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Search Results - Samson-Bouma, M E
Search Results - Samson-Bouma, M E
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The role of the microsomal triglygeride transfer protein in abetalipoproteinemia
by
BERRIOT-VAROQUEAUX, N
,
AGGERBECK, L. P
,
SAMSON-BOUMA, M.-E
,
WETTERAU, J. R
Published in
Annual review of nutrition
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Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities
by
Silvain, M
,
Bligny, D
,
Aparicio, T
,
Laforêt, P
,
Grodet, A
,
Peretti, N
,
Ménard, D
,
Djouadi, F
,
Jardel, C
,
Bégué, JM
,
Walker, F
,
Schmitz, J
,
Lachaux, A
,
Aggerbeck, LP
,
Samson-Bouma, ME
Published in
Clinical genetics
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Apolipoprotein B production and very low density lipoprotein secretion by calf liver slices
by
Gruffat-Mouty, D
,
Graulet, B
,
Durand, D
,
Samson-Bouma, M.E
,
Bauchart, D
Published in
Journal of biochemistry (Tokyo)
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Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia
by
Di Filippo, Mathilde
,
Moulin, Philippe
,
Roy, Pascal
,
Samson-Bouma, Marie Elisabeth
,
Collardeau-Frachon, Sophie
,
Chebel-Dumont, Sabrina
,
Peretti, Noël
,
Dumortier, Jérôme
,
Zoulim, Fabien
,
Fontanges, Thierry
,
Parini, Rossella
,
Rigoldi, Miriam
,
Furlan, Francesca
,
Mancini, Grazia
,
Bonnefont-Rousselot, Dominique
,
Bruckert, Eric
,
Schmitz, Jacques
,
Scoazec, Jean Yves
,
Charrière, Sybil
,
Villar-Fimbel, Sylvie
,
Gottrand, Frederic
,
Dubern, Béatrice
,
Doummar, Diane
,
Joly, Francesca
,
Liard-Meillon, Marie Elisabeth
,
Lachaux, Alain
,
Sassolas, Agnès
Published in
Journal of hepatology
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Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes
by
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
Published in
Histochemistry and cell biology
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Postprandial lipid absorption in seven heterozygous carriers of deleterious variants of MTTP in two abetalipoproteinemic families
by
Di Filippo, Mathilde
,
Varret, Mathilde
,
Boehm, Vanessa
,
Rabès, Jean-Pierre
,
Ferkdadji, Latifa
,
Abramowitz, Laurent
,
Dumont, Sabrina
,
Lenaerts, Catherine
,
Boileau, Catherine
,
Joly, Francisca
,
Schmitz, Jacques
,
Samson-Bouma, Marie-Elisabeth
,
Bonnefont-Rousselot, Dominique
Published in
Journal of clinical lipidology
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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 w...
by
Rehberg, E F
,
Samson-Bouma, M E
,
Kienzle, B
,
Blinderman, L
,
Jamil, H
,
Wetterau, J R
,
Aggerbeck, L P
,
Gordon, D A
Published in
The Journal of biological chemistry
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Effects of dietary coconut oil on apolipoprotein B synthesis and VLDL secretion by calf liver slices
by
Gruffat-mouty, Dominique
,
Graulet, Benoît
,
Durand, Denys
,
Samson-Bouma, Marie Elisabeth
,
Bauchart, Dominique
Published in
British journal of nutrition
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Ultrastructural immunogold labeling of lipid-laden enterocytes from patients with genetic malabsorption syndromes
by
Samson-Bouma, Marie-Elisabeth
,
Verthier, Nicole
,
Ginsel, Leo A
,
Feldmann, Gérard
,
Fransen, Jack AM
,
Aggerbeck, Lawrence P
Published in
Biology of the cell
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43 NEW GAIN OF FUNCTIONS MUTATIONS IN PCSK9 AND THEIR IMPACT IN FAMILIAL HYPERCHOLESTEROLEMIA
by
AbiFadel, M.
,
Rabès, J.-P.
,
Guérin, M.
,
Carreau, V.
,
Carrié, A.
,
Varret, M.
,
Samson-Bouma, M.-E.
,
Tosolini, L.
,
Erlich, D.
,
Couvert, P.
,
Bonnefont-Rousselot, D.
,
Bruckert, E.
,
Prat, A.
,
Seidah, N.
,
Boileau, C.
Published in
Atherosclerosis. Supplements
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MS91 PCSK9: FROM GENE AND VARIANTS TO PROTEIN AND PLASMA LEVELS
by
AbiFadel, M.
,
Rabès, J.-P.
,
Varret, M.
,
Samson-Bouma, M.-E.
,
Bruckert, E.
,
Devillers, M.
,
Carreau, V.
,
Tosolini, L.
,
Marduel, M.
,
Marques, A.
,
Couvert, P.
,
Bonnefont-Rousselot, D.
,
Guérin, M.
,
Carrié, A.
,
Prat, A.
,
Seidah, N.
,
Boileau, C.
Published in
Atherosclerosis. Supplements
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SFP-P057 – Hépatologie, gastro-entérologie et nutrition – La maladie d’Anderson : identification d’une nouvelle mutation du gène SARA2
by
Georges, A.
,
Varret, M.
,
Bonnefont-Rousselot, D.
,
Champigneulle, J.
,
Guedenet, J.-C.
,
Abifadel, M.
,
Rabes, J.-P.
,
Bruckert, E.
,
Boileau, C.
,
Bouma-Samson, M.E.
,
Morali, A.
Published in
Archives de pédiatrie : organe officiel de la Société française de pédiatrie
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