Article Cited by others

LETTER TO THE EDITOR

Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation

Wang Xiong, Jin Hai-Rong, Cui Yuan-Qing, Chen Jie, Sha Yan-Wei, Gao Zhen-Li

Year : 2018| Volume: 20| Issue : 1 | Page no: 101-102

   This article has been cited by
 
1 The mutation c.346-1G?>?A in SOHLH1 impairs sperm production in the homozygous but not in the heterozygous condition
Mohan Liu, Yihong Yang, Yan Wang, Suren Chen, Ying Shen
Human Molecular Genetics. 2021;
[Pubmed]  [Google Scholar] [DOI]
2 Functional role of piRNAs in animal models and its prospects in aquaculture
Christy Lite,Vasisht Varsh Sridhar,Swati Sriram,Melita Juliet,Aziz Arshad,Jesu Arockiaraj
Reviews in Aquaculture. 2021;
[Pubmed]  [Google Scholar] [DOI]
3 Human testis-expressed (TEX) genes: a review focused on spermatogenesis and male fertility
Hela Bellil,Farah Ghieh,Emeline Hermel,Béatrice Mandon-Pepin,François Vialard
Basic and Clinical Andrology. 2021; 31(1)
[Pubmed]  [Google Scholar] [DOI]
4 Preconception genome medicine: current state and future perspectives to improve infertility diagnosis and reproductive and health outcomes based on individual genomic data
Antonio Capalbo,Maurizio Poli,Antoni Riera-Escamilla,Vallari Shukla,Miya Kudo Høffding,Csilla Krausz,Eva R Hoffmann,Carlos Simon
Human Reproduction Update. 2020;
[Pubmed]  [Google Scholar] [DOI]
5 Novel compound heterozygous DNAAF2 mutations cause primary ciliary dyskinesia in a Han Chinese family
Minghan Sun,Yi Zhang,Yi JiyunYang,Yi Wang,Hao Tan,Hailian Wang,Tiantian Lei,Xiaojie Li,Xiaojian Zhang,Wen Xiong,Ke Dou,Yongxin Ma
Journal of Assisted Reproduction and Genetics. 2020;
[Pubmed]  [Google Scholar] [DOI]
6 Kartagener syndrome
Bi-cui Liu,Ting-xuan Huang,Chun-Tao Liu
The American Journal of the Medical Sciences. 2020;
[Pubmed]  [Google Scholar] [DOI]
7 Dyskinésies ciliaires primitives de l’enfant
S. Blanchon,J.F. Papon,N. Beydon,A. Tamalet,E. Escudier,M. Legendre,G. Thouvenin
Journal de Pédiatrie et de Puériculture. 2020;
[Pubmed]  [Google Scholar] [DOI]
8 TEX15 is an essential executor of MIWI2-directed transposon DNA methylation and silencing
Theresa Schöpp,Ansgar Zoch,Rebecca V. Berrens,Tania Auchynnikava,Yuka Kabayama,Lina Vasiliauskaite,Juri Rappsilber,Robin C. Allshire,Dónal O’Carroll
Nature Communications. 2020; 11(1)
[Pubmed]  [Google Scholar] [DOI]
9 Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes
T. F. Araujo,C. Friedrich,C. H. P. Grangeiro,L. R. Martelli,J. D. Grzesiuk,J. Emich,M. J. Wyrwoll,S. Kliesch,A. L. Simões,F. Tüttelmann
Andrology. 2019;
[Pubmed]  [Google Scholar] [DOI]
10 Loss-of-function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype
Yanwei Sha,Xiong Wang,JinTing Yuan,Xingshen Zhu,Zhiying Su,Xuequan Zhang,Xiaohui Xu,Xiaoli Wei
Clinical Genetics. 2019;
[Pubmed]  [Google Scholar] [DOI]
11 Genetic causes of nonsyndromic forms of azoospermia and severe oligozoospermia in infertility men
O. A. Solovova,V. B. Chernykh
Andrology and Genital Surgery. 2019; 20(2): 16
[Pubmed]  [Google Scholar] [DOI]
12 Novel IFT140 variants cause spermatogenic dysfunction in humans
Xiong Wang,Yan-wei Sha,Wen-ting Wang,Yuan-qing Cui,Jie Chen,Wei Yan,Xiao-tao Hou,Li-bin Mei,Cui-cui Yu,Jiahui Wang
Molecular Genetics & Genomic Medicine. 2019;
[Pubmed]  [Google Scholar] [DOI]
13 SCSA results correlated with rate of motility reduction after ejaculation in Asthenozoospermia
Zohreh Moradian Fard,Majid Naghdi,Peyman Salehi,Seyedeh Zahra Shahrokhi,Ali Ajami,Mohammad Reza Deemeh,Mohammad Hassan Meshkibaf
Andrologia. 2018; : e13146
[Pubmed]  [Google Scholar] [DOI]

 

Read this article