Bingwu Xiang

发表

Targeted deletion of Insm2 in mice result in reduced insulin secretion and glucose intolerance

M. Lan, Zhongsheng Sun, Guanjie Chen, 2018, Journal of Translational Medicine.

Identification of novel mutations in the HbF repressor gene BCL11A in patients with autism and intelligence disabilities

Jinchen Li, T. Cai, Zhouwen He, 2017, American journal of hematology.

A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia

T. Cai, Xiang Chen, Haixia Zhang, 2019, BMC Medical Genetics.

Three novel recessive mutations in LAMA2, SYNE1, and TTN are identified in a single case with congenital muscular dystrophy

T. Cai, Xiang Chen, B. Xiang, 2017, Neuromuscular Disorders.

A De novo Loss-of-Function Mutation in PAFAH1B1 Identified in a Single Case with Agyria–Pachygyria Complex

Wei Chen, T. Cai, Xiang Chen, 2019, Journal of Pediatric Neurology.

Treadmill Exercise Promotes Neurogenesis in Ischemic Rat Brains via Caveolin-1/VEGF Signaling Pathways

Chan Liu, Fengxia Tu, Qiongyi Pang, 2016, Neurochemical Research.

Three intellectual disability-associated de novo mutations in MECP2 identified by trio-WES analysis

T. Cai, Xiang Chen, Yi Gu, 2020, BMC Medical Genetics.

Case report: a novel mutation in ZIC2 in an infant with microcephaly, holoprosencephaly, and arachnoid cyst

T. Cai, Xiang Chen, Bingwu Xiang, 2019, Medicine.

Targeted deletion of Insm2 in mice result in reduced insulin secretion and glucose intolerance

M. Lan, Zhongsheng Sun, Guanjie Chen, 2018, Journal of Translational Medicine.