Haiou Jiang

No. 492, Jinxi South Road
Huaihua, 418000, China

Last Updated: 09/26/2026

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Found 11 publications

Molecular Dissection of Permanent vs. Reperfused Ischemia: Multi-Omics Divergence and Precision Therapeutic Implications.

Molecular Dissection of Permanent vs. Reperfused Ischemia: Multi-Omics Divergence and Precision Therapeutic Implications.

Journal: Current issues in molecular biology

Published: December 16, 2025

A novel duplication mutation in the MYO7A gene associated with autosomal recessive hearing loss in a Chinese family.

A novel duplication mutation in the MYO7A gene associated with autosomal recessive hearing loss in a Chinese family.

Journal: Genes & genomics

Published: August 25, 2025

Synthesis and multi-target evaluation of 2-(2-phenylethyl)/2,3-styrylchromone derivatives as potential anti-Alzheimer's disease agents.

Synthesis and multi-target evaluation of 2-(2-phenylethyl)/2,3-styrylchromone derivatives as potential anti-Alzheimer's disease agents.

Journal: Molecular diversity

Published: May 07, 2025

Identification of a novel POU4F3 frameshift variant in a Chinese family with autosomal dominant hearing loss.

Identification of a novel POU4F3 frameshift variant in a Chinese family with autosomal dominant hearing loss.

Journal: European journal of medical research

Published: March 20, 2025

Identification of a Novel NF1 Frameshift Variant in a Chinese Family with Neurofibromatosis Type 1.

Identification of a Novel NF1 Frameshift Variant in a Chinese Family with Neurofibromatosis Type 1.

Journal: BioMed research international

Published: August 25, 2019

A novel compound heterozygous mutation in the GJB2 gene is associated with non-syndromic hearing loss in a Chinese family.

A novel compound heterozygous mutation in the GJB2 gene is associated with non-syndromic hearing loss in a Chinese family.

Journal: Bioscience trends

Published: November 27, 2018

11 cases of ichthyosis vulgaris from a family

11 cases of ichthyosis vulgaris from a family

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 10, 2016

Identification of novel compound heterozygous mutations of USH2A gene in a family with Usher syndrome type II

Identification of novel compound heterozygous mutations of USH2A gene in a family with Usher syndrome type II

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: June 04, 2015

Seven patients with congenital finger flexion contracture deformity in a family

Seven patients with congenital finger flexion contracture deformity in a family

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 12, 2015

Eight affected subjects in a Chinese family with autosomal dominant nonsyndromic hearing loss

Eight affected subjects in a Chinese family with autosomal dominant nonsyndromic hearing loss

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 12, 2015

Clinical investigation of a Chinese family with hypotrichosis simplex of the scalp and mutational analysis of CDSN gene

Clinical investigation of a Chinese family with hypotrichosis simplex of the scalp and mutational analysis of CDSN gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: August 10, 2012

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Last Updated: 09/26/2026