Xiaojian Yang

No. 600, Tianhe Road
Guangzhou, 510630, China

Last Updated: 09/26/2026

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Found 11 publications

Florasulam impairs Leydig cell function by blocking autophagic flux and triggering PERK-eIF2α-ATF4-CHOP-mediated ER stress.

Florasulam impairs Leydig cell function by blocking autophagic flux and triggering PERK-eIF2α-ATF4-CHOP-mediated ER stress.

Journal: Ecotoxicology and environmental safety

Published: December 12, 2025

Decoding cytarabine-induced damage in the prepubertal testis: A multi-omics atlas of ecosystem and inheritance.

Decoding cytarabine-induced damage in the prepubertal testis: A multi-omics atlas of ecosystem and inheritance.

Journal: iScience

Published: November 14, 2025

ELOVL2 restrains cell proliferation, migration, and invasion of prostate cancer via regulation of the tumor suppressor INPP4B.

ELOVL2 restrains cell proliferation, migration, and invasion of prostate cancer via regulation of the tumor suppressor INPP4B.

Journal: Cellular signalling

Published: April 07, 2022

Heterogeneous spectrum of CFTR gene mutations in Chinese patients with CAVD and the dilemma of genetic blocking strategy.

Heterogeneous spectrum of CFTR gene mutations in Chinese patients with CAVD and the dilemma of genetic blocking strategy.

Journal: Reproduction (Cambridge, England)

Published: August 07, 2021

Integrative bioinformatics approaches for identifying potential biomarkers and pathways involved in non-obstructive azoospermia.

Integrative bioinformatics approaches for identifying potential biomarkers and pathways involved in non-obstructive azoospermia.

Journal: Translational andrology and urology

Published: February 03, 2021

Long non-coding RNA SNHG8 promotes prostate cancer progression through repressing miR-384 and up-regulating HOXB7.

Long non-coding RNA SNHG8 promotes prostate cancer progression through repressing miR-384 and up-regulating HOXB7.

Journal: The journal of gene medicine

Published: June 13, 2020

Mutation analysis of the cystic fibrosis transmembrane conductance regulator gene in Chinese congenital absence of vas deferens patients.

Mutation analysis of the cystic fibrosis transmembrane conductance regulator gene in Chinese congenital absence of vas deferens patients.

Journal: Gene

Published: April 15, 2020

A novel mutation (-195C>A) in the promoter region of CFTR gene is associated with Chinese Congenital Bilateral Absence of Vas Deferens (CBAVD).

A novel mutation (-195C>A) in the promoter region of CFTR gene is associated with Chinese Congenital Bilateral Absence of Vas Deferens (CBAVD).

Journal: Gene

Published: June 23, 2019

Detection of promoter region of CFTR gene in Chinese congenital bilateral absence of vas deferens

Detection of promoter region of CFTR gene in Chinese congenital bilateral absence of vas deferens

Journal: Zhonghua yi xue za zhi

Published: January 28, 2016

Novel mutations and polymorphisms in the CFTR gene associated with three subtypes of congenital absence of vas deferens.

Novel mutations and polymorphisms in the CFTR gene associated with three subtypes of congenital absence of vas deferens.

Journal: Fertility and sterility

Published: April 06, 2015

Microsurgical varicocelectomy with transfixing of the difficult-to-isolate periarterial vein using microsutures.

Microsurgical varicocelectomy with transfixing of the difficult-to-isolate periarterial vein using microsutures.

Journal: Urology

Published: September 20, 2014

Showing 1-11 of 11

Last Updated: 09/26/2026