139 related articles for article (PubMed ID: 3018358)
1. Lymphoid cell lines as a model system for the study of Wolman's disease: enzymatic, metabolic and ultrastructural investigations.
Nègre A; Salvayre R; Maret A; Vieu C; Bes JC; Borrone C; Durand P; Douste-Blazy L
J Inherit Metab Dis; 1986; 9(2):193-201. PubMed ID: 3018358
[TBL] [Abstract][Full Text] [Related]
2. Enzyme studies on Epstein-Barr virus-transformed lymphoid cell lines from Wolman's disease. Lipases, cholesterol esterase and 4-methylumbelliferyl acyl ester hydrolases.
Negre A; Salvayre R; Durand P; Lenoir G; Douste-Blazy L
Biochim Biophys Acta; 1984 Jun; 794(1):89-95. PubMed ID: 6329310
[TBL] [Abstract][Full Text] [Related]
3. Acid lipase and carboxylesterases in EBV-transformed lymphoid cell line from Wolman's disease: influence of fatty acid structure of substrate.
Negre A; Salvayre R; Vuillaume M; Durand P; Douste-Blazy L
Enzyme; 1984; 31(4):241-6. PubMed ID: 6088221
[TBL] [Abstract][Full Text] [Related]
4. Cholesterol ester and triglyceride metabolism in intact fibroblasts from patients with Wolman's disease and cholesterol ester storage disease.
Burton BK; Remy WT; Rayman L
Pediatr Res; 1984 Dec; 18(12):1242-5. PubMed ID: 6522136
[TBL] [Abstract][Full Text] [Related]
5. Neutral lipid storage with acid lipase deficiency: a new variant of Wolman's disease with features of the Senior syndrome.
Philippart M; Durand P; Borrone C
Pediatr Res; 1982 Nov; 16(11):954-9. PubMed ID: 7155665
[TBL] [Abstract][Full Text] [Related]
6. [Acid lipases and acid cholesterol esterases: Wolman's disease and cholesteryl ester storage disease].
Nègre A; Salvayre R; Douste-Blazy L
Pathol Biol (Paris); 1988 Feb; 36(2):167-81. PubMed ID: 3279387
[TBL] [Abstract][Full Text] [Related]
7. Two cases of cholesteryl ester storage disease (CESD) acid lipase deficiency.
Tylki-Szymanska A; Maciejko D; Wozniewicz B; Muszynska B
Hepatogastroenterology; 1987 Jun; 34(3):98-9. PubMed ID: 3610021
[TBL] [Abstract][Full Text] [Related]
8. [Wolman disease and cholesterol ester storage disease in adults. New means of study and diagnosis].
Salvayre R; Nègre A; Maret A; Radom J; Douste-Blazy L
Ann Biol Clin (Paris); 1986; 44(6):611-7. PubMed ID: 3826777
[TBL] [Abstract][Full Text] [Related]
9. Extracellular origin of the lipid lysosomal storage in cultured fibroblasts from Wolman's disease.
Salvayre R; Negre A; Maret A; Radom J; Douste-Blazy L
Eur J Biochem; 1987 Dec; 170(1-2):453-8. PubMed ID: 3691534
[TBL] [Abstract][Full Text] [Related]
10. Genetic variation of lysosomal acid lipase.
Cortner JA; Coates PM; Swoboda E; Schnatz JD
Pediatr Res; 1976 Nov; 10(11):927-32. PubMed ID: 10546
[TBL] [Abstract][Full Text] [Related]
11. [Hepatic cholesterolosis. Histological, histochemical and ultrastructural study of 2 cases].
Verola O; de Roquancourt A; Chanu B; Rouffy J; Brocheriou C
Sem Hop; 1983 Jun; 59(23):1753-9. PubMed ID: 6308802
[TBL] [Abstract][Full Text] [Related]
12. Lysosomal acid lipase deficiency in rats: lipid analyses and lipase activities in liver and spleen.
Kuriyama M; Yoshida H; Suzuki M; Fujiyama J; Igata A
J Lipid Res; 1990 Sep; 31(9):1605-12. PubMed ID: 2246613
[TBL] [Abstract][Full Text] [Related]
13. New spectrophotometric assays of acid lipase and their use in the diagnosis of Wolman and cholesteryl ester storage diseases.
Nègre A; Salvayre R; Dagan A; Borrone C; Gatt S
Anal Biochem; 1985 Mar; 145(2):398-405. PubMed ID: 4014671
[TBL] [Abstract][Full Text] [Related]
14. Morphological characteristics of lipid accumulation in liver-constituting cells of acid lipase deficiency rats (Wolman's disease model rats).
Kuriwaki K; Yoshida H
Pathol Int; 1999 Apr; 49(4):291-7. PubMed ID: 10365847
[TBL] [Abstract][Full Text] [Related]
15. [Cholesterol ester storage disease in children. Comparative biochemistry of hepatocyte and fibroblast cultures].
Gautier M; Lapous D; Raulin J
Arch Fr Pediatr; 1978 Dec; 35(10 Suppl):38-49. PubMed ID: 749752
[TBL] [Abstract][Full Text] [Related]
16. Expression and functional characterization of human lysosomal acid lipase gene (LIPA) mutation responsible for cholesteryl ester storage disease (CESD) phenotype.
Rajamohan F; Reyes AR; Ruangsiriluk W; Hoth LR; Han S; Caspers N; Tu M; Ward J; Kurumbail RG
Protein Expr Purif; 2015 Jun; 110():22-9. PubMed ID: 25620107
[TBL] [Abstract][Full Text] [Related]
17. Ultrastructural investigations on two lymphoid cell lines from Niemann-Pick disease type B.
Bes JC; Salvayre R; Levade T; Caratero C; Planel H
Biol Cell; 1984; 50(3):299-302. PubMed ID: 6087964
[TBL] [Abstract][Full Text] [Related]
18. Wolman's disease: clinical, biochemical and ultrastructural studies in an unusual case without striking adrenal calcification.
Schaub J; Janka GE; Christomanou H; Sandhoff K; Permanetter W; Hübner G; Meister P
Eur J Pediatr; 1980 Oct; 135(1):45-53. PubMed ID: 7449788
[TBL] [Abstract][Full Text] [Related]
19. Metabolism of pyrenedecanoic acid in Epstein-Barr virus-transformed lymphoid cell lines from normal subjects and from a patient with multisystemic lipid storage myopathy.
Radom J; Salvayre R; Negre A; Douste-Blazy L
Biochim Biophys Acta; 1989 Sep; 1005(2):130-6. PubMed ID: 2550076
[TBL] [Abstract][Full Text] [Related]
20. Partial deficiency of acid lipase with storage of triglycerides and cholesterol esters in liver. Genetic variant of Wolman's disease?
Suzuki Y; Kawai S; Kobayashi A; Ohbe Y; Endo H
Clin Chim Acta; 1976 Jun; 69(2):219-24. PubMed ID: 1277555
[No Abstract] [Full Text] [Related]
[Next] [New Search]
