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Mingtai Wang
Zhengzhou University
4Publications
4H-index
91Citations
Publications 4
Newest
Published on Sep 1, 2005in Archives of Dermatological Research2.31
Qinghe Xing26
Estimated H-index: 26
(CAS: Chinese Academy of Sciences),
Mingtai Wang4
Estimated H-index: 4
(Zhengzhou University)
+ 7 AuthorsLin He56
Estimated H-index: 56
(CAS: Chinese Academy of Sciences)
Dyschromatosis symmetrica hereditaria (DSH [MIM 127400]) is characterized by the presence of hyperpigmented and hypopigmented macules mostly on the dorsal aspects of the extremities. Genetic studies have identified mutations in the ADAR gene, encoding double-stranded RNA-specific adenosine deaminase, to be responsible for this disorder. Here, we found a novel deletion mutation in the ADAR gene, 2929delA, in a Chinese family with DSH. This mutation is located in codon 977 (AGC→GC), and leads to a...
Published on Jul 1, 2005in Human Genetics5.21
Qinghe Xing26
Estimated H-index: 26
(CAS: Chinese Academy of Sciences),
Xiangdong Chen3
Estimated H-index: 3
+ 9 AuthorsJianjun Gao16
Estimated H-index: 16
(CAS: Chinese Academy of Sciences)
Generalized lentiginosis (GL) is characterized by widespread lentigines without associated noncutaneous abnormalities. In this study we performed a genome-wide linkage search in a Chinese family with GL and localized the familial GL locus to chromosome 4q21.1–q22.3, with a maximum two-point LOD score of 3.01 for D4S395 and D4S423 at a recombination fraction of 0. Multipoint analysis (maximum LOD score of 5.08 between markers D4S395 and D4S1563) and haplotype construction showed strong evidence o...
Published on Dec 1, 2003in Schizophrenia Research4.57
Qinghe Xing26
Estimated H-index: 26
(CAS: Chinese Academy of Sciences),
Shengnan Wu9
Estimated H-index: 9
(CAS: Chinese Academy of Sciences)
+ 6 AuthorsLin He56
Estimated H-index: 56
(CAS: Chinese Academy of Sciences)
Abstract Several studies have suggested that the transcriptional activity of the DRD4 gene may exert an important role in susceptibility to schizophrenia. To address this issue, we studied the association of schizophrenia and polymorphisms including −616C>G, −603T>del, −602G>del, 600G>C, −521C>T, −376C>T and a 120 bp tandem duplication polymorphism (120 bp repeat) in 1.2 kb upstream from the initiation codon in the promoter region of the DRD4 gene with 210 schizophrenic cases and 206 healthy con...
Published on Aug 1, 2003in American Journal of Human Genetics9.92
Qinghe Xing26
Estimated H-index: 26
(CAS: Chinese Academy of Sciences),
Xiangdong Chen3
Estimated H-index: 3
+ 8 AuthorsMingtai Wang4
Estimated H-index: 4
(Zhengzhou University)
Dyschromatosis symmetrica hereditaria (DSH) is a hereditary skin disease characterized by the presence of hyperpigmented and hypopigmented macules on extremities and face. The gene, or even its chromosomal location, for DSH has not yet been identified. In this study, two Chinese families with DSH were identified and subjected to a genomewide screen for linkage analysis. Two-point linkage analysis for pedigree A (maximum LOD score [Zmax] = 7.28 at recombination fraction [θ] = 0.00) and pedigree B...
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