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Maria Vittoria Cubellis

Observed names: Cubellis, Maria, Cubellis, Maria Vittoria, Cubellis, Maria, Vittoria, M V Cubellis, M. V. CUBELLIS, M. V. Cubellis, M. VITTORIA CUBELLIS, M. Vittoria CUBELLIS, M. Vittoria Cubellis, M.V. CUBELLIS, M.V. Cubellis, M.Vittoria Cubellis, MV Cubellis, Maria Cubellis, Maria V Cubellis, Maria V. Cubellis, Maria Vittoria CUBELLIS
Observed institutions: University of Copenhagen, University of Milan, University of Campania "Luigi Vanvitelli", University of Cambridge, Stazione Zoologica Anton Dohrn, Accademia di Belle Arti di Napoli, Institute of Applied Science and Intelligent Systems, Federico II University Hospital, Institute of Protein Biochemistry, Institute of Biostructure and Bioimaging, Institute of Genetics and Biophysics, Istituto di Chimica Biomolecolare, National Research Council, University of Naples Federico II, Sapienza University of Rome
ORCID: 0000-0001-6147-6553
Observed ORCID: 0000-0001-6147-6553
OpenAlex ID: A5010599632
Cloning and expression of the receptor for human urokinase plasminogen activator, a central molecule in cell surface, plasmin dependent proteolysis.
1990 · A.L. Roldan, M.V. Cubellis, et al. · The EMBO Journal · 603
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Receptor‐mediated internalization and degradation of urokinase is caused by its specific inhibitor PAI‐1.
1990 · M.V. Cubellis, T.C. Wun, et al. · The EMBO Journal · 375
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Autocrine saturation of pro-urokinase receptors on human A431 cells
1986 · M.Patrizia Stoppelli, Carlo Tacchetti, et al. · Cell · 357
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome
2008 · Jet Bliek, Gaetano Verde, et al. · European Journal of Human Genetics · 229
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(Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome
2015 · Alessandro Mussa, Silvia Russo, et al. · European Journal of Human Genetics · 200
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Binding of single-chain prourokinase to the urokinase receptor of human U937 cells.
1986 · M V Cubellis, M L Nolli, et al. · Journal of Biological Chemistry · 188
Accessibility of receptor-bound urokinase to type-1 plasminogen activator inhibitor.
1989 · M V Cubellis, P Andreasen, et al. · Proceedings of the National Academy of Sciences · 180
Pharmacological Chaperones: A Therapeutic Approach for Diseases Caused by Destabilizing Missense Mutations
2020 · Ludovica Liguori, Maria Monticelli, et al. · International Journal of Molecular Sciences · 139
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Regulation of urokinase receptors in monocytelike U937 cells by phorbol ester phorbol myristate acetate.
1989 · R Picone, E L Kajtaniak, et al. · The Journal of Cell Biology · 139
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The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases
2011 · Nicoletta Chiesa, Agostina De Crescenzo, et al. · Human Molecular Genetics · 126
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Properties of polyproline II, a secondary structure element implicated in protein–protein interactions
2005 · M. V. Cubellis, F. Caillez, et al. · Proteins Structure Function and Bioinformatics · 110
Isolation and sequencing of a new β-galactosidase-encoding archaebacterial gene
1990 · Maria Vittoria Cubellis, Carla Rozzo, et al. · Gene · 110
CDKN1C mutations: two sides of the same coin
2014 · Thomas Eggermann, Gerhard Binder, et al. · Trends in Molecular Medicine · 99
The pharmacological chaperone 1-deoxynojirimycin increases the activity and lysosomal trafficking of multiple mutant forms of acid alpha-glucosidase
2009 · John J. Flanagan, Barbara Rossi, et al. · Human Mutation · 99
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The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites
2012 · Jasmin Beygo, Valentina Citro, et al. · Human Molecular Genetics · 98
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The receptor for urokinase‐plasminogen activator
1986 · Francesco Blasi, M. Patrizia Stoppelli, et al. · Journal of Cellular Biochemistry · 96
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour
2008 · F. Cerrato, A. Sparago, et al. · Human Molecular Genetics · 87
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Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
2020 · Maria Vittoria Cubellis, Laura Pignata, et al. · Clinical Epigenetics · 78
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Cloning and sequencing of the gene coding for aspartate aminotransferase from the thermoacidophilic archaebacterium Sulfolobus solfataricus
1989 · Maria Vittoria CUBELLIS, Carla ROZZO, et al. · European Journal of Biochemistry · 78
The urokinase receptor and regulation of cell surface plasminogen activation
1990 · Francesco Blasi, M. Vittoria Cubellis, et al. · Cell Differentiation and Development · 76
Secondary structure assignment that accurately reflects physical and evolutionary characteristics
2005 · Maria Vittoria Cubellis, Fabien Cailliez, et al. · BMC Bioinformatics · 65
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Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women
2021 · Maria Monticelli, Bruno Hay Mele, et al. · Genes · 62
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The urokinase receptor: Structure, regulation and inhibitor-mediated internalization
1994 · F. Blasi, M. Conese, et al. · Fibrinolysis and Proteolysis · 62
Looking for protein stabilizing drugs with thermal shift assay
2015 · Giuseppina Andreotti, Maria Monticelli, et al. · Drug Testing and Analysis · 61
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Inherited and Sporadic Epimutations at the IGF2-H19 Locus in Beckwith-Wiedemann Syndrome and Wilms’ Tumor
2009 · Andrea Riccio, Angela Sparago, et al. · Endocrine development · 51
Works count: 175
Citation count: 5,351
H-index: 37
I10-index: 78
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