Liang-Liang Fan (Liangliang Fan, L-L Fan)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 21

Top Topics

Dna Methylation

Pulmonary Fibrosis

Top Venues

BioMed research international

Disease markers

DNA and cell biology

This page only lists publications with an associated author ORCID identifier.

Publications

Mei-Fang Zhao, Song-Lin Zhang, YangZiYu Xiang, Qian Wang, Gao-Hui Cao, Ping-Ping Zhang, Liang-Liang Fan, Rong Yu, Ya-Li Li
A de novo Mutation (p.Gln277X) of Cyclin D2 is Responsible for a Child with Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome. DNA and cell biology (2024)
Jie-Yuan Jin, Si-Hua Chang, Ya-Qin Chen, Meng-Wei Liu, Yi Dong, Ji-Shi Liu, Qin Wang, Hao Huang, Liang-Liang Fan, Rong Xiang
Reticulon 3 regulates sphingosine-1-phosphate synthesis in endothelial cells to control blood pressure. MedComm 5 (2) (2024)
Jie-Yuan Jin, Si-Hua Chang, Ya-Qin Chen, Meng-Wei Liu, Yi Dong, Ji-Shi Liu, Qin Wang, Hao Huang, Liang-Liang Fan, Rong Xiang
Reticulon 3 regulates sphingosine-1-phosphate synthesis in endothelial cells to control blood pressure. MedComm 5 (2) (2024)
Chen-Yu Wang, Si-Hua Chang, Cheng-Feng Hu, Yi-Qiao Hu, Hong Luo, Lv Liu, Liang-Liang Fan
ZCCHC8 p.P410A disrupts nucleocytoplasmic localization, promoting idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease. Molecular medicine (Cambridge, Mass.) 30 (1) (2024)
Mei-Fang Zhao, Song-Lin Zhang, YangZiYu Xiang, Qian Wang, Gao-Hui Cao, Ping-Ping Zhang, Liang-Liang Fan, Rong Yu, Ya-Li Li
A de novo Mutation (p.Gln277X) of Cyclin D2 is Responsible for a Child with Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome. DNA and cell biology 43 (7) (2024)
Mei-Fang Zhao, Song-Lin Zhang, YangZiYu Xiang, Qian Wang, Gao-Hui Cao, Ping-Ping Zhang, Liang-Liang Fan, Rong Yu, Ya-Li Li
A de novo Mutation (p.Gln277X) of Cyclin D2 is Responsible for a Child with Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome. DNA and cell biology 43 (7) (2024)
Zhao-Jing Lin, Jun-Mei Xu, He-Yu Ji, Ya-Qing Jiang, Jun Su, Liang-Liang Fan, Rong Yu
Silencing MYOT Expression May Inhibit Autophagy in Human Skeletal Muscle Cells. Disease markers 2023 (2023)
Hao Huang, Shuai Guo, Ya-Qin Chen, Yu-Xing Liu, Jie-Yuan Jin, Yun Liang, Liang-Liang Fan, Rong Xiang
Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK-IDH2 pathway. MedComm 4 (2) (2023)
Hao Huang, Shuai Guo, Ya-Qin Chen, Yu-Xing Liu, Jie-Yuan Jin, Yun Liang, Liang-Liang Fan, Rong Xiang
Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK-IDH2 pathway. MedComm 4 (2) (2023)
Zhao-Jing Lin, Jun-Mei Xu, He-Yu Ji, Ya-Qing Jiang, Jun Su, Liang-Liang Fan, Rong Yu
Silencing MYOT Expression May Inhibit Autophagy in Human Skeletal Muscle Cells. Disease markers 2023 (2023)
Zhao-Jing Lin, Jun-Mei Xu, He-Yu Ji, Ya-Qing Jiang, Jun Su, Liang-Liang Fan, Rong Yu
Silencing MYOT Expression May Inhibit Autophagy in Human Skeletal Muscle Cells. Disease markers 2023 (2023)
Liang-Liang Fan, L Liu, C-Y Wang, T Guo, Hong Luo
A novel nonsense mutation of ABCA8 in a patient with reduced HDL-c levels and atherosclerosis. QJM : monthly journal of the Association of Physicians 115 (5) (2022)
Rong Yu, Lv Liu, Ya-Li Li, Liang-Liang Fan
MITF p.Arg217Thr Variant Identified in a Han Chinese Family with Tietz/Waardenburg Syndrome. BioMed research international 2021 (2021)
Yi Dong, Ran Du, Liang-Liang Fan, Jie-Yuan Jin, Hao Huang, Ya-Qin Chen, Dan-Dong Bi, Rong Xiang
Whole-Exome Sequencing Identifies a Novel TRPM4 Mutation in a Chinese Family with Atrioventricular Block. BioMed research international 2021 (2021)
Hao Huang, Yaqin Chen, Jieyuan Jin, Ran Du, Ke Tang, Liang-Liang Fan, Rong Xiang
CSRP3, p.Arg122*, is responsible for hypertrophic cardiomyopathy in a Chinese family. The journal of gene medicine (2021)
Zhuang-Zhuang Yuan, Chen-Yu Wang, Jie-Yuan Jin, Yue Sheng, Mei-Fang Zhao, Liang-Liang Fan, Ai-Qian Zhang
A novel POF1B variant in a Chinese patient is associated with premature ovarian failure. Clinical genetics 100 (6) (2021)
Zhao-Xia Wang, Yi-Hui Liu, Yi Dong, Ya-Li Li, Tie-Yu Tang, Liang-Liang Fan
Whole-Exome Sequencing Identified a Novel Homozygous Frameshift Mutation of HPS3 in a Consanguineous Family with Hermansky-Pudlak Syndrome. BioMed research international 2021 (2021)
Liang-Liang Fan, Lv Liu, Fang-Mei Luo, Ran Du, Chen-Yu Wang, Yi Dong, Ji-Shi Liu
A novel heterozygous variant of the COL4A4 gene in a Chinese family with hematuria and proteinuria leads to focal segmental glomerulosclerosis and chronic kidney disease. Molecular genetics & genomic medicine 8 (12) (2020)
Bo-Da Wu, Yong-Jun Wang, Liang-Liang Fan, Hui Huang, Peng Zhou, Mei Yang, Xiao-Liu Shi
Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome. BioMed research international 2020 (2020)
Jian-Xia Tang, Xiang-Shui Xiao, Kai Wang, Jie-Yuan Jin, Liang-Liang Fan, Rong Xiang
Identification of a Novel Variant of ARHGAP29 in a Chinese Family with Nonsyndromic Cleft Lip and Palate. BioMed research international 2020 (2020)
Cong Ma, Lv Liu, Fang-Na Wang, Hai-Shen Tian, Yan Luo, Rong Yu, Liang-Liang Fan, Ya-Li Li
Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling. BMC medical genetics 20 (1) (2019)