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Genomics publications search

2,677 publications found

Use of Buccal Swabs for Sampling DNA from Nestling and Adult Birds

Methods of DNA extraction and PCR amplification for individual freshwater mussel (Bivalvia Unionidae) glochidia, with the first report of multiple paternity in these organisms

Bartonella DNA in Dog Saliva

Human herpesvirus 6 integrates within telomeric region as evidenced by five different chromosomal sites

DNA Fingerprinting in a Forensic Teaching Experiment.

Rapid Identification of the Mediterranean Fruit Fly (Diptera: Tephritidae) by loop-mediated isothermal amplification

Genetic variation in brain-derived neurotrophic factor and human fear conditioning

Telephone Assessment of Cognitive Function in the Late Onset Alzheimer’s Disease Family Study

Improving Molecular Detection of Fungal DNA in Formalin-Fixed Paraffin-Embedded Tissues: Comparison of Five Tissue DNA Extraction Methods Using Panfungal PCR.

Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals

Fat Distribution, Aerobic Fitness, Blood Lipids, and Insulin Sensitivity in African-American and European-American Women

High-Risk Human Papillomavirus in Esophageal Squamous Cell Carcinoma.

Characterization of Apomictic BC7 and BC8 Pearl Millet: Meiotic Chromosome Behavior and Construction of an ASGR-carrier Chromosome-specific Library

Effects of the adenosine deaminase polymorphism and caffeine intake on sleep parameters in a large population sample

Frequency and Large T (LT) sequence of JC Polyomavirus DNA in oligodendrocytes, astrocytes and granular cells in non-PML Brain

Immunohistochemical and Taqman real-time detection of mycobacterial infections in fish.

Arabidopsis Pht1 ; 5 Mobilizes Phosphate between Source and Sink Organs and Influences the Interaction between Phosphate Homeostasis and Ethylene Signaling.

PIK3CA Mutations May Be Discordant between Primary and Corresponding Metastatic Disease in Breast Cancer

The Lysis-Lysogeny Decision of Bacteriophage 933W: a 933W Repressor-Mediated Long-Distance Loop Has No Role in Regulating 933W PRM Activity.

Direct Recruitment of ERK Cascade Components to Inducible Genes Is Regulated by Heterogeneous Nuclear Ribonucleoprotein (hnRNP) K.

Practical application of self-organizing maps to interrelate biodiversity and functional data in NGS-based metagenomics

Identification of polymorphisms in the malic enzyme 1, NADP (+)-dependent, cytosolic and nuclear receptor subfamily 0, group B, member 2 genes and their associations with meat and carcass quality traits in commercial Angus cattle

PPARγ2 gene Pro12Ala and PPARα gene Leu162Val SNPs interact with dietary intake of fat in determination of plasma lipid concentrations

Variants at chromosome 20 (ASIP locus) and melanoma risk

Fibrillin-1 genotype and risk of prevalent hypertension: A study in two independent populations

Common genetic variants at the 11q13. 3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression

Assessment of the value of a genetic risk score in improving the estimation of coronary risk

Characterization and investigation of zebrafish models of filamin-related myofibrillar myopathy

Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases

Comprehensive Evaluation of the Impact of 14 Genetic Variants on Colorectal Cancer Phenotype and Risk

Identification of candidate genes carrying polymorphisms associated with the risk of colorectal cancer by analyzing the colorectal mutome and microRNAome

Polymorphisms in miRNA binding sites of nucleotide excision repair genes and colorectal cancer risk

SNP discovery using Paired‐End RAD‐tag sequencing on pooled genomic DNA of Sisymbrium austriacum (Brassicaceae)

Application of real-time PCR-based SNP detection for mapping of Net2, a causal D-genome gene for hybrid necrosis in interspecific crosses between tetraploid wheat and Aegilops tauschii

Targeted re‐sequencing of the allohexaploid wheat exome

Variants in the 3′ UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression

Influence of Genetic Variants in Type I Interferon Genes on Melanoma Survival and Therapy

Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot

Interleukin-6 receptor pathways in abdominal aortic aneurysm

Genetic variation in the natriuretic peptide system, circulating natriuretic peptide levels, and blood pressure: an ambulatory blood pressure study

The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis

Variaciones genéticas de TLR2 y asociación con estenosis aórtica degenerativa

Matrix Metalloproteinase-9 Genotype as a Potential Genetic Marker for Abdominal Aortic Aneurysm

Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot

An acenocoumarol dosing algorithm using clinical and pharmacogenetic data in Spanish patients with thromboembolic disease

WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk

Are myocardial infarction–associated single-nucleotide polymorphisms associated with ischemic stroke?

TFPI gene variation and ischemic stroke

The association between genetic variations of CHI3L1, levels of the encoded glycoprotein YKL-40 and the lipid profile in a danish population

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