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Cancer Genetics and Cytogenetics
|
March 1, 1993
Genetic analysis of repeated, biparental, diploid, hydatidiform moles
L Sunde, L O Vejerslev, M P Jensen, et al.
Journal of Inherited Metabolic Disease
|
June 19, 2001
The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disorders
N Gregersen, P Bross, B S Andrese, et al.
Clinical Genetics
|
April 1, 1996
A G-1-to-A acceptor splice site LDLR mutant allele leads to reduced relative transcript levels in patients with heterozygous familial hypercholesterolemia
H K Jensen, L G Jensen, P S Hansen, et al.
The Journal of Biological Chemistry
|
March 15, 1988
Characterization of a camptothecin-resistant human DNA topoisomerase I
E Kjeldsen, B J Bonven, T Andoh, et al.
Clinical Genetics
|
June 1, 1991
DNA deletions in the low density lipoprotein (LDL) receptor gene in Danish families with familial hypercholesterolemia
N S Rüdiger, E M Heinsvig, F A Hansen, et al.
Cloning and Stem Cells
|
September 24, 2005
High overall in vitro efficiency of porcine handmade cloning (HMC) combining partial zona digestion and oocyte trisection with sequential culture
Y Du, P M Kragh, X Zhang, et al.
The Biochemical Journal
|
May 16, 1998
A human homologue of Escherichia coli ClpP caseinolytic protease: recombinant expression, intracellular processing and subcellular localization
T J Corydon, P Bross, H U Holst, et al.
Human Genetics
|
November 1, 1986
Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12
S Kølvraa, T A Kruse, P K Jensen, et al.
Human Mutation
|
January 1, 1996
An LDL receptor promoter mutation in a heterozygous FH patient with dramatically skewed ratio between the two allelic mRNA variants
L G Jensen, H K Jensen, H Nissen, et al.
Progress in Clinical and Biological Research
|
January 1, 1992
Molecular analysis of medium-chain acyl-CoA dehydrogenase deficiency: a diagnostic approach
N Gregersen, V Winter, S Kølvraa, et al.
Page
of 15
Search research articles
Search
Showing results (71-80 of 146) with videos related to
Sort By:
Page
of 15
Cancer Genetics and Cytogenetics
|
March 1, 1993
Genetic analysis of repeated, biparental, diploid, hydatidiform moles
L Sunde, L O Vejerslev, M P Jensen, et al.
Journal of Inherited Metabolic Disease
|
June 19, 2001
The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disorders
N Gregersen, P Bross, B S Andrese, et al.
Clinical Genetics
|
April 1, 1996
A G-1-to-A acceptor splice site LDLR mutant allele leads to reduced relative transcript levels in patients with heterozygous familial hypercholesterolemia
H K Jensen, L G Jensen, P S Hansen, et al.
The Journal of Biological Chemistry
|
March 15, 1988
Characterization of a camptothecin-resistant human DNA topoisomerase I
E Kjeldsen, B J Bonven, T Andoh, et al.
Clinical Genetics
|
June 1, 1991
DNA deletions in the low density lipoprotein (LDL) receptor gene in Danish families with familial hypercholesterolemia
N S Rüdiger, E M Heinsvig, F A Hansen, et al.
Cloning and Stem Cells
|
September 24, 2005
High overall in vitro efficiency of porcine handmade cloning (HMC) combining partial zona digestion and oocyte trisection with sequential culture
Y Du, P M Kragh, X Zhang, et al.
The Biochemical Journal
|
May 16, 1998
A human homologue of Escherichia coli ClpP caseinolytic protease: recombinant expression, intracellular processing and subcellular localization
T J Corydon, P Bross, H U Holst, et al.
Human Genetics
|
November 1, 1986
Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12
S Kølvraa, T A Kruse, P K Jensen, et al.
Human Mutation
|
January 1, 1996
An LDL receptor promoter mutation in a heterozygous FH patient with dramatically skewed ratio between the two allelic mRNA variants
L G Jensen, H K Jensen, H Nissen, et al.
Progress in Clinical and Biological Research
|
January 1, 1992
Molecular analysis of medium-chain acyl-CoA dehydrogenase deficiency: a diagnostic approach
N Gregersen, V Winter, S Kølvraa, et al.
Page
of 15