated epigenetic phen
123 r results suggest that highly desynchronized germ cell development and the maintenance of a small pop
124 ight the importance to understand primordial germ cell development and the timing of gametogenesis wi
125 ion by NRF1 and epigenetic modulation during germ cell development and unequivocally demonstrate a no
126  germline, how this affects other aspects of germ cell development and what studies in Drosophila can
127 t with the absolute requirement for Sin3A in germ cells' development and/or viability.
128 stem for discovering novel genes involved in germ-cell development and malignancy.
129 umber of genes specifically involved in male germ cell development, and deletion of the AZFc region a
130 atic cells of the gonad that is required for germ cell development, and highlight the importance of s
131  that it is essential for Gryllus primordial germ cell development, and is regulated by upstream inpu
132  for silencing transposons during primordial germ cell development, and MIWI-bound piRNAs are require
133 ing at the pachytene stage of meiosis during germ cell development; and (3) negative selection to pur
134 was observed in 4-week-old mutant testes but germ cell development appeared to be normal.
135 tility of male mammals, and abnormalities in germ cell development are apparent in the XXY testis wit
136                             Defects in human germ cell development are common and yet little is known
137    In this review, two major aspects of male germ cell development are discussed: underlying mechanis
138                             Studies of human germ cell development are limited in large part by inacc
139     However, most of the reports on SAGE and germ cell development are limited to descriptive analyse
140 yndrome and control individuals and examined germ cell development as a function of X chromosome comp
141 es, loss of GLP-1 leads to a severe block in germ cell development as early as E17.5.
142 omosome acquired this prominent role in male germ-cell development as it evolved from an ordinary, un
143     This may include a fundamental effect on germ-cell development because PG but not AG cells can di
144                       In human reproduction, germ cell development begins with the specification of p
145                However, Cdk2 is required for germ cell development; both male and female Cdk2(-/-) mi
146 -interacting RNAs (piRNAs) are essential for germ cell development, but analysis of the molecular mec
147  hematopoiesis, melanogenesis and primordial germ cell development, but is critical in spermatogenesi
148 ssociated proteins and MSY2 to regulate male germ cell development by controlling several gamete-spec
149 G) play crucial roles in early embryonic and germ cell development by mediating DNA demethylation.
150 itional exposures during critical windows of germ cell development can impact the male germline methy
151 e genes encoding proteins important for male germ cell development, chromosomal segregation and the D
152 standing of regeneration, tissue patterning, germ cell development, chromosome evolution, aging, and
153 utosomal DAZL1 gene, potentially involved in germ cell development, created a unique opportunity to s
154 , multiple genes controlling many aspects of germ-cell development depend on tauCstF-64 for their nor
155                                              Germ cell development depends on the capacity of somatic
156 actors that act during the initial stages of germ cell development, differentiation of germ cells in
157 esticular teratomas result from anomalies in germ cell development during embryogenesis.
158  required for anteroposterior patterning and germ cell development during embryogenesis.
159  RNA-binding protein required for primordial germ cell development during later stages of embryogenes
160 nt study, I use a molecular marker to follow germ cell development during P. hawaiensis embryogenesis
161 are critical for BTB function and subsequent germ cell development during spermatogenesis.
162 r understanding of human embryonic and fetal germ cell development, encompassing germ cell specificat
163 iniferous epithelium segregates post-meiotic germ cell development from the systemic circulation and
164 e events of meiotic division and postmeiotic germ cell development from the systemic circulation.
165 anding of molecular genetic aspects of human germ cell development has been limited, at least in part
166 ral states and a fuller understanding of how germ cell development has evolved in different arthropod
167        We show here that during normal mouse germ cell development, hnRNP G-T protein is strongly exp
168 ccur during the initial stages of primordial germ cell development; however, all consequences of this
169 redominantly expressed during embryonic male germ cell development; however, it is also expressed in
170 ad, suggesting an unexpected role for Wt1 in germ cell development in addition to a role in the devel
171  proteins to silence transposons and promote germ cell development in animals.
172                                              Germ cell development in C. elegans requires that the X
173 ing RNA and protein, and required for proper germ cell development in C. elegans.
174 ed an ortholog of nanos, a gene required for germ cell development in diverse organisms, from Schmidt
175 ily of RNA binding proteins are required for germ cell development in Drosophila, Xenopus, and Caenor
176 n apoptosis beginning with the first wave of germ cell development in juvenile mice.
177 anisms, including humans and is required for germ cell development in males and/or females.
178 nes of the DAZ family play critical roles in germ cell development in mammals and other animals.
179 r progression through the earliest stages of germ cell development in mammals.
180 nd yet little is known of genes required for germ cell development in men and women.
181              Piwi proteins are important for germ cell development in most animals.
182 s homologs required for both female and male germ cell development in other organisms; and BOULE, a g
183 ults reveal a conserved function of nanos in germ cell development in planarians and suggest that the
184 and post-transcriptional mechanisms regulate germ cell development in planarians.
185 ment of sexual identity is a crucial step of germ cell development in sexually reproducing organisms.
186 use immunodetection of Vasa protein to study germ cell development in the amphipod crustacean Parhyal
187                       In fact, evaluation of germ cell development in the Arid4a(-/-)Arid4b(+/-) mice
188 e find that TLS is essential for pre-meiotic germ cell development in the embryo.
189 with abnormal fusome morphology and arrested germ cell development in the germaria.
190 e nervous system have been shown to regulate germ cell development in the planarian Schmidtea mediter
191 We conclude that TAF7L is essential for male germ cell development in the rat.
192 pport the notion that genes governing normal germ cell development in utero are implicated in the dev
193 have defined new roles for TUBD1 during male germ cell development in vivo using a conditional knocko
194 ression, which is critical for stem-cell and germ-cell development in Drosophila.
195 Bam may regulate somewhat different steps of germ-cell development in oogenesis and spermatogenesis.
196 sive and in-depth nucleome analysis of mouse germ-cell development in vitro, encompassing pluripotent
197 ms, a few thousand genes may be required for germ cell development including meiosis.
198 ntal evidence that NANOS3 functions in human germ cell development; indeed, NANOS3 is now one of just
199 la melanogaster embryos, we show that normal germ cell development involves extensive programmed cell
200                                              Germ cell development involves extensive remodeling of t
201                                              Germ cell development involves major reprogramming of th
202 e regulation of CDK2 kinase activity in male germ cell development is crucial for the gonocyte-to-spe
203                                         Male germ cell development is dependent on the orchestrated r
204              Yet, our understanding of human germ cell development is poor, at least in part due to t
205                                   Yet, human germ cell development is poorly understood, at least in
206 omatic differentiation, but its role in male germ cell development is unknown.
207                Although a Dazl role in early germ cell development is well established, no function h
208 ecifically in the testis and is required for germ cell development, it is likely that PTCH2 mediates
209 ross species and was shown to be crucial for germ cell development, its mechanism, function, and stru
210 tion provides new insights for understanding germ cell development, neuronal diversity, and transgene
211 polyadenylation-induced translation controls germ cell development, neuronal synaptic plasticity and
212 s to understand the mechanisms that regulate germ cell development opens promising new avenues to dev
213 ether pseudo-tetraploid cells arise early in germ cell development or just prior to meiosis has remai
214 ression of target genes at earlier stages of germ cell development, our results suggest that a simila
215 ssays and supported by normal lymphocyte and germ cell development, Parp1(+/A) cells are hypersensiti
216   It plays important roles in epithelial and germ cell development, particularly by repressing c-Myc
217 l maturation and how BTB dynamics coordinate germ cell development remain unclear.
218  precise molecular role of these proteins in germ-cell development remains enigmatic; however, they a
219                                         Male germ cell development requires precise regulation of gen
220 be biologically relevant for male and female germ cell development, respectively.
221                Many genes essential for late germ cell development showed dramatic downregulation, wh
222                                         Male germ cell development starts when pluripotent cells unde
223                                       During germ cell development, SUMO-1 was observed at low but de
224                Thus, meiosis and postmeiotic germ cell development take place in the seminiferous epi
225      In addition to its utility for studying germ cell development, this EST collection will be an im
226 activate translationally silent mRNAs during germ cell development through the direct recruitment of
227 ants with defects ranging from problems with germ cell development to abnormal sperm morphology.
228 olog, DAZL (DAZ-like), are required early in germ cell development to maintain initial germ cell popu
229 f detectable RBM expression we see stages of germ cell development up to early meiosis, but not past
230                                   Primordial germ cell development uses programmed cell death to remo
231 hese potent signaling molecules in embryonic germ cell development, using JHs in Drosophila melanogas
232 viable system to probe the genetics of human germ cell development via use of induced pluripotent ste
233 effects of telomere dysfunction on mammalian germ cell development, we examined the meiotic progressi
234                                 Focussing on germ cell development, we found that Tra2b PE deletion c
235 core PRC2 subunits EED and SUZ12 during male germ cell development, we identified a requirement for P
236   To systematically investigate early murine germ cell development, we lineage marked the progeny of
237         To investigate Ifitm function during germ cell development, we used targeted chromosome engin
238 ade methylation more effectively during male germ cell development, whereas other subfamilies show th
239 opose a de novo DNA methylation model during germ cell development whereby a pattern is established b
240  elucidate the molecular mechanisms of human germ cell development, which has implications not only f
241         Knowledge of the mechanisms of human germ cell development will enable its in vitro reconstit
242  provide the first systematic description of germ cell development with molecular markers in a myriap
243 AGE) representing major stages in mouse male germ cell development, with 150,000 sequence tags in eac
244 ome plays an essential role in prefollicular germ cell development within insects such as Drosophila
245 hways that promote TGCT susceptibility: male germ cell development within its somatic niche and regul
246 dent on the outcomes of recombination during germ cell development, yet systems to study mammalian ge

 
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