نتایج جستجو برای: haplotype frequency

تعداد نتایج: 496718  

2013
Alexandre Dobly Sara Van der Heyden Stefan Roels

In sheep, susceptibility to scrapie is mainly determined by codons 136, 154, and 171 of the PRNP gene. Five haplotypes are usually present (ARR, ARQ, ARH, AHQ, and VRQ). The ARR haplotype confers the greatest resistance to classical scrapie while VRQ renders animals most susceptible. In 2004, the European Union implemented a breeding program that promotes selection of the ARR haplotype while re...

Background: Recurrent Pregnancy Loss (RPL) is a multifactorial disease that affects 1-3% of couples. Since Human Leukocyte Antigen-G (HLA-G) gene is involved in fetal maternal immune tolerance, mutations in the HLA-G gene can affect the success rate of pregnancy. Objective: The present study aims to investigate the haplotype effect of rs1736933 and rs2735022 polymorphisms found in the HLA-G ge...

Journal: :Genetics 2005
Michael T Schouten Christopher K I Williams Chris S Haley

Recent studies have highlighted the dangers of using haplotypes reconstructed directly from population data for a fine-scale mapping analysis. Family data may help resolve ambiguity, yet can be costly to obtain. This study is concerned with the following question: How much family data (if any) should be used to facilitate haplotype reconstruction in a population study? We conduct a simulation s...

Journal: :modares journal of medical sciences: pathobiology 2011
arezou sayad mahdi zamani mohammad taghi akbari feridoon mostafavi anooshirvan kazemnejad

objective: survey of the influence of hla-drb1, -dqb1 alleles, genotypes and haplotypes on age at onset of type 1 diabetes (t1d) in an iranian population materials and methods: 105 iranian t1d patients of different ethnic group and 100 ethnically, age and sex matched individuals were selected from tehran's hospitals and hla-drb, -dqb typing was performed. according to the age at onset of t1d, ...

Journal: :European Journal of Human Genetics 2012

Journal: :Genetics 1990
C Denniston J F Crow

For any set of one- or two-locus genotypic fitnesses there are alternative sets, usually frequency-dependent and often with quite different biological meanings, that give rise to the same equations for change of allele or haplotype frequencies. Therefore, it is not possible to distinguish among alternative fitness models from allele or haplotype frequency trajectories or equilibrium distributio...

Journal: :Human molecular genetics 1996
G Cooper W Amos D Hoffman D C Rubinsztein

To investigate the utility of Y chromosome microsatellites for studying human male-lineage evolution, we typed samples from three populations for five tetranucleotide repeats and an Alu insertion polymorphism. We found very high levels of haplotype diversity and evidence that most mutations involve the gain or loss of only one repeat unit, implying that any given microsatellite haplotype may ha...

Journal: :Genetics 1997
D Durand K Ardlie L Buttel S A Levin L M Silver

The t-haplotype is a chromosomal region in Mus musculus characterized by meiotic drive such that heterozygous males transmit t-bearing chromosomes to roughly 90% of their offspring. Most naturally occurring t-haplotypes express a recessive embryonic lethality, preventing fixation of the t-haplotype. Surprisingly, the t-haplotype occurs in nature as a persistent, low-frequency polymorphism. Earl...

2004
Lei M. Li Jong Hyun Kim Michael S. Waterman Lei Li

In some sequencing projects, the targets contains two homologous chromosomes and our aim is to distinguish between polymorphisms and sequencing errors. Duplication is an important aspect of evolution, and paralogous regions could be mis-aligned together in one assembly. In this case our goal is to unravel duplicated regions. The difficulty lies in the fact that origins of fragments are unknown....

2005
C L Noble E R Nimmo H Drummond L Smith I D R Arnott J Satsangi

Introduction: Recent data have suggested that specific haplotypic variants of the DLG5 gene on chromosome 10q23 may be associated with susceptibility to inflammatory bowel disease (IBD) in Germany. Haplotype D, notably characterised by the presence of a GRA substitution at nucleotide 113, was associated with susceptibility to Crohn’s disease (CD) whereas an extended haplotype A conferred protec...

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