Literature DB >> 7092849

Metabolism of sphingomyelin by intact cultured fibroblasts: differentiation of Niemann-Pick disease type A and B.

A L Beaudet, A A Manschreck.   

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Year:  1982        PMID： 7092849     DOI： 10.1016/s0006-291x(82)80004-1

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN： 0006-291X            Impact factor:   3.575


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  10 in total

1.  A new variant of sphingomyelinase deficiency (Niemann-Pick): visceromegaly, minimal neurological lesions and low in vivo degradation rate of sphingomyelin.

Authors:  M Elleder; J Nevoral; V Spicáková; H Hyniová; J Kraus; J Krásný; M T Vanier
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

2.  High-resolution loading tests in the study of genetic heterogeneity in gangliosidosis fibroblasts.

Authors:  V S Akhunov; T V Mirenburg; X D Krasnopolskaya
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

3.  Uptake and degradation of several pyrenesphingomyelins by skin fibroblasts from control subjects and patients with Niemann-Pick disease. Effect of the structure of the fluorescent fatty acyl residue.

Authors:  T Levade; S Gatt; R Salvayre
Journal:  Biochem J       Date:  1991-04-01       Impact factor: 3.857

4.  Mutations of glucocerebrosidase: discrimination of neurologic and non-neurologic phenotypes of Gaucher disease.

Authors:  E I Ginns; R O Brady; S Pirruccello; C Moore; S Sorrell; F S Furbish; G J Murray; J Tager; J A Barranger
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

5.  The role of sphingomyelin in phosphatidylcholine metabolism in cultured human fibroblasts from control and sphingomyelin lipidosis patients and in Chinese hamster ovary cells.

Authors:  M W Spence; H W Cook; D M Byers; F B Palmer
Journal:  Biochem J       Date:  1990-06-15       Impact factor: 3.857

6.  Deletion of arginine (608) in acid sphingomyelinase is the prevalent mutation among Niemann-Pick disease type B patients from northern Africa.

Authors:  M T Vanier; K Ferlinz; R Rousson; S Duthel; P Louisot; K Sandhoff; K Suzuki
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132

7.  Evidence for both endogenous and exogenous sources of the sphingomyelin storage in lymphoid cell lines from patients with Niemann-Pick disease types A and B.

Authors:  T Levade; R Salvayre; A Maret; L Douste-Blazy
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

8.  A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rate.

Authors:  W Sperl; G Bart; M T Vanier; H Christomanou; I Baldissera; E Steichen-Gersdorf; E Paschke
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

9.  Separation of subcellular compartments containing distinct functional forms of MHC class II.

Authors:  Y Qiu; X Xu; A Wandinger-Ness; D P Dalke; S K Pierce
Journal:  J Cell Biol       Date:  1994-05       Impact factor: 10.539

10.  Sorting of an internalized plasma membrane lipid between recycling and degradative pathways in normal and Niemann-Pick, type A fibroblasts.

Authors:  M Koval; R E Pagano
Journal:  J Cell Biol       Date:  1990-08       Impact factor: 10.539
  10 in total

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