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Barbara Cellini

Showing results (61-70 of 104) with videos related to

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Biochimie|August 14, 2022
CRISPR/Cas9-mediated knock-out of AGXT1 in HepG2 cells as a new in vitro model of Primary Hyperoxaluria Type 1Leonardo Gatticchi, Silvia Grottelli, Giulia Ambrosini, et al.
Frontiers in Molecular Biosciences|May 9, 2024
Harnessing inter-kingdom metabolic disparities at the human-fungal interface for novel therapeutic approachesClaudio Costantini, Marilena Pariano, Matteo Puccetti, et al.
The International Journal of Biochemistry & Cell Biology|December 27, 2011
The N-terminal extension is essential for the formation of the active dimeric structure of liver peroxisomal alanine:glyoxylate aminotransferaseRiccardo Montioli, Sonia Fargue, Jackie Lewin, et al.
Human Molecular Genetics|July 4, 2014
S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementationRiccardo Montioli, Alessandro Roncador, Elisa Oppici, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type IBarbara Cellini, Riccardo Montioli, Alessandro Paiardini, et al.
Plos One|March 3, 2012
Identification by virtual screening and in vitro testing of human DOPA decarboxylase inhibitorsFrederick Daidone, Riccardo Montioli, Alessandro Paiardini, et al.
ACS Chemical Biology|June 19, 2014
S-Glutathionylation at Cys328 and Cys542 impairs STAT3 phosphorylationElena Butturini, Elena Darra, Giulia Chiavegato, et al.
Journal of Chemical Information and Modeling|August 23, 2024
Molecular Dynamics-Ensemble Docking and Biophysical Studies for Structure-Based Identification of Non-Amino Acidic Ligands of DDAH-1Carlo Bigiotti, Elisa Bianconi, Luana Ruta, et al.
Human Molecular Genetics|July 23, 2015
Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type IElisa Oppici, Sonia Fargue, Emma S Reid, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 26, 2018
Molecular and cellular basis of ornithine δ-aminotransferase deficiency caused by the V332M mutation associated with gyrate atrophy of the choroid and retinaRiccardo Montioli, Maria Andrea Desbats, Silvia Grottelli, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
Biochimie|August 14, 2022
CRISPR/Cas9-mediated knock-out of AGXT1 in HepG2 cells as a new in vitro model of Primary Hyperoxaluria Type 1Leonardo Gatticchi, Silvia Grottelli, Giulia Ambrosini, et al.
Frontiers in Molecular Biosciences|May 9, 2024
Harnessing inter-kingdom metabolic disparities at the human-fungal interface for novel therapeutic approachesClaudio Costantini, Marilena Pariano, Matteo Puccetti, et al.
The International Journal of Biochemistry & Cell Biology|December 27, 2011
The N-terminal extension is essential for the formation of the active dimeric structure of liver peroxisomal alanine:glyoxylate aminotransferaseRiccardo Montioli, Sonia Fargue, Jackie Lewin, et al.
Human Molecular Genetics|July 4, 2014
S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementationRiccardo Montioli, Alessandro Roncador, Elisa Oppici, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type IBarbara Cellini, Riccardo Montioli, Alessandro Paiardini, et al.
Plos One|March 3, 2012
Identification by virtual screening and in vitro testing of human DOPA decarboxylase inhibitorsFrederick Daidone, Riccardo Montioli, Alessandro Paiardini, et al.
ACS Chemical Biology|June 19, 2014
S-Glutathionylation at Cys328 and Cys542 impairs STAT3 phosphorylationElena Butturini, Elena Darra, Giulia Chiavegato, et al.
Journal of Chemical Information and Modeling|August 23, 2024
Molecular Dynamics-Ensemble Docking and Biophysical Studies for Structure-Based Identification of Non-Amino Acidic Ligands of DDAH-1Carlo Bigiotti, Elisa Bianconi, Luana Ruta, et al.
Human Molecular Genetics|July 23, 2015
Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type IElisa Oppici, Sonia Fargue, Emma S Reid, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 26, 2018
Molecular and cellular basis of ornithine δ-aminotransferase deficiency caused by the V332M mutation associated with gyrate atrophy of the choroid and retinaRiccardo Montioli, Maria Andrea Desbats, Silvia Grottelli, et al.
Pageof 11