Literature DB >> 11945425

Phosphorylase kinase deficiency in mice.

F Huijing1.   

Abstract

Entities:  

Year:  1970        PMID： 11945425     DOI： 10.1016/0014-5793(70)80465-3

Source DB:  PubMed          Journal:  FEBS Lett        ISSN： 0014-5793            Impact factor:   4.124


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  7 in total

1.  Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency.

Authors:  B Lederer; F Van Hoof; G Van den Berghe; H Hers
Journal:  Biochem J       Date:  1975-04       Impact factor: 3.857

2.  Glycogen-storage disease associated with phosphorylase kinase deficiency: evidence for X inactivation.

Authors:  B R Migeon; F Huijing
Journal:  Am J Hum Genet       Date:  1974-05       Impact factor: 11.025

Review 3.  Glycogen storage diseases in animals and their potential value as models of human disease.

Authors:  H C Walvoort
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

4.  The phosphorylase kinase deficiency (Phk) locus in the mouse: evidence that the mutant allele codes for an enzyme with an abnormal structure.

Authors:  S R Gross; M A Longshore; S Pangburn
Journal:  Biochem Genet       Date:  1975-10       Impact factor: 1.890

5.  X-linked dominant inheritance of partial phosphorylase kinase deficiency in mice.

Authors:  M Varsányi; A Vrbica; L M Heilmeyer
Journal:  Biochem Genet       Date:  1980-04       Impact factor: 1.890

6.  Location of phosphorylase kinase (Phk) in the mouse X chromosome.

Authors:  F Huijing; E M Eicher; D L Coleman
Journal:  Biochem Genet       Date:  1973-06       Impact factor: 1.890

Review 7.  Inherited metabolic disease in laboratory animals: a review.

Authors:  G Bulfield
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982
  7 in total

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