Literature DB >> 22503279

Mutations in WNT4 are not responsible for Müllerian duct abnormalities in Chinese women.

Xinyue Chang1, Yingying Qin, Chengyan Xu, Guangyu Li, Xiaoming Zhao, Zi-Jiang Chen.   

Abstract

The WNT4 gene plays a crucial role in sexual differentiation and female genital tract development. This study screened WNT4 for mutation in 189 Chinese women with Müllerian duct abnormalities (10 Mayer-Rokitansky-Küster-Hauser syndrome, five Müllerian aplasia and 174 incomplete Müllerian fusion) and detected no perturbation that would indicate a major role for WNT4. Only one novel synonymous mutation (c.1091G>A) in exon 5 and one known single-nucleotide polymorphism (rs16826648) in exon 2 were found. The results suggest that WNT4 might not contribute to the aetiology of Müllerian duct abnormalities in Chinese women.
Copyright © 2012 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22503279     DOI: 10.1016/j.rbmo.2012.03.008

Source DB:  PubMed          Journal:  Reprod Biomed Online        ISSN: 1472-6483            Impact factor:   3.828


  8 in total

1.  The SNP in the promoter region of the bovine ELOVL5 gene influences economic traits including subcutaneous fat thickness.

Authors:  Hirokazu Matsumoto; Yumiko Shimizu; Atsuko Tanaka; Takuya Nogi; Ichiro Tabuchi; Kenji Oyama; Masaaki Taniguchi; Hideyuki Mannen; Shinji Sasazaki
Journal:  Mol Biol Rep       Date:  2012-12-27       Impact factor: 2.316

Review 2.  Mechanistic Drivers of Müllerian Duct Development and Differentiation Into the Oviduct.

Authors:  Laura Santana Gonzalez; Ioanna A Rota; Mara Artibani; Matteo Morotti; Zhiyuan Hu; Nina Wietek; Abdulkhaliq Alsaadi; Ashwag Albukhari; Tatjana Sauka-Spengler; Ahmed A Ahmed
Journal:  Front Cell Dev Biol       Date:  2021-03-08

3.  Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.

Authors:  Wenqing Ma; Ya Li; Man Wang; Haixia Li; Tiefen Su; Yan Li; Shixuan Wang
Journal:  PLoS One       Date:  2015-06-15       Impact factor: 3.240

4.  Gene expression profile of patients with Mayer-Rokitansky-Küster-Hauser syndrome: new insights into the potential role of developmental pathways.

Authors:  Cristina Nodale; Simona Ceccarelli; Mariateresa Giuliano; Marcella Cammarota; Sirio D'Amici; Enrica Vescarelli; Diana Maffucci; Filippo Bellati; Pierluigi Benedetti Panici; Ferdinando Romano; Antonio Angeloni; Cinzia Marchese
Journal:  PLoS One       Date:  2014-03-07       Impact factor: 3.240

Review 5.  Identification of Genetic Causes in Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome: A Systematic Review of the Literature.

Authors:  Varvara Ermioni Triantafyllidi; Despoina Mavrogianni; Andreas Kalampalikis; Michael Litos; Stella Roidi; Lina Michala
Journal:  Children (Basel)       Date:  2022-06-27

6.  Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies.

Authors:  Ying Zhu; Ruyi Wang; Yun Cheng; Yang Han; Tengyan Li; Yunxia Cao; Binbin Wang
Journal:  Orphanet J Rare Dis       Date:  2021-06-07       Impact factor: 4.123

7.  Disorders of sex development: a genetic study of patients in a multidisciplinary clinic.

Authors:  Luigi Laino; Silvia Majore; Nicoletta Preziosi; Barbara Grammatico; Carmelilia De Bernardo; Salvatore Scommegna; Anna Maria Rapone; Giacinto Marrocco; Irene Bottillo; Paola Grammatico
Journal:  Endocr Connect       Date:  2014-09-23       Impact factor: 3.335

Review 8.  Studying Müllerian duct anomalies - from cataloguing phenotypes to discovering causation.

Authors:  Laura Santana González; Mara Artibani; Ahmed Ashour Ahmed
Journal:  Dis Model Mech       Date:  2021-06-23       Impact factor: 5.758

  8 in total

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