Liangliang Fan

Changsha, 410011, China

Last Updated: 09/26/2026

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Found 24 publications

Effects of Thap6 gene knockout on emotional and social behaviors in mice

Effects of Thap6 gene knockout on emotional and social behaviors in mice

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
Published: August 07, 2026

Novel MORC2 variants in Charcot-Marie-Tooth disease type 2Z: genetic and functional insights.

Novel MORC2 variants in Charcot-Marie-Tooth disease type 2Z: genetic and functional insights.

Journal: Frontiers in medicine
Published: April 25, 2026

Research progress of genetic research on POIKTMP syndrome

Research progress of genetic research on POIKTMP syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 31, 2026

Corrigendum to "Accumulation of neutral lipids in dystrophic neurites surrounding amyloid plaques in Alzheimer's disease" [2024 Apr;1870(4):167086.].

Corrigendum to "Accumulation of neutral lipids in dystrophic neurites surrounding amyloid plaques in Alzheimer's disease" [2024 Apr;1870(4):167086.].

Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: March 01, 2026

Bioinformatics analysis of a CLCN5 geneframeshift mutation in a patient with Dent disease.

Bioinformatics analysis of a CLCN5 geneframeshift mutation in a patient with Dent disease.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
Published: September 08, 2025

A Novel LAMA2 Mutation (c.7412G>A) Was Found in a Chinese Patient With Congenital Muscular Dystrophy.

A Novel LAMA2 Mutation (c.7412G>A) Was Found in a Chinese Patient With Congenital Muscular Dystrophy.

Journal: Journal of cellular and molecular medicine
Published: January 13, 2025

Research progress of genetic research on Char syndrome

Research progress of genetic research on Char syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 31, 2024

Identification of a de novo CACNA1B variant and a start-loss ADRA2B variant in paroxysmal kinesigenic dyskinesia.

Identification of a de novo CACNA1B variant and a start-loss ADRA2B variant in paroxysmal kinesigenic dyskinesia.

Journal: Heliyon
Published: November 18, 2023

Accumulation of neutral lipids in dystrophic neurites surrounding amyloid plaques in Alzheimer's disease.

Accumulation of neutral lipids in dystrophic neurites surrounding amyloid plaques in Alzheimer's disease.

Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: November 04, 2023

Identification of a novel MYO1D variant associated with laterality defects, congenital heart diseases, and sperm defects in humans.

Identification of a novel MYO1D variant associated with laterality defects, congenital heart diseases, and sperm defects in humans.

Journal: Frontiers of medicine
Published: August 03, 2023

Haploinsufficiency of Lipin3 leads to hypertriglyceridemia and obesity by disrupting the expression and nucleocytoplasmic localization of Lipin1.

Haploinsufficiency of Lipin3 leads to hypertriglyceridemia and obesity by disrupting the expression and nucleocytoplasmic localization of Lipin1.

Journal: Frontiers of medicine
Published: December 16, 2022

Case report: A de novo Non-sense SOX9 mutation (p.Q417*) located in transactivation domain is Responsible for Campomelic Dysplasia.

Case report: A de novo Non-sense SOX9 mutation (p.Q417*) located in transactivation domain is Responsible for Campomelic Dysplasia.

Journal: Frontiers in pediatrics
Published: November 04, 2022
Showing 1-12 of 24

Last Updated: 09/26/2026