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Human Mutation
|
January 1, 1996
Allele-specific measurement of low-density lipoprotein receptor transcript levels
L G Jensen, H K Jensen, F Heath, et al.
Nature Genetics
|
June 1, 1993
Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1
N Tommerup, W Schempp, P Meinecke, et al.
Cloning and Stem Cells
|
January 2, 2007
Chemically assisted handmade enucleation of porcine oocytes
J Li, Y Du, Y H Zhang, et al.
Clinical Genetics
|
August 1, 1994
An alanine29-serine variant in exon 2 of the low density lipoprotein receptor gene: no association with hypercholesterolemia
H K Jensen, L G Jensen, P S Hansen, et al.
Clinical Genetics
|
November 1, 1996
Phenotypic characterization of a patient homozygous for the D558N LDL receptor gene mutation
H K Jensen, L G Jensen, F Heath, et al.
Progress in Clinical and Biological Research
|
January 1, 1992
Characterization of medium-chain acyl-CoA dehydrogenase (MCAD) with a point mutation associated with MCAD deficiency
P Bross, T Jensen, F Kräutle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 26, 2000
Human and mouse mitochondrial orthologs of bacterial ClpX
T J Corydon, M Wilsbech, C Jespersgaard, et al.
Ugeskrift for Laeger
|
April 15, 2000
[Keratin diseases]
P K Jensen, C B Sørensen, B S Andresen, et al.
The Journal of Biological Chemistry
|
July 25, 2000
Grp78 is involved in retention of mutant low density lipoprotein receptor protein in the endoplasmic reticulum
M M Jørgensen, O N Jensen, H U Holst, et al.
Biochemical Medicine and Metabolic Biology
|
June 1, 1994
Characterization of wild-type human medium-chain acyl-CoA dehydrogenase (MCAD) and mutant enzymes present in MCAD-deficient patients by two-dimensional gel electrophoresis: evidence for post-translational modification of the enzyme
P Bross, T G Jensen, B S Andresen, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 146) with videos related to
Sort By:
Page
of 15
Human Mutation
|
January 1, 1996
Allele-specific measurement of low-density lipoprotein receptor transcript levels
L G Jensen, H K Jensen, F Heath, et al.
Nature Genetics
|
June 1, 1993
Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1
N Tommerup, W Schempp, P Meinecke, et al.
Cloning and Stem Cells
|
January 2, 2007
Chemically assisted handmade enucleation of porcine oocytes
J Li, Y Du, Y H Zhang, et al.
Clinical Genetics
|
August 1, 1994
An alanine29-serine variant in exon 2 of the low density lipoprotein receptor gene: no association with hypercholesterolemia
H K Jensen, L G Jensen, P S Hansen, et al.
Clinical Genetics
|
November 1, 1996
Phenotypic characterization of a patient homozygous for the D558N LDL receptor gene mutation
H K Jensen, L G Jensen, F Heath, et al.
Progress in Clinical and Biological Research
|
January 1, 1992
Characterization of medium-chain acyl-CoA dehydrogenase (MCAD) with a point mutation associated with MCAD deficiency
P Bross, T Jensen, F Kräutle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 26, 2000
Human and mouse mitochondrial orthologs of bacterial ClpX
T J Corydon, M Wilsbech, C Jespersgaard, et al.
Ugeskrift for Laeger
|
April 15, 2000
[Keratin diseases]
P K Jensen, C B Sørensen, B S Andresen, et al.
The Journal of Biological Chemistry
|
July 25, 2000
Grp78 is involved in retention of mutant low density lipoprotein receptor protein in the endoplasmic reticulum
M M Jørgensen, O N Jensen, H U Holst, et al.
Biochemical Medicine and Metabolic Biology
|
June 1, 1994
Characterization of wild-type human medium-chain acyl-CoA dehydrogenase (MCAD) and mutant enzymes present in MCAD-deficient patients by two-dimensional gel electrophoresis: evidence for post-translational modification of the enzyme
P Bross, T G Jensen, B S Andresen, et al.
Page
of 15