Results 21 to 30 of about 499,359 (306)

SNP-SNP interactions in breast cancer susceptibility [PDF]

open access: yesBMC Cancer, 2006
AbstractBackgroundBreast cancer predisposition genes identified to date (e.g., BRCA1 and BRCA2) are responsible for less than 5% of all breast cancer cases. Many studies have shown that the cancer risks associated with individual commonly occurring single nucleotide polymorphisms (SNPs) are incremental.
Onay, Venüs Ü   +9 more
openaire   +4 more sources

Relationship of FTO gene variations with NAFLD risk in Chinese men

open access: yesOpen Life Sciences, 2020
Fat mass and obesity-associated (FTO) gene is an obesity susceptibility gene and its relationship with the nonalcoholic fatty liver disease (NAFLD) remains unclear.
Chen Xuefen   +5 more
doaj   +1 more source

A Genome-Wide Association Study To Understand the Effect of Fusarium verticillioides Infection on Seedlings of a Maize Diversity Panel

open access: yesG3: Genes, Genomes, Genetics, 2020
Fusarium verticillioides, which causes ear, kernel and stem rots, has been reported as the most prevalent species on maize worldwide. Kernel infection by F. verticillioides results in reduced seed yield and quality as well as fumonisin contamination, and
Lorenzo Stagnati   +7 more
doaj   +1 more source

Association between GLS Gene Polymorphisms and the Susceptibility to Lung Cancer in the Chinese Han Population

open access: yesFrontiers in Bioscience-Landmark, 2023
Background: Lung cancer is one of the most serious malignant tumors endangering human health and life. This study focused on evaluating the association between single nucleotide polymorphisms (SNPs) of the glutaminase (GLS) and lung cancer susceptibility
Yuhe Wang   +8 more
doaj   +1 more source

A second generation human haplotype map of over 3.1 million SNPs

open access: yesNature, 2007
We describe the Phase II HapMap, which characterizes over 3.1 million human single nucleotide polymorphisms (SNPs) genotyped in 270 individuals from four geographically diverse populations and includes 25–35% of common SNP variation in the populations ...
K. Frazer   +236 more
semanticscholar   +1 more source

DNA methylation and single nucleotide variants in the brain-derived neurotrophic factor (BDNF) and oxytocin receptor (OXTR) genes are associated with anxiety/depression in older women

open access: yesFrontiers in Genetics, 2015
Background: Environmental effects and personal experiences could be expressed in individuals through epigenetic non-structural changes such as DNA methylation. This methylation could up- regulate or down-regulate corresponding gene expressions and modify
Yvon eChagnon   +3 more
doaj   +1 more source

GENETIC VARIATION IN HOST IMMUNE RESPONSE TO MAJOR INFECTIOUS DISEASES IN BOVINES AND ITS APPLICATION IN ANIMAL BREEDING : A REVIEW [PDF]

open access: yesExploratory Animal and Medical Research, 2023
Livestock infectious diseases pose a significant threat to animal health and welfare on a worldwide scale, and efficient management of these diseases is essential for maintaining agronomic health, securing national and international food supply, and ...
Chhaya Rani   +8 more
doaj   +1 more source

SNP-sites: rapid efficient extraction of SNPs from multi-FASTA alignments

open access: yesbioRxiv, 2016
Rapidly decreasing genome sequencing costs have led to a proportionate increase in the number of samples used in prokaryotic population studies. Extracting single nucleotide polymorphisms (SNPs) from a large whole genome alignment is now a routine task ...
A. Page   +6 more
semanticscholar   +1 more source

SNP interaction pattern identifier (SIPI): an intensive search for SNP–SNP interaction patterns [PDF]

open access: yesBioinformatics, 2016
Abstract Motivation Testing SNP–SNP interactions is considered as a key for overcoming bottlenecks of genetic association studies. However, related statistical methods for testing SNP–SNP interactions are underdeveloped.
Hui-Yi Lin   +41 more
openaire   +6 more sources

ErbB polymorphisms: Insights and implications for response to targeted cancer therapeutics

open access: yesFrontiers in Genetics, 2015
Advances in high-throughput genomic-scanning have expanded the repertory of genetic variations in DNA sequences encoding ErbB tyrosine kinase receptors in humans, including single nucleotide polymorphisms (SNPs), polymorphic repetitive elements ...
Moulay A Alaoui-Jamali   +2 more
doaj   +1 more source

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