Literature DB >> 28199199

Association of MAMLD1 single-nucleotide polymorphisms  with hypospadias in Chinese Han population.

Yidong Liu1, Weijing Ye1, Ming Wu1, Yiran Huang2.   

Abstract

Hypospadias is one of the most common congenital malformations among children. Both gene mutations and environmental factors are thought to be involved in the development of hypospadias. The mastermind-like domain-containing 1 gene (MAMLD1, formerly CXorf6) is a new candidate gene and its mutation has been shown in some cases of hypospadias. Here, by direct sequencing of PCR products, we assessed and found mutations that occur in 220 sporadic cases of hypospadias. The mutations p.N589S (c.1766A>G) was found at a significantly higher rate among patients with hypospadias.

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Year:  2017        PMID: 28199199     DOI: 10.2741/4540

Source DB:  PubMed          Journal:  Front Biosci (Landmark Ed)        ISSN: 2768-6698


  4 in total

1.  Single-nucleotide and copy-number variance related to severity of hypospadias.

Authors:  Neetu Singh; Devendra Kumar Gupta; Shilpa Sharma; Dinesh Kumar Sahu; Archana Mishra; Devendra Kumar Yadav; Jiledar Rawat; Arun Kumar Singh
Journal:  Pediatr Surg Int       Date:  2018-08-04       Impact factor: 1.827

2.  A New MAMLD1 Variant in an Infant With Microphallus and Hypospadias With Hormonal Pattern Suggesting Partial Hypogonadotropic Hypogonadism-Case Report.

Authors:  Diego Yeste; Cristina Aguilar-Riera; Gennaro Canestrino; Paula Fernández-Alvarez; María Clemente; Núria Camats-Tarruella
Journal:  Front Endocrinol (Lausanne)       Date:  2022-06-28       Impact factor: 6.055

Review 3.  New frontiers on the molecular underpinnings of hypospadias according to severity.

Authors:  Coriness Piñeyro-Ruiz; Horacio Serrano; Marcos R Pérez-Brayfield; Juan Carlos Jorge
Journal:  Arab J Urol       Date:  2020-05-24

Review 4.  Clinical and molecular spectrum of 46,XY disorders of sex development that harbour MAMLD1 variations: case series and review of literature.

Authors:  Lele Li; Chang Su; Lijun Fan; Fenqi Gao; Xuejun Liang; Chunxiu Gong
Journal:  Orphanet J Rare Dis       Date:  2020-07-20       Impact factor: 4.123

  4 in total

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