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The Pediatric Infectious Disease Journal
|
November 26, 1999
Klebsiella pneumoniae with extended spectrum beta-lactamase activity associated with a necrotizing enterocolitis outbreak
N Gregersen, W Van Nierop, A Von Gottberg, et al.
American Journal of Human Genetics
|
June 1, 1993
Three RFLPs defining a haplotype associated with the common mutation in human medium-chain acyl-CoA dehydrogenase (MCAD) deficiency occur in Alu repeats
Z Zhang, S Kolvraa, Y Zhou, et al.
European Journal of Biochemistry
|
May 23, 1991
Repetitive sequences involved in the recombination leading to deletion of exon 5 of the low-density-lipoprotein receptor gene in a patient with familial hypercholesterolemia
N S Rüdiger, P S Hansen, M Jørgensen, et al.
Bone
|
March 1, 1997
A sequence variation: 713-8delC in the transforming growth factor-beta 1 gene has higher prevalence in osteoporotic women than in normal women and is associated with very low bone mass in osteoporotic women and increased bone turnover in both osteoporotic and normal women
B L Langdahl, J Y Knudsen, H K Jensen, et al.
Pediatric Research
|
October 1, 1982
C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects
N Gregersen, H Wintzensen, S K Christensen, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
October 1, 1995
A polymerase chain reaction-based method for the semiquantitative study of interleukin-8 mRNA in human basophil leukocytes
P Markvardsen, T Bjerke, N Rüdiger, et al.
Nucleic Acids Research
|
November 11, 1988
Treatment of genomic DNA with T4 DNA ligase improves Southern blot analysis
J E Koch, S Kølvraa, M Corneliusen, et al.
Human Genetics
|
March 1, 1993
A PvuII polymorphism of the low density lipoprotein receptor gene is not associated with plasma concentrations of low density lipoproteins including LP(a)
I C Klausen, P S Hansen, L U Gerdes, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency due to heterozygosity for the common mutation and an allele resulting in low levels of MCAD mRNA
B S Andresen, P Bross, I Knudsen, et al.
Human Mutation
|
September 8, 1999
Protein misfolding and degradation in genetic diseases
P Bross, T J Corydon, B S Andresen, et al.
Page
of 21
Search research articles
Search
Showing results (91-100 of 208) with videos related to
Sort By:
Page
of 21
The Pediatric Infectious Disease Journal
|
November 26, 1999
Klebsiella pneumoniae with extended spectrum beta-lactamase activity associated with a necrotizing enterocolitis outbreak
N Gregersen, W Van Nierop, A Von Gottberg, et al.
American Journal of Human Genetics
|
June 1, 1993
Three RFLPs defining a haplotype associated with the common mutation in human medium-chain acyl-CoA dehydrogenase (MCAD) deficiency occur in Alu repeats
Z Zhang, S Kolvraa, Y Zhou, et al.
European Journal of Biochemistry
|
May 23, 1991
Repetitive sequences involved in the recombination leading to deletion of exon 5 of the low-density-lipoprotein receptor gene in a patient with familial hypercholesterolemia
N S Rüdiger, P S Hansen, M Jørgensen, et al.
Bone
|
March 1, 1997
A sequence variation: 713-8delC in the transforming growth factor-beta 1 gene has higher prevalence in osteoporotic women than in normal women and is associated with very low bone mass in osteoporotic women and increased bone turnover in both osteoporotic and normal women
B L Langdahl, J Y Knudsen, H K Jensen, et al.
Pediatric Research
|
October 1, 1982
C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects
N Gregersen, H Wintzensen, S K Christensen, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
October 1, 1995
A polymerase chain reaction-based method for the semiquantitative study of interleukin-8 mRNA in human basophil leukocytes
P Markvardsen, T Bjerke, N Rüdiger, et al.
Nucleic Acids Research
|
November 11, 1988
Treatment of genomic DNA with T4 DNA ligase improves Southern blot analysis
J E Koch, S Kølvraa, M Corneliusen, et al.
Human Genetics
|
March 1, 1993
A PvuII polymorphism of the low density lipoprotein receptor gene is not associated with plasma concentrations of low density lipoproteins including LP(a)
I C Klausen, P S Hansen, L U Gerdes, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency due to heterozygosity for the common mutation and an allele resulting in low levels of MCAD mRNA
B S Andresen, P Bross, I Knudsen, et al.
Human Mutation
|
September 8, 1999
Protein misfolding and degradation in genetic diseases
P Bross, T J Corydon, B S Andresen, et al.
Page
of 21