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Journal of Inherited Metabolic Disease
|
January 26, 2006
Mutation spectrum of type I glycogen storage disease in Hungary
G Miltenberger-Miltenyi, L Szonyi, L Balogh, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1989
Defects in the low density lipoprotein receptor gene affect lipoprotein (a) levels: multiplicative interaction of two gene loci associated with premature atherosclerosis
G Utermann, F Hoppichler, H Dieplinger, et al.
Molecular & General Genetics : MGG
|
October 28, 1998
Molecular characterization of the human protein kinase C theta gene locus (PRKCQ)
K Kofler, S Köchl, W Parson, et al.
Clinical Genetics
|
June 1, 1981
Lecithin-cholesterol-acyltransferase deficiency: autosomal recessive transmission in a large kindred
G Utermann, H J Menzel, P Dieker, et al.
Cytogenetics and Cell Genetics
|
September 8, 1998
The human gene encoding SCYB9B, a putative novel CXC chemokine, maps to human chromosome 4q21 like the closely related genes for MIG (SCYB9) and INP10 (SCYB10)
M Erdel, A Laich, G Utermann, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 17, 2000
Lipoprotein(a) in homozygous familial hypercholesterolemia
H G Kraft, A Lingenhel, F J Raal, et al.
Diabetologia
|
September 24, 1999
Is apolipoprotein(a) a susceptibility gene for type I diabetes mellitus and related to long-term survival?
F Kronenberg, M Auinger, E Trenkwalder, et al.
American Journal of Medical Genetics
|
July 27, 2001
Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorder
M Witsch-Baumgartner, J Loeffler, H J Menzel, et al.
Molecular Genetics and Genomics : MGG
|
July 12, 2002
Direct interaction of the extracellular matrix protein DANCE with apolipoprotein(a) mediated by the kringle IV-type 2 domain
A Kapetanopoulos, F Fresser, G Millonig, et al.
Human Genetics
|
November 1, 1992
The apolipoprotein (a) gene: a transcribed hypervariable locus controlling plasma lipoprotein (a) concentration
H G Kraft, S Köchl, H J Menzel, et al.
Page
of 21
Search research articles
Search
Showing results (91-100 of 208) with videos related to
Sort By:
Page
of 21
Journal of Inherited Metabolic Disease
|
January 26, 2006
Mutation spectrum of type I glycogen storage disease in Hungary
G Miltenberger-Miltenyi, L Szonyi, L Balogh, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1989
Defects in the low density lipoprotein receptor gene affect lipoprotein (a) levels: multiplicative interaction of two gene loci associated with premature atherosclerosis
G Utermann, F Hoppichler, H Dieplinger, et al.
Molecular & General Genetics : MGG
|
October 28, 1998
Molecular characterization of the human protein kinase C theta gene locus (PRKCQ)
K Kofler, S Köchl, W Parson, et al.
Clinical Genetics
|
June 1, 1981
Lecithin-cholesterol-acyltransferase deficiency: autosomal recessive transmission in a large kindred
G Utermann, H J Menzel, P Dieker, et al.
Cytogenetics and Cell Genetics
|
September 8, 1998
The human gene encoding SCYB9B, a putative novel CXC chemokine, maps to human chromosome 4q21 like the closely related genes for MIG (SCYB9) and INP10 (SCYB10)
M Erdel, A Laich, G Utermann, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 17, 2000
Lipoprotein(a) in homozygous familial hypercholesterolemia
H G Kraft, A Lingenhel, F J Raal, et al.
Diabetologia
|
September 24, 1999
Is apolipoprotein(a) a susceptibility gene for type I diabetes mellitus and related to long-term survival?
F Kronenberg, M Auinger, E Trenkwalder, et al.
American Journal of Medical Genetics
|
July 27, 2001
Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorder
M Witsch-Baumgartner, J Loeffler, H J Menzel, et al.
Molecular Genetics and Genomics : MGG
|
July 12, 2002
Direct interaction of the extracellular matrix protein DANCE with apolipoprotein(a) mediated by the kringle IV-type 2 domain
A Kapetanopoulos, F Fresser, G Millonig, et al.
Human Genetics
|
November 1, 1992
The apolipoprotein (a) gene: a transcribed hypervariable locus controlling plasma lipoprotein (a) concentration
H G Kraft, S Köchl, H J Menzel, et al.
Page
of 21