Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Binghua Dou"'
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundGlutamic acid decarboxylase (GAD) is the rate-limiting enzyme for the synthesis of gamma-aminobutyric acid (GABA), the major inhibitory neurotransmitter in the central nervous system. Antibodies against glutamic acid decarboxylase (GAD) are
Externí odkaz:
https://doaj.org/article/8f3a567a83be41edbff1865ad8035bd0
Autor:
Jing Wu, Mengru Wang, Zhouyang Jiao, Binghua Dou, Bo Li, Jianjiang Zhang, Haohao Zhang, Yue Sun, Xin Tu, Xiangdong Kong, Ying Bai
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Acromesomelic dysplasia, Maroteaux type (AMDM) is a rare skeletal dysplasia characterized by severe disproportionate short stature, short hands and feet, normal intelligence, and facial dysmorphism. Homozygous or compound heterozygous mutations in th
Externí odkaz:
https://doaj.org/article/e763f90f540e45c9a8c685f8a3e18ed5
Oncogenic Long Noncoding RNA DARS-AS1 in Childhood Acute Myeloid Leukemia by Binding to microRNA-425
Autor:
Binghua Dou MM, Zhu Jiang MM, Xiaoguang Chen MM, Chunmei Wang MD, Jing Wu MD, Jindou An MB, Guangyao Sheng MM
Publikováno v:
Technology in Cancer Research & Treatment, Vol 19 (2020)
Objective: Acute myeloid leukemia (AML) represents a hematological cancer. The aim of the investigation was to probe the regulatory relevance of long non-coding RNA (lncRNA) aspartyl-tRNA synthetase anti-sense 1 (DARS-AS1)/microRNA-425 (miR-425)/tran
Externí odkaz:
https://doaj.org/article/fae0d6527ca54ec2acf120b2b59f92dd
Autor:
Jing, Wu, Mengru, Wang, Zhouyang, Jiao, Binghua, Dou, Bo, Li, Jianjiang, Zhang, Haohao, Zhang, Yue, Sun, Xin, Tu, Xiangdong, Kong, Ying, Bai
Publikováno v:
Frontiers in genetics. 13
Acromesomelic dysplasia, Maroteaux type (AMDM) is a rare skeletal dysplasia characterized by severe disproportionate short stature, short hands and feet, normal intelligence, and facial dysmorphism. Homozygous or compound heterozygous mutations in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d06b2db783772c570cea0fbcf3a2291
https://pubmed.ncbi.nlm.nih.gov/35368703
https://pubmed.ncbi.nlm.nih.gov/35368703
[Gene variant analysis of a child presented with neonatal diabetes and multiple organ malformations]
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(12)
To explore the genetic basis for an infant with neonatal diabetes (NDM) and multiple malformations.Genetic variants were detected by next generation sequencing (NGS). Suspected variant was verified by Sanger sequencing.A de novo heterozygous variant,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0421d2140a0f741ec6ab4db2e4d9c86
https://pubmed.ncbi.nlm.nih.gov/33306825
https://pubmed.ncbi.nlm.nih.gov/33306825
Autor:
Jing, Wu, Binghua, Dou, Ge, Meng, Huifang, Wang, Yaqin, Hou, Junke, Xia, Ying, Bai, Xiangdong, Kong
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(8)
To explore the genetic basis for a child with multiple malformation and growth retardation.The child was subjected to low-coverage massively parallel copy number variation sequencing (CNV-seq) based on next generation sequencing (NGS) technique.G-ban
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03967f95c1b910a43657b3f4fdffddb7
https://pubmed.ncbi.nlm.nih.gov/32761594
https://pubmed.ncbi.nlm.nih.gov/32761594