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1 ic (primary and secondary spermatocytes) and postmeiotic.
2 0.6 mm), meiotic (0.8, 1.0, and 1.4 mm), and postmeiotic (1.8 mm) anthers, for which we then investig
3 estricted expression in testis, and a unique postmeiotic alternative splicing pattern supported the i
4 testes revealed that Taf7l(-/Y) mice develop postmeiotic arrest at the first stage of spermiogenesis,
5  species Capsella (Capsella rubella), caused postmeiotic arrest of pollen development at the microspo
6 eased apoptosis of meiotic spermatocytes and postmeiotic arrest of spermatid differentiation.
7 ilure is caused by CENH3 dilution during the postmeiotic cell divisions that precede gamete formation
8 ntington disease mutations were found in the postmeiotic cell population, suggesting that expansions
9 rtially condensed chromosomes accumulate and postmeiotic cells are lacking.
10 rted populations of premeiotic, meiotic, and postmeiotic cells.
11 s developmental stages, including in haploid postmeiotic cells.
12 nd providing immune privilege to meiotic and postmeiotic cells.
13 18% of mouse X-linked genes are expressed in postmeiotic cells.
14 and that this expression is predominantly in postmeiotic cells.
15 like SAM68, predominantly within meiotic and postmeiotic cells.
16 nally regulated are initially transcribed in postmeiotic cells.
17 demonstrate that SSTK is required for proper postmeiotic chromatin remodeling and male fertility.
18 st that, for healthy men, (a) sperm carrying postmeiotic chromosomal breaks appear to be more prevale
19 hase II and consequently leads to defects in postmeiotic cytokinesis and cell wall formation.
20                      Consequently, the first postmeiotic cytokinesis was abolished without the format
21    However, in the absence of both kinesins, postmeiotic development of the male gametophyte was seve
22 genesis, specifically disrupting meiotic and postmeiotic development, resulting in male infertility r
23 alternative 3'-processing during meiosis and postmeiotic development.
24 are enriched in multicopy genes required for postmeiotic differentiation of round spermatids into spe
25 on and analysis of five mutations induced by postmeiotic ENU treatment.
26 ase homolog that is required to regulate the postmeiotic events of spore wall assembly.
27         Many classes of genes show increased postmeiotic expression in the germlines of older flies.
28 is limited to meiotic spermatocytes and that postmeiotic expression of sex-linked genes is variable.
29 d altering bursting frequency contributes to postmeiotic expression.
30                                 Treatment of postmeiotic gametes with ENU induces specific-locus muta
31 -locus mutations observed after treatment of postmeiotic gametes with ENU.
32 In higher plants this is achieved in part by postmeiotic gene activity controlling the development of
33                                              Postmeiotic gene expression is essential for development
34 rant expression of transposable elements and postmeiotic gene expression.
35 e that TAF7L binds to promoters of activated postmeiotic genes in testis.
36                               The paucity of postmeiotic genes on the X chromosome has been interpret
37 rectly with TRF2 at promoters of a subset of postmeiotic genes to regulate spermiogenesis.
38 deed, we find that Taf7l and Trf2 coregulate postmeiotic genes, but none of Taf4b-regulated germ stem
39 c lineage tracing that Foxa3 is expressed in postmeiotic germ and interstitial Leydig cells.
40 ssion of ZFP628 in the mouse and uncovered a postmeiotic germ cell arrest at the round spermatid stag
41 uestering the events of meiotic division and postmeiotic germ cell development from the systemic circ
42                            Thus, meiosis and postmeiotic germ cell development take place in the semi
43 ling of transcription and translation during postmeiotic germ cell differentiation is critical for su
44 or Pf20 in mouse spermatogenesis, sustaining postmeiotic germ cell viability.
45 pstream start site, is transcribed solely in postmeiotic germ cells and is translationally regulated
46 egeneration of late spermatids, sloughing of postmeiotic germ cells from the seminiferous epithelium,
47  spermatids and irregular head morphology in postmeiotic germ cells in the seminiferous epithelium, w
48      Nkx-1.2 mRNA was shown to be present in postmeiotic germ cells of the testis and in mature sperm
49 ers an immunological barrier for meiotic and postmeiotic germ cells, and its dynamic permeability fac
50 is abundantly expressed in mouse meiotic and postmeiotic germ cells, and that methylation of histone
51 threonine kinase (SSTK) that is expressed in postmeiotic germ cells, associates with HSP90, and is in
52 ation factor (CstF-64), in mouse meiotic and postmeiotic germ cells.
53 The variant form was specific to meiotic and postmeiotic germ cells.
54 1 transcripts were most abundant in pre- and postmeiotic germ cells.
55 have globally altered chromatin structure in postmeiotic germ cells.
56 cific CREM-regulated mRNAs in mammalian male postmeiotic germ cells.
57 s meiotic/spermatogonial genes and activates postmeiotic haploid gene programs during meiotic exit, w
58 The transition from meiotic spermatocytes to postmeiotic haploid germ cells constitutes an essential
59 ns are significantly elevated in meiotic and postmeiotic haploid germ cells when chromatin modificati
60 t at the stages of meiotic spermatocytes and postmeiotic haploid spermatids.
61 c spermatocytes and during the maturation of postmeiotic haploid spermatids.
62 negative genetic interaction results because postmeiotic haploids that are supposed to be under negat
63 he frequency of minisatellite mutation after postmeiotic irradiation of spermatids was similar to tha
64 les deficient for h1-h3 or h4-h9 displayed a postmeiotic lesion with disrupted individualization comp
65 c spindle, divide asymmetrically in a single postmeiotic lineage.
66 eveal large reductions in the mRNA levels of postmeiotic male germ cell mRNAs and smaller reductions
67 ouse protamines are expressed exclusively in postmeiotic male germ cells and are crucial for the comp
68 A storage/translational delay in meiotic and postmeiotic male germ cells of the mouse.
69 notype that was only detected in meiotic and postmeiotic male germ cells, giving us the opportunity t
70 eas the 35-kDa protein, which accumulates in postmeiotic male germ cells, is abundant in the nucleus.
71  are needed to activate mP2 transcription in postmeiotic male germ cells.
72 nd then extended our analysis to meiotic and postmeiotic male germ cells.
73 ark of active sex chromosome-linked genes in postmeiotic male germ cells.
74 e mouse genome is dedicated to expression in postmeiotic male germ cells.
75 he vegetative cell, and their precursor, the postmeiotic microspore, and found that unlike in mammals
76 ting that this process is different from the postmeiotic mitoses observed in other fungi.
77                                          The postmeiotic mitoses were normal in the homozygous lines;
78 G1 phase prior to DNA synthesis of the first postmeiotic mitosis.
79 reports, many of the translationally delayed postmeiotic mRNAs shift from the RNPs into the polysomes
80 te than premeiotic regimens, suggesting that postmeiotic mutagenesis protocols could be useful in som
81              Spermatogenesis is disrupted in postmeiotic null germ cells with many misshapen and mult
82 last premeiotic mitosis and before the first postmeiotic one of a parental genome-the "perigametic in
83 a nonconcordant normal embryo, pointing to a postmeiotic or microgametophytic origin.
84  separation of centriole pairs in M-phase or postmeiotic organization of gamma Tub23C at centrioles.
85                   During spermiogenesis, the postmeiotic phase of mammalian spermatogenesis, transcri
86             Akap4 is transcribed only in the postmeiotic phase of spermatogenesis and encodes the mos
87  the de novo transcription of RNA during the postmeiotic phases.
88  Saccharomyces cerevisiae that regulates the postmeiotic program of spore formation.
89                                The extent of postmeiotic reactivation of germ-cell-specific X-linked
90 nked genes we examined showed some degree of postmeiotic reactivation.
91 ed a specific requirement for Smed-TTBK-d in postmeiotic regulation of spermatogenesis.
92 t members of the TTBK family of proteins are postmeiotic regulators of sperm development and also con
93 iotically, and we provide evidence that this postmeiotic repression is a downstream consequence of MS
94 is show that the maintenance of X chromosome postmeiotic repression is incomplete.
95                                   While this postmeiotic repression occurs after the loss of MSUC-rel
96    The early meiotic role of Cak1p, like the postmeiotic role in the Smk1p pathway, is CDC28 independ
97 gh levels in the testes, particularly in the postmeiotic round spermatid compartment of the seminifer
98                                              Postmeiotic round spermatids advance at most to step 7 o
99 nner, is present in cytoplasmic fractions of postmeiotic round spermatids where the protamine mRNAs a
100                                           In postmeiotic round spermatids, genomic compartmentalizati
101 nia, and pachytene spermatocytes, but not in postmeiotic round spermatids.
102 sion of mouse Rad30b occurs predominantly in postmeiotic round spermatids.
103 Msh2-Msh3 activate the MutL homolog 1 (Mlh1)-postmeiotic segregation 1 (Pms1) endonuclease in the pre
104  mispairs whereas addition of MutL homolog 1-postmeiotic segregation 1 had no affect on MMR.
105 tability during DNA replication within human postmeiotic segregation 2 (hPMS2)-deficient and proficie
106                             It is shown that postmeiotic segregation 2 (PMS2), an MMR protein, is req
107            In the absence of mei-9 activity, postmeiotic segregation associated with noncrossovers oc
108 se mutants did not accumulate high levels of postmeiotic segregation at the ARG4 recombination hotspo
109 c transmission distortions which manifest as postmeiotic segregation events and gene conversions.
110 s during meiosis: in a pms1 mutant, frequent postmeiotic segregation indicates a defect in the correc
111 n a mlh2 mutant, crossing-over is normal and postmeiotic segregation is not observed but non-Mendelia
112 f the arrangement of heteroduplex DNA in the postmeiotic segregation products reveals different patte
113 in an Msh6 mutant, leading to high levels of postmeiotic segregation; however, hDNA and gene conversi
114                     Most of these events are postmeiotic segregations that represent unrepaired heter
115 omes in haploid spermatids via regulation of postmeiotic sex chromatin (PMSC) [8-11] and opposing eff
116                     We demonstrate that this postmeiotic sex chromatin (PMSC) persists throughout spe
117  into spermatids with the silent compartment postmeiotic sex chromatin (PMSC).
118 aternal germ line and persists thereafter as postmeiotic sex chromatin (PMSC).
119 is required for the epigenetic regulation of postmeiotic sex chromosome expression.
120 st strikingly, profiles of escape genes from postmeiotic silencing diverge significantly between huma
121 and may allow mammals to cope with conserved postmeiotic silencing during the evolutionary past.
122  males for haploid gene transcription during postmeiotic sperm differentiation.
123 he X and Y occupy a novel compartment in the postmeiotic spermatid and adopt a non-Rabl configuration
124  body, creates an immune-privileged site for postmeiotic spermatid development to avoid the productio
125                                       During postmeiotic spermatid differentiation, gamma Tub23C was
126 phila spermatogenesis, mitochondria in early postmeiotic spermatids aggregate, fuse, and elongate bes
127 70-2 -/-) did not synthesize HSP70-2, lacked postmeiotic spermatids and mature sperm, and were infert
128 clusively in testis and more specifically in postmeiotic spermatids and sperm cells.
129                        The iDKO males lacked postmeiotic spermatids and spermatocytes after meiosis I
130                                              Postmeiotic spermatids are the only cells of the seminif
131 -64 was limited to meiotic spermatocytes and postmeiotic spermatids in testis.
132 mammals and teleosts, the differentiation of postmeiotic spermatids to spermatozoa (spermiogenesis) i
133                                              Postmeiotic spermatids use a unique strategy to coordina
134 al body is detached from the nucleus in asun postmeiotic spermatids, resulting in abnormalities later
135 lar degeneration with increased apoptosis of postmeiotic spermatids.
136  gene promoter to express Cre recombinase in postmeiotic spermatids.
137 stis, coinciding with low SAFB expression in postmeiotic spermatids.
138 ident with the onset of MSCI and persists in postmeiotic spermatids.
139 division, and is present in the cytoplasm of postmeiotic spermatids.
140 terochromatin in mammalian meiotic and newly postmeiotic spermatocytes.
141 clear extracts from premeiotic, meiotic, and postmeiotic spermatogenic cell types obtained from young
142 rcc1 mRNAs correlated with meiotic and early postmeiotic spermatogenic cells.
143 af7l ablation impairs the expression of many postmeiotic spermatogenic-specific as well as metabolic
144 essed in testes tissues and is necessary for postmeiotic spermiogenesis, but loss of Blanks is not ac
145 uggesting a role for the gene product in the postmeiotic stages of male germ cell development.
146  The mRNA is expressed during the meiotic or postmeiotic stages of spermatogenesis, and the protein i
147 on with x-rays was studied at premeiotic and postmeiotic stages of spermatogenesis.
148 omal mRNAs during the late meiotic and early postmeiotic stages of spermatogenesis.
149 ly regulated and correlates with the meiotic/postmeiotic stages of spermatogenesis.
150 ayed pleiotropic defects, beginning at early postmeiotic stages.
151 s on the Y short arm induce defects at early postmeiotic stages.
152 hasiRNAs were present in both premeiotic and postmeiotic stages.
153 rentiation during fetal development and into postmeiotic stages.
154 g meiotic prophase and nucleosome removal at postmeiotic stages.
155 and sporophytes, which may be explained by a postmeiotic survivorship bias.
156 ts strengthen the newly emerging notion that postmeiotic transcription is dynamic and integral to the
157 elongation, which coordinates the meiotic-to-postmeiotic transcriptome switch in alliance with the SO
158 ase-independent manner during the meiotic-to-postmeiotic transition in spermatogenesis.
159 early round spermatids during the meiotic-to-postmeiotic transition, which is associated with robust
160 ytene spermatocytes was required for the two postmeiotic transitions, but not for the two premeiotic
161 ermatocytes produce RA to coordinate the two postmeiotic transitions.
162 es now reveal that RA also regulates the two postmeiotic transitions: initiation of spermatid elongat
163 tic cells, the range of mutations induced in postmeiotic zebrafish germ cells has been less thoroughl

 
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