Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants.
about
Complex signatures of natural selection at the Duffy blood group locusArchaic African and Asian lineages in the genetic ancestry of modern humansInteraction-based evolution: how natural selection and nonrandom mutation work togetherα-thalassaemiaParallel adaptive divergence among geographically diverse human populations.Autosomal, mtDNA, and Y-chromosome diversity in Amerinds: pre- and post-Columbian patterns of gene flow in South AmericaGenetic variability in response to infection: malaria and after.Beta-thalassemia in the Korean population.Molecular and population genetic analysis of allelic sequence diversity at the human beta-globin locus.A method for fine mapping quantitative trait loci in outbred animal stocks.Beta-globin haplotype analysis suggests that a major source of Malagasy ancestry is derived from Bantu-speaking NegroidsErythrocyte variants and the nature of their malaria protective effect.Environmental Correlation Analysis for Genes Associated with Protection against MalariaEpidemiological profile of common haemoglobinopathies in Arab countriesMolecular analysis of the beta-globin gene cluster in the Niokholo Mandenka population reveals a recent origin of the beta(S) Senegal mutation.Hemoglobinopathies in North Africa: a review.Selection for carriers of recessive diseases: a common phenomenon?Identification of Two Novel β-Thalassemia Mutations (HBB: c.335-346del and HBB: c.108 C > G) in Han Chinese.The course of gastric cancer following surgery is associated with genetic variations of the interleukin-1 receptor antagonist and interleukin-1β.Prevalence of α(+)-Thalassemia in the Scheduled Tribe and Scheduled Caste Populations of Damoh District in Madhya Pradesh, Central India.Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic areaMultiple mutations in a specific gene in a small geographic area: a common phenomenon?Effect of age, gender and calciotropic hormones on the relationship between vitamin D receptor gene polymorphisms and bone mineral density.Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.The spectrum of β-thalassemia mutations in Baghdad, Central Iraq.Global meta-analysis of the C-11377G alteration in the ADIPOQ gene indicates the presence of population-specific effects: challenge for global health initiatives.Factor V Leiden in an Urartian, dating back to 1000 BC.The 'hot-spot' of Hb E [beta26(B8)Glu-->Lys] in Southeast Asia: beta-globin anomalies in the Lao Theung population of southern Laos.Characterization of beta-globin haplotypes using blood spots from a population-based cohort of newborns with homozygous HbS.The role of Factor V Leiden in adult patients with venous thromboembolism: a meta-analysis of published studies from Turkey.Whole-Genome-Sequence-Based Haplotypes Reveal Single Origin of the Sickle Allele during the Holocene Wet PhaseGenotype distribution of the mutations in the coagulation factor V gene in the Korean population: Absence of its association with coronary artery disease
P2860
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P2860
Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Why are some genetic diseases ...... lysis of globin gene variants.
@en
Why are some genetic diseases ...... lysis of globin gene variants.
@nl
type
label
Why are some genetic diseases ...... lysis of globin gene variants.
@en
Why are some genetic diseases ...... lysis of globin gene variants.
@nl
prefLabel
Why are some genetic diseases ...... lysis of globin gene variants.
@en
Why are some genetic diseases ...... lysis of globin gene variants.
@nl
P2093
P356
P1433
P1476
Why are some genetic diseases ...... lysis of globin gene variants.
@en
P2093
P2888
P304
P356
10.1007/BF00222709
P577
1993-03-01T00:00:00Z