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1 s their repressive state when present in the spermatogonial stem cell.
2 ach for purification and characterization of spermatogonial stem cells.
3 on, and resulted in a 166-fold enrichment of spermatogonial stem cells.
4 tial for reproduction, little is known about spermatogonial stem cells.
5 rat model made by germline gene targeting in spermatogonial stem cells.
6 te-determining HoxC transcription factors in spermatogonial stem cells.
7 ide an epigenetic paradigm for regulation of spermatogonial stem cells.
8 (ENU) to induce single base substitutions in spermatogonial stem cells.
9 es impaired differentiation of embryonic and spermatogonial stem cells.
10 e cyst cells break apart and probably become spermatogonial stem cells.
11 nuclear factor-Y is required for maintaining spermatogonial stem cells.
12 is: regulation of meiosis and maintenance of spermatogonial stem cells.
13 pment, hematopoiesis, and differentiation of spermatogonial stem cells.
14 l systems, we used primary cultures of mouse spermatogonial stem cells, a mouse spermatogonial stem c
15 arch surrounds the regenerative potential of spermatogonial stem cells, a recent article highlights t
16                        Thus, to proliferate, spermatogonial stem cells activate mechanisms that are s
17 n provides insight into the amplification of spermatogonial stem cells and the origin of primordial f
18 are prospermatogonia), increases steadily as spermatogonial stem cells appear, plateaus as the first
19                       Age-related changes in spermatogonial stem cells appeared modest, whereas age-r
20    This results, in part, from the fact that spermatogonial stem cells are an extremely rare cell pop
21 e generated a transgenic mouse line in which spermatogonial stem cells are marked by expression of an
22                                              Spermatogonial stem cells are required for the initiatio
23                                     Although spermatogonial stem cells are unipotent, these cells are
24 ovessels may contribute to the regulation of spermatogonial stem cells, as well.
25          In contrast, the recently developed spermatogonial stem cell assay system allows quantitatio
26                               We demonstrate spermatogonial stem cell-associated antigens by using an
27 tal period in the non-dividing precursors of spermatogonial stem cells at a stage where retrotranspos
28  required for the survival of mouse PGCs and spermatogonial stem cells by suppressing apoptosis.
29          Mice lacking DOT1L fail to maintain spermatogonial stem cells, characterized by a sequential
30                      CBX2 is up-regulated as spermatogonial stem cells differentiate and is required
31      Spermatogenesis is the process by which spermatogonial stem cells divide and differentiate to pr
32                                              Spermatogonial stem cells divide throughout life, mainta
33 losely related species with similar rates of spermatogonial stem cell divisions but a shorter mean ag
34                                 The lifelong spermatogonial stem cell divisions unique to male germ c
35         Thus, molecular markers specific for spermatogonial stem cells establish a reliable and rapid
36 ike primordial germ cells toward a unipotent spermatogonial stem cell fate.
37     Recently, transplantation of mouse donor spermatogonial stem cells from a fertile testis to an in
38                     Thus, transplantation of spermatogonial stem cells from an infertile donor to a p
39  we examine the feasibility of transplanting spermatogonial stem cells from other species to the mous
40 highlights the in-vitro propagation of human spermatogonial stem cells from testicular biopsies for f
41                                       First, spermatogonial stem cells from the adult cryptorchid tes
42                                              Spermatogonial stem cells functionality reside in the sl
43  consistent with germline selection: mutated spermatogonial stem cells gained an advantage that allow
44                               In contrast to spermatogonial stem cells, gonocytes can be identified e
45              Whereas in-vitro propagation of spermatogonial stem cells has been established in animal
46                                  Human adult spermatogonial stem cells (hSSCs) must balance self-rene
47 ve clonal fate studies of transplanted mouse spermatogonial stem cells in host seminiferous tubules.
48 antation experiments revealed a depletion of spermatogonial stem cells in the adult.
49                               We establish a spermatogonial stem cell index (SSCI) that reliably pred
50                                          The spermatogonial stem cell initiates and maintains spermat
51 rmatogenesis involves the differentiation of spermatogonial stem cells into spermatocytes via mitotic
52  of the genome, and telomerase expression in spermatogonial stem cells is responsible for the mainten
53                              Self-renewal of spermatogonial stem cells is vital to lifelong productio
54 sequent extensive apoptosis occurring at the spermatogonial stem-cell level.
55  of mouse spermatogonial stem cells, a mouse spermatogonial stem cell line and freshly isolated testi
56                                   Vertebrate spermatogonial stem cells maintain sperm production over
57  and revealed a novel function in regulating spermatogonial stem cell maintenance.
58 erm cells and the identification of a set of spermatogonial stem cell marker transcripts.
59 adhesion receptor ADGRA3 (GPR125) is a known spermatogonial stem cell marker, but its impact on male
60  proliferation is impaired and expression of spermatogonial stem cell markers c-Ret, Plzf, and Stra8
61 cteristics - a partial rejuvenation - of the spermatogonial stem cell niche and, in addition, detecte
62 he present study shows that GAHT changes the spermatogonial stem cell niche by partially rejuvenating
63  manner, implying failure of maintaining the spermatogonial stem cell niche in somatic cells.
64 istological and transcriptomic analysis, the spermatogonial stem cell niche of 106 trans women who un
65 urotrophic factor (GDNF), a component of the spermatogonial stem cell niche produced by the somatic S
66 g a classic stem cell system, the Drosophila spermatogonial stem cell niche, we reveal daily rhythms
67 nd blood flow are known to contribute to the spermatogonial stem cell niche.
68 vitro retroviral-mediated gene delivery into spermatogonial stem cells of both adult and immature mic
69 permatogenesis in mouse testes suggests that spermatogonial stem cells of many species could be trans
70 was not functionally redundant with NSun2 in spermatogonial stem cells or Sertoli cells.
71 id not substantially impact the diversity of spermatogonial stem cell pools in these individuals.
72                                    The adult spermatogonial stem cell population arises from pluripot
73                          The identity of the spermatogonial stem cell population in the undisturbed t
74                                  Division of spermatogonial stem cells produces daughter cells that e
75            We report here that GDNF promotes spermatogonial stem cell proliferation through activatio
76                                     Although spermatogonial stem cells remain unaffected, proliferati
77 ave now devised culture conditions where rat spermatogonial stem cells renew and proliferate in cultu
78  sexes, with males also exhibiting defective spermatogonial stem-cell renewal.
79                               Maintenance of spermatogonial stem cells requires the transcriptional r
80 view the developments that have been made in spermatogonial stem cell research and potential future u
81                                              Spermatogonial stem cells reside in specific niches with
82 estigation of molecular mechanisms governing spermatogonial stem cell self renewal and hierarchical d
83 ruption of ERM have a loss of maintenance of spermatogonial stem cell self-renewal without a block in
84 ole H3K79 methyltransferase, is required for spermatogonial stem cell self-renewal.
85 toli cells in the testis and is required for spermatogonial stem cell self-renewal.
86  TAF4b may be required for the regulation of spermatogonial stem cell specification and proliferation
87 om the center of seminiferous tubules to the spermatogonial stem cell (SSC) 'niche' in its periphery
88                                 We evaluated spermatogonial stem cell (SSC) activity in the developin
89            The intricate interaction between spermatogonial stem cell (SSC) and testicular niche is e
90 importance of individual miRs in controlling spermatogonial stem cell (SSC) homeostasis has not been
91 malian spermatogenic lineage, a foundational spermatogonial stem cell (SSC) pool arises from prosperm
92  their lives depends upon establishment of a spermatogonial stem cell (SSC) pool from gonocyte progen
93       Consequently, neither the foundational spermatogonial stem cell (SSC) pool nor progenitor sperm
94 and pale (Ap) spermatogonia that make up the spermatogonial stem cell (SSC) pool.
95 enile quiescence of germ cells with immature spermatogonial stem cell (SSC) precursors (gonocytes) pr
96                                              Spermatogonial stem cell (SSC) self-renewal and differen
97 s suggest that exogenous factors crucial for spermatogonial stem cell (SSC) self-renewal are conserve
98 NADPH1 oxidase 1 (NOX1) are thought to drive spermatogonial stem cell (SSC) self-renewal through feed
99 DNF, an essential growth factor required for spermatogonial stem cell (SSC) self-renewal.
100 , a Bmp type I receptor inhibitor, prolonged spermatogonial stem cell (SSC) survival in culture and e
101                                          The spermatogonial stem cell (SSC) that supports spermatogen
102   The mechanisms that guide the continuum of spermatogonial stem cell (SSC) to progenitor spermatogon
103                                              Spermatogonial stem cell (SSC) transplantation has been
104 how that conditional deletion of Tert in the spermatogonial stem cell (SSC)-containing population in
105                               In this study, spermatogonial stem cells (SSC) that harbor paternalized
106  selfish mutations: substitutions that grant spermatogonial stem cells (SSCs) a selective advantage i
107                                              Spermatogonial stem cells (SSCs) are a subpopulation of
108                                              Spermatogonial stem cells (SSCs) are at the foundation o
109                             Male germline or spermatogonial stem cells (SSCs) are conserved across ma
110                                              Spermatogonial stem cells (SSCs) are essential for adult
111                                              Spermatogonial stem cells (SSCs) are essential for the g
112                                              Spermatogonial stem cells (SSCs) are generally character
113                                              Spermatogonial stem cells (SSCs) are responsible for mai
114                                              Spermatogonial stem cells (SSCs) are the basis of sperma
115                                              Spermatogonial stem cells (SSCs) are the foundation for
116                                              Spermatogonial stem cells (SSCs) are unipotent germ cell
117                                              Spermatogonial stem cells (SSCs) are unique among tissue
118 he untimely and excessive differentiation of spermatogonial stem cells (SSCs) by disturbing the expre
119                                              Spermatogonial stem cells (SSCs) capable of self-renewal
120                                              Spermatogonial stem cells (SSCs) form the basis of male
121                                              Spermatogonial stem cells (SSCs) have the dual capacity
122 ction of functional sperm from self-renewing spermatogonial stem cells (SSCs) in cell culture conditi
123 erm line stem cells (GSCs) in Drosophila, or spermatogonial stem cells (SSCs) in mammals.
124          Self-renewal and differentiation by spermatogonial stem cells (SSCs) is the foundation for c
125                              Self-renewal of spermatogonial stem cells (SSCs) is the foundation for m
126                                              Spermatogonial stem cells (SSCs) maintain spermatogenesi
127                                              Spermatogonial stem cells (SSCs) maintain spermatogenesi
128                                    Postnatal spermatogonial stem cells (SSCs) progress through prolif
129          Self-renewal and differentiation of spermatogonial stem cells (SSCs) provide the foundation
130                                              Spermatogonial stem cells (SSCs) self-renew and produce
131 self-renewal and differentiation programs of spermatogonial stem cells (SSCs) that is regulated by re
132 permatogenesis is initiated and sustained by spermatogonial stem cells (SSCs) through self-renewal an
133 ent results have demonstrated the ability of spermatogonial stem cells (SSCs) to de-differentiate int
134                                           In spermatogonial stem cells (SSCs), Myc controls SSC fate
135              We observed a paucity of mutant spermatogonial stem cells (SSCs), which appears independ
136 eating transchromosomic mice by manipulating spermatogonial stem cells (SSCs), which exhibited superi
137 easonal spermatogenesis in fish is driven by spermatogonial stem cells (SSCs), which undergo a comple
138  epigenetic reprogramming, and spermatogonia/spermatogonial stem cells (SSCs).
139 enesis and lifelong fertility is provided by spermatogonial stem cells (SSCs).
140 level is essential for homeostasis in murine spermatogonial stem cells (SSCs).
141  population size and differentiation fate of spermatogonial stem cells (SSCs).
142 n the GFRA1(+) spermatogonia, which includes spermatogonial stem cells (SSCs).
143 gametes originate from a small population of spermatogonial stem cells (SSCs).
144  testis, sustained spermatogenesis relies on spermatogonial stem cells (SSCs); their progeny either r
145 ermore, the presence of surface integrins on spermatogonial stem cells suggests that these cells shar
146  fetal testes, resulting in the formation of spermatogonial stem cells: the foundational stem cells r
147        Despite the central importance of the spermatogonial stem cell to male reproduction, little is
148 ideal surrogate for transplantation of donor spermatogonial stem cells to expand the availability of
149                                              Spermatogonial stem cell transplantation (SSCT) is an ex
150                                              Spermatogonial stem cell transplantation began as a theo
151           Restoration of fertility following spermatogonial stem cell transplantation in animals sugg
152              Given STAT3's function in mouse spermatogonial stem cells, we suggest that this interact
153  after treatment, suggesting that persistent spermatogonial stem cells were not sensitive to NOVP.
154 ence of Pramef12 expression, there are fewer spermatogonial stem cells which exhibit lower expression
155 al germ cells in the embryo and give rise to spermatogonial stem cells, which establish and maintain
156                          Transfection of the spermatogonial stem cells with a plasmid containing the
157 ance and differentiation of gonocytes and/or spermatogonial stem cells would be modulated through thi

 
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