Xiangrong Tang

Chongqing, 400010, China

Last Updated: 09/26/2026

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Found 11 publications

IQUB mutation induces radial spoke 1 deficiency causing asthenozoospermia with normal sperm morphology in humans and mice.

IQUB mutation induces radial spoke 1 deficiency causing asthenozoospermia with normal sperm morphology in humans and mice.

Journal: Cell communication and signaling : CCS

Published: December 03, 2024

DNAH3 deficiency causes flagellar inner dynein arm loss and male infertility in humans and mice.

DNAH3 deficiency causes flagellar inner dynein arm loss and male infertility in humans and mice.

Journal: eLife

Published: November 06, 2024

Patients with mutations in DNAH2, DNAH6 and DNAH10 causing multiple morphological abnormalities of human sperm flagella achieve good ICSI outcomes.

Patients with mutations in DNAH2, DNAH6 and DNAH10 causing multiple morphological abnormalities of human sperm flagella achieve good ICSI outcomes.

Journal: Reproductive biomedicine online

Published: August 08, 2024

Prader-Willi syndrome protein necdin regulates the nucleocytoplasmic distribution and dopaminergic neuron development.

Prader-Willi syndrome protein necdin regulates the nucleocytoplasmic distribution and dopaminergic neuron development.

Journal: Scientific reports

Published: August 08, 2024

Prenatal low-dose Bisphenol A exposure impacts cortical development via cAMP-PKA-CREB pathway in offspring.

Prenatal low-dose Bisphenol A exposure impacts cortical development via cAMP-PKA-CREB pathway in offspring.

Journal: Frontiers in integrative neuroscience

Published: April 18, 2024

Novel variants in DNAH17 cause sperm flagellar outer dynein arm defects but not total fertilization failure after ICSI.

Novel variants in DNAH17 cause sperm flagellar outer dynein arm defects but not total fertilization failure after ICSI.

Journal: Reproductive biomedicine online

Published: April 18, 2024

A novel homozygous LRRC6 mutation causes male infertility with asthenozoospermia and primary ciliary dyskinesia in humans.

A novel homozygous LRRC6 mutation causes male infertility with asthenozoospermia and primary ciliary dyskinesia in humans.

Journal: Andrology

Published: December 07, 2023

Deletion of ACTRT1 is associated with male infertility as sperm acrosomal ultrastructural defects and fertilization failure in human.

Deletion of ACTRT1 is associated with male infertility as sperm acrosomal ultrastructural defects and fertilization failure in human.

Journal: Human reproduction (Oxford, England)

Published: June 06, 2023

Novel biallelic variants in DNAH1 cause multiple morphological abnormalities of sperm flagella with favorable outcomes of fertility after ICSI in Han Chinese males.

Novel biallelic variants in DNAH1 cause multiple morphological abnormalities of sperm flagella with favorable outcomes of fertility after ICSI in Han Chinese males.

Journal: Andrology

Published: May 07, 2023

A novel variant in CFAP69 causes asthenoteratozoospermia with treatable ART outcomes and a literature review.

A novel variant in CFAP69 causes asthenoteratozoospermia with treatable ART outcomes and a literature review.

Journal: Journal of assisted reproduction and genetics

Published: February 09, 2023

FMRP binds Per1 mRNA and downregulates its protein expression in mice.

FMRP binds Per1 mRNA and downregulates its protein expression in mice.

Journal: Molecular brain

Published: January 27, 2023

Showing 1-11 of 11

Last Updated: 09/26/2026