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Journal of Personalized Medicine
|
April 30, 2021
Dimerization Drives Proper Folding of Human Alanine:Glyoxylate Aminotransferase But Is Dispensable for Peroxisomal Targeting
Mirco Dindo, Giulia Ambrosini, Elisa Oppici, et al.
Journal of Nephrology
|
February 26, 2022
Primary hyperoxaluria in Italy: the past 30 years and the near future of a (not so) rare disease
Giorgia Mandrile, Alessandra Pelle, Veronica Sciannameo, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 26, 2022
Amniotic fluid stem cell-derived extracellular vesicles are independent metabolic units capable of modulating inflammasome activation in THP-1 cells
Letizia Mezzasoma, Ilaria Bellezza, Pierluigi Orvietani, et al.
Cell Reports
|
August 17, 2017
The IL-17F/IL-17RC Axis Promotes Respiratory Allergy in the Proximal Airways
Antonella De Luca, Marilena Pariano, Barbara Cellini, et al.
Human Molecular Genetics
|
September 15, 2018
Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses
Encarnación Medina-Carmona, Isabel Betancor-Fernández, Jaime Santos, et al.
Scientific Reports
|
October 19, 2016
A Novel Pathway for Metabolism of the Cardiovascular Risk Factor Homoarginine by alanine:glyoxylate aminotransferase 2
Roman N Rodionov, Elisa Oppici, Jens Martens-Lobenhoffer, et al.
Molecular Oncology
|
April 28, 2016
Mutant p53 proteins counteract autophagic mechanism sensitizing cancer cells to mTOR inhibition
Marco Cordani, Elisa Oppici, Ilaria Dando, et al.
International Journal of Biological Macromolecules
|
January 1, 2026
Nanobodies as therapies for loss-of-function misfolding diseases: the example of Primary Hyperoxaluria Type 1
Mirco Dindo, Atanasio Gómez-Mulas, Juan Luis Pacheco-García, et al.
EMBO Molecular Medicine
|
January 17, 2023
Liver-directed gene therapy for ornithine aminotransferase deficiency
Iolanda Boffa, Elena Polishchuk, Lucia De Stefano, et al.
Molecular Genetics and Metabolism
|
July 25, 2024
Extending diagnostic practices in gyrate atrophy: Enzymatic characterization and the development of an in vitro pyridoxine responsiveness assay
Berith M Balfoort, Gioena Pampalone, Jos P N Ruiter, et al.
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of 11
Search research articles
Search
Showing results (91-100 of 104) with videos related to
Sort By:
Page
of 11
Journal of Personalized Medicine
|
April 30, 2021
Dimerization Drives Proper Folding of Human Alanine:Glyoxylate Aminotransferase But Is Dispensable for Peroxisomal Targeting
Mirco Dindo, Giulia Ambrosini, Elisa Oppici, et al.
Journal of Nephrology
|
February 26, 2022
Primary hyperoxaluria in Italy: the past 30 years and the near future of a (not so) rare disease
Giorgia Mandrile, Alessandra Pelle, Veronica Sciannameo, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 26, 2022
Amniotic fluid stem cell-derived extracellular vesicles are independent metabolic units capable of modulating inflammasome activation in THP-1 cells
Letizia Mezzasoma, Ilaria Bellezza, Pierluigi Orvietani, et al.
Cell Reports
|
August 17, 2017
The IL-17F/IL-17RC Axis Promotes Respiratory Allergy in the Proximal Airways
Antonella De Luca, Marilena Pariano, Barbara Cellini, et al.
Human Molecular Genetics
|
September 15, 2018
Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses
Encarnación Medina-Carmona, Isabel Betancor-Fernández, Jaime Santos, et al.
Scientific Reports
|
October 19, 2016
A Novel Pathway for Metabolism of the Cardiovascular Risk Factor Homoarginine by alanine:glyoxylate aminotransferase 2
Roman N Rodionov, Elisa Oppici, Jens Martens-Lobenhoffer, et al.
Molecular Oncology
|
April 28, 2016
Mutant p53 proteins counteract autophagic mechanism sensitizing cancer cells to mTOR inhibition
Marco Cordani, Elisa Oppici, Ilaria Dando, et al.
International Journal of Biological Macromolecules
|
January 1, 2026
Nanobodies as therapies for loss-of-function misfolding diseases: the example of Primary Hyperoxaluria Type 1
Mirco Dindo, Atanasio Gómez-Mulas, Juan Luis Pacheco-García, et al.
EMBO Molecular Medicine
|
January 17, 2023
Liver-directed gene therapy for ornithine aminotransferase deficiency
Iolanda Boffa, Elena Polishchuk, Lucia De Stefano, et al.
Molecular Genetics and Metabolism
|
July 25, 2024
Extending diagnostic practices in gyrate atrophy: Enzymatic characterization and the development of an in vitro pyridoxine responsiveness assay
Berith M Balfoort, Gioena Pampalone, Jos P N Ruiter, et al.
Page
of 11