Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

Motility enhancement of human spermatozoa using electrical stimulation in the nano-Ampere range with enzymatic biofuel cells

(2020) Tai Eun Shin et al.   PLoS One

A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia

(2020) Xiaoqing Ni et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility

(2020) Chunyu Liu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Quantitative High-Speed Video Profiling Discriminates Between DNAH11 and HYDIN Variants of Primary Ciliary Dyskinesia

(2019) Maurizio Chioccioli et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia

(2019) Yanwei Sha et al.   Molecular Genetics & Genomic Medicine

Asthenozoospermia: Cellular and molecular contributing factors and treatment strategies

(2019) Seyedeh Zahra Shahrokhi et al.   ANDROLOGIA

Sperm defects in primary ciliary dyskinesia and related causes of male infertility

(2019) Anu Sironen et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: First results from Turkey

(2019) Nagehan Emiralioğlu et al.   PEDIATRIC PULMONOLOGY

Global, regional, and national prevalence and disability-adjusted life-years for infertility in 195 countries and territories, 1990–2017: results from a global burden of disease study, 2017

(2019) Hui Sun et al.   Aging-US

Fertility and infertility: Definition and epidemiology

(2018) Mélodie Vander Borght et al.   CLINICAL BIOCHEMISTRY

Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus

(2018) Mahmoud R. Fassad et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects

(2018) Niki T. Loges et al.   AMERICAN JOURNAL OF HUMAN GENETICS

DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population

(2017) Yanwei Sha et al.   FERTILITY AND STERILITY

Genes and molecular pathways underpinning ciliopathies

(2017) Jeremy F. Reiter et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Testicular sperm aspiration (TESA) for infertile couples with severe or complete asthenozoospermia

(2017) A. H. Al-Malki et al.   Andrology

European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia

(2016) Jane S. Lucas et al.   EUROPEAN RESPIRATORY JOURNAL

Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals newDNAH1mutations

(2016) Amir Amiri-Yekta et al.   HUMAN REPRODUCTION

Variation in DNAH1 may contribute to primary ciliary dyskinesia

(2015) Faiqa Imtiaz et al.   BMC Medical Genetics

T26248G-transversion mutation in exon7 of the putative methyltransferase Nsun7 gene causes a change in protein folding associated with reduced sperm motility in asthenospermic men

(2015) Nahid Khosronezhad et al.   REPRODUCTION FERTILITY AND DEVELOPMENT

Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella

(2013) Mariem Ben Khelifa et al.   AMERICAN JOURNAL OF HUMAN GENETICS