نتایج جستجو برای: single nucleotide polymorphisms snps

تعداد نتایج: 992379  

Journal: :Annals of medical research 2022

Objective: NRG1 is one of the genes that was reported to have susceptibility alleles effecting phenotype schizophrenia. There are many SNPs (single nucleotide polymorphisms) located in gene with suspected which were associated In this study, we investigated potential associations between schizophrenia and polymorphisms rs4560751 rs3802160. Material Methods: We collected DNA samples 96 patients ...

Journal: :Singmulbullyuhakoeji 2023

We have determined the complete chloroplast genome of <i>Erigeron canadensis</i> isolated in Korea. The circular <i>E. is 152,767 bp long and has four subregions: 84,317 large single-copy 18,446 small regions are separated by 25,004 inverted repeat including 133 genes (88 protein-coding genes, eight rRNAs, 37 tRNAs). Korea differs from Chinese isolate 103 single-nucleotide pol...

Journal: :Egyptian Journal of Medical Human Genetics 2022

Abstract Objective This study was conducted to accomplish a better insight into the impact of single nucleotide polymorphisms (SNPs) nicotinic acetylcholine receptors (nAChR) at risk Alzheimer’s disease (AD) and their possible pathogenicity. Methods We carried out systemic review accessible studies. The case–control studies were assessed by an electronic search international local databases ide...

2017
Fengkai Zhang

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 ...

2017
Fengkai Zhang

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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