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Sean Froese

Showing results (11-20 of 63) with videos related to

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Cellular and Molecular Life Sciences : CMLS|September 15, 2021
Mitochondrial disease, mitophagy, and cellular distress in methylmalonic acidemiaAlessandro Luciani, Matthew C S Denley, Larissa P Govers, et al.
Biochemistry|February 27, 2026
5,10-Methylenetetrahydrofolate Reductase─the Key Allosteric Regulator in One-Carbon MetabolismLinnea K M Blomgren, Shuning Guo, D Sean Froese, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2011
Conformational plasticity of glycogenin and its maltosaccharide substrate during glycogen biogenesisApirat Chaikuad, D Sean Froese, Georgina Berridge, et al.
Human Mutation|May 13, 2017
Protein destabilization and loss of protein-protein interaction are fundamental mechanisms in cblA-type methylmalonic aciduriaTanja Plessl, Céline Bürer, Seraina Lutz, et al.
Plos One|March 26, 2015
Zip4 mediated zinc influx stimulates insulin secretion in pancreatic beta cellsAlexandre B Hardy, Kacey J Prentice, Sean Froese, et al.
Journal of Inherited Metabolic Disease|October 16, 2016
Functional characterization of missense mutations in severe methylenetetrahydrofolate reductase deficiency using a human expression systemPatricie Burda, Terttu Suormala, Dorothea Heuberger, et al.
Biochimie|November 21, 2024
Evidence for interaction of 5,10-methylenetetrahydrofolate reductase (MTHFR) with methylenetetrahydrofolate dehydrogenase (MTHFD1) and general control nonderepressible 1 (GCN1)Linda R Büchler, Linnea K M Blomgren, Céline Bürer, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|October 25, 2016
Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHCChristine Bassila, Rose Ghemrawi, Justine Flayac, et al.
Human Mutation|May 12, 2016
Molecular Genetic Characterization of 151 Mut-Type Methylmalonic Aciduria Patients and Identification of 41 Novel Mutations in MUTPatrick Forny, Anne-Sophie Schnellmann, Celine Buerer, et al.
Biochemistry|April 5, 2014
Enzymatic and structural characterization of rTSγ provides insights into the function of rTSβDaniel J Wichelecki, D Sean Froese, Jolanta Kopec, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Cellular and Molecular Life Sciences : CMLS|September 15, 2021
Mitochondrial disease, mitophagy, and cellular distress in methylmalonic acidemiaAlessandro Luciani, Matthew C S Denley, Larissa P Govers, et al.
Biochemistry|February 27, 2026
5,10-Methylenetetrahydrofolate Reductase─the Key Allosteric Regulator in One-Carbon MetabolismLinnea K M Blomgren, Shuning Guo, D Sean Froese, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2011
Conformational plasticity of glycogenin and its maltosaccharide substrate during glycogen biogenesisApirat Chaikuad, D Sean Froese, Georgina Berridge, et al.
Human Mutation|May 13, 2017
Protein destabilization and loss of protein-protein interaction are fundamental mechanisms in cblA-type methylmalonic aciduriaTanja Plessl, Céline Bürer, Seraina Lutz, et al.
Plos One|March 26, 2015
Zip4 mediated zinc influx stimulates insulin secretion in pancreatic beta cellsAlexandre B Hardy, Kacey J Prentice, Sean Froese, et al.
Journal of Inherited Metabolic Disease|October 16, 2016
Functional characterization of missense mutations in severe methylenetetrahydrofolate reductase deficiency using a human expression systemPatricie Burda, Terttu Suormala, Dorothea Heuberger, et al.
Biochimie|November 21, 2024
Evidence for interaction of 5,10-methylenetetrahydrofolate reductase (MTHFR) with methylenetetrahydrofolate dehydrogenase (MTHFD1) and general control nonderepressible 1 (GCN1)Linda R Büchler, Linnea K M Blomgren, Céline Bürer, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|October 25, 2016
Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHCChristine Bassila, Rose Ghemrawi, Justine Flayac, et al.
Human Mutation|May 12, 2016
Molecular Genetic Characterization of 151 Mut-Type Methylmalonic Aciduria Patients and Identification of 41 Novel Mutations in MUTPatrick Forny, Anne-Sophie Schnellmann, Celine Buerer, et al.
Biochemistry|April 5, 2014
Enzymatic and structural characterization of rTSγ provides insights into the function of rTSβDaniel J Wichelecki, D Sean Froese, Jolanta Kopec, et al.
Pageof 7