Literature DB >> 2896

Cobalamins in fibroblasts cultured from normal control subjects and patients with methylmalonic aciduria.

J C Linnell, D M Matthews, S H Mudd, B W Uhlendorf, I J Wise.   

Abstract

The intracellular content and proportional distribution of B12 (cobalamin) derivatives in fibroblasts cultured from patients with various forms of methylmalonic aciduria, as well as from normal control subjects, has been determined by a two-dimensional chromatobioautographic technique. Each line of fibroblasts was grown in the presence of four concentrations of cobalamin, ranging from the 0.04-0.07 pmol/ml contained in the basal medium to 74 pmol/ml (100 ng/ml), added in form of hydroxocobalamin (OH-CHl). Control cells grown in the basal medium contained substantial proportions of both methylcobalamin (MeCbl) and adenysylcobalamin (AdoCbl), with the former predominating. As increasing concentrations of OH-CBl were added to the growth medium, the total cellular cobalamin content increased without marked changes in the relative proportions of MeCbl, AdoCbl, and OH-Cbl. Three different patterns were discernable in the cobalamin distributions of the cells cultured from patients with methylmalonic aciduria (Table 1 and Fig. 1).

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Year:  1976        PMID: 2896     DOI: 10.1203/00006450-197603000-00007

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  8 in total

1.  Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant.

Authors:  H F Willard; I S Mellman; L E Rosenberg
Journal:  Am J Hum Genet       Date:  1978-01       Impact factor: 11.025

2.  Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts.

Authors:  I Mellman; H F Willard; L E Rosenberg
Journal:  J Clin Invest       Date:  1978-11       Impact factor: 14.808

Review 3.  Cobalamin deficiency and related disorders in infancy and childhood.

Authors:  D M Matthews; J C Linnell
Journal:  Eur J Pediatr       Date:  1982-02       Impact factor: 3.183

4.  Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts.

Authors:  H F Willard; L E Rosenberg
Journal:  Biochem Genet       Date:  1979-02       Impact factor: 1.890

5.  Phenotype of disease in three patients with identical mutations in methylmalonyl CoA mutase.

Authors:  A M Crane; L S Martin; D Valle; F D Ledley
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

6.  Binding and uptake of transcobalamin II by human fibroblasts.

Authors:  P Youngdahl-Turner; L E Rosenberg; R H Allen
Journal:  J Clin Invest       Date:  1978-01       Impact factor: 14.808

7.  Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression.

Authors:  H F Willard; L E Rosenberg
Journal:  J Clin Invest       Date:  1980-03       Impact factor: 14.808

8.  Defective adenosylcobalamin synthesis in a case of transcobalamin II deficiency.

Authors:  J C Linnell; E V Quadros; P G Elliott; P Malleson
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

  8 in total

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