نتایج جستجو برای: snp polymorphism

تعداد نتایج: 116808  

Journal: :Biodiversitas 2023

Abstract. Setyorini YW, Kurnianto E, Sutopo, Sutiyono. 2023. Identification polymorphism of LHR and FSHR genes in Indonesian Holstein dairy cattle associated with productive reproductive traits. Biodiversitas 24: 2898-2905. Luteinizing follicle-stimulating hormones their receptors play an important role the system’s hormonal activity physiological function. This study aimed to identify genotype...

Journal: :archives of medical laboratory sciences 0
hossain hajghani neurology research center, department of neurology, kerman university of medical sciences, kerman, iran soosan bagherzadeh neurology research center, department of neurology, kerman university of medical sciences, kerman, iran hossain-ali ebrahimi neurology research center, department of neurology, kerman university of medical sciences, kerman, iran arezu khosravimashizi maryam nemati motahereh ghazizadeh

background: ccl22 is a chemokine that induces the migration of th2- and regulatory t cells to the inflammatory sites. the aim of this study was to investigate the association of a single nucleotide polymorphism (snp), rs4359426, in ccl22 gene, with multiple sclerosis (ms) in patients from southeast of iran. materials and methods: the blood samples collected from 150 patients with ms and 150 hea...

Journal: :Agronomy 2022

Sclerotinia sclerotiorum is a serious disease of oil crop. The P5CR gene the first reported to be associated with resistance infection in soybeans, and its closest homologs are located on chromosomes A10 C09 Brassica napus. We named these BnP5CR1 BnP5CR2, respectively. purpose this study was examine single-nucleotide polymorphism (SNP) haplotype diversity (Hd) BnP5CR2 among canola cultivars dif...

Journal: :Current issues in molecular biology 2003
Pui-Yan Kwok Xiangning Chen

Single nucleotide polymorphism (SNP) detection technologies are used to scan for new polymorphisms and to determine the allele(s) of a known polymorphism in target sequences. SNP detection technologies have evolved from labor intensive, time consuming, and expensive processes to some of the most highly automated, efficient, and relatively inexpensive methods. Driven by the Human Genome Project,...

2017
Wei-Lin Wu Xue-Wen Feng Chen-Feng Qiu Jing Lin Xian-Jun Bao

Previous studies identified that phosphodiesterase 4D (PDE4D) gene polymorphism might be associated with cerebral infarction or ischemic stroke, and hemorrhagic stroke in human populations. However, as yet, no meta-analysis has revealed any detailed association. We retrospectively reviewed studies regarding the relationship of PDE4D gene polymorphism with ischemic stroke (IS) published during t...

2011
J. A. UJAN H. B. WANG S. A. UJAN

In the present study, we evaluated polymorphism of myogenic factor 5, involved in growth and meat quality traits. Based on PCR-SSCP technology, a novel missense substitution SNP (single-nucleotide polymorphism) g.1142 A > G was identifi ed in the intron1 region of the MyF-5 gene, it causes an amino acid substitution (1142Glutamine/ Glycine1142). Allele frequencies, gene heterozygosity, eff ecti...

Journal: :International heart journal 2015
Jia-Lu Yao Ya-Feng Zhou Xiang-Jun Yang Xiao-Dong Qian Wen-Ping Jiang

To investigate the relationship between KCNN3 SNP (single-nucleotide polymorphism) rs13376333 and risk of atrial fibrillation (AF) and to provide evidence for prevention and treatment for AF.The PubMed, Embase, OVID, Cochrane library, CNKI, and Wan Fang databases were searched to identify studies on the relationship between KCNN3 SNP rs13376333 polymorphism and atrial fibrillation. Two authors ...

2008
Eugene Lin Po See Chen Lung-Cheng Huang Sen-Yen Hsu

Major depressive disorder (MDD) is one of the most common mental disorders worldwide. Single nucleotide polymorphisms (SNPs) can be used in clinical association studies to determine the contribution of genes to drug efficacy. A common SNP in the brain-derived neurotrophic factor (BDNF) gene, a methionine (Met) substitution for valine (Val) at codon 66 (Val66Met), is a candidate SNP for influenc...

Journal: :Genome 2006
Catherine Ravel Sébastien Praud Alain Murigneux Aurélie Canaguier Frédéric Sapet Delphine Samson François Balfourier Philippe Dufour Boulos Chalhoub Dominique Brunel Michel Beckert Gilles Charmet

Information on single-nucleotide polymorphisms (SNPs) in hexaploid bread wheat is still scarce. The goal of this study was to detect SNPs in wheat and examine their frequency. Twenty-six bread wheat lines from different origins worldwide were used. Specific PCR-products were obtained from 21 genes and directly sequenced. SNPs were discovered from the alignment of these sequences. The overall se...

Journal: :Haematologica 2009
Ana I Antón Raúl Teruel Javier Corral Antonia Miñano Irene Martínez-Martínez Adriana Ordóñez Vicente Vicente Beatriz Sánchez-Vega

Genetic factors involved in the interindividual variability of antithrombin have not been identified. We studied two polymorphisms of the gene coding for antithrombin (SER-PINC1) in 298 Spanish Caucasian blood donors: rs3138521, a DNA length polymorphism located on the promoter region and rs2227589, a SNP located on intron 1 that has been described as a mild thrombotic risk factor. We detected ...

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