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1 bud, mesonephric tubules, Wolffian duct, and Mullerian duct.
2 equently the non-cell-autonomous loss of the Mullerian duct.
3 , represses the expression of Hoxa-10 in the Mullerian duct.
4 pothesized to occur at its target organ, the Mullerian duct.
5 receptor for beta-catenin activation in the Mullerian duct.
6 lffian duct does not contribute cells to the Mullerian duct.
7 atenin specifically in the mesenchyme of the Mullerian duct.
8 d for the development and maintenance of the Mullerian duct.
9 anephric tubules and caudal extension of the Mullerian duct.
10 in beta-catenin expression in the embryonic Mullerian duct.
11 Lhx1 is expressed in both the Wolffian and Mullerian ducts.
12 ype I receptor for Amh-induced regression of Mullerian ducts.
13 e the specialized epithelia derived from the mullerian ducts.
14 sufficient MIS was produced to eliminate the MUllerian ducts.
15 allows sexually dimorphic development of the Mullerian ducts.
16 s epithelium of the urogenital sinus or from mullerian ducts.
17 t is still responsible for regression of the Mullerian ducts.
18 development) by the former and the uterus by Mullerian ducts.
19 es that are embryologically derived from the Mullerian ducts.
20 two pairs of genital ducts, the Wolffian and Mullerian ducts.
21 o arise from the coelomic epithelium and the Mullerian ducts.
22 ervix and upper vagina, are derived from the Mullerian ducts, a pair of epithelial tubes that form wi
23 ian duct showed that epithelial cells of the Mullerian duct actively migrate along the anterior-poste
25 ession in males causes the regression of the Mullerian ducts, an essential process in male sexual dif
27 ien, Wolffian (mesonephric) ducts instead of Mullerian ducts and sinovaginal bulbs, give rise to the
29 male reproductive tracts are developed from Mullerian ducts and Wolffian ducts, respectively, involv
30 , including the ureteric bud, Wolffian duct, Mullerian duct, and developing tubules in the mesonephro
35 sis reveals that the cells of the developing Mullerian duct are mesoepithelial when deposited, and su
36 ule Wnt-7a fail to undergo regression of the Mullerian duct as a result of the absence of the recepto
39 MRKH) syndrome is a congenital defect of the Mullerian ducts characterized by uterovaginal agenesis a
43 phologic features that resemble those of the mullerian duct-derived epithelia of the reproductive tra
44 inclusion cysts in normal ovaries and in the mullerian duct-derived epithelium of normal fallopian tu
45 en exhibit morphologic features of embryonic Mullerian duct-derived tissue lineages and colonize peri
47 ound that HOX genes, which normally regulate mullerian duct differentiation, are not expressed in nor
51 epubertal testes, promotes involution of the mullerian ducts during normal male sexual differentiatio
54 Mullerian duct epithelium led to a block in Mullerian duct elongation and uterine hypoplasia charact
57 deciding vaginal epithelial cell fate in the Mullerian duct epithelial cells (MDECs) via direct bindi
58 f the tip of the duct; however, migration of Mullerian duct epithelial cells proximal to the tip rema
59 ranscription factor that is essential in the Mullerian duct epithelial progenitor cells for female re
60 genesis in mesenchymal cells adjacent to the Mullerian duct epithelium and in Sertoli and granulosa c
61 3K/AKT signaling pathway is activated in the Mullerian duct epithelium and is required for elongation
62 Cervicovaginal mesenchyme induced p63 in Mullerian duct epithelium and subsequent squamous differ
66 termine the role of Lhx1 specifically in the Mullerian duct epithelium, we performed a Mullerian duct
71 erstanding of the mechanisms contributing to Mullerian duct formation and to the general process of e
81 amic morphological changes in the elongating Mullerian duct in rat urogenital ridges in organ culture
84 iological modifier that causes regression of Mullerian ducts in male embryos, is effective as a singl
85 e (AMH) is responsible for regression of the Mullerian ducts in males during embryonic development.
87 ian epithelial tumors arise from remnants of mullerian ducts in the vicinity of the ovary therefore m
90 ed in the formation and morphogenesis of the Mullerian duct into various parts of the female reproduc
91 r, Wnt-4-mutant females are masculinized-the Mullerian duct is absent while the Wolffian duct continu
95 own as Alk3) in the mesenchymal cells of the Mullerian ducts leads to retention of oviducts and uteri
97 1 (serine threonine kinase 11), in the fetal Mullerian duct mesenchyme (MDM), the caudal remnant of w
98 und that Fzd1 is one receptor present in the Mullerian duct mesenchyme and could be the putative rece
99 conditional deletion of beta-catenin in the Mullerian duct mesenchyme before postnatal differentiati
100 that male-specific Wnt4 expression in mouse Mullerian duct mesenchyme depends upon AMH signaling, im
102 d not affect AMH signaling activation in the Mullerian duct mesenchyme, but did block Mullerian duct
104 bstance (MIS) causes regression of the fetal Mullerian duct on binding a heteromeric complex of types
105 substance (MIS), initiates regression of the Mullerian duct or female reproductive tract anlagen; thi
107 the uterine cervix is derived from the same Mullerian duct precursor as the epithelium of the ovary,
108 hat precursor cells at the caudal tip of the Mullerian duct proliferate to deposit a cord of cells al
109 We were intrigued that both the limb and the Mullerian duct px phenotypes are similar to those caused
111 that beta-catenin mediates AMH signaling for Mullerian duct regression during male sexual differentia
112 Smad proteins that are required in vivo for Mullerian duct regression have not yet been identified.
113 Here, we show that apoptosis occurs during Mullerian duct regression in male embryos beginning at E
119 molecular and cellular mechanisms leading to Mullerian duct regression, the present findings provide
130 he Mullerian duct epithelium, we performed a Mullerian duct-specific knockout study using Wnt7a-Cre m
131 also be a contributing factor in persistent Mullerian duct syndrome, a form of male pseudohermaphrod
133 xpressed by mesenchymal cells underlying the Mullerian duct that are thought to mediate regression of
134 expression, the epithelium of the developing Mullerian duct that gives rise to the oviduct, uterus an
135 nic) and metanephric (adult) kidneys and the Mullerian duct, the anlage of much of the female reprodu
136 e elongation and maintenance of the adjacent Mullerian duct, the anlage of the female reproductive tr
137 e fetal testes and induces regression of the Mullerian ducts, the primordia of the female reproductiv
138 tance (Mis)), which causes regression of the Mullerian ducts, the primordia of the oviducts, uterus a
139 required in both sexes for formation of the Mullerian duct, then Wnt-4 in the developing ovary appea
141 udies indicate that caudal elongation of the Mullerian duct towards the urogenital sinus occurs in pa
143 ive from a pair of tubular structures called Mullerian ducts, which are composed of three elements: a
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