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

Guilmeau, S; Niot, I; Laigneau, J P; Devaud, H; Petit, V; Brousse, N; Bouvier, R; Ferkdadji, L; Besmond, C; Aggerbeck, L P; Bado, A; Samson-Bouma, M E

Guilmeau, S; Niot, I; Laigneau, J P; Devaud, H; Petit, V; Brousse, N; Bouvier, R; Ferkdadji, L; Besmond, C; Aggerbeck, L P; Bado, A; Samson-Bouma, M E.

Affiliation

Guilmeau S; Institut National de la Santé et de la Recherche Médicale (INSERM), U773, Centre de Recherche Bichat Beaujon CRB3, Université Paris 7 Denis Diderot, site Bichat, BP 416, 75018, Paris, France.

Histochem Cell Biol ; 128(2): 115-23, 2007 Aug.

Article in En | MEDLINE | ID: mdl-17605029

Subject(s)

Abetalipoproteinemia/metabolism; Fatty Acid-Binding Proteins/metabolism; Intestinal Mucosa/metabolism; Lipid Metabolism, Inborn Errors/metabolism; Malabsorption Syndromes/metabolism; Abetalipoproteinemia/genetics; Adolescent; Adult; Child; Fatty Acid-Binding Proteins/genetics; Female; Humans; Immunohistochemistry; Lipid Metabolism, Inborn Errors/genetics; Malabsorption Syndromes/genetics; Male; RNA, Messenger/metabolism

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Collection: 01-internacional Database: MEDLINE Main subject: Abetalipoproteinemia / Fatty Acid-Binding Proteins / Intestinal Mucosa / Lipid Metabolism, Inborn Errors / Malabsorption Syndromes Limits: Adolescent / Adult / Child / Female / Humans / Male Language: En Journal: Histochem Cell Biol Journal subject: CITOLOGIA / HISTOCITOQUIMICA Year: 2007 Type: Article Affiliation country: France

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