國家衛生研究院 NHRI:Item 3990099045/3259
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    題名: Chromosomal Abnormalities and Gene Discovery in Schizophrenia
    其他題名: 精神分裂症的細胞遺傳學研究
    作者: Fang, JS;Chen, CH
    貢獻者: Division of Mental Health and Substance Abuse Research
    摘要: Background: Schizophrenia is a complex disease in its clinical aspect, it is also complex in genetic aspect. Hence, schizophrenia can be considered a complex genetic disease. Currently, there are several approaches to investigate the genetic underpinnings of schizophrenia, such as genetic linkage analysis, genome-wide association study, chromosome analysis, and genomic study. Lilerature Reviews: The results from these studies show that schizophrenia can be associated with common variants of many genes, and each gene contributes a small to modest risk to schizophrenia. In addition, schizophrenia can also be associated with rare mutations in a single gene that plays an essential role in brain function. Schizophrenia patients with chromosomal abnormalities belong to this category. The incidence of chromosomal abnormalities in the schizophrenic population is rare, and psychiatrists rarely refer schizophrenia patients for cytogenetic examinations. However, with the progress of molecular genetic technology, the new molecular cytogenetics becomes an important tool to discover genes-associated with schizophrenia. Chromosomal rearrangement is a common biological phenomenon in human genome, which can lead to inversion, translocation, deletion, and duplication of chromosome segments. Some rearrangements can cause diseases including psychiatric disorders. The accurate localization of these regions can help identify the disease-associated genes. Results: There are increasing reports of chromosomal aberrations associated with schizophrenia in the literature, and multiple schizophrenia genes have been identified through these chromosomal aberrations. Furthermore, the recent development of high density array comparative genome hybridization has greatly improved the resolution of conventional karyotype analysis, and studies have shown that this new technology is useful in detecting submicroscopic deletion and duplication in patients with developmental disorder and mental illness. Conclusion: The combination of conventional karyotype examination and new molecular cytogenetic analysis will offer an invaluable opportunity to discover genes associated with schizophrenia, leading to new insights into the pathogenesis of schizophrenia, and to better treatment of patients with schizophrenia in the future.
    日期: 2007-12
    關聯: Taiwanese Journal of Psychiatry. 2007 Dec;21(4):242-253.
    Link to: http://www.airitilibrary.com/searchdetail.aspx?DocIDs=10283684-200712-21-4-242-253-a
    顯示於類別:[陳嘉祥(2009-2013)] 期刊論文

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