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Clinical Genetics
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July 17, 2001
LDL-receptor gene mutations and the hypocholesterolemic response to statin therapy
J U Brorholt-Petersen, H K Jensen, B Raungaard, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 31, 1994
Genotyping compared with protein phenotyping of the common apolipoprotein E polymorphism
P S Hansen, L U Gerdes, I C Klausen, et al.
Human Mutation
|
January 1, 1996
Two point mutations (313 + 1G --> A and 313 + 1G --> T) in the splice donor site of intron 3 of the low-density lipoprotein receptor gene are associated with familial hypercholesterolemia
H K Jensen, L G Jensen, P S Hansen, et al.
Human Genetics
|
March 1, 1993
Polymorphisms in the apolipoprotein B-100 gene contributes to normal variation in plasma lipids in 464 Danish men born in 1948
P S Hansen, L U Gerdes, I C Klausen, et al.
Molecular Pathology : MP
|
November 25, 2000
Analysis of the Epstein-Barr virus (EBV) latent membrane protein 1 (LMP-1) gene and promoter in Hodgkin's disease isolates: selection against EBV variants with mutations in the LMP-1 promoter ATF-1/CREB-1 binding site
K Sandvej, B S Andresen, X G Zhou, et al.
Clinical Genetics
|
February 1, 1996
An Iranian-Armenian LDLR frameshift mutation causing familial hypercholesterolemia
H K Jensen, L G Jensen, P S Hansen, et al.
European Journal of Pediatrics
|
June 1, 1995
The prevalence of the G985 allele of medium-chain acyl-CoA dehydrogenase deficiency among sudden infant death victims and healthy newborns in northern Germany
R Santer, N Gregersen, K Tanaka, et al.
Clinical Chemistry
|
August 1, 1996
High sensitivity of the single-strand conformation polymorphism method for detecting sequence variations in the low-density lipoprotein receptor gene validated by DNA sequencing
H K Jensen, L G Jensen, P S Hansen, et al.
Atherosclerosis
|
February 1, 1996
The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark
H K Jensen, L G Jensen, P S Hansen, et al.
Nucleic Acids Research
|
January 11, 1988
Detection of alpha 1-antitrypsin genotypes by analysis of amplified DNA sequences
K B Petersen, S Kølvraa, L Bolund, et al.
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of 21
Search research articles
Search
Showing results (81-90 of 208) with videos related to
Sort By:
Page
of 21
Clinical Genetics
|
July 17, 2001
LDL-receptor gene mutations and the hypocholesterolemic response to statin therapy
J U Brorholt-Petersen, H K Jensen, B Raungaard, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 31, 1994
Genotyping compared with protein phenotyping of the common apolipoprotein E polymorphism
P S Hansen, L U Gerdes, I C Klausen, et al.
Human Mutation
|
January 1, 1996
Two point mutations (313 + 1G --> A and 313 + 1G --> T) in the splice donor site of intron 3 of the low-density lipoprotein receptor gene are associated with familial hypercholesterolemia
H K Jensen, L G Jensen, P S Hansen, et al.
Human Genetics
|
March 1, 1993
Polymorphisms in the apolipoprotein B-100 gene contributes to normal variation in plasma lipids in 464 Danish men born in 1948
P S Hansen, L U Gerdes, I C Klausen, et al.
Molecular Pathology : MP
|
November 25, 2000
Analysis of the Epstein-Barr virus (EBV) latent membrane protein 1 (LMP-1) gene and promoter in Hodgkin's disease isolates: selection against EBV variants with mutations in the LMP-1 promoter ATF-1/CREB-1 binding site
K Sandvej, B S Andresen, X G Zhou, et al.
Clinical Genetics
|
February 1, 1996
An Iranian-Armenian LDLR frameshift mutation causing familial hypercholesterolemia
H K Jensen, L G Jensen, P S Hansen, et al.
European Journal of Pediatrics
|
June 1, 1995
The prevalence of the G985 allele of medium-chain acyl-CoA dehydrogenase deficiency among sudden infant death victims and healthy newborns in northern Germany
R Santer, N Gregersen, K Tanaka, et al.
Clinical Chemistry
|
August 1, 1996
High sensitivity of the single-strand conformation polymorphism method for detecting sequence variations in the low-density lipoprotein receptor gene validated by DNA sequencing
H K Jensen, L G Jensen, P S Hansen, et al.
Atherosclerosis
|
February 1, 1996
The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark
H K Jensen, L G Jensen, P S Hansen, et al.
Nucleic Acids Research
|
January 11, 1988
Detection of alpha 1-antitrypsin genotypes by analysis of amplified DNA sequences
K B Petersen, S Kølvraa, L Bolund, et al.
Page
of 21