Candidate Genes and Single Nucleotide Polymorphisms (SNPs) in the Study of Human Disease
نویسندگان
چکیده
منابع مشابه
Candidate Genes and Single Nucleotide Polymorphisms (SNPs) in the Study of Human Disease
The genomic revolution has generated an extraordinary resource, the catalog of variation within the human genome, for investigating biological, evolutionary and medical questions. Together with new, more efficient platforms for high-throughput genotyping, it is possible to begin to dissect genetic contributions to complex trait diseases, specifically examining common variants, such as the singl...
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Introduction: Schizophrenia is a chronic heterogenic neurodevelopment disorder. Many genes interfere in the development of SCZ. All four genes, NrCAM, PRODH, ANK3, and ANKK1, which were evaluated in this study, were previously reported to be associated with Schizophrenia. The NrCAM contributes to creating cognitive deficiencies through the CAM’s signaling pathway. PRODH plays a vital role in cr...
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Lymphedema is abnormal accumulation of interstitial fluid, due to Introduction inefficient uptake and reduced flow, leading to swelling and disability, mostly in the extremities. Hereditary lymphedema usually occurs as an autosomal dominant trait with allelic heterogeneity. We identified single Methods: nucleotide polymorphisms (SNPs) in the FOXC2 gene using dbSNP, analyzed their effect on the ...
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Lymphedema is an abnormal accumulation of interstitial fluid, Introduction due to inefficient uptake and reduced flow, leading to swelling and disability, mostly in the extremities. Hereditary lymphedema usually occurs as an autosomal dominant trait with allelic heterogeneity. : We identified single nucleotide polymorphisms (SNPs) in the FOXC2 Methods gene using dbSNP, analyzed their effect on ...
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ژورنال
عنوان ژورنال: Disease Markers
سال: 2001
ISSN: 0278-0240,1875-8630
DOI: 10.1155/2001/858760