Literature DB >> 4953285

Hurler's syndrome: demonstration of an inherited disorder of connective tissue in cell culture.

B S Danes, A G Bearn.   

Abstract

Skin fibroblasts from three patients with Hurler's syndrome were grown in tissue culture and shown to contain metachromatic granules when stained for mucopolysaccharides with toluidine blue O. Similar inclusions were observed in cultures of fibroblasts from other members of the families, who appeared to be clinically normal but who were, judged from studies of pedigree, heterozygous or hemizygous for the abnormal gene.

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Year:  1965        PMID: 4953285     DOI: 10.1126/science.149.3687.987

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  21 in total

1.  Neuropsychological deficits in obligatory heterozygotes for metachromatic leukodystrophy.

Authors:  H Kohn; P Manowitz; M Miller; A Kling
Journal:  Hum Genet       Date:  1988-05       Impact factor: 4.132

2.  The mucopolysaccharidoses.

Authors:  C A Pennock; I C Barnes
Journal:  J Med Genet       Date:  1976-06       Impact factor: 6.318

3.  Quantitation of phospholipid analysis using P32 by a digital computer method in metabolic experiments on Niemann-Pick disease.

Authors:  A I Holtz
Journal:  J Am Oil Chem Soc       Date:  1967-02       Impact factor: 1.849

4.  The role of cytochemistry in human genetic research.

Authors:  H Galjaard
Journal:  Histochemistry       Date:  1986

5.  The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide.

Authors:  J C Fratantoni; C W Hall; E F Neufeld
Journal:  Proc Natl Acad Sci U S A       Date:  1968-06       Impact factor: 11.205

6.  The William Allan Memorial Award Lecture: Genetic nosology: three approaches.

Authors:  V A McKusick
Journal:  Am J Hum Genet       Date:  1978-03       Impact factor: 11.025

Review 7.  Adventures in viscous solutions.

Authors:  A Dorfman
Journal:  Mol Cell Biochem       Date:  1974-08-01       Impact factor: 3.396

8.  Serum dependency of cellular phenotype in mucopolysaccharidoses: the influence of autologous serum on metachromasia.

Authors:  L P ten Kate; G J Anders; C J de Groot
Journal:  Humangenetik       Date:  1973-03-23

9.  The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolism.

Authors:  M Cantz; J Gehler
Journal:  Hum Genet       Date:  1976-06-29       Impact factor: 4.132

10.  Simulation of genetic mucopolysaccharidoses in normal human fibroblasts by alteration of pH of the medium.

Authors:  S O Lie; V A McKusick; E F Neufeld
Journal:  Proc Natl Acad Sci U S A       Date:  1972-09       Impact factor: 11.205

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