Pengfei Lin

A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42)

Pengfei Lin, Jianwei Li, Qiji Liu et al. · The American Journal of Human Genetics · 2008 · 128 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Clinical features and <i>ETFDH</i> mutation spectrum in a cohort of 90 Chinese patients with late‐onset multiple acyl‐CoA dehydrogenase deficiency

Jianying Xi, Bing Wen, Jie Lin et al. · Journal of Inherited Metabolic Disease · 2013 · 106 citations

Life Sciences, Genetics, Molecular Genetics +10

Glymphatic dysfunction in patients with early-stage amyotrophic lateral sclerosis

Shuangwu Liu, Xiaohan Sun, Qingguo Ren et al. · Brain · 2023 · 76 citations

Life Sciences, Neurology, Neuroscience +15

The β6-integrin-ERK/MAP kinase pathway contributes to chemo resistance in colon cancer

Song Liu, Jian Wang, Weibo Niu et al. · Cancer Letters · 2012 · 60 citations

Medicine, Cell Biology, Oncology +14

Identification of miRNA, lncRNA and mRNA-associated ceRNA networks and potential biomarker for MELAS with mitochondrial DNA A3243G mutation

Wei Wang, Qianqian Zhuang, Kunqian Ji et al. · Scientific Reports · 2017 · 52 citations · Full text

Life Sciences, Genetics, Molecular Biology +17