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1  mutant germ cells unable to progress beyond round spermatid.
2 ndent retrotransposon LINE1 de-repression in round spermatids.
3 hytene spermatocytes, but not in postmeiotic round spermatids.
4 in a cDNA library prepared from fractionated round spermatids.
5 e Rad30b occurs predominantly in postmeiotic round spermatids.
6  co-cultured with pachytene spermatocytes or round spermatids.
7 ing that Prbp acts to repress translation in round spermatids.
8 ment of late-stage meiotic cells and haploid round spermatids.
9  pachytene spermatocytes and in post-meiotic round spermatids.
10 ar tissue revealed an arrest at the stage of round spermatids.
11 at SMG6 and PIWIL1 co-regulate many genes in round spermatids.
12  the late stage of meiosis or early stage of round spermatids.
13 spermatogenesis, preventing formation beyond round spermatids.
14 signs of meiosis as noted by the presence of round spermatids.
15 n reorganization property of Brdt in haploid round spermatids.
16 a- and Dicer-null pachytene spermatocytes or round spermatids.
17 es of control versus Brdt(DeltaBD1/DeltaBD1) round spermatids.
18 heir 3'-untranslated region (UTR) typical of round spermatids.
19 ns Tes and Mena in the subacrosomal layer of round spermatids.
20 enes on the X chromosome remain repressed in round spermatids.
21 nd adult pachytene spermatocytes, as well as round spermatids.
22 the most significant differences apparent in round spermatids.
23 , could be detected only in the germ line in round spermatids.
24 ed in late-stage pachytene spermatocytes and round spermatids.
25  of phospho-GRTH in the chromatoid bodies of round spermatids.
26  to the haploid expression of its members in round spermatids.
27 s restricted mainly in the spermatocytes and round spermatids.
28 ctivator in late pachytene spermatocytes and round spermatids 1).
29 t Jam-C is essential for the polarization of round spermatids, a function that we attribute to its ro
30 confined to late pachytene spermatocytes and round spermatids, a time window concomitant with the occ
31                                  Postmeiotic round spermatids advance at most to step 7 of differenti
32                                   Rnf17-null round spermatids advanced to step 4 but failed to produc
33 mplete arrest of spermiogenesis at step 8 of round spermatids and failure to elongate.
34 asm and nucleus of meiotic spermatocytes and round spermatids and functions as a component of mRNP pa
35 eduction in the size of chromatoid bodies of round spermatids and germ cell apoptosis.
36 ay-old prepubertal mice, which contain early round spermatids and lack elongated spermatids.
37 SUMO-1 localized in chromocenters of certain round spermatids and perinuclear ring and centrosomes of
38  Ddx5 and Hnrnpk mRNAs were longer in mutant round spermatids and resulted in reduced protein levels.
39 es and is expressed at the highest levels in round spermatids and Sertoli cells.
40 and embryonic development are established in round spermatids and spermatozoa of these animals, even
41 rich protein is translationally repressed in round spermatids and translationally active in elongated
42 tocytes (midstage of meiotic division I) and round spermatids and weakly in Leydig cells (somatic cel
43 atogenesis (spermatogonia, spermatocytes and round spermatids) and testicular somatic Sertoli cells.
44       ADAD1, previously shown to localize to round spermatids, and ADAD2 had distinct localization pa
45 plasmic protein present in spermatocytes and round spermatids, and it is required for the expression
46 ched in RNPs from pachytene spermatocytes to round spermatids, and the enrichment of shorter 3' UTR m
47  fertile offspring when their spermatozoa or round spermatids are injected into oocytes of normal fem
48         These translation defects in haploid round spermatids are likely indirect, as neither MAEL no
49                              Coincident with round spermatid arrest, we find reduced mRNA expression
50 where it is highly expressed in post-meiotic round spermatids as well as in Sertoli cells.
51 As containing the Gfp coding region in early round spermatids at the same transcription start site as
52                 PAF-1 reaches high levels in round spermatids at the time of mP2 transcription.
53 ative homeodomain transcription factor 1 and round spermatid basic protein 1.
54                                        Their round spermatids bear "ghost" CBs, whose architecture is
55  as in the reorganization of hyperacetylated round spermatid chromatin.
56  the testes, particularly in the postmeiotic round spermatid compartment of the seminiferous tubules.
57 mmunoreactivity was detected in protein from round spermatids, condensing spermatids, and mature sper
58 s were not found in pachytene spermatocytes, round spermatids, condensing spermatids, or sperm, sugge
59 e sterile and exhibited a complete arrest in round spermatids, demonstrating that Rnf17 encodes a nov
60 und spermatids into zygotes in ROSI and that round spermatid-derived H3K27me3 is associated with less
61 lasses of Utp14b transcripts were highest in round spermatids despite the transcription of Utp14a in
62                                The Rfx2-null round spermatids detached from the seminiferous tubules,
63                                     However, round spermatids did not progress beyond step 6, reveali
64 tive and inactive pools, results in abnormal round spermatid differentiation and impaired fertility.
65 t that progression through meiosis and early-round spermatid differentiation are surprisingly unaffec
66                                          The round spermatids display normal centrosomes consisting o
67 s expression detectable in spermatocytes and round spermatids during spermatogenesis.
68 of Rlim in male reproduction specifically in round spermatids during spermiogenesis.
69 tch from the late spermatocytes to the early round spermatids during the meiotic-to-postmeiotic trans
70 rkable cellular transformation, during which round spermatids elongate into chromatin-condensed sperm
71 atocytes arrest at metaphase I, compromising round spermatid formation.
72                               In postmeiotic round spermatids, genomic compartmentalization increases
73                                           In round spermatids, hCG caused a significant decrease of 6
74 olecular logic, in which chromatin states in round spermatids impinge on chromatin accessibility and
75 These modulations alter 3'-UTR processing in round spermatids; importantly, the BD1 is essential for
76 tment and further progressed to the level of round spermatids in control samples at 4 weeks.
77 ast through the steps of meiosis to generate round spermatids in testes of rats treated with an acute
78 matozoa, in Sertoli cells, Leydig cells, and round spermatids in the testis, and in the principal cel
79 d gene, most abundantly expressed in haploid round spermatids in the testis, and the protein is local
80 nly expressed in pachytene spermatocytes and round spermatids in the testis.
81                                              Round spermatid injection (ROSI) results in a lower birt
82 zation, intracytoplasmic sperm injection, or round spermatid injection.
83 ation, intracytoplasmic sperm injection, and round spermatid injection.
84 ng spermiogenesis, a process that transforms round spermatids into mature sperm.
85 le in spermiogenesis, the differentiation of round spermatids into mature spermatozoa.
86 ular morphogenesis that converts unpolarized round spermatids into polarized amoeboid spermatozoa cap
87  required for postmeiotic differentiation of round spermatids into sperm.
88 itically required for the differentiation of round spermatids into spermatozoa in mice.
89  histone mark, H3K27me3, persists from mouse round spermatids into zygotes in ROSI and that round spe
90 A erasure in the nuclei of spermatocytes and round spermatids is essential for correct splicing and t
91 and Prm2 mRNA in pachytene spermatocytes and round spermatids is essential for their timely translati
92  Sertoli cells, pachytene spermatocytes, and round spermatids isolated from wild-type animals.
93 spermatocytes the Golgi is spherical and, in round spermatids, it is localized over the acrosomal ves
94 an NF-kappaB-activating cytokine produced by round spermatids located adjacent to Sertoli cells, stim
95     However, only punctate expression of the round spermatid marker SP-10 in the acrosomal granule of
96 ressed specifically in the spermatocytes and round spermatids of a transgenic line, confirming that s
97                                              Round spermatids of the null mice showed marked diminuti
98 ter gene in late pachytene spermatocytes and round spermatids of transgenic mice.
99 -prone meiosis and spermatogenic arrest with round spermatids of type Sa as the most advanced populat
100 d in germ cells (pachytene spermatocytes and round spermatids) of the rat testis.
101 chment is then specified in the transcribing round spermatid, recapitulating the organization of the
102 pecially abundant in spermatocytes and early round spermatids, regardless of the type of the genomic
103 stly elevated in pachytene spermatocytes and round spermatids relative to other spermatogenic cells.
104 , in isolated pachytene spermatocytes (PtS), round spermatids (RS), and later spermatids (LS), the mR
105  mouse SP-10 gene was sufficient to maintain round spermatid-specific expression.
106               Our previous studies using the round spermatid-specific mouse SP-10 gene, which codes f
107 anscription in spermatocytes of an otherwise round spermatid-specific promoter.
108  (Spga), pachytene spermatocytes (Spcy), and round spermatids (Sptd) were determined by sequencing th
109 a (Spga), pachytene spermatocytes (Spcy) and round spermatids (Sptd) were included.
110  (Spga), pachytene spermatocytes (Spcy), and round spermatids (Sptd).
111 ize, lack sperm with spermatogenic arrest at round spermatid stage and loss of the cytoplasmic phosph
112 overed a postmeiotic germ cell arrest at the round spermatid stage in the seminiferous tubules of the
113 rthermore, spermatogenesis is blocked at the round spermatid stage, causing a total absence of the el
114 bundantly expressed from the spermatocyte to round spermatid stage, coinciding with the widespread ex
115 with a significant loss of germ cells at the round spermatid stage, in association with disorganizati
116 spermatogenic arrest at the beginning of the round spermatid stage, resembling the phenotype of CREM,
117 stages of meiotic prophase and ending in the round spermatid stage.
118 togenesis, ranging from the pachytene to the round spermatid stage.
119 s being most highly expressed in the haploid round spermatid stage.
120 ential for spermatogenesis to proceed to the round spermatid stage.
121 fects of JQ1 evident at the spermatocyte and round spermatid stages cause a complete and reversible c
122 sis in Bsg KO mice was arrested at the early round spermatid stages.
123 to the arrest of spermatogenesis at an early round spermatid step.
124 is, expression of MBD3L1 is observed only in round spermatids, suggesting a role for the gene product
125 ve been localized in the acrosomal region of round spermatids, they resemble a major component of the
126 enorhabditis elegans as they activate from a round spermatid to a mature, crawling spermatozoon.
127 imals further shows that progression of late-round spermatids to elongating steps is sensitive to los
128  disruption, even though it fails to support round spermatids to enter spermiogenesis.
129 sis, the final phase of spermatogenesis when round spermatids transform to spermatozoa, is defective
130                  We found that, in Ewsr1 CKO round spermatids, transition from a meiotic gene-express
131                   It was also noted that the round spermatids underwent eventual degeneration with th
132                                              Round spermatids were present but no elongated spermatid
133  spermatocytes, pachytene spermatocytes, and round spermatids were purified from enzymatically disper
134 ormally in the absence of Boule, and haploid round spermatids were readily detected.
135 sent in cytoplasmic fractions of postmeiotic round spermatids where the protamine mRNAs are translati
136                                           In round spermatids where the SP-10 gene is expressed, this
137 erm line of the testis from zygotene through round spermatids, whereas mUtp14a, although well express
138 , however, TDP-43 remains at the promoter in round spermatids, which express acrv1 mRNA.
139 cells of 12-day-old mice and subsequently in round spermatids, which is consistent with androgen regu
140 is-specific (H1fnt) protein in Brdt(BD1/BD1) round spermatids, which may be linked to the previously
141 aggregate, genetic effects were strongest in round spermatids, which parallels their increased transc
142 n addition, long-frozen samples showed fewer round spermatids with detectable protamine expression, s

 
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