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1 n Leydig cells (somatic cells outside of the seminiferous tubules).
2 is in the fluctuating environment within the seminiferous tubule.
3 re elongate spermatids into the lumen of the seminiferous tubule.
4 ozoa, which takes place in the epithelium of seminiferous tubules.
5      Both radionuclides gained access to the seminiferous tubules.
6  testicular size and no spermatozoa in their seminiferous tubules.
7  reduced sperm counts, and disruption of the seminiferous tubules.
8 within the thin vascular layer overlying the seminiferous tubules.
9 storage vesicles within Sertoli cells of the seminiferous tubules.
10 stmeiotic round spermatid compartment of the seminiferous tubules.
11 questered behind the Sertoli cell barrier in seminiferous tubules.
12 permatocytes in the basal compartment of the seminiferous tubules.
13 rized by calcifications within the lumina of seminiferous tubules.
14  in the kidney collecting tubules and testis seminiferous tubules.
15 g, oviduct, epididymis, ductus deferens, and seminiferous tubules.
16 erstitial tissue that normally surrounds the seminiferous tubules.
17 aled that UT3 is located in Sertoli cells of seminiferous tubules.
18 ble to generate spermatogenesis in recipient seminiferous tubules.
19 facilitate seminoma disseminating beyond the seminiferous tubules.
20 orescent staining showed fewer germ cells in seminiferous tubules.
21 study mechanisms of virus persistence in the seminiferous tubules.
22 nted mouse spermatogonial stem cells in host seminiferous tubules.
23 oordinated spatiotemporally across and along seminiferous tubules.
24 sulting in cell death and destruction of the seminiferous tubules.
25 creased mitotic index and disorganization of seminiferous tubules.
26 ring formation of structures resembling male seminiferous tubules.
27 , which are however found in the wall of the seminiferous tubules.
28 a PEDF, may prevent vascularization of human seminiferous tubules.
29 d18 foci were increased in the lumina of the seminiferous tubules.
30 genesis in juvenile mice results in agametic seminiferous tubules.
31 r for the identification of Sertoli cells in seminiferous tubules.
32 ecifically in the nuclei of Sertoli cells in seminiferous tubules.
33 es, which in turn are composed of convoluted seminiferous tubules.
34 icle-stimulating hormone receptor within the seminiferous tubules.
35 the proportion of abnormal sperm and clogged seminiferous tubules.
36 ce of active spermatogenesis in 24 +/- 7% of seminiferous tubules.
37 oimaging, and in situ confocal microscopy of seminiferous tubules.
38 n of germ cells localized at the base of the seminiferous tubules.
39 ressed primarily in Sertoli cells within the seminiferous tubules.
40 als, including human, can replicate in mouse seminiferous tubules after transplantation, the growth f
41 IKV to establish persistent infection in the seminiferous tubules, an immune-privileged site in the t
42 lls migrated to the basement membrane of the seminiferous tubule and were maintained similar to SSCs.
43 rm counts and a high frequency of degenerate seminiferous tubules and abnormal sperm.
44    Testes from PTU-treated male tadpoles had seminiferous tubules and advanced stage male germ cells,
45 the establishment of the avascular nature of seminiferous tubules and after puberty androgens may fur
46  stem cells reside in specific niches within seminiferous tubules and continuously generate different
47 zation success and caused disorganization of seminiferous tubules and dysregulated spermatogenic gene
48 were evident in light micrographs of testis' seminiferous tubules and epithelial cells lining the epi
49 e when administered intratesticularly enters seminiferous tubules and exerts effects beyond BTB is cu
50 PAC1R(3a) mRNA is preferentially detected in seminiferous tubules and is expressed at the highest lev
51 ar space, creating a microenvironment within seminiferous tubules and providing immune privilege to m
52 fertile and sired offspring but had abnormal seminiferous tubules and reduced sperm counts.
53 the testes of adult males showed dilation of seminiferous tubules and reduction in their density when
54 nockout resulted in disruption of developing seminiferous tubules and subsequent progressive loss of
55 , almost all Sertoli cells are lost from the seminiferous tubules and the Leydig cell population is r
56 scent protein (GFP) transgenic mice into the seminiferous tubules and the testicular interstitium of
57 ased apoptotic cells within the walls of the seminiferous tubules, and a decrease in the number, moti
58  progenitor cells, macrophage penetration of seminiferous tubules, and increased tumor necrosis facto
59           Treatment of mice with JQ1 reduced seminiferous tubule area, testis size, and spermatozoa n
60 ules were approximated by a cross-section of seminiferous tubules arranged in a hexagonal pattern, wi
61          ZIKV antigens were only detected in seminiferous tubules at 14 DPI.
62                                          Rat seminiferous tubules at stages I, II-III, IV-V, VI, VIIa
63                                        Focal seminiferous tubule atrophy accompanied by Leydig cell h
64                                              Seminiferous tubule basement membrane (STBM) plays an im
65 , we observed a lower mutation frequency for seminiferous tubule cell preparations, which contain all
66 tion studies, non-selected, freshly isolated seminiferous tubule cells were transferred to the testis
67 ically significant decrease in the number of seminiferous tubules containing germ cells.
68                In isolated 7 days postpartum seminiferous tubules containing mostly germ line stem ce
69 c expression of I-CREBs in germ cells of the seminiferous tubules correlates with the cyclical down-r
70 optosis of germ cells, spermatogenic arrest, seminiferous tubule degeneration, and infertility.
71 ce have excessive spermatocyte apoptosis and seminiferous tubule degeneration.
72 tion, there was some impairment of renal and seminiferous tubule development.
73 ertile by 3 mo of age and eventually exhibit seminiferous tubules devoid of germ cells.
74 ndrogen effects, such as testicular atrophy, seminiferous tubule diameter reduction and hyperplasia o
75 ter testicular atrophy and decreased average seminiferous tubule diameter when compared with K48R-age
76 ls and hyperplastic Leydig cells, leading to seminiferous tubule dilation and degeneration of germ ce
77 animals produces sexual hormone dysfunction, seminiferous tubule dystrophy and spermatogenesis blocka
78 rum of phenotypes, including thinning of the seminiferous tubule epithelia, dilation of the rete test
79 ired in PTM-ARKO males, indicated by reduced seminiferous tubule fluid production and reduced express
80 from the basal to apical compartments of the seminiferous tubules for further development and maturat
81 h spermatozoa formation in 13% to 17% of the seminiferous tubules formed in the grafts.
82 zed that Ct may infect the epithelium of the seminiferous tubule, formed by Sertoli cells, thus leadi
83 Rfx2-null round spermatids detached from the seminiferous tubules, forming large multinucleated giant
84 ed by GFP fluorescence in squashes of living seminiferous tubules from adult testes, and the presence
85 hese pathological responses are conserved in seminiferous tubules from Gravin(-/-) mice where an over
86 tis displayed typical signs of aging (patchy seminiferous tubules, germ cell depletion, and vacuoliza
87                   When transplanted into the seminiferous tubules, hGaSCs formed embryo-like structur
88  males are infertile and the analysis of the seminiferous tubules identified disrupted acrosomal deve
89 n of germ cells in a substantial fraction of seminiferous tubules in aged mice.
90 e adult testis and to a lesser degree in the seminiferous tubules in spermatogonia and Sertoli cells.
91 tis barrier showed increased permeability of seminiferous tubules in the Arid4a(-/-)Arid4b(+/-) teste
92 ial for the maintenance of Sertoli cells and seminiferous tubules in the developing testes.
93 d mild interstitial edema and closely packed seminiferous tubules in the left testes, indicating reve
94                     Histological analysis of seminiferous tubules in the testes, caput and corpus epi
95 tive dysfunction associated with hypoplastic seminiferous tubules in the testis and perturbed corpus
96 ced testis size and numbers of germ cells in seminiferous tubules, increased germ cell apoptosis, and
97            Sperm develop from puberty in the seminiferous tubules, inside the blood-testis barrier to
98           Here we show that cells from adult seminiferous tubules interact with mammary epithelial ce
99 d in a second-level tubule CNN, which places seminiferous tubules into one of 12 distinct tubule stag
100 ural networks (CNNs) to classify nuclei from seminiferous tubules into seven distinct cell types with
101 e Sertoli cells of the adult mouse and human seminiferous tubules into testicular interstitial fluid
102  expression of RAR-dependent genes along the seminiferous tubules is disrupted.
103 lls, which are an important component of the seminiferous tubules, is robust and induces a strong ant
104 showed hypoplastic and dysgenic testes, with seminiferous tubules lacking spermatogonia.
105 yma to be mostly replaced by bone tissue and seminiferous tubule-like structures.
106 decreased number of germ cells, degenerating seminiferous tubules, maturation arrest and apoptosis, i
107 ermatids, and the bicarbonate present in the seminiferous tubule may be a signal that regulates cAMP
108 m cells caused their premature exit from the seminiferous tubule niche, resulting in germ cell deplet
109                                       In the seminiferous tubules of busulfan-treated mice, GFP-posit
110        Consistent with enhanced apoptosis in seminiferous tubules of C/C testes, we recorded a drasti
111  of undifferentiated iPSCs directly into the seminiferous tubules of germ cell-depleted immunodeficie
112    When rat PGCLCs are transplanted into the seminiferous tubules of germline-less rats, functional s
113  spermatogenesis was totally compromised, as seminiferous tubules of homozygous mutant animals were d
114 , identifiable mutations directly within the seminiferous tubules of human testes.
115 at clump-forming rabbit germ cells colonized seminiferous tubules of immunodeficient mice, proliferat
116  a rare population of macrophages within the seminiferous tubules of Mlh3(-/-) and Hormad1(-/-) mice,
117 8(Ink4c) and p19(Ink4d) are expressed in the seminiferous tubules of postnatal wild-type mice, being
118   We detected MPXV in interstitial cells and seminiferous tubules of testes as well as epididymal lum
119 hest level of expression was detected in the seminiferous tubules of testis.
120 nor cells established spermatogenesis in the seminiferous tubules of the host, and normal spermatozoa
121 genesis takes place in the epithelium of the seminiferous tubules of the testes, producing millions o
122 on becomes XY-specific and restricted to the seminiferous tubules of the testis as gonadogenesis proc
123 l arrest at the round spermatid stage in the seminiferous tubules of the testis in ZFP628-deficient m
124 ransdifferentiation to structures resembling seminiferous tubules of the testis, including Sertoli-li
125 larin family, is expressed at high levels in seminiferous tubules of the testis, specifically in Sert
126 on spermatogenesis, which takes place in the seminiferous tubules of the testis.
127 ed mainly by spermatocytes and spermatids in seminiferous tubules of the testis.
128 d that both mRNAs were strongly expressed in seminiferous tubules of the testis.
129           However, this was not found in the seminiferous tubules of W/W(v) mice.
130  not DeltaNp73KO mice, display a "near-empty seminiferous tubule" phenotype due to massive premature
131 s of cells: (i) epithelial germ cells of the seminiferous tubules, primarily spermatids and spermatoc
132 s while OSKM cells that remained outside the seminiferous tubule proliferated extensively and formed
133 e Sertoli cell, the only somatic cell within seminiferous tubules, provides the stem cell niche throu
134 how impaired testis development, degenerated seminiferous tubules, reduced sperm count and low fertil
135 tis and mechanisms by which the virus enters seminiferous tubules remain unclear.
136 yclic peptide exposure of cultures from mice seminiferous tubules resulted in significant inhibition
137 are small, compared with the diameter of the seminiferous tubules, resulting in high energy depositio
138 was small, compared with the diameter of the seminiferous tubules, resulting in high energy depositio
139 The CSS pipeline comprises four parts: (i) A seminiferous tubule segmentation model is developed to e
140  More detailed analysis of specific cells in seminiferous tubules shows localization of Atr to the nu
141                                              Seminiferous tubule staging shows that stages X to XII,
142 UB1 is involved in cellular functions in the seminiferous tubules such as spermatogenesis.
143 expressed in both the podocyte and the basal seminiferous tubule, suggesting that the loss of CD2AP i
144 sues only in the developing spermatocytes of seminiferous tubules, suggesting that mSgy is a spermato
145 meiotic spermatids are the only cells of the seminiferous tubules that express HIP1.
146 n the Sertoli-Sertoli tight junctions in the seminiferous tubules, the approximately 32 kDa murine JA
147 iremia, ZIKV must establish infection in the seminiferous tubules, the site of spermatozoon developme
148  integrate local and global information of a seminiferous tubule to distinguish Stages I-V from Stage
149 l stem cells from other species to the mouse seminiferous tubule to generate spermatogenesis.
150 ProSG subset translocates from the center of seminiferous tubules to the spermatogonial stem cell (SS
151  disruptive distribution of AKAP9 across the seminiferous tubules was also noted during adjudin-induc
152           Focal vacuolization in some of the seminiferous tubules was observed in 4-week-old mutant t
153                                          The seminiferous tubules were divided into concentric layers
154        Adult testicular cells, isolated from seminiferous tubules, were mixed with limiting dilutions
155  testis and was localized to a region of the seminiferous tubule where secondary spermatocytes and ea
156 eir radial migration to the periphery of the seminiferous tubule where the spermatogenic niche will f
157 uptake into the testis as a whole and to the seminiferous tubules where the germ cells are located.
158 ed that the testes were composed of atrophic seminiferous tubules, whereas germ cells were found in 1
159      The testis cords give rise to the adult seminiferous tubules, whereas steroidogenic Leydig cells
160 n culminates in complete degeneration of the seminiferous tubules, which become acellular, empty spac
161 unostaining for Mamu-AG5 in cells within the seminiferous tubules, which was corroborated by localiza
162 is normally provided by Sertoli cells of the seminiferous tubules, whose function depends on testoste
163 t cells (MGC) were found lining the lumen of seminiferous tubules with many of them undergoing apopto
164 roliferate and migrate within the developing seminiferous tubule, with proper niche interaction and m

 
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