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L P Aggerbeck

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Journal of Molecular Biology|July 5, 1988
Crystallization and preliminary X-ray diffraction studies on the amino-terminal (receptor-binding) domain of human apolipoprotein E3 from serum very low density lipoproteinsL P Aggerbeck, J R Wetterau, K H Weisgraber, et al.
The Journal of Biological Chemistry|May 5, 1988
Human apolipoprotein E3 in aqueous solution. II. Properties of the amino- and carboxyl-terminal domainsL P Aggerbeck, J R Wetterau, K H Weisgraber, et al.
Biology of the Cell|January 1, 1996
Ultrastructural immunogold labeling of lipid-laden enterocytes from patients with genetic malabsorption syndromesM E Samson-Bouma, N Verthier, L A Ginsel, et al.
La Revue De Medecine Interne|July 1, 1990
[Familial hypobetalipoproteinemia. Familial study of 4 cases]G Gay, M Pessah, M E Bouma, et al.
The Journal of Biological Chemistry|November 22, 1996
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 isomeraseE F Rehberg, M E Samson-Bouma, B Kienzle, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 16, 1999
Anderson's disease: exclusion of apolipoprotein and intracellular lipid transport genesA H Dannoura, N Berriot-Varoqueaux, P Amati, et al.
Science (New York, N.Y.)|November 6, 1992
Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemiaJ R Wetterau, L P Aggerbeck, M E Bouma, et al.
Gastroenterology|October 26, 2001
Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's diseaseN Berriot-Varoqueaux, A H Dannoura, A Moreau, et al.
Histochemistry and Cell Biology|July 3, 2007
Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromesS Guilmeau, I Niot, J P Laigneau, et al.
Clinical Genetics|September 13, 2008
Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalitiesM Silvain, D Bligny, T Aparicio, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Journal of Molecular Biology|July 5, 1988
Crystallization and preliminary X-ray diffraction studies on the amino-terminal (receptor-binding) domain of human apolipoprotein E3 from serum very low density lipoproteinsL P Aggerbeck, J R Wetterau, K H Weisgraber, et al.
The Journal of Biological Chemistry|May 5, 1988
Human apolipoprotein E3 in aqueous solution. II. Properties of the amino- and carboxyl-terminal domainsL P Aggerbeck, J R Wetterau, K H Weisgraber, et al.
Biology of the Cell|January 1, 1996
Ultrastructural immunogold labeling of lipid-laden enterocytes from patients with genetic malabsorption syndromesM E Samson-Bouma, N Verthier, L A Ginsel, et al.
La Revue De Medecine Interne|July 1, 1990
[Familial hypobetalipoproteinemia. Familial study of 4 cases]G Gay, M Pessah, M E Bouma, et al.
The Journal of Biological Chemistry|November 22, 1996
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 isomeraseE F Rehberg, M E Samson-Bouma, B Kienzle, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 16, 1999
Anderson's disease: exclusion of apolipoprotein and intracellular lipid transport genesA H Dannoura, N Berriot-Varoqueaux, P Amati, et al.
Science (New York, N.Y.)|November 6, 1992
Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemiaJ R Wetterau, L P Aggerbeck, M E Bouma, et al.
Gastroenterology|October 26, 2001
Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's diseaseN Berriot-Varoqueaux, A H Dannoura, A Moreau, et al.
Histochemistry and Cell Biology|July 3, 2007
Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromesS Guilmeau, I Niot, J P Laigneau, et al.
Clinical Genetics|September 13, 2008
Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalitiesM Silvain, D Bligny, T Aparicio, et al.
Pageof 3