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Clinical Chemistry
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October 31, 2002
Liquid chromatographic-tandem mass spectrometric method for the determination of 5-hydroxyindole-3-acetic acid in urine
Charles A Kroll, Mark J Magera, Janice K Helgeson, et al.
Molecular Genetics and Metabolism
|
August 24, 2019
Rare Saposin A deficiency: Novel variant and psychosine analysis
Laurel Calderwood, David A Wenger, Dietrich Matern, et al.
Human Gene Therapy
|
February 6, 2015
Long-term sex-biased correction of circulating propionic acidemia disease markers by adeno-associated virus vectors
Adam J Guenzel, Renata Collard, Jan P Kraus, et al.
Molecular Genetics and Metabolism
|
December 14, 2004
Influence of dietary fatty acid chain-length on metabolic tolerance in mouse models of inherited defects in mitochondrial fatty acid beta-oxidation
A Michele Schuler, Barbara A Gower, Dietrich Matern, et al.
Molecular Genetics and Metabolism
|
July 29, 2014
Succinylacetone as primary marker to detect tyrosinemia type I in newborns and its measurement by newborn screening programs
Víctor R De Jesús, Barbara W Adam, Daniel Mandel, et al.
Analytical and Bioanalytical Chemistry
|
August 27, 2024
A multiplexed targeted method for profiling of serum gangliosides and glycosphingolipids: application to GM2-gangliosidosis
Jinyong Kim, Seul Kee Byeon, Devin Oglesbee, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
September 26, 2013
Altered body composition and energy expenditure but normal glucose tolerance among humans with a long-chain fatty acid oxidation disorder
Melanie B Gillingham, Cary O Harding, Dale A Schoeller, et al.
The Journal of Molecular Diagnostics : JMD
|
August 25, 2024
Genotype and Phenotype Correlation of the TPMT∗8 Allele in Thiopurine Metabolism
Rosalie M Sterner, Patricia L Hall, Dietrich Matern, et al.
Molecular Genetics and Metabolism
|
March 29, 2026
Biochemical genetic testing for congenital disorders of glycosylation after sequencing produces equivocal results
Matthew J Schultz, Kristen L Liedtke, Coleman T Turgeon, et al.
Molecular Genetics and Metabolism
|
April 20, 2006
In vitro characterization and in vivo expression of human very-long chain acyl-CoA dehydrogenase
J Lawrence Merritt, Dietrich Matern, Jerry Vockley, et al.
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of 16
Search research articles
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Showing results (31-40 of 152) with videos related to
Sort By:
Page
of 16
Clinical Chemistry
|
October 31, 2002
Liquid chromatographic-tandem mass spectrometric method for the determination of 5-hydroxyindole-3-acetic acid in urine
Charles A Kroll, Mark J Magera, Janice K Helgeson, et al.
Molecular Genetics and Metabolism
|
August 24, 2019
Rare Saposin A deficiency: Novel variant and psychosine analysis
Laurel Calderwood, David A Wenger, Dietrich Matern, et al.
Human Gene Therapy
|
February 6, 2015
Long-term sex-biased correction of circulating propionic acidemia disease markers by adeno-associated virus vectors
Adam J Guenzel, Renata Collard, Jan P Kraus, et al.
Molecular Genetics and Metabolism
|
December 14, 2004
Influence of dietary fatty acid chain-length on metabolic tolerance in mouse models of inherited defects in mitochondrial fatty acid beta-oxidation
A Michele Schuler, Barbara A Gower, Dietrich Matern, et al.
Molecular Genetics and Metabolism
|
July 29, 2014
Succinylacetone as primary marker to detect tyrosinemia type I in newborns and its measurement by newborn screening programs
Víctor R De Jesús, Barbara W Adam, Daniel Mandel, et al.
Analytical and Bioanalytical Chemistry
|
August 27, 2024
A multiplexed targeted method for profiling of serum gangliosides and glycosphingolipids: application to GM2-gangliosidosis
Jinyong Kim, Seul Kee Byeon, Devin Oglesbee, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
September 26, 2013
Altered body composition and energy expenditure but normal glucose tolerance among humans with a long-chain fatty acid oxidation disorder
Melanie B Gillingham, Cary O Harding, Dale A Schoeller, et al.
The Journal of Molecular Diagnostics : JMD
|
August 25, 2024
Genotype and Phenotype Correlation of the TPMT∗8 Allele in Thiopurine Metabolism
Rosalie M Sterner, Patricia L Hall, Dietrich Matern, et al.
Molecular Genetics and Metabolism
|
March 29, 2026
Biochemical genetic testing for congenital disorders of glycosylation after sequencing produces equivocal results
Matthew J Schultz, Kristen L Liedtke, Coleman T Turgeon, et al.
Molecular Genetics and Metabolism
|
April 20, 2006
In vitro characterization and in vivo expression of human very-long chain acyl-CoA dehydrogenase
J Lawrence Merritt, Dietrich Matern, Jerry Vockley, et al.
Page
of 16