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1 eferens, and seminal vesicle from a straight Wolffian duct.
2 and FGFs reminiscent of UB budding from the wolffian duct.
3 ced ectopic ureteric bud formation along the Wolffian duct.
4 ubules, ureteric bud, developing ureter, and Wolffian duct.
5 c reproductive tracts from the Mullerian and Wolffian ducts.
6 in the regionalization of the Mullerian and Wolffian ducts.
7 ates, the Mullerian duct elongates along the Wolffian duct, a mesonephric structure that is required
8 ude any significant influx of cells from the Wolffian duct and also the view of a tube forming by coe
9 ckout of Lhx1 results in degeneration of the Wolffian duct and consequently the non-cell-autonomous l
10 hese mutants retained the cranial end of the Wolffian duct and formed the epididymis and vas deferens
12 early events-ureteric bud outgrowth from the Wolffian duct and initial induction of Pax-2 expression
13 the ureteric bud, a caudal outgrowth of the Wolffian duct and progenitor for the collecting duct net
14 acellular matrix protein associated with the Wolffian duct and the ureteric bud, epithelial structure
15 of the cranial mesonephric tubules from the Wolffian duct and to the development of major portions o
18 tor tyrosine kinase that is expressed in the Wolffian duct and ureteric bud of the developing excreto
19 ls show a limited distribution in the caudal Wolffian duct and ureteric bud, similar to Ret(-/-) cell
22 aused by failure of ureters to separate from Wolffian ducts and migrate to their definitive position.
23 for beta-catenin in maintaining cells of the Wolffian ducts and the duct derived ureteric bud/collect
24 present in mesenchyme surrounding the lower Wolffian ducts and, at later stages, FGF10 transcripts b
26 ed epithelial outgrowth from the base of the Wolffian ducts, and that the distal ureter abnormalities
27 rowing tip is intimately associated with the Wolffian duct as it elongates to the urogenital sinus.
28 ureteric buds that fail to separate from the wolffian duct as well as decreased branching morphogenes
29 ial evagination of the ureteric bud from the Wolffian duct, as well as its subsequent growth and bran
30 ecifically in the mesenchyme of the anterior Wolffian duct at embryonic day 12.5 before the productio
31 ian kidney development is initiated when the Wolffian duct branches and invades the overlying metanep
32 nephros development, it was expressed in the Wolffian duct but not in the mesonephric mesenchyme.
33 itial outgrowth of the ureteric bud from the Wolffian duct by controlling the expression of Gdnf in t
34 evated or reduced RET activity, we find that Wolffian duct cells compete, based on RET signaling leve
36 erm, revealed that the cranial region of the Wolffian duct degenerated prematurely and the cranial me
39 enetic fate mapping, we demonstrate that the Wolffian duct does not contribute cells to the Mullerian
40 ry1 is to modulate GDNF/RET signaling in the Wolffian duct, ensuring that kidney induction is restric
41 movements and Ret-independent changes in the Wolffian duct epithelium contribute to ureteric bud form
42 iated removal of beta-catenin from the mouse Wolffian duct epithelium leads to the premature expressi
43 ellular signal-regulated kinase signaling in Wolffian duct epithelium was responsible for the retenti
44 bryonic day 15.5, mutant Mullerian ducts and Wolffian ducts have elongated but their duct tips are en
45 /3 arising too high and 1/3 too low from the Wolffian duct; however, apoptosis was unaltered in E12.5
47 efault because the male reproductive tracts (Wolffian ducts) in the female degenerate owing to a lack
48 es, testosterone promotes differentiation of Wolffian ducts into the epididymis, vas deferens and sem
49 studies have shown that the presence of the Wolffian duct is required for the development and mainte
50 ms due to inductive interactions between the Wolffian duct, its derivative the ureteric bud, and thei
52 eam promoter transcription factor II) in the Wolffian duct mesenchyme became intersex-possessing both
53 ss Ksp-cadherin, including the ureteric bud, Wolffian duct, Mullerian duct, and developing tubules in
54 as Inhba was also expressed in the anterior Wolffian duct of female embryos where no testosterone wa
56 ependently of the bladder, from the ureters, Wolffian ducts or a combination of both; however, these
58 Dmrt1 is expressed in the genital ridge and Wolffian duct prior to sexual differentiation and is exp
60 racts are developed from Mullerian ducts and Wolffian ducts, respectively, involving initiation, elon
62 ated whether Fgfr2 acts specifically in peri-Wolffian duct stroma (ST) to regulate UB induction and d
63 rosine kinase promotes cell movements in the Wolffian duct that give rise to the first ureteric bud t
64 The GFRA1 gene encodes a receptor on the Wolffian duct that regulates ureteric bud outgrowth in t
67 d as the key factor for morphogenesis of the Wolffian duct, the precursor of several male reproductiv
68 ects are due to increased sensitivity of the Wolffian duct to GDNF/RET signaling, and reducing Gdnf g
69 c mesenchyme, activates Ret signaling in the Wolffian duct to initiate the formation of the metanephr
70 ove from their primary insertion site in the Wolffian ducts to the trigone, a muscular structure comp
71 quentially induces an epithelial tubule (the Wolffian duct) to undergo in vitro budding, followed by
73 m from their initial integration site in the Wolffian ducts up to the base of the bladder in a proces
76 pressed in mesenchymal cells surrounding the Wolffian duct (WD) and ureter stalk, whereas bone morpho
78 the morphogenesis and differentiation of the Wolffian duct (WD) into the epididymis, an essential org
79 common nephric ducts (CND), the caudal-most Wolffian duct (WD) segment, depends on Y1015 signals.
82 pted development of the Mullerian ducts (MD)/Wolffian ducts (WD) through multifactorial mechanisms ha
84 use Osr1 was expressed prenatally in MDs and Wolffian ducts (WDs), from rostral to caudal segments, i
85 -dependent cell rearrangements in the caudal Wolffian duct, which generate a specialized epithelial d