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[1]Increased RTN3 Leads to Obesity and Hypertriglyceridemia by Interacting with HSPA5[J].Circulation, 2018, 138 (17) : 1828-1838.
[2]Loss of RTN3 phenocopies chronic kidney disease and results in activation of the IGF2-JAK2 pathway in proximal tubular epithelial cells.Exp Mol Med, 54 (5) : 653-661.
[3]Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK-IDH2 pathway.Medcomm, 3 (2) : e226.
[4]A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation[J].QJM: An International Journal of Medicine, 2018, 111 (6) : 373-377.
[5]Novel heterozygous mutation of MCTP2 gene in a patient with coarctation of the aorta.QJM, 115 (3) : 157-159.
[6]A novel nonsense mutation of ABCA8 in a patient with reduced HDL-c levels and atherosclerosis.QJM, 115 (5) : 321-322.
[7]A de novo mutation of SMYD1 (p. F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient[J].Clinical Chemistry and Laboratory Medicine, 2019, 57 (4) : 532-539.
[8]A novel mutation (p.Y24N) in NHP2 leads to idiopathic pulmonary fibrosis and lung carcinoma chronic obstructive lung disease by disrupting the expression and nucleocytoplasmic localization of NHP2.Biochim Biophys Acta Mol Basis Dis, 1869 (5) : 166692.
[9]Haploinsufficiency of syncoilin leads to hypertrophic cardiomyopathy.GENES & DISEASES
[10]The genetic spectrum of familial hypercholesterolemia in the central south region of China[J].Atherosclerosis, 2017, 258: 84-88.
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