Zobrazeno 1 - 10
of 24
pro vyhledávání: '"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
https://doi.org/10.1146/annurev.nutr.20.1.663
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⟩
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
https://pubmed.ncbi.nlm.nih.gov/17605029
Publikováno v:
Annales d'endocrinologie. 61(2)
Microsomal triglyceride transfer protein (MTP) is a dimeric protein complex consisting of protein disulfide isomerase and a unique 97 kDa subunit. In vitro, MTP accelerates the transport of triglyceride, cholesteryl ester, and phospholipid between ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c75169f2c2c5115e8971dee22ab0faa
https://pubmed.ncbi.nlm.nih.gov/10891663
https://pubmed.ncbi.nlm.nih.gov/10891663
Publikováno v:
Molecular and cellular biology. 17(3)
Cleavage and polyadenylation factor I (CF I) is one of four factors required in vitro for yeast pre-mRNA 3'-end processing. Two protein components of this factor, encoded by genes RNA14 and RNA15, have already been identified. We describe here anothe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26582aa39241e0cc02855cca7018c39f
https://pubmed.ncbi.nlm.nih.gov/9032237
https://pubmed.ncbi.nlm.nih.gov/9032237
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
https://pubmed.ncbi.nlm.nih.gov/8939939
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
https://pubmed.ncbi.nlm.nih.gov/9075328
Autor:
G, Gay, M, Pessah, M E, Bouma, J F, Roche, J P, Aymard, I, Beucler, L P, Aggerbeck, R, Infante
Publikováno v:
La Revue de medecine interne. 11(4)
A familial study of four cases with hypobetalipoproteinemia is reported. Three members are heterozygous and one is homozygous. This congenital fat malabsorption in homozygous state is commonly associated with an absence of serum apoprotein B and LDL.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c194a85f58b00bc703bb154790e7674e
https://pubmed.ncbi.nlm.nih.gov/2096430
https://pubmed.ncbi.nlm.nih.gov/2096430
Autor:
M. Bernard, L. Ferkdadji, Jean Navarro, L. P. Aggerbeck, J.P. Cézard, Michel Peuchmaur, Anne Munck, M. E. Samson-Bouma, I. Beucler
Publikováno v:
Archives de Pédiatrie. 3:1183-1184
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe0fa7081fe6134ff36bb0796dd73d93
https://doi.org/10.1016/s0929-693x(96)89608-4
https://doi.org/10.1016/s0929-693x(96)89608-4
Publikováno v:
Journal of Biological Chemistry. 263:6249-6258
Hydrodynamic, chromatographic, and spectroscopic techniques were used to study the aqueous solution properties of the two structural domains of human apolipoprotein (apo) E3. An amino-terminal thrombolytic fragment of apoE (22 kDa, residues 1-191) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b51fa6fc2b1695e224933c841c68f8b7
https://doi.org/10.1016/s0021-9258(18)68779-4
https://doi.org/10.1016/s0021-9258(18)68779-4
Publikováno v:
Journal of Biological Chemistry. 263:4882-4890
The glycoprotein Ib.IX complex is a major component of the platelet membrane. It mediates the adhesion of platelets to exposed subendothelium and provides an attachment site for the membrane skeleton on the plasma membrane. The present study was desi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e20a4d38aadf82ce72aa4c754b9bd9f
https://doi.org/10.1016/s0021-9258(18)68868-4
https://doi.org/10.1016/s0021-9258(18)68868-4