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#TitleJournalYearCitations
1STAT1 drives M1 microglia activation and neuroinflammation under hypoxiaArchives of Biochemistry and Biophysics201998
2Metastatic Breast Cancer Cells Enter Into Dormant State and Express Cancer Stem Cells Phenotype Under Chronic HypoxiaJournal of Cellular Biochemistry201791
3The chaperone role of the pyridoxal 5′-phosphate and its implications for rare diseases involving B6-dependent enzymesClinical Biochemistry201480
4Redox Regulation of STAT1 and STAT3 SignalingInternational Journal of Molecular Sciences202076
5Tumor Dormancy and Interplay with Hypoxic Tumor MicroenvironmentInternational Journal of Molecular Sciences201974
6Molecular basis of primary hyperoxaluria: clues to innovative treatmentsUrolithiasis201955
7Structural effects of Mg2+ on the regulatory states of three neuronal calcium sensors operating in vertebrate phototransductionBiochimica Et Biophysica Acta - Molecular Cell Research201554
8Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type IHuman Molecular Genetics201550
9Allosteric communication pathways routed by Ca2+/Mg2+ exchange in GCAP1 selectively switch target regulation modesScientific Reports201643
10Delivery success rate of engineered nanoparticles in the presence of the protein corona: a systems-level screeningNanomedicine: Nanotechnology, Biology, and Medicine201238
11Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overviewBiochimica Et Biophysica Acta - Proteins and Proteomics201538
12Divalent cations modulate membrane binding and pore formation of a potent antibiotic peptide analog of alamethicinCell Calcium201336
13Two retinal dystrophy-associated missense mutations inGUCA1Awith distinct molecular properties result in a similar aberrant regulation of the retinal guanylate cyclaseHuman Molecular Genetics201536
14Biochemical 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 IMolecular Genetics and Metabolism201234
15Nanodevice-induced conformational and functional changes in a prototypical calcium sensor proteinNanoscale201434
16Dysfunction of cGMP signalling in photoreceptors by a macular dystrophy-related mutation in the calcium sensor GCAP1Human Molecular Genetics201734
17Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferaseBiochimica Et Biophysica Acta - Molecular Basis of Disease201333
18Structural plasticity of calmodulin on the surface of CaF2nanoparticles preserves its biological functionNanoscale201433
19A novel p.(Glu111Val) missense mutation in GUCA1A associated with cone-rod dystrophy leads to impaired calcium sensing and perturbed second messenger homeostasis in photoreceptorsHuman Molecular Genetics201832
20The N-terminal extension is essential for the formation of the active dimeric structure of liver peroxisomal alanine:glyoxylate aminotransferaseInternational Journal of Biochemistry and Cell Biology201229
21S-glutathionylation exerts opposing roles in the regulation of STAT1 and STAT3 signaling in reactive microgliaFree Radical Biology and Medicine201829
22Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analysesHuman Molecular Genetics201929
23A Novel Pathway for Metabolism of the Cardiovascular Risk Factor Homoarginine by alanine:glyoxylate aminotransferase 2Scientific Reports201627
24Molecular insights into primary hyperoxaluria Type I pathogenesisFrontiers in Bioscience - Landmark201226
25Impact of cone dystrophy-related mutations in GCAP1 on a kinetic model of phototransductionCellular and Molecular Life Sciences201426
26Targeting Cystalysin, a Virulence Factor of Treponema denticola‐Supported PeriodontitisChemMedChem201426
27Preferential Binding of Mg2+ Over Ca2+ to CIB2 Triggers an Allosteric Switch Impaired in Usher Syndrome Type 1JFrontiers in Molecular Neuroscience201826
28A physiological role for the supramolecular organization of rhodopsin and transducin in rod photoreceptorsFEBS Letters201325
29Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implicationsProteins: Structure, Function and Bioinformatics201324
30Mutations in PLS1 , encoding fimbrin, cause autosomal dominant nonsyndromic hearing lossHuman Mutation201923
31Biochemical and Computational Approaches to Improve the Clinical Treatment of Dopa Decarboxylase-Related Diseases: An OverviewThe Open Biochemistry Journal201223
32Deficit of human ornithine aminotransferase in gyrate atrophy: Molecular, cellular, and clinical aspectsBiochimica Et Biophysica Acta - Proteins and Proteomics202122
33Rapid Profiling of Disease Alleles Using a Tunable Reporter of Protein MisfoldingGenetics201220
34Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type INanomedicine: Nanotechnology, Biology, and Medicine201720
35The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type IACS Chemical Biology201519
36New variants of AADC deficiency expand the knowledge of enzymatic phenotypesArchives of Biochemistry and Biophysics202019
37Correlation between the molecular effects of mutations at the dimer interface of alanine–glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B6Journal of Inherited Metabolic Disease201818
38Evolutionary-Conserved Allosteric Properties of Three Neuronal Calcium Sensor ProteinsFrontiers in Molecular Neuroscience201918
39Aromatic Amino Acid Decarboxylase Deficiency: The Added Value of BiochemistryInternational Journal of Molecular Sciences202118
40Allele-specific Characterization of Alanine: Glyoxylate Aminotransferase Variants Associated with Primary HyperoxaluriaPLoS ONE201417
41Fingerprints of Calcium-Binding Protein Conformational Dynamics Monitored by Surface Plasmon ResonanceACS Chemical Biology201617
42Normal GCAPs partly compensate for altered cGMP signaling in retinal dystrophies associated with mutations in GUCA1AScientific Reports201917
43Electrostatic interactions drive native‐like aggregation of human alanine:glyoxylate aminostransferaseFEBS Journal201715
44Gut microbiota modulates seizure susceptibilityEpilepsia202115
45Astrocytes Regulate the Expression of Insulin-Like Growth Factor 1 Receptor (IGF1-R) in Primary Cortical Neurons During In Vitro SenescenceJournal of Molecular Neuroscience201014
46Polymorphism −2604G>A variants in TLR4 promoter are associated with different gene expression level in peripheral blood of atherosclerotic patientsJournal of Human Genetics201314
47Natural Sesquiterpene Lactones Enhance Chemosensitivity of Tumor Cells through Redox Regulation of STAT3 SignalingOxidative Medicine and Cellular Longevity201914
48A medieval case of digitalis poisoning: the sudden death of Cangrande della Scala, lord of verona (1291–1329)Journal of Archaeological Science201513
49CaF2nanoparticles as surface carriers of GCAP1, a calcium sensor protein involved in retinal dystrophiesNanoscale201713
50Folding Defects Leading to Primary HyperoxaluriaHandbook of Experimental Pharmacology201713