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Riccardo Montioli Selected Research

Alanine-glyoxylate transaminase (alanine-glyoxylate aminotransferase)

1/2016Caenorhabditis elegans AGXT-1 is a mitochondrial and temperature-adapted ortholog of peroxisomal human AGT1: New insights into between-species divergence in glyoxylate metabolism.
1/2016Natural and Unnatural Compounds Rescue Folding Defects of Human Alanine: Glyoxylate Aminotransferase Leading to Primary Hyperoxaluria Type I.
10/2015The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I.
9/2015Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overview.
11/2014S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementation.
12/2013Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase.
1/2012Molecular insights into primary hyperoxaluria type 1 pathogenesis.
1/2012Biochemical 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 I.
11/2011Human liver peroxisomal alanine:glyoxylate aminotransferase: characterization of the two allelic forms and their pathogenic variants.
2/2010Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I.
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Riccardo Montioli Research Topics

Disease

9Primary Hyperoxaluria (Oxaluria, Primary)
01/2016 - 11/2007
6Gyrate Atrophy
01/2021 - 02/2014
5Primary hyperoxaluria type 1
01/2016 - 03/2009
4Parkinson Disease (Parkinson's Disease)
01/2016 - 12/2011
3Inborn Genetic Diseases (Disease, Hereditary)
09/2021 - 01/2012
3Rare Diseases (Rare Disease)
10/2015 - 02/2014
2Neurodegenerative Diseases (Neurodegenerative Disease)
09/2021 - 01/2012
2Blindness (Hysterical Blindness)
01/2021 - 01/2017
2Aromatic amino acid decarboxylase deficiency
10/2014 - 04/2013
1Neoplasms (Cancer)
11/2017
1Hydroxykynureninuria
02/2014
1Homocystinuria
02/2014
1Hypokinesia (Bradykinesia)
01/2012
1Tremor (Tremors)
01/2012
1Nervous System Diseases (Neurological Disorders)
01/2012
1Schizophrenia (Dementia Praecox)
12/2011
1Periodontitis
11/2006

Drug/Important Bio-Agent (IBA)

13EnzymesIBA
01/2020 - 11/2007
11Alanine-glyoxylate transaminase (alanine-glyoxylate aminotransferase)IBA
01/2016 - 11/2007
10PyridoxalIBA
01/2020 - 11/2006
4OrnithineIBA
01/2021 - 01/2017
4Transaminases (Aminotransferases)IBA
01/2021 - 01/2017
4Dopamine (Intropin)FDA LinkGeneric
01/2020 - 12/2011
4Serotonin (5 Hydroxytryptamine)IBA
01/2020 - 12/2011
3Aromatic-L-Amino-Acid DecarboxylasesIBA
09/2021 - 01/2012
3Ornithine-Oxo-Acid Transaminase (Ornithine Aminotransferase)IBA
01/2021 - 01/2019
3glyoxylic acid (glyoxylate)IBA
01/2016 - 01/2012
3Dopa DecarboxylaseIBA
01/2016 - 12/2011
2Proteins (Proteins, Gene)FDA Link
09/2021 - 10/2015
2OxalatesIBA
01/2016 - 03/2009
2Calcium OxalateIBA
09/2015 - 12/2013
2Pyridoxine (Pyridoxin)FDA LinkGeneric
02/2014 - 04/2013
1angiogeninIBA
09/2021
1Retinaldehyde (Retinal)IBA
01/2021
15-fluoromethylornithineIBA
01/2019
1SaltsIBA
01/2019
1ranpirnase (Pannon)IBA
11/2017
1BenserazideIBA
01/2016
1Carbidopa (Lodosyn)FDA LinkGeneric
01/2016
1Levodopa (L Dopa)FDA LinkGeneric
01/2016
1Aromatic Amino Acid Decarboxylase InhibitorsIBA
01/2016
1AcidsIBA
10/2015
1Coenzymes (Enzyme Cofactors)IBA
02/2014
1Neurotransmitter Agents (Neurotransmitter)IBA
12/2011
1Glycine (Aminoacetic Acid)FDA LinkGeneric
02/2010
1Histidine (L-Histidine)FDA Link
01/2008
1carbon-sulfur lyaseIBA
11/2006
1cystalysinIBA
11/2006
1Virulence Factors (Pathogenicity Factors)IBA
11/2006

Therapy/Procedure

1Therapeutics
10/2014