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Sean Froese

Showing results (1-10 of 63) with videos related to

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Expert Reviews in Molecular Medicine|December 1, 2010
Genetic disorders of vitamin B₁₂ metabolism: eight complementation groups--eight genesD Sean Froese, Roy A Gravel
Journal of Inherited Metabolic Disease|January 30, 2019
Vitamin B<sub>12</sub> , folate, and the methionine remethylation cycle-biochemistry, pathways, and regulationD Sean Froese, Brian Fowler, Matthias R Baumgartner
Topics in Current Chemistry|May 22, 2012
The role of protein structural analysis in the next generation sequencing eraWyatt W Yue, D Sean Froese, Paul E Brennan
Practical Laboratory Medicine|December 30, 2022
Reference ranges for the polyethylene glycol (PEG) precipitation activity (%PPA) of eight routine enzyme activitiesCarmen Bürki, Martin Volleberg, Linnea Blomgren, et al.
Journal of Inherited Metabolic Disease|January 21, 2023
The complex machinery of human cobalamin metabolismThomas J McCorvie, Douglas Ferreira, Wyatt W Yue, et al.
Journal of Inherited Metabolic Disease|November 13, 2022
Cellular and computational models reveal environmental and metabolic interactions in MMUT-type methylmalonic aciduriaCharlotte Ramon, Florian Traversi, Céline Bürer, et al.
Human Mutation|August 16, 2014
Functional characterization and categorization of missense mutations that cause methylmalonyl-CoA mutase (MUT) deficiencyPatrick Forny, D Sean Froese, Terttu Suormala, et al.
JIMD Reports|March 17, 2021
Decrease of disease-related metabolites upon fasting in a hemizygous knock-in mouse model (<i>Mut</i>-ko/ki) of methylmalonic aciduriaMarie Lucienne, Déborah Mathis, Nathan Perkins, et al.
Journal of Inherited Metabolic Disease|April 12, 2014
Characterization of functional domains of the cblD (MMADHC) gene productJehona Jusufi, Terttu Suormala, Patricie Burda, et al.
Human Genetics|November 19, 2021
Spectrum and characterization of bi-allelic variants in MMAB causing cblB-type methylmalonic aciduriaPatrick Forny, Tanja Plessl, Caroline Frei, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Expert Reviews in Molecular Medicine|December 1, 2010
Genetic disorders of vitamin B₁₂ metabolism: eight complementation groups--eight genesD Sean Froese, Roy A Gravel
Journal of Inherited Metabolic Disease|January 30, 2019
Vitamin B<sub>12</sub> , folate, and the methionine remethylation cycle-biochemistry, pathways, and regulationD Sean Froese, Brian Fowler, Matthias R Baumgartner
Topics in Current Chemistry|May 22, 2012
The role of protein structural analysis in the next generation sequencing eraWyatt W Yue, D Sean Froese, Paul E Brennan
Practical Laboratory Medicine|December 30, 2022
Reference ranges for the polyethylene glycol (PEG) precipitation activity (%PPA) of eight routine enzyme activitiesCarmen Bürki, Martin Volleberg, Linnea Blomgren, et al.
Journal of Inherited Metabolic Disease|January 21, 2023
The complex machinery of human cobalamin metabolismThomas J McCorvie, Douglas Ferreira, Wyatt W Yue, et al.
Journal of Inherited Metabolic Disease|November 13, 2022
Cellular and computational models reveal environmental and metabolic interactions in MMUT-type methylmalonic aciduriaCharlotte Ramon, Florian Traversi, Céline Bürer, et al.
Human Mutation|August 16, 2014
Functional characterization and categorization of missense mutations that cause methylmalonyl-CoA mutase (MUT) deficiencyPatrick Forny, D Sean Froese, Terttu Suormala, et al.
JIMD Reports|March 17, 2021
Decrease of disease-related metabolites upon fasting in a hemizygous knock-in mouse model (<i>Mut</i>-ko/ki) of methylmalonic aciduriaMarie Lucienne, Déborah Mathis, Nathan Perkins, et al.
Journal of Inherited Metabolic Disease|April 12, 2014
Characterization of functional domains of the cblD (MMADHC) gene productJehona Jusufi, Terttu Suormala, Patricie Burda, et al.
Human Genetics|November 19, 2021
Spectrum and characterization of bi-allelic variants in MMAB causing cblB-type methylmalonic aciduriaPatrick Forny, Tanja Plessl, Caroline Frei, et al.
Pageof 7