Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG 2 alleles-Reference-Cited by-同舟云学术

Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG 2 alleles

Published:2019-02-27 Issue:3 Volume:7 Page:329-340
ISSN:2047-2919
Container-title:Andrology
language:en
Short-container-title:Andrology

Author:

Yuan P.¹^ORCID,Liang Z. K.¹,Liang H.²,Zheng L. Y.¹,Li D.¹,Li J.¹,Zhang J.³,Tian J.⁴,Lai L. H.²,Zhang K.⁵,He Z. Y.⁵,Zhang Q. X.¹,Wang W. J.¹

Affiliation:

1. IVF Center Department of Obstetrics and Gynecology Sun Yat‐sen Memorial Hospital Sun Yat‐sen University Guangzhou China

2. BNLMS State Key Laboratory for Structural Chemistry of Unstable and Stable Species Peking‐Tsinghua Center for Life Sciences at College of Chemistry and Molecular Engineering, and Center for Quantitative Biology Peking University Beijing China

3. Reproductive Medicine Center Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou China

4. Ultrasonography Department Sun Yat‐sen Memorial Hospital Sun Yat‐sen University Guangzhou China

5. State Key Laboratory of Biocontrol School of Life Sciences Sun Yat‐sen University Guangzhou China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/andr.12592

Reference49 articles.

1. Congenital Bilateral Absence of the Vas Deferens

2. CFTR gene mutations in Japanese individuals with congenital bilateral absence of the vas deferens

3. Recommendations for the classification of diseases as CFTR-related disorders

4. Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

5. Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital unilateral absence of the vas deferens;Journal of Case Reports and Images in Urology;2024-02-13

2. An overview of CFTR mutation profiles and assisted reproductive technology outcomes in Chinese patients with congenital obstructive azoospermia;Journal of Assisted Reproduction and Genetics;2023-12-20

3. Proteomic approach towards identification of seminal fluid biomarkers from individuals with severe oligozoospermia, cryptozoospermia and non-obstructive azoospermia: a pilot study;Translational Andrology and Urology;2023-10

4. Clinical features and microsurgical reconstruction of congenital unilateral absence of the vas deferens with obstructive azoospermia: a tertiary care center experience;Asian Journal of Andrology;2023

5. Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis;Asian Journal of Andrology;2023