Testicular CFTR Splice Variants in Patients with Congenital Absence of the Vas Deferens-Reference-Cited by-同舟云学术

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Testicular CFTR Splice Variants in Patients with Congenital Absence of the Vas Deferens

Published:1998-10-01 Issue:11 Volume:7 Page:1739-1744
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Larriba S.,Bassas L.,Gimenez J.,Ramos M. D.,Segura A.,Nunes V.,Estivill X.,Casals T.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/7/11/1739/6951520/7-11-1739.pdf

Reference38 articles.

1. Identification of the Cystic Fibrosis Gene: Genetic Analysis

2. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

3. Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping

4. Sickly channels in mild disease

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1. A novel role for CFTR interaction with LH and FGF in azoospermia and epididymal maldevelopment caused by cryptorchidism;Basic and Clinical Andrology;2022-06-21

2. Congenital absence of the vas deferens: Cystic fibrosis transmembrane regulatory gene mutations;Best Practice & Research Clinical Endocrinology & Metabolism;2020-12

3. Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations ‐ Evaluated in a cohort of 639 non‐vasectomized azoospermic men;Andrology;2020-11-07

4. A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR;Scientific Reports;2017-10-27

5. Cystic Fibrosis, CFTR Gene, and Male Infertility;Male Infertility: Understanding, Causes and Treatment;2017

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