Literature DB >> 885551

Phosphoglucose isomerase (PGI) variants in the Netherlands.

S G Welch, H A Bartstra, R A Geerdink.   

Abstract

Six hundred individuals of pure Dutch ancestry have been typed for their erythrocyte phosphoglucose isomerase phenotypes by starch gel and cellulose acetate electrophoresis. In two individuals a variant phenotype was discovered. One phenotype was found to be indistinguishable from PGI-Phillips. The other variant would appear to be a new phenotype and has been designated PGI-Jager.

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Year:  1977        PMID： 885551     DOI： 10.1007/bf00393614

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  10 in total

1.  A point mutation increasing the stability of human phosphoglucose isomerase.

Authors:  B E Tilley; R W Gracy; S G Welch
Journal:  J Biol Chem       Date:  1974-07-25       Impact factor: 5.157

2.  Qualitative and quantitative variants of human phosphoglucose isomerase.

Authors:  S G Welch
Journal:  Hum Hered       Date:  1971       Impact factor: 0.444

3.  Inherited variations in human phosphohexose isomerase.

Authors:  J C Detter; P O Ways; E R Giblett; M A Baughan; D A Hopkinson; S Povey; H Harris
Journal:  Ann Hum Genet       Date:  1968-05       Impact factor: 1.670

4.  Phosphoglucose isomerase variation in man.

Authors:  L I Fitch; C W Parr; S G Welch
Journal:  Biochem J       Date:  1968-12       Impact factor: 3.857

5.  Rapid detection of 6-phosphogluconate dehydrogenase variants by electrophoresis on cellulose acetate gel.

Authors:  P Meera Khan; M C Rattazzi
Journal:  Biochem Genet       Date:  1968-11       Impact factor: 1.890

6.  [Formal genetics of phosphoglucose isomerase (EC:5.3.1.9). Studies of a family with PGI-deficiency].

Authors:  G Tariverdian; H Arnold; K G Blume; U Lenkeit; G W Löhr
Journal:  Humangenetik       Date:  1970

7.  Inherited variations in red cell phosphoglucose isomerase among Japanese.

Authors:  T Shinoda
Journal:  Jinrui Idengaku Zasshi       Date:  1970-12

8.  [Populationgenetics of phosphoglucoseisomerase. (EC:5.3.1.9)].

Authors:  G Tariverdian; H Obracaj; H Ritter; G G Wendt
Journal:  Humangenetik       Date:  1971

9.  Occurrence of defective hexosephosphate isomerization in human erythrocytes and leukocytes.

Authors:  D E Paglia; P Holland; M A Baughan; W N Valentine
Journal:  N Engl J Med       Date:  1969-01-09       Impact factor: 91.245

10.  Hereditary hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency--a new enzyme defect of human erythrocytes.

Authors:  M A Baughan; W N Valentine; D E Paglia; P O Ways; E R Simons; Q B DeMarsh
Journal:  Blood       Date:  1968-08       Impact factor: 22.113
  10 in total

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