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1 d germ cells at the basal compartment in the seminiferous epithelium.
2 express stage-specifically at the BTB in the seminiferous epithelium.
3 epresenting spermatogenic development in the seminiferous epithelium.
4 totic germ cells by Sertoli cells lining the seminiferous epithelium.
5 with apical ES and BTB restructuring in the seminiferous epithelium.
6 or of cell adhesion and BTB integrity in the seminiferous epithelium.
7 hich leads to germ cell exfoliation from the seminiferous epithelium.
8 occurs within a highly organized tissue, the seminiferous epithelium.
9 tis in germ cells at the basal aspect of the seminiferous epithelium.
10 ween spermatids and Sertoli cells within the seminiferous epithelium.
11 .g., residual bodies, phagosomes) across the seminiferous epithelium.
12 t by controlling the microenvironment of the seminiferous epithelium.
13 function, leading to germ cell loss from the seminiferous epithelium.
14 ype A spermatogonia in the basal part of the seminiferous epithelium.
15 s is compromised, germ cells detach from the seminiferous epithelium and infertility often results.
16 connexin43, which was present throughout the seminiferous epithelium and not restricted to the BTB as
17 and distance are designated the cycle of the seminiferous epithelium and the spermatogenic wave, resp
19 permiogenesis, age-dependent degeneration of seminiferous epithelium, and disorder of cholesterol hom
20 and sloughing off of spermatogenic cells in seminiferous epithelium, and lack of mature spermatids i
21 sloughing of postmeiotic germ cells from the seminiferous epithelium, and marked reduction in the num
22 ed tracks, and laid perpendicular across the seminiferous epithelium, and prominently expressed at th
23 of germ cells, vacuole formation within the seminiferous epithelium, and reduced sperm production.
24 n the transport of synthetic F5-peptide into seminiferous epithelium, and thus Slc15a1 is a novel tar
26 inus, was found to be transported across the seminiferous epithelium at stages VIII-IX of the epithel
28 e same stage in development, stage IV of the seminiferous epithelium cycle, equivalent to mid-pachyne
29 ligand JAGGED-1 (JAG1) at stage VIII of the seminiferous epithelium cycle, therefore mediating germ
30 ogonia located in a niche at the base of the seminiferous epithelium delimited by Sertoli cells and p
31 that reside at the basal compartment of the seminiferous epithelium differentiate into more advanced
35 s cellular events that take place across the seminiferous epithelium during the epithelial cycle of s
36 modeling near the BM at opposite ends of the seminiferous epithelium during the epithelial cycle, kno
37 ce) to coordinate cellular events across the seminiferous epithelium during the epithelial cycle.
39 involvement in junction restructuring in the seminiferous epithelium, especially at the ectoplasmic s
40 ed Sertoli cells, a somatic component of the seminiferous epithelium, exhibited significantly lower a
41 es to enter the adluminal compartment of the seminiferous epithelium for development into spermatozoa
42 Although the cycle and the wave of the adult seminiferous epithelium have been well characterised, pa
45 nally, expression of Aire was evident in the seminiferous epithelium in an age-dependent manner, as w
46 o critical cellular events that occur across seminiferous epithelium in mammalian testis during sperm
47 tects against late-onset degeneration of the seminiferous epithelium in mice and inhibits Leydig cell
50 of molecules between cells, and separate the seminiferous epithelium into basal and adluminal compart
52 ion of spermatids and their release from the seminiferous epithelium is AR dependent and maximally se
54 to survey all laminin chains in cells of the seminiferous epithelium, it was noted that alpha 2, alph
55 triking testicular pathology, with disrupted seminiferous epithelium, multinucleated giant cells, unc
58 expression was the highest at the ES in the seminiferous epithelium of adult rat testes, most notabl
61 co-localized to the site of apical ES in the seminiferous epithelium of the rat testis in immunohisto
62 specific adherens junction (AJ) type] in the seminiferous epithelium of the rat testis, we sought to
63 oses a challenge to deliver any drugs to the seminiferous epithelium of the testis, such as a nonhorm
64 iminate expression of a reporter gene in the seminiferous epithelium of transgenic mice, whereas the
65 as an adhesion and maturation factor of the seminiferous epithelium orchestrating spermiogenesis.
66 a show that the cycle and wave of the murine seminiferous epithelium originate at a much earlier stag
68 ) conferred by adjacent Sertoli cells in the seminiferous epithelium segregates post-meiotic germ cel
70 od-testis barrier (BTB) restructuring in the seminiferous epithelium that occur concurrently at stage
72 preferentially expressed in stages VII-VIII seminiferous epithelium, the androgen-dependent stages d
73 ere is a lack of data on Ct infection of the seminiferous epithelium; therefore, we aimed to characte
74 y disrupts Sertoli-germ cell adhesion in the seminiferous epithelium to facilitate germ cell migratio
77 tact during the transit of spermatids in the seminiferous epithelium, which is associated with extens
78 averse the blood-testis barrier (BTB) in the seminiferous epithelium, which is reminiscent of viral p
79 morphology in postmeiotic germ cells in the seminiferous epithelium, which led to the complete arres
80 d Sertoli cells as the only cell type in the seminiferous epithelium with detectable ApoER2 expressio