コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 e and higher claudin-11 expression along the blood-testis barrier.
2 t spermatogenesis and create the impermeable blood-testis barrier.
3 partment, thus completing transit across the blood-testis barrier.
4 this plasma insulin cannot pass through the blood-testis barrier.
5 or male contraception may interfere with the blood-testis barrier.
6 terstitial fluid (TIF) that is "outside" the blood-testis barrier.
7 ation and maintaining the homeostasis of the blood-testis barrier.
8 These tight junctions form the basis of the blood-testis barrier, a structure whose function and dyn
9 ivileged site in the testis protected by the blood-testis barrier, also called the Sertoli cell (SC)
11 in-based adhesion junctions, to maintain the blood-testis barrier and support spermatid transport and
13 to the adhesion between Sertoli cells at the blood-testis barrier, as well as between Sertoli and dev
14 that it is localized in Sertoli cells at the blood-testis barrier (BTB) and at the apical ectoplasmic
15 calized to actin-based cell junctions at the blood-testis barrier (BTB) and the apical ectoplasmic sp
16 e from type B spermatogonia and traverse the blood-testis barrier (BTB) at stage VIII of the seminife
17 oss the murine blood-brain barrier (BBB) and blood-testis barrier (BTB) by a saturable transport syst
19 es permanent infertility due to irreversible blood-testis barrier (BTB) disruption even though the po
20 sforming growth factor (TGF)-beta3 regulates blood-testis barrier (BTB) dynamics in vivo, plausibly b
22 r the basement membrane, associated with the blood-testis barrier (BTB) in stage VIII-IX tubules.
23 sis, preleptotene spermatocytes traverse the blood-testis barrier (BTB) in the seminiferous epitheliu
28 Throughout spermatogenesis, the Sertoli cell blood-testis barrier (BTB) is strictly regulated by cyto
29 s, would disrupt spermatogenesis because the blood-testis barrier (BTB) must remain intact during the
30 be used to enhance the transport across the blood-testis barrier (BTB) of contraceptive drugs or to
32 rmore, gap and tight junctions essential for blood-testis barrier (BTB) organization are disrupted.
33 tes testis function by inducing Sertoli cell blood-testis barrier (BTB) remodeling and is also capabl
34 such as rats, the mechanism(s) that regulate blood-testis barrier (BTB) restructuring at stages VIII-
35 and coordinate the events of spermiation and blood-testis barrier (BTB) restructuring in the seminife
36 g apical ectoplasmic specialization (ES) and blood-testis barrier (BTB) restructuring in the testis.
38 ates the timely and selective opening of the blood-testis barrier (BTB) to migrating preleptotene/lep
41 axis between the basement membrane (BM), the blood-testis barrier (BTB), and the apical ectoplasmic s
45 ein, using an in vitro model of Sertoli cell blood-testis barrier (BTB), PFOS was found to induce Ser
47 oside transporters (ENTs) are present at the blood-testis barrier (BTB), where they can facilitate an
56 hibited no toxicity, efficiently crossed the blood-testis barrier, did not accumulate in brain, and i
58 ic antigen-presenting cells, and sustain the blood-testis barrier formed by their tight junctions.
61 nal blood-testis barrier reversibly perturbs blood-testis barrier integrity in vitro and in the rat t
63 es infertility with compromised integrity of blood-testis barrier, leading to germ cells unable to tr
64 ally, germ cell sloughing and rupture of the blood-testis barrier occur and are correlated with decre
65 ding spermatogenic failures and the impaired blood-testis barrier, recapitulated the defects found in
66 ility assessment, and overexpression of BTB (blood-testis barrier) regulatory genes such as FAK and i
67 Sertoli cells with an established functional blood-testis barrier reversibly perturbs blood-testis ba
69 1 and ENT2 substrates and can circumvent the blood-testis barrier through this transepithelial transp
70 tor results in increased permeability of the blood-testis barrier to biotin, suggesting claudin 3 reg
71 erty in the seminiferous tubules, inside the blood-testis barrier to prevent their recognition as "no
73 gh thiamin transporter expression beyond the blood-testis barrier, were more susceptible to apoptosis
74 permiation and mediates restructuring of the blood-testis barrier, which facilitates the transit of p
75 degeneration of Sertoli cells, including the blood-testis barrier, which leads to disruption of the a