Literature DB >> 4430156

Detection of inborn errors of metabolism. III. Defects in urea cycle metabolism.

H Z Hill, S I Goodman.   

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Year:  1974        PMID： 4430156

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


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  6 in total

1.  Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts.

Authors:  R A Gravel; K F Lam; K J Scully; Y Hsia
Journal:  Am J Hum Genet       Date:  1977-07       Impact factor: 11.025

2.  Analysis of genetic complementation by whole-cell microtechniques in fibroblast heterokaryons.

Authors:  R A Gravel; A Leung; M Saunders; P Hösli
Journal:  Proc Natl Acad Sci U S A       Date:  1979-12       Impact factor: 11.205

3.  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

4.  Cell genetic studies on propionyl-CoA carboxylase deficient cell lines.

Authors:  G H Van Leeuwen; G De Vrieze; J A Gimpel; H J Huisjes; F A Hommes
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

5.  Interallelic complementation in an inborn error of metabolism: genetic heterogeneity in argininosuccinate lyase deficiency.

Authors:  R R McInnes; V Shih; S Chilton
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

6.  Argininosuccinic acid synthetase deficiency in a hamster cell line and its complementation of argininosuccinic aciduria human fibroblasts.

Authors:  A González-Noriega; J Verduzco; E Prieto; A Velázquez
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982
  6 in total

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