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S Harvey Mudd

Showing results (1-10 of 27) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 11, 2011
Hypermethioninemias of genetic and non-genetic origin: A reviewS Harvey Mudd
The Journal of Nutrition|May 17, 2006
The 5th workshop on the assessment of adequate intake of dietary amino acids: general discussion 1John D Fernstrom, S Harvey Mudd
The New England Journal of Medicine|April 18, 2003
Population screeningSally P Stabler, S Harvey Mudd
Molecular Genetics and Metabolism|October 13, 2009
A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiencyFlemming Skovby, Mette Gaustadnes, S Harvey Mudd
The Journal of Biological Chemistry|June 2, 2009
Glycine N-methyltransferase and regulation of S-adenosylmethionine levelsZigmund Luka, S Harvey Mudd, Conrad Wagner
Human Mutation|January 30, 2009
S-adenosylhomocysteine hydrolase (AHCY) deficiency: two novel mutations with lethal outcomeOliver Vugrek, Robert Beluzić, Nikolina Nakić, et al.
AJNR. American Journal of Neuroradiology|November 16, 2005
Characteristic MR imaging changes in severe hypermethioninemic statesNancy E Braverman, S Harvey Mudd, Peter B Barker, et al.
The Biochemical Journal|July 29, 2006
A single mutation at Tyr143 of human S-adenosylhomocysteine hydrolase renders the enzyme thermosensitive and affects the oxidation state of bound cofactor nicotinamide-adenine dinucleotideRobert Beluzić, Mario Cuk, Tea Pavkov, et al.
Molecular Genetics and Metabolism|January 12, 2016
Molecular and biochemical investigations of patients with intermediate or severe hyperhomocysteinemiaJannie Tanderup Sørensen, Mette Gaustadnes, Sally P Stabler, et al.
Journal of Inherited Metabolic Disease|September 21, 2010
S-adenosylhomocysteine hydrolase deficiency: two siblings with fetal hydrops and fatal outcomesRandall Grubbs, Oliver Vugrek, Jeremy Deisch, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 11, 2011
Hypermethioninemias of genetic and non-genetic origin: A reviewS Harvey Mudd
The Journal of Nutrition|May 17, 2006
The 5th workshop on the assessment of adequate intake of dietary amino acids: general discussion 1John D Fernstrom, S Harvey Mudd
The New England Journal of Medicine|April 18, 2003
Population screeningSally P Stabler, S Harvey Mudd
Molecular Genetics and Metabolism|October 13, 2009
A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiencyFlemming Skovby, Mette Gaustadnes, S Harvey Mudd
The Journal of Biological Chemistry|June 2, 2009
Glycine N-methyltransferase and regulation of S-adenosylmethionine levelsZigmund Luka, S Harvey Mudd, Conrad Wagner
Human Mutation|January 30, 2009
S-adenosylhomocysteine hydrolase (AHCY) deficiency: two novel mutations with lethal outcomeOliver Vugrek, Robert Beluzić, Nikolina Nakić, et al.
AJNR. American Journal of Neuroradiology|November 16, 2005
Characteristic MR imaging changes in severe hypermethioninemic statesNancy E Braverman, S Harvey Mudd, Peter B Barker, et al.
The Biochemical Journal|July 29, 2006
A single mutation at Tyr143 of human S-adenosylhomocysteine hydrolase renders the enzyme thermosensitive and affects the oxidation state of bound cofactor nicotinamide-adenine dinucleotideRobert Beluzić, Mario Cuk, Tea Pavkov, et al.
Molecular Genetics and Metabolism|January 12, 2016
Molecular and biochemical investigations of patients with intermediate or severe hyperhomocysteinemiaJannie Tanderup Sørensen, Mette Gaustadnes, Sally P Stabler, et al.
Journal of Inherited Metabolic Disease|September 21, 2010
S-adenosylhomocysteine hydrolase deficiency: two siblings with fetal hydrops and fatal outcomesRandall Grubbs, Oliver Vugrek, Jeremy Deisch, et al.
Pageof 3