Výsledky vyhledávání - "M. E. Samson-Bouma"

The Role of the Microsomal Triglygeride Transfer Protein in Abetalipoproteinemia

Autor: M.-E. Samson-Bouma, J. R. Wetterau, Nathalie Berriot-Varoqueaux, L. P. Aggerbeck

Publikováno v: Annual Review of Nutrition. 20:663-697

The microsomal triglyceride transfer protein (MTP) is a dimeric lipid transfer protein consisting of protein disulfide isomerase and a unique 97-kDa subunit. In vitro, MTP accelerates the transport of triglyceride, cholesteryl ester, and phospholipid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45a975b53a2083f91eaf86385bae93db
https://doi.org/10.1146/annurev.nutr.20.1.663

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Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes

Autor: André Bado, Claude Besmond, Sandra Guilmeau, J. P. Laigneau, V. Petit, H. Devaud, L. Ferkdadji, M. E. Samson-Bouma, R. Bouvier, L. P. Aggerbeck, N. Brousse, Isabelle Niot

Publikováno v: Histochemie / Histochemistry Histochimie
Histochemie / Histochemistry Histochimie, 2007, 128 (2), pp.115-23. 〈10.1007/s00418-007-0302-x〉
Histochemie / Histochemistry Histochimie, 2007, 128 (2), pp.115-23. ⟨10.1007/s00418-007-0302-x⟩

We investigated, for the first time, the expression of I- and L-FABP in two very rare hereditary lipid malabsorption syndromes as compared with normal subjects. Abetalipoproteinemia (ABL) and Anderson's disease (AD) are characterized by an inability

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a7155837c5d59a498759816b7a7d75e
https://pubmed.ncbi.nlm.nih.gov/17605029

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A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomerase

Autor: E F, Rehberg, M E, Samson-Bouma, B, Kienzle, L, Blinderman, H, Jamil, J R, Wetterau, L P, Aggerbeck, D A, Gordon

Publikováno v: The Journal of biological chemistry. 271(47)

The microsomal triglyceride transfer protein (MTP) is a heterodimer composed of the ubiquitous multifunctional protein, protein disulfide isomerase, and a unique 97-kDa subunit. Mutations that lead to the absence of a functional 97-kDa subunit cause

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8ecb6c128843a73d675e1bb27b800432
https://pubmed.ncbi.nlm.nih.gov/8939939

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Ultrastructural immunogold labeling of lipid-laden enterocytes from patients with genetic malabsorption syndromes

Autor: M E, Samson-Bouma, N, Verthier, L A, Ginsel, G, Feldmann, J A, Fransen, L P, Aggerbeck

Publikováno v: Biology of the cell. 87(3)

Intestinal biopsies from patients having genetic disorders of lipoprotein assembly and secretion, such as abetalipoproteinemia (ABL) or Anderson's disease (AD), contain large amounts of lipids which are accumulated in the enterocytes. Determination o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fc7e004f5a3010558271630bb0b3ef77
https://pubmed.ncbi.nlm.nih.gov/9075328

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