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Atherosclerosis
|
November 9, 2004
No genetic linkage or molecular evidence for involvement of the PCSK9, ARH or CYP7A1 genes in the Familial Hypercholesterolemia phenotype in a sample of Danish families without pathogenic mutations in the LDL receptor and apoB genes
Dorte Damgaard, Jesper Moeller Jensen, Mogens Lytken Larsen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 22, 2003
A comparison of in vitro acylcarnitine profiling methods for the diagnosis of classical and variant short chain acyl-CoA dehydrogenase deficiency
Sarah P Young, Dietrich Matern, Niels Gregersen, et al.
Journal of Neurology
|
April 11, 2007
A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegia
Jakob Hansen, Kirsten Svenstrup, Debbie Ang, et al.
Stem Cell Research
|
April 18, 2017
Induced pluripotent stem cells derived from a patient with autosomal dominant familial neurohypophyseal diabetes insipidus caused by a variant in the AVP gene
Lise Bols Toustrup, Yan Zhou, Helene Kvistgaard, et al.
Ugeskrift for Laeger
|
August 1, 2019
[Psychological, neurological and cell-mediated mechanisms by mindfulness-based therapy]
Rasmus Jentoft Boutrup, Malene Munk Jørgensen, Niels Gregersen, et al.
Annals of the New York Academy of Sciences
|
June 29, 2006
Heat-shock protein 70 genes and human longevity: a view from Denmark
Ripudaman Singh, Steen Kølvraa, Peter Bross, et al.
Metabolism: Clinical and Experimental
|
December 17, 2009
Metabolic profiling of heat or anoxic stress in mouse C2C12 myotubes using multinuclear magnetic resonance spectroscopy
Ida K Straadt, Jette F Young, Bent O Petersen, et al.
Biochemistry
|
September 11, 2002
Purification and characterization of two polymorphic variants of short chain acyl-CoA dehydrogenase reveal reduction of catalytic activity and stability of the Gly185Ser enzyme
Tien V Nguyen, Charles Riggs, Dusica Babovic-Vuksanovic, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
July 17, 2010
A UPLC-MS/MS application for profiling of intermediary energy metabolites in microdialysis samples--a method for high-throughput
Rune Isak Dupont Birkler, Nicolaj Brejnholt Støttrup, Sigurd Hermannson, et al.
Pediatrics
|
November 5, 2003
Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder
Levinus A Bok, Peter Vreken, Frits A Wijburg, et al.
Page
of 17
Search research articles
Search
Showing results (101-110 of 161) with videos related to
Sort By:
Page
of 17
Atherosclerosis
|
November 9, 2004
No genetic linkage or molecular evidence for involvement of the PCSK9, ARH or CYP7A1 genes in the Familial Hypercholesterolemia phenotype in a sample of Danish families without pathogenic mutations in the LDL receptor and apoB genes
Dorte Damgaard, Jesper Moeller Jensen, Mogens Lytken Larsen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 22, 2003
A comparison of in vitro acylcarnitine profiling methods for the diagnosis of classical and variant short chain acyl-CoA dehydrogenase deficiency
Sarah P Young, Dietrich Matern, Niels Gregersen, et al.
Journal of Neurology
|
April 11, 2007
A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegia
Jakob Hansen, Kirsten Svenstrup, Debbie Ang, et al.
Stem Cell Research
|
April 18, 2017
Induced pluripotent stem cells derived from a patient with autosomal dominant familial neurohypophyseal diabetes insipidus caused by a variant in the AVP gene
Lise Bols Toustrup, Yan Zhou, Helene Kvistgaard, et al.
Ugeskrift for Laeger
|
August 1, 2019
[Psychological, neurological and cell-mediated mechanisms by mindfulness-based therapy]
Rasmus Jentoft Boutrup, Malene Munk Jørgensen, Niels Gregersen, et al.
Annals of the New York Academy of Sciences
|
June 29, 2006
Heat-shock protein 70 genes and human longevity: a view from Denmark
Ripudaman Singh, Steen Kølvraa, Peter Bross, et al.
Metabolism: Clinical and Experimental
|
December 17, 2009
Metabolic profiling of heat or anoxic stress in mouse C2C12 myotubes using multinuclear magnetic resonance spectroscopy
Ida K Straadt, Jette F Young, Bent O Petersen, et al.
Biochemistry
|
September 11, 2002
Purification and characterization of two polymorphic variants of short chain acyl-CoA dehydrogenase reveal reduction of catalytic activity and stability of the Gly185Ser enzyme
Tien V Nguyen, Charles Riggs, Dusica Babovic-Vuksanovic, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
July 17, 2010
A UPLC-MS/MS application for profiling of intermediary energy metabolites in microdialysis samples--a method for high-throughput
Rune Isak Dupont Birkler, Nicolaj Brejnholt Støttrup, Sigurd Hermannson, et al.
Pediatrics
|
November 5, 2003
Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder
Levinus A Bok, Peter Vreken, Frits A Wijburg, et al.
Page
of 17