Literature DB >> 4673517

Rare GPT-phenotypes in a random sample of Southern Germany: evidence for a third allele.

S Gussmann, F Schwarzfischer.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1972        PMID： 4673517     DOI： 10.1007/bf02079691

Source DB:  PubMed          Journal:  Z Rechtsmed        ISSN： 0044-3433


× No keyword cloud information.
  3 in total

1.  Soluble glutamic-pyruvic transaminase (EC:2.6.1.2): formal genetics and linkage relations.

Authors:  J Kömpf
Journal:  Humangenetik       Date:  1971

2.  Population genetics of soluble glutamic-pyruvic transaminase (EC: 2.6.1.2): gene frequencies in Southwestern Germany.

Authors:  J Kömpf
Journal:  Humangenetik       Date:  1971

3.  Polymorphism of soluble glutamic-pyruvic transaminase: a new genetic marker in man.

Authors:  S H Chen; E R Giblett
Journal:  Science       Date:  1971-07-09       Impact factor: 47.728
  3 in total
  7 in total

1.  Red cell glutamic-pyruvic transaminase gene frequencies in the region of the Po Delta (Ferrara, northern Italy).

Authors:  R Scozzari; G Trippa; C Barberio; P Menini
Journal:  Humangenetik       Date:  1975

2.  Phenotypic distributions of red cell glutamate-pyruvate transaminase (E.C.2.6.1.2) isoenzymes in British and New York populations.

Authors:  S G Welch; P R Mills; R E Gaensslen
Journal:  Humangenetik       Date:  1975

3.  Studies on the polymorphism of the soluble glutamic-pyruvic-transaminase in the population of Northern Bavaria (Germany).

Authors:  D Wiebecke; H D Brackebusch
Journal:  Humangenetik       Date:  1974

4.  [GPT system, with special reference to the silent gene GPT].

Authors:  W Spielmann; P Kühnl; C Rexrodt; G Hänsel
Journal:  Humangenetik       Date:  1973

5.  Population genetics of soluble glutamic-pyruvic-transaminase in North Germans (Lübeck).

Authors:  S Seth
Journal:  Humangenetik       Date:  1974

6.  Two rare GPT phenotypes in a Norwegian family. Evidence of a seventh allele.

Authors:  B Olaisen
Journal:  Humangenetik       Date:  1973-09-20

7.  Polymorphism of alanine aminotransferase (E.C.2.7.6.1): common and rare alleles.

Authors:  J Kömpf; H Ritter
Journal:  Hum Genet       Date:  1979-10-02       Impact factor: 4.132
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.