نتایج جستجو برای: weinberg disequilibrium p

تعداد نتایج: 1279161  

2017
A. Arbiol-Roca A. Padró-Miquel M. Hueso E. Navarro P. Alía-Ramos M.T. González-Álvarez I. Rama J. Torras J.M. Grinyó J.M. Cruzado N. Lloberas

A long non-coding RNA called ANRIL located on chromosome 9p21.3 has been identified as a novel genetic factor associated with cardiovascular disease. Investigation of several single nucleotide polymorphisms (SNPs) of Noncoding Antisense RNA in the INK4 Locus (ANRIL) gene are of particular interest. This article reports data related to the research article entitled: "Association of ANRIL gene po...

Journal: :Genetics and molecular research : GMR 2015
S G Liu L Ma Q H Cen J S Huang J X Zhang J J Zhang

Genome-wide association studies in several ethnic groups have reported that polymorphisms of the telomerase reverse transcriptase (TERT) and cleft lip and palate transmembrane 1-like (CLPTM1L) genes, located on 5p15.33, are associated with susceptibility to lung cancer. However, whether genetic variants of TERT-CLPTM1L are associated with an increased risk of lung cancer in the Chinese Han popu...

Journal: :Methods in Ecology and Evolution 2021

Linkage disequilibrium (LD) is an important genetic parameter used to infer the diversity of natural populations and their evolutionary history. Traditionally, LD defined as non-random association non-alleles at different loci in gametes for diploids, but has a limited use polyploids. We formulate framework define tetraploid-specific including (a) Hardy–Weinberg disequilibria each locus, (b) co...

Journal: :Conservation Genetics Resources 2021

Largemouth bass (Micropterus salmoides) is an economically important species in China. Contrary to its rapidly increasing yield during the last decades, domestic genetic diversity of largemouth has gradually declined. In this study, 37 single nucleotide polymorphism (SNP) markers were developed based on genotyping-by-sequencing data and characterized by genotyping 32 individuals using PCR–restr...

2013
Na Young Kim Young Ho Kim Ji Wan Park Seung-Hak Baek

The purpose of this study was to investigate the contribution of MSX1 gene to the risk of nonsyndromic cleft lip with or without cleft palate (NS-CL ± P) in the Korean population. The samples consisted of 142 NS-CL ± P families (9 with cleft lip, 26 with cleft lip and alveolus, and 107 with cleft lip and palate; 76 trios and 66 dyads). Three single nucleotide polymorphisms (SNPs: rs3821949, rs1...

2005
ALAN W. MEEROW

Sixteen microsatellite loci isolated from Halesia tetraptera are described. All 16 are polymorphic, with four to 13 alleles across 15–19 members of a single half-sib family. Heterozygosity ranged from 0.067 to 1. One locus departs significantly from Hardy–Weinberg equilibrium in our test family. The test population shows significant heterozygote deficiency at this and two other loci. Thirteen l...

Journal: :Molecular ecology resources 2009
Marloes Poortvliet Jeanine L Olsen Kimberly A Selkoe James A Coyer Giacomo Bernardi

Eleven microsatellites were characterized for Semicossyphus pulcher (California sheephead) using an enrichment protocol. The number of alleles varied from three to 14 for a sample of 40 individuals from two populations. Expected heterozygosities ranged from 0.311 to 0.891. All loci but one were in Hardy-Weinberg equilibrium. No evidence for linkage disequilibrium was observed. These polymorphic...

Journal: :Rheumatology 2005
J S Seo S-S Lee S I Kim W H Ryu K H Sa S U Kim S W Han E J Nam J Y Park W K Lee S Y Kim Y M Kang

OBJECTIVES To investigate the role of polymorphisms of the vascular endothelial growth factor (VEGF) gene in susceptibility to ankylosing spondylitis (AS), and their relationship to clinical features and radiographic severity. METHODS This study included 157 patients with AS and 140 healthy unrelated controls. Polymorphisms of the VEGF gene were analysed by the polymerase chain reaction (PCR)...

Journal: :Human molecular genetics 2007
Xingguang Luo Henry R Kranzler Lingjun Zuo Shuang Wang Nicholas J Schork Joel Gelernter

Drug dependence (DD) is commonly co-morbid with alcohol dependence (AD). Many studies have also shown common genetic risk factors for these disorders. We previously reported associations of AD with seven alcohol dehydrogenase (ADH) genes. The present study examines the relationship between these genes and DD. We genotyped 16 markers within the ADH gene cluster and 38 unlinked ancestry-informati...

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