Miao Jiang

NHC Key Laboratory Of Reproductive Health And Medical Genetics & Liaoning Key Laboratory Of Reproductive Health
Shenyang, China

Last Updated: 09/26/2026

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Found 10 publications

MicroRNAs in spermatogenesis dysfunction and male infertility: clinical phenotypes, mechanisms and potential diagnostic biomarkers.

MicroRNAs in spermatogenesis dysfunction and male infertility: clinical phenotypes, mechanisms and potential diagnostic biomarkers.

Journal: Frontiers in endocrinology

Published: September 13, 2023

In vitro enzymatic degradation of the PTMC/cross-linked PEGDA blends.

In vitro enzymatic degradation of the PTMC/cross-linked PEGDA blends.

Journal: Frontiers in bioengineering and biotechnology

Published: July 05, 2023

Growth factors in the treatment of Achilles tendon injury.

Growth factors in the treatment of Achilles tendon injury.

Journal: Frontiers in bioengineering and biotechnology

Published: July 03, 2023

Multimodal imaging findings in a patient with type I sialidosis with a compound heterozygous mutation in the NEU1 gene.

Multimodal imaging findings in a patient with type I sialidosis with a compound heterozygous mutation in the NEU1 gene.

Journal: Quantitative imaging in medicine and surgery

Published: July 21, 2020

A novel c.287G>T NDP missense mutation in a Chinese family with Norrie disease.

A novel c.287G>T NDP missense mutation in a Chinese family with Norrie disease.

Journal: Ophthalmic genetics

Published: May 13, 2020

Increased hydrophobicity of CRYGD p.(Ala159ProfsTer9): Suspected cause of congenital cataracts in a large Chinese family.

Increased hydrophobicity of CRYGD p.(Ala159ProfsTer9): Suspected cause of congenital cataracts in a large Chinese family.

Journal: Molecular genetics & genomic medicine

Published: April 08, 2020

Extremely severe scoliosis, heterotopic ossification, and osteoarthritis in a three-generation family with Crouzon syndrome carrying a mutant c.799T>C FGFR2.

Extremely severe scoliosis, heterotopic ossification, and osteoarthritis in a three-generation family with Crouzon syndrome carrying a mutant c.799T>C FGFR2.

Journal: Molecular genetics & genomic medicine

Published: November 01, 2018

Mutation analysis and first-trimester prenatal diagnosis for a Chinese family with hidrotic ectodermal dysplasia

Mutation analysis and first-trimester prenatal diagnosis for a Chinese family with hidrotic ectodermal dysplasia

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

Published: August 09, 2013

Mutation analysis of CRYBB1 gene and prenatal diagnosis for a Chinese kindred featuring autosomal dominant congenital nuclear cataract

Mutation analysis of CRYBB1 gene and prenatal diagnosis for a Chinese kindred featuring autosomal dominant congenital nuclear cataract

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

Published: June 08, 2013

Detection of ED1 gene mutations in six pedigrees with hypohidrotic ectodermal dysplasia

Detection of ED1 gene mutations in six pedigrees with hypohidrotic ectodermal dysplasia

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

Published: August 10, 2012

Showing 1-10 of 10

Last Updated: 09/26/2026