Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice

Chaofeng Tu, Jiangshan Cong, Xiaojin He, +23

The American Journal of Human Genetics

InfertilityAndrologyBi-allelic MutationsFertilityGenetics +9

Biallelic mutations in <i>CFAP65</i> lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations

Weili Wang, Chaofeng Tu, Hongchuan Nie, +10

Journal of Medical Genetics

Propranolol induced G0/G1/S phase arrest and apoptosis in melanoma cells via AKT/MAPK pathway

Chengfang Zhou, Xiang Chen, Weiqi Zeng, +15

Oncotarget

Acral MelanomaApoptosisImmunologyCell DeathPharmacotherapy +16

Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD

Chaofeng Tu, Hongchuan Nie, Lanlan Meng, +11

Human Genetics

Cilia BridgeMedicineGeneticsPathogenesisNovel Mutations +8

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis

Weili Wang, Shixong Tian, Hongchuan Nie, +13

Human Molecular Genetics

SpermatogenesisMitochondrial Sheath AssemblyGeneticsCfap65-associated Sperm MalformationMolecular Genetics +17

EBV infection and MSI status significantly influence the clinical outcomes of gastric cancer patients

Hua Shen, Meizuo Zhong, Weili Wang, +10

Clinica Chimica Acta

EpidemiologyCancer-associated VirusGastrointestinal OncologyMedicineClinical Epidemiology +8

Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans

Dongyan Li, Xiaoxuan Yang, Chaofeng Tu, +5

Asian Journal of Andrology

SpermatogenesisGeneticsMolecular BiologySperm Flagellar 2Molecular Genetics +18

An <i>M1AP</i> homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family

Chaofeng Tu, Ying Wang, Hongchuan Nie, +9

Clinical Genetics

GeneticsPathologyMolecular GeneticsDisease Gene IdentificationGenomics +16

Biallelic variants in <i>KCTD19</i> associated with male factor infertility and oligoasthenoteratozoospermia

Weili Wang, Lilan Su, Lanlan Meng, +11

Human Reproduction

A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans

Yong Li, Weili Wang, Chaofeng Tu, +6

Asian Journal of Andrology

SpermatogenesisCytogeneticsGeneticsMolecular GeneticsGenomics +26