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American Journal of Human Genetics
|
October 3, 2000
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism
B S Andresen, E Christensen, T J Corydon, et al.
American Journal of Human Genetics
|
May 12, 2001
Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency
B S Andresen, S F Dobrowolski, L O'Reilly, et al.
Human Molecular Genetics
|
April 1, 1996
Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene
B S Andresen, P Bross, C Vianey-Saban, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
May 5, 2004
Assessment of the safety of foods derived from genetically modified (GM) crops
A König, A Cockburn, R W R Crevel, et al.
Human Molecular Genetics
|
May 1, 1997
The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?
B S Andresen, P Bross, S Udvari, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
March 15, 2002
Hazard identification by methods of animal-based toxicology
S M Barlow, J B Greig, J W Bridges, et al.
Page
of 17
Search research articles
Search
Showing results (161-170 of 166) with videos related to
Sort By:
Page
of 17
You have reached the last page of results.
This site can display upto 166 results.
American Journal of Human Genetics
|
October 3, 2000
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism
B S Andresen, E Christensen, T J Corydon, et al.
American Journal of Human Genetics
|
May 12, 2001
Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency
B S Andresen, S F Dobrowolski, L O'Reilly, et al.
Human Molecular Genetics
|
April 1, 1996
Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene
B S Andresen, P Bross, C Vianey-Saban, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
May 5, 2004
Assessment of the safety of foods derived from genetically modified (GM) crops
A König, A Cockburn, R W R Crevel, et al.
Human Molecular Genetics
|
May 1, 1997
The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?
B S Andresen, P Bross, S Udvari, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
March 15, 2002
Hazard identification by methods of animal-based toxicology
S M Barlow, J B Greig, J W Bridges, et al.
Page
of 17