Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Sanduo Jiang"'
Publikováno v:
NeuroReport. 16:1023-1026
We investigated insertion (Ins)/deletion(Del) polymorphism in alpha-2-macroglobulin (A2M), G/C variant in the beta-site amyloid precursor protein-cleaving enzyme 1 (BACE1) and apolipoprotein E (APOE) gene epsilon2/epsilon3/epsilon4 polymorphism in 38
Publikováno v:
Molecular Psychiatry. 10:669-677
The etiology of schizophrenia is unclear, although family, twin, and linkage studies implicate genetic factors. Here, we identified adenomatous polyposis coli (APC), a tumor suppressor gene, as a risk factor for schizophrenia. We compared leukocytic
Autor:
Mingyuan Zhang, Sicui Lin, Daming Ren, Kaida Jiang, Ye Zhang, Guomei Tang, Fei Li, Yiping Qian, Dongxiang Wang, Sanduo Jiang
Publikováno v:
American Journal of Medical Genetics. :99-102
Previous studies have suggested the involvement of amyloid precursor protein (APP) in Alzheimer's disease (AD), as exons 16 and 17 of the APP gene mutations have been found in some familial AD patients. Furthermore, overexpression and deposition of t
Publikováno v:
American Journal of Medical Genetics. 105:783-788
Attention-deficit hyperactivity disorder (ADHD) is a prevalent behavioral disorder in children and the etiology of this disorder is not clear. Molecular genetic and pharmacological studies suggest the involvement of dopaminergic and noradrenergic neu
Publikováno v:
American Journal of Medical Genetics. :16-18
Serotonin (5-hydroxytryptamine; 5-HT) is a neurotransmitter that occupies a uniquely important place in neurobiology because of its role in many physiologic processes such as sleep, appetite, thermoregulation, pain perception, hormone secretion, and
Autor:
Yixin Hao, Yinyu Wang, Lishan Chen, Daming Ren, Lin Xu, Hui-jun Xie, Guomei Tang, Hekui Lan, Sanduo Jiang, Dayu Lin, Mingyuan Zhang, Zucheng Wang
Publikováno v:
Neuroscience Letters. 328:195-197
Several lines of evidence have revealed some overlapping pathologies in Alzheimer's disease (AD) and Parkinson's disease (PD). Although the alpha-2 macroglobulin gene (A2M) might be a risk factor of these two neurodegenerative diseases, conclusions f
Publikováno v:
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry. 13(2)
To study the involvement of the N-acylsphingosine amidohydrolase 1 gene (ASAH1) in the susceptibility to schizophrenia in the Han Chinese population.We performed cDNA microarray analysis to exam the gene expression profile in six schizophrenic patien
Autor:
Sanduo Jiang, Yipin Qian, Dongxiang Wang, Niufan Gu, Mingyuan Zhang, Tongguan Jin, Xiaodong Wu, Guomei Tang, Sicui Lin
Publikováno v:
American Journal of Medical Genetics. 96:133-135
We investigated a common signal peptide polymorphism in the α 1-antichymotrypsin (ACT) gene in 125 sporadic Alzheimer disease (AD) patients and 141 healthy control subjects in Chinese Han population. We found no significant difference in the distrib
Publikováno v:
American Journal of Medical Genetics. 96:12-14
To ascertain whether mood disorders, including bipolar and unipolar, are genetically associated with the monoamine oxidase A (MAOA) or monoamine oxidase B (MAOB) gene in the Chinese population, 132 cases of mood disorder and 88 normal controls were g
Publikováno v:
American Journal of Medical Genetics. 88:598-600
From the fact that DXS7 polymorphism is closely related to monoamine oxidase (MAO) genes and MAO inhibitors are widely used in the treatment of unipolar depression, it is of particular interest to study the relationship between the DXS7 polymorphism