Xinying Wang

Changsha, 410078, China

Last Updated: 09/26/2026

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Found 13 publications

Gestational NO₂ exposure induces anxiety- and depression-like behaviors in mice via hippocampal PTGDS-PGD2 activation and tryptophan metabolism reprogramming.

Gestational NO₂ exposure induces anxiety- and depression-like behaviors in mice via hippocampal PTGDS-PGD2 activation and tryptophan metabolism reprogramming.

Journal: Neurotoxicology

Published: May 20, 2026

Smart self-assembled peptide-based hydrogels: Mechanism, design and biomedical applications.

Smart self-assembled peptide-based hydrogels: Mechanism, design and biomedical applications.

Journal: Colloids and surfaces. B, Biointerfaces

Published: December 17, 2024

Cry1Δ11 mutation induces ADHD-like symptoms through hyperactive dopamine D1 receptor signaling.

Cry1Δ11 mutation induces ADHD-like symptoms through hyperactive dopamine D1 receptor signaling.

Journal: JCI insight

Published: March 10, 2023

A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.

A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.

Journal: Human molecular genetics

Published: October 08, 2022

ANOS1 variants in a large cohort of Chinese patients with congenital hypogonadotropic hypogonadism.

ANOS1 variants in a large cohort of Chinese patients with congenital hypogonadotropic hypogonadism.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Published: August 30, 2022

SLIT2 Rare Sequencing Variants Identified in Idiopathic Hypogonadotropic Hypogonadism.

SLIT2 Rare Sequencing Variants Identified in Idiopathic Hypogonadotropic Hypogonadism.

Journal: Hormone research in paediatrics

Published: November 25, 2021

Discovery of a Novel Variant of SEMA3A in a Chinese Patient with Isolated Hypogonadotropic Hypogonadism.

Discovery of a Novel Variant of SEMA3A in a Chinese Patient with Isolated Hypogonadotropic Hypogonadism.

Journal: International journal of endocrinology

Published: August 05, 2021

Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism.

Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism.

Journal: Molecular genetics & genomic medicine

Published: June 03, 2021

Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism.

Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism.

Journal: Journal of medical genetics

Published: December 17, 2019

Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism.

Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism.

Journal: European journal of endocrinology

Published: December 14, 2019

Locus-specific DNA methylation of Mecp2 promoter leads to autism-like phenotypes in mice.

Locus-specific DNA methylation of Mecp2 promoter leads to autism-like phenotypes in mice.

Journal: Cell death & disease

Published: October 01, 2019

Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort.

Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 23, 2019

Showing 1-12 of 13

Last Updated: 09/26/2026