Shengran Liang

Whole exome sequencing identified a novel <i><scp>DAG</scp>1</i> mutation in a patient with rare, mild and late age of onset muscular dystrophy‐dystroglycanopathy

Yi Dai, Shengran Liang, Xue Dong et al. · Journal of Cellular and Molecular Medicine · 2018 · 106 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Whole Exome Sequencing Identified a Novel Heterozygous Mutation in HMBS Gene in a Chinese Patient With Acute Intermittent Porphyria With Rare Type of Mild Anemia

Yongjiang Zheng, Jiehua Xu, Shengran Liang et al. · Frontiers in Genetics · 2018 · 67 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

An LMNB1 Duplication Caused Adult-Onset Autosomal Dominant Leukodystrophy in Chinese Family: Clinical Manifestations, Neuroradiology and Genetic Diagnosis

Yi Dai, Yaling Ma, Shengde Li et al. · Frontiers in Molecular Neuroscience · 2017 · 18 citations · Full text

Life Sciences, Genetics, Neurology +17

Targeted next generation sequencing identified novel mutations in <i>RPGRIP1</i> associated with both retinitis pigmentosa and Leber’s congenital amaurosis in unrelated Chinese patients

Hui Huang, Ying Wang, Huishuang Chen et al. · Oncotarget · 2017 · 17 citations · Full text

Medicine, Genetics, Molecular Genetics +17

CpG oligodeoxynucleotides enhance chemosensitivity of 5-fluorouracil in HepG2 human hepatoma cells via downregulation of the antiapoptotic factors survivin and livin

Shengran Liang, Guangrui Hu, Lijuan Fang et al. · Cancer Cell International · 2013 · 13 citations · Full text

Medicine, Oncology, Pharmacology +16