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Barbara Cellini

Showing results (31-40 of 104) with videos related to

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Biochimie|August 18, 2010
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variantBarbara Cellini, Antonio Lorenzetto, Riccardo Montioli, et al.
The Journal of Biological Chemistry|January 22, 2009
Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I MutationBarbara Cellini, Riccardo Montioli, Alessandro Paiardini, et al.
The Biochemical Journal|August 19, 2007
Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implicationsBarbara Cellini, Mariarita Bertoldi, Riccardo Montioli, et al.
Biochemical and Biophysical Research Communications|January 22, 2023
Biochemical and cellular effects of a novel missense mutation of the AGXT gene associated with Primary Hyperoxaluria Type 1Leonardo Gatticchi, Mirco Dindo, Gioena Pampalone, et al.
IUBMB Life|February 27, 2019
Biochemical properties and oxalate-degrading activity of oxalate decarboxylase from bacillus subtilis at neutral pHCarolina Conter, Elisa Oppici, Mirco Dindo, et al.
Molecular and Cellular Neurosciences|November 16, 2018
Cyclo(His-Pro) inhibits NLRP3 inflammasome cascade in ALS microglial cellsSilvia Grottelli, Letizia Mezzasoma, Paolo Scarpelli, et al.
Urolithiasis|November 16, 2018
Molecular basis of primary hyperoxaluria: clues to innovative treatmentsMirco Dindo, Carolina Conter, Elisa Oppici, et al.
The Biochemical Journal|January 10, 2003
Treponema denticola cystalysin exhibits significant alanine racemase activity accompanied by transamination: mechanistic implicationsMariarita Bertoldi, Barbara Cellini, Alessandro Paiardini, et al.
Molecular Genetics and Metabolism|October 25, 2011
Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associated with primary hyperoxaluria type IElisa Oppici, Riccardo Montioli, Antonio Lorenzetto, et al.
Frontiers in Bioscience (Landmark Edition)|January 7, 2022
Role of misfolding in rare enzymatic deficits and use of pharmacological chaperones as therapeutic approachGioena Pampalone, Silvia Grottelli, Leonardo Gatticchi, et al.
Pageof 11

Showing results (31-40 of 104) with videos related to

Sort By:
Pageof 11
Biochimie|August 18, 2010
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variantBarbara Cellini, Antonio Lorenzetto, Riccardo Montioli, et al.
The Journal of Biological Chemistry|January 22, 2009
Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I MutationBarbara Cellini, Riccardo Montioli, Alessandro Paiardini, et al.
The Biochemical Journal|August 19, 2007
Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implicationsBarbara Cellini, Mariarita Bertoldi, Riccardo Montioli, et al.
Biochemical and Biophysical Research Communications|January 22, 2023
Biochemical and cellular effects of a novel missense mutation of the AGXT gene associated with Primary Hyperoxaluria Type 1Leonardo Gatticchi, Mirco Dindo, Gioena Pampalone, et al.
IUBMB Life|February 27, 2019
Biochemical properties and oxalate-degrading activity of oxalate decarboxylase from bacillus subtilis at neutral pHCarolina Conter, Elisa Oppici, Mirco Dindo, et al.
Molecular and Cellular Neurosciences|November 16, 2018
Cyclo(His-Pro) inhibits NLRP3 inflammasome cascade in ALS microglial cellsSilvia Grottelli, Letizia Mezzasoma, Paolo Scarpelli, et al.
Urolithiasis|November 16, 2018
Molecular basis of primary hyperoxaluria: clues to innovative treatmentsMirco Dindo, Carolina Conter, Elisa Oppici, et al.
The Biochemical Journal|January 10, 2003
Treponema denticola cystalysin exhibits significant alanine racemase activity accompanied by transamination: mechanistic implicationsMariarita Bertoldi, Barbara Cellini, Alessandro Paiardini, et al.
Molecular Genetics and Metabolism|October 25, 2011
Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associated with primary hyperoxaluria type IElisa Oppici, Riccardo Montioli, Antonio Lorenzetto, et al.
Frontiers in Bioscience (Landmark Edition)|January 7, 2022
Role of misfolding in rare enzymatic deficits and use of pharmacological chaperones as therapeutic approachGioena Pampalone, Silvia Grottelli, Leonardo Gatticchi, et al.
Pageof 11