Bingwu Xiang
Wenzhou, China
Last Updated: 09/26/2026
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Found 8 publications
Identification of biallelic mutations in MCM3AP and comprehensive literature analysis.
Journal: Frontiers in genetics
Published: March 23, 2024
Three intellectual disability-associated de novo mutations in MECP2 identified by trio-WES analysis.
Three intellectual disability-associated de novo mutations in MECP2 identified by trio-WES analysis.
Journal: BMC medical genetics
Published: April 02, 2020
A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia.
Journal: BMC medical genetics
Published: November 01, 2018
Targeted deletion of Insm2 in mice result in reduced insulin secretion and glucose intolerance.
Journal: Journal of translational medicine
Published: September 18, 2018
Identification of novel mutations in the HbF repressor gene BCL11A in patients with autism and intelligence disabilities.
Journal: American journal of hematology
Published: September 04, 2017
Three novel recessive mutations in LAMA2, SYNE1, and TTN are identified in a single case with congenital muscular dystrophy.
Journal: Neuromuscular disorders : NMD
Published: March 05, 2017
Treadmill Exercise Promotes Neurogenesis in Ischemic Rat Brains via Caveolin-1/VEGF Signaling Pathways.
Journal: Neurochemical research
Published: November 12, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026