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M J Hoffer

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Biochemical and Biophysical Research Communications|July 13, 2000
Familial chylomicronemia caused by a novel type of mutation in the APOE-CI-CIV-CII gene cluster encompassing both the APOCII gene and the first APOCIV gene mutation: APOCII-CIV(Nijmegen)J de Graaf, M J Hoffer, P M Stuyt, et al.
Genomics|January 1, 1993
Evolutionary conservation of the mouse apolipoprotein e-c1-c2 gene cluster: structure and genetic variability in inbred miceM J Hoffer, M H Hofker, M M van Eck, et al.
Genomics|May 1, 1994
The apolipoprotein C2-linked (Acl) gene: a new gene within the mouse apolipoprotein e-c1-c2 gene clusterM M van Eck, M J Hoffer, L M Havekes, et al.
Genomics|July 1, 1993
Structure and expression of the mouse apolipoprotein C2 geneM J Hoffer, M M van Eck, L M Havekes, et al.
Genomics|October 1, 1993
The mouse apolipoprotein C1 gene: structure and expressionM J Hoffer, M M van Eck, L M Havekes, et al.
European Journal of Clinical Investigation|October 30, 1998
Increased risk for endogenous hypertriglyceridaemia is associated with an apolipoprotein C3 haplotype specified by the SstI polymorphismM J Hoffer, E J Sijbrands, F H De Man, et al.
Atherosclerosis|August 5, 2000
The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemiaM J Hoffer, H Snieder, S J Bredie, et al.
Atherosclerosis|December 1, 1993
An acceptor splice site mutation in intron 16 of the low density lipoprotein receptor gene leads to an elongated, internalization defective receptorP Lombardi, M J Hoffer, B Top, et al.
Atherosclerosis|August 2, 1996
Apolipoprotein E1-Hammersmith (Lys146-->Asn;Arg147-->Trp), due to a dinucleotide substitution, is associated with early manifestation of dominant type III hyperlipoproteinaemiaM J Hoffer, S Niththyananthan, R P Naoumova, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 13, 1999
Severe hyperlipidemia in apolipoprotein E2 homozygotes due to a combined effect of hyperinsulinemia and an SstI polymorphismE J Sijbrands, M J Hoffer, A E Meinders, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Biochemical and Biophysical Research Communications|July 13, 2000
Familial chylomicronemia caused by a novel type of mutation in the APOE-CI-CIV-CII gene cluster encompassing both the APOCII gene and the first APOCIV gene mutation: APOCII-CIV(Nijmegen)J de Graaf, M J Hoffer, P M Stuyt, et al.
Genomics|January 1, 1993
Evolutionary conservation of the mouse apolipoprotein e-c1-c2 gene cluster: structure and genetic variability in inbred miceM J Hoffer, M H Hofker, M M van Eck, et al.
Genomics|May 1, 1994
The apolipoprotein C2-linked (Acl) gene: a new gene within the mouse apolipoprotein e-c1-c2 gene clusterM M van Eck, M J Hoffer, L M Havekes, et al.
Genomics|July 1, 1993
Structure and expression of the mouse apolipoprotein C2 geneM J Hoffer, M M van Eck, L M Havekes, et al.
Genomics|October 1, 1993
The mouse apolipoprotein C1 gene: structure and expressionM J Hoffer, M M van Eck, L M Havekes, et al.
European Journal of Clinical Investigation|October 30, 1998
Increased risk for endogenous hypertriglyceridaemia is associated with an apolipoprotein C3 haplotype specified by the SstI polymorphismM J Hoffer, E J Sijbrands, F H De Man, et al.
Atherosclerosis|August 5, 2000
The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemiaM J Hoffer, H Snieder, S J Bredie, et al.
Atherosclerosis|December 1, 1993
An acceptor splice site mutation in intron 16 of the low density lipoprotein receptor gene leads to an elongated, internalization defective receptorP Lombardi, M J Hoffer, B Top, et al.
Atherosclerosis|August 2, 1996
Apolipoprotein E1-Hammersmith (Lys146-->Asn;Arg147-->Trp), due to a dinucleotide substitution, is associated with early manifestation of dominant type III hyperlipoproteinaemiaM J Hoffer, S Niththyananthan, R P Naoumova, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 13, 1999
Severe hyperlipidemia in apolipoprotein E2 homozygotes due to a combined effect of hyperinsulinemia and an SstI polymorphismE J Sijbrands, M J Hoffer, A E Meinders, et al.
Pageof 2