Literature DB >> 984045

Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.

A Rinaldi, G Filippi, M Siniscalco.   

Abstract

The distribution of G6PD red blood phenotypes in an unbiased sample of 77 Sardinian certain heterozygotes for the GdMediterranean mutant was found to be skewed in favor of the G6PD (+) cells. Four of these individuals exhibited the normal hemizygous phenotype in all of their cells, but two of them had a mosaic population of G6PD (+) and (-) red blood cells when reexamined after 1 year. These findings suggest that somatic selection may be the main factor determining the phenotype variability of individual somatic cells in highly differentiated tissues of heterozygotes at the G6PD locozygotes for the GdMediterranean mutant should not be used as a criterion for precise estimation of the embryonic or stem tissue cell pool at X inactivation.

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Year:  1976        PMID: 984045      PMCID: PMC1685117     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  17 in total

1.  SURVIVAL OF 51 CR-LABELLED RED CELLS IN SUBJECTS WITH THALASSAEMIA-TRAIT OR G6PD DEFICIENCY OR BOTH ABNORMALITIES.

Authors:  L BERNINI; B LATTE; M SINISCALCO; S PIOMELLI; U SPADA; M ADINOLFI; P L MOLLISON
Journal:  Br J Haematol       Date:  1964-04       Impact factor: 6.998

2.  GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

Authors:  W E NANCE
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1964

3.  SELECTION IN MAMMALIAN MOSAIC CELL POPULATIONS.

Authors:  S M GARTLER; D LINDER
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1964

4.  Studies of Glucose-6-Phosphate Dehydrogenase Activity of Individual Erythrocytes: The Methemoglobin-Elution Test for Identification of Females Heterozygous for G6PD Deficiency.

Authors:  J C Gall; G J Brewer; R J Dern
Journal:  Am J Hum Genet       Date:  1965-07       Impact factor: 11.025

5.  Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type).

Authors:  G Romeo; A Rinaldi; F Urbano; G Filippi
Journal:  Am J Hum Genet       Date:  1976-09       Impact factor: 11.025

6.  Lesch-Nyhan syndrome: absence of the mutant enzyme in erythrocytes of a heterozygote for both normal and mutant hypoxanthine-guanine phosphoribosyl transferase.

Authors:  J A McDonald; W N Kelley
Journal:  Biochem Genet       Date:  1972-02       Impact factor: 1.890

7.  Mosaicism of peripheral blood lymphocyte populations in females heterozygous for the Lesch-Nyhan mutation.

Authors:  R J Albertini; R DeMars
Journal:  Biochem Genet       Date:  1974-05       Impact factor: 1.890

8.  Glucose-6 phosphate dehydrogenase mosaicism: utilization as a tracer in the study of the development of hair root cells.

Authors:  S M Gartler; E Gandini; G Angioni; N Argiolas
Journal:  Ann Hum Genet       Date:  1969-10       Impact factor: 1.670

9.  The haematological effects of glucose-6-phosphate dehydrogenase deficiency and thalassaemia trait: interaction between the two genes at the phenotype level.

Authors:  S Piomelli; M Siniscalco
Journal:  Br J Haematol       Date:  1969-06       Impact factor: 6.998

10.  Glucose-6-phosphate dehydrogenase deficient red cells: resistance to infection by malarial parasites.

Authors:  L Luzzatto; F A Usanga; S Reddy
Journal:  Science       Date:  1969-05-16       Impact factor: 47.728

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  27 in total

1.  Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type).

Authors:  G Romeo; A Rinaldi; F Urbano; G Filippi
Journal:  Am J Hum Genet       Date:  1976-09       Impact factor: 11.025

2.  Triplo-X constitution of mother explains apparent occurrence of two recombinants in sibship segregating at two closely X-linked loci (G6PD and deutan).

Authors:  A Rinaldi; M Velivasakis; B Latte; G Filippi; M Siniscalco
Journal:  Am J Hum Genet       Date:  1978-07       Impact factor: 11.025

3.  On the incidence of unilateral and bilateral colour blindness in heterozygous females.

Authors:  K Feig; H H Ropers
Journal:  Hum Genet       Date:  1978-04-24       Impact factor: 4.132

4.  Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect.

Authors:  M Rocchi; N Archidiacono; A Rinaldi; G Filippi; G Bartolucci; G S Fancello; M Siniscalco
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

5.  Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for rasburicase therapy in the context of G6PD deficiency genotype.

Authors:  M V Relling; E M McDonagh; T Chang; K E Caudle; H L McLeod; C E Haidar; T Klein; L Luzzatto
Journal:  Clin Pharmacol Ther       Date:  2014-05-02       Impact factor: 6.875

6.  X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency.

Authors:  G Filippi; A Rinaldi; G Crisponi; G L Daniels; M Siniscalco
Journal:  J Med Genet       Date:  1979-06       Impact factor: 6.318

7.  Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.

Authors:  A Rinaldi; N Archidiacono; M Rocchi; G Filippi
Journal:  J Med Genet       Date:  1979-06       Impact factor: 6.318

8.  Glucose 6-phosphate dehydrogenase deficiency and incidence of hematologic malignancy.

Authors:  A M Ferraris; G Broccia; T Meloni; G Forteleoni; G F Gaetani
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

9.  Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.

Authors:  G Filippi; P M Mannucci; R Coppola; A Farris; A Rinaldi; M Siniscalco
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

10.  A cell surface abnormality in Duchenne muscular dystrophy: intercellular adhesiveness of skin fibroblasts from patients and carriers.

Authors:  G E Jones; J A Witkowski
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

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