Literature DB >> 6244018

Alpha globin gene number: population and restriction endonuclease studies.

G Brittenham, B Lozoff, J W Harris, Y W Kan, A M Dozy, N V Nayudu.   

Abstract

Restriction endonuclease analysis was used to test a proposed genetic model using alpha-globin gene number to account for the observed distributions of the proportions of hemoglobin (Hb) S in sickle cell trait. In a subsample of specimens collected during a population survey in India, these studies confirmed that the postulated genotype was present in 22 of the 23 individuals examined. In the study population, the number of alpha-globin genes explains about 90% of the variance in the proportion of HbS in sickle cell trait (r2 = 0.895, p less than 10(-10)).

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Year:  1980        PMID: 6244018

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  7 in total

1.  Hemoglobin abnormalities. An evaluation on new-born infants and their mothers in a maternity unit close to Brazzaville (P.R. Congo).

Authors:  M Lallemant; F Galacteros; S Lallemant-Lecoeur; J Feingold; P Carnevale; V Boukila; J Mouchet; J Rosa
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

2.  Alpha thalassaemia in British people.

Authors:  D R Higgs; H Ayyub; J B Clegg; A V Hill; R D Nicholls; H Teal; J S Wainscoat; D J Weatherall
Journal:  Br Med J (Clin Res Ed)       Date:  1985-05-04

3.  Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India.

Authors:  R Fodde; M Losekoot; M H van den Broek; M Oldenburg; N Rashida; A Schreuder; J T Wijnen; P C Giordano; N V Nayudu; P M Khan
Journal:  Hum Genet       Date:  1988-10       Impact factor: 4.132

4.  Some observations on the measurement of haemoglobin A2 and S percentages by high performance liquid chromatography in the presence and absence of alpha thalassaemia.

Authors:  C E Head; M Conroy; M Jarvis; L Phelan; B J Bain
Journal:  J Clin Pathol       Date:  2004-03       Impact factor: 3.411

5.  Genotypic influence of α-deletions on the phenotype of Indian sickle cell anemia patients.

Authors:  Sanjay Pandey; Sweta Pandey; Rahasya Mani Mishra; Monica Sharma; Renu Saxena
Journal:  Korean J Hematol       Date:  2011-09-30

6.  Mechanistic Studies of the Negative Epistatic Malaria-protective Interaction Between Sickle Cell Trait and α+thalassemia.

Authors:  D Herbert Opi; Lucy B Ochola; Metrine Tendwa; Bethsheba R Siddondo; Harold Ocholla; Harry Fanjo; Ashfaq Ghumra; David J P Ferguson; J Alexandra Rowe; Thomas N Williams
Journal:  EBioMedicine       Date:  2014-11-01       Impact factor: 8.143

Review 7.  World distribution, population genetics, and health burden of the hemoglobinopathies.

Authors:  Thomas N Williams; David J Weatherall
Journal:  Cold Spring Harb Perspect Med       Date:  2012-09-01       Impact factor: 6.915

  7 in total

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