Literature DB >> 4430155

Detection of inborn errors of metabolism. II. Defects in propionic acid metabolism.

H Z Hill, S I Goodman.   

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Year:  1974        PMID： 4430155

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

1.  Propionyl-CoA-carboxylase determination: study of enzyme parameters in cultured skin fibroblasts from enzyme-deficient and normal subjects.

Authors:  P Divry; M O Rolland; N Dingeon; M Mathieu; J Cotte; P Guibaud
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

2.  Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells.

Authors:  H F Willard; L M Ambani; A C Hart; M J Mahoney; L E Rosenberg
Journal:  Hum Genet       Date:  1976-12-15       Impact factor: 4.132

3.  Import of TAT-Conjugated Propionyl Coenzyme A Carboxylase Using Models of Propionic Acidemia.

Authors:  Renata Collard; Tomas Majtan; Insun Park; Jan P Kraus
Journal:  Mol Cell Biol       Date:  2018-02-27       Impact factor: 4.272

4.  Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism.

Authors:  R A Gravel; M J Mahoney; F H Ruddle; L E Rosenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1975-08       Impact factor: 11.205
  4 in total

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