G. Maga

G. Maga, U. Hübscher, Kristijan Ramadan, 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Human Proliferating Cell Nuclear Antigen, Poly(ADP-ribose) Polymerase-1, and p21waf1/cip1

G. Maga, M. Savio, F. Riva, 2003, Journal of Biological Chemistry.

Cell cycle‐dependent dynamic association of cyclin/Cdk complexes with human DNA replication proteins

G. Biamonti, G. Maga, U. Hübscher, 2002, The EMBO journal.

De novo DNA synthesis by human DNA polymerase lambda, DNA polymerase mu and terminal deoxyribonucleotidyl transferase.

G. Maga, U. Hübscher, Kristijan Ramadan, 2004, Journal of molecular biology.

Human DNA polymerase lambda possesses terminal deoxyribonucleotidyl transferase activity and can elongate RNA primers: implications for novel functions.

G. Maga, L. Blanco, U. Hübscher, 2003, Journal of molecular biology.

Microhomology-mediated DNA strand annealing and elongation by human DNA polymerases λ and β on normal and repetitive DNA sequences

E. Crespan, G. Maga, U. Hübscher, 2012, Nucleic acids research.

Two Birds with a Stone: Molecular Cancer Therapy Targeting Signal Transduction and DNA Repair Pathways

E. Crespan, G. Maga, M. Kissová, 2013 .

Synthesis and biological activity evaluation of 3-(hetero) arylideneindolin-2-ones as potential c-Src inhibitors

E. Crespan, G. Maga, N. Zaffaroni, 2022, Journal of enzyme inhibition and medicinal chemistry.

Correction: Real-Time Analysis of Imatinib- and Dasatinib-Induced Effects on Chronic Myelogenous Leukemia Cell Interaction with Fibronectin

G. Maga, A. Obr, Pavla Rö Selová, 2014, PLoS ONE.

Human DNA Polymerase λ Functionally and Physically Interacts with Proliferating Cell Nuclear Antigen in Normal and Translesion DNA Synthesis*

G. Maga, L. Blanco, U. Hübscher, 2002, The Journal of Biological Chemistry.

Selective interactions of human kin17 and RPA proteins with chromatin and the nuclear matrix in a DNA damage- and cell cycle-regulated manner.

G. Maga, D. Biard, F. Harper, 2003, Nucleic acids research.

Chiral Indolylarylsulfone Non-Nucleoside Reverse Transcriptase Inhibitors as New Potent and Broad Spectrum Anti-HIV-1 Agents.

C. Limatola, E. Novellino, A. Coluccia, 2017, Journal of medicinal chemistry.

Living on the Edge: DNA Polymerase Lambda between Genome Stability and Mutagenesis.

G. Maga, U. Hübscher, B. van Loon, 2017, Chemical research in toxicology.

DNA Elongation by the Human DNA Polymerase λ Polymerase and Terminal Transferase Activities Are Differentially Coordinated by Proliferating Cell Nuclear Antigen and Replication Protein A*

G. Maga, U. Hübscher, Kristijan Ramadan, 2005, Journal of Biological Chemistry.

DNA polymerase θ purified from human cells is a high-fidelity enzyme

G. Maga, U. Hübscher, Kristijan Ramadan, 2002 .

DNA Polymerases: Discovery, Characterization and Functions in Cellular DNA Transactions

G. Maga, U. Hübscher, S. Spadari, 2010 .

Phosphorylation of the PCNA binding domain of the large subunit of replication factor C by Ca2+/calmodulin-dependent protein kinase II inhibits DNA synthesis.

G. Maga, U. Hübscher, R. Fischer, 1997, Biochemistry.

Dual mode of interaction of DNA polymerase epsilon with proliferating cell nuclear antigen in primer binding and DNA synthesis.

G. Maga, Z. Jónsson, U. Hübscher, 1999, Journal of molecular biology.

DNA replication machinery: functional characterization of a complex containing DNA polymerase alpha, DNA polymerase delta, and replication factor C suggests an asymmetric DNA polymerase dimer.

G. Maga, U. Hübscher, 1996, Biochemistry.

Targeting Cellular Cofactors in HIV Therapy

U. Dietrich, E. Crespan, G. Maga, 2014 .

Vif is an auxiliary factor of the HIV-1 reverse transcriptase and facilitates abasic site bypass.

G. Maga, S. Spadari, R. Cancio, 2004, The Biochemical journal.

DNA polymerase switching: I. Replication factor C displaces DNA polymerase α prior to PCNA loading

G. Maga, U. Hübscher, M. Stucki, 2000 .

Expansion of CAG triplet repeats by human DNA polymerases λ and β in vitro, is regulated by flap endonuclease 1 and DNA ligase 1.

E. Crespan, G. Maga, U. Hübscher, 2015, DNA repair.

Human base excision repair complex is physically associated to DNA replication and cell cycle regulatory proteins

G. Maga, E. Parlanti, E. Dogliotti, 2007, Nucleic acids research.

DNA replication: a complex matter

G. Maga, A. Montecucco, S. Spadari, 2003, EMBO reports.

Reconstitution of the base excision repair pathway for 7,8-dihydro-8-oxoguanine with purified human proteins.

E. Seeberg, G. Maga, E. Dogliotti, 2002, Nucleic acids research.

Genetic divergence of influenza A NS1 gene in pandemic 2009 H1N1 isolates with respect to H1N1 and H3N2 isolates from previous seasonal epidemics

F. Rovida, F. Baldanti, G. Maga, 2010, Virology Journal.

Biochemical Characterization of Arabidopsis thaliana DNA Polymerase λ: Role in the Oxidative DNA Damage Bypass

E. Crespan, G. Maga, A. Amoroso, 2009 .

Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors: Synthesis and Biological Evaluation of Novel Quinoxalinylethylpyridylthioureas as Potent Antiviral Agents

A. Bergamini, E. Novellino, G. Greco, 2000, Antiviral chemistry & chemotherapy.

5-Alkyl-2-alkylamino-6-(2,6-difluorophenylalkyl)-3,4-dihydropyrimidin-4(3H)-ones, a new series of potent, broad-spectrum non-nucleoside reverse transcriptase inhibitors belonging to the DABO family.

A. Mai, G. Maga, M. Artico, 2005, Bioorganic & medicinal chemistry.

Synthesis, biological evaluation and docking studies of 4-amino substituted 1H-pyrazolo[3,4-d]pyrimidines.

C. Tintori, C. Brullo, E. Crespan, 2008, European journal of medicinal chemistry.

A Motif Unique to the Human Dead-Box Protein DDX3 Is Important for Nucleic Acid Binding, ATP Hydrolysis, RNA/DNA Unwinding and HIV-1 Replication

U. Dietrich, G. Maga, A. Garbelli, 2011, PloS one.

Dual Src and Abl inhibitors target wild type Abl and the AblT315I Imatinib-resistant mutant with different mechanisms.

M. Radi, E. Crespan, S. Zanoli, 2010, Bioorganic & medicinal chemistry.

Multi-Target CFTR Modulators Endowed with Multiple Beneficial Side Effects for Cystic Fibrosis Patients: Toward a Simplified Therapeutic Approach.

M. Radi, C. Zamperini, E. Dreassi, 2019, Journal of medicinal chemistry.

The human tyrosine kinase Kit and its gatekeeper mutant T670I, show different kinetic properties: Implications for drug design.

E. Crespan, G. Maga, M. Kissová, 2016, Bioorganic & medicinal chemistry.

AKAP149 binds to HIV-1 reverse transcriptase and is involved in the reverse transcription.

J. Rain, G. Maga, R. Benarous, 2008, Journal of molecular biology.

Host DDX Helicases as Possible SARS-CoV-2 Proviral Factors: A Structural Overview of Their Hijacking Through Multiple Viral Proteins

R. Berisio, G. Maga, A. Ruggiero, 2020, Frontiers in Chemistry.

Discovery of the First Potent and Selective Inhibitors of Human dCTP Pyrophosphatase 1.

L. Meijer, P. Artursson, E. Crespan, 2016, Journal of medicinal chemistry.

DNA replication and repair bypass machines.

G. Maga, U. Hübscher, 2011, Current opinion in chemical biology.

Identification, partial purification and inhibition by guanine analogues of a novel enzymic activity which phosphorylates guanosine to GMP in the protozoan parasite Eimeria tenella.

G. Maga, F. Focher, S. Spadari, 1994, Biochemical Journal.

Diketo Hexenoic Acid Derivatives Are Novel Selective Non-Nucleoside Inhibitors of Mammalian Terminal Deoxynucleotidyl Transferases, with Potent Cytotoxic Effect against Leukemic Cells

E. Crespan, G. Maga, U. Hübscher, 2005, Molecular Pharmacology.

Crystal structure of HIV-1 reverse transcriptase bound to a non-nucleoside inhibitor with a novel mechanism of action.

M. Radi, E. Crespan, G. Maga, 2010, Angewandte Chemie.

Mutational analysis of the HIV-1 auxiliary protein Vif identifies independent domains important for the physical and functional interaction with HIV-1 reverse transcriptase

G. Maga, C. Bovolenta, R. Lupo, 2014, Nucleic acids research.

A conserved domain of the large subunit of replication factor C binds PCNA and acts like a dominant negative inhibitor of DNA replication in mammalian cells.

G. Maga, R. Fotedar, A. Fotedar, 1996, The EMBO journal.

A new proofreading mechanism for lesion bypass by DNA polymerase‐λ

E. Crespan, G. Maga, U. Hübscher, 2012, EMBO reports.

Mutagenesis of human DNA polymerase lambda: essential roles of Tyr505 and Phe506 for both DNA polymerase and terminal transferase activities.

G. Maga, U. Hübscher, Kristijan Ramadan, 2003, Nucleic acids research.

DNA Polymerase λ from Calf Thymus Preferentially Replicates Damaged DNA*

G. Maga, U. Hübscher, Kristijan Ramadan, 2002, The Journal of Biological Chemistry.

New nucleotide-competitive non-nucleoside inhibitors of terminal deoxynucleotidyl transferase: discovery, characterization, and crystal structure in complex with the target.

M. Delarue, E. Novellino, B. Maresca, 2013, Journal of medicinal chemistry.

Silencing of human DNA polymerase λ causes replication stress and is synthetically lethal with an impaired S phase checkpoint

G. Mazzini, G. Dianov, G. Maga, 2012, Nucleic acids research.

Expanding the repertoire of DNA polymerase substrates: template-instructed incorporation of non-nucleoside triphosphate analogues by DNA polymerases β and λ

E. Crespan, G. Maga, M. Kukhanova, 2006, Nucleic acids research.

Human replication protein A can suppress the intrinsic in vitro mutator phenotype of human DNA polymerase λ

G. Maga, U. Hübscher, I. Shevelev, 2006, Nucleic acids research.

Human DNA polymerase β, but not λ, can bypass a 2-deoxyribonolactone lesion together with proliferating cell nuclear antigen.

E. Crespan, G. Maga, U. Hübscher, 2013, ACS chemical biology.

A Role for Human DNA Polymerase λ in Alternative Lengthening of Telomeres

S. Bione, E. Crespan, G. Maga, 2021, International journal of molecular sciences.

Replication protein A and proliferating cell nuclear antigen coordinate DNA polymerase selection in 8-oxo-guanine repair

E. Crespan, G. Maga, U. Hübscher, 2008, Proceedings of the National Academy of Sciences.

Error-free bypass of 2-hydroxyadenine by human DNA polymerase λ with Proliferating Cell Nuclear Antigen and Replication Protein A in different sequence contexts

E. Crespan, G. Maga, U. Hübscher, 2007, Nucleic acids research.

Novel alternative ribonucleotide excision repair pathways in human cells by DDX3X and specialized DNA polymerases

G. Maga, F. Casiraghi, A. Gagliardi, 2020, Nucleic acids research.

Impact of ribonucleotide incorporation by DNA polymerases β and λ on oxidative base excision repair

E. Crespan, G. Maga, U. Hübscher, 2016, Nature Communications.

DNA Polymerases

G. Maga, 2019, Reference Module in Biomedical Sciences.

Ribonucleotide incorporation by human DNA polymerase η impacts translesion synthesis and RNase H2 activity

E. Crespan, G. Maga, U. Hübscher, 2016, Nucleic acids research.

Indolyl-pyrrolone as a new scaffold for Pim1 inhibitors.

Fabrizio Manetti, Maurizio Botta, Silvia Schenone, 2009, Bioorganic & medicinal chemistry letters.

From the magic bullet to the magic target: exploiting the diverse roles of DDX3X in viral infections and tumorigenesis.

G. Maga, V. Riva, 2019, Future medicinal chemistry.

The resveratrol analogue 4,4'-dihydroxy-trans-stilbene inhibits cell proliferation with higher efficiency but different mechanism from resveratrol.

G. Maga, M. Savio, L. Stivala, 2009, The international journal of biochemistry & cell biology.

Identification of a new family of pyrazolo[3,4-d]pyrimidine derivatives as multitarget Fyn-Blk-Lyn inhibitors active on B- and T-lymphoma cell lines.

F. Musumeci, A. L. Fallacara, E. Crespan, 2019, European journal of medicinal chemistry.

DNA polymerase switching: I. Replication factor C displaces DNA polymerase alpha prior to PCNA loading.

G. Maga, U. Hübscher, M. Stucki, 2000, Journal of molecular biology.

The Arabidopsis STRESS RESPONSE SUPPRESSOR DEAD-box RNA helicases are nucleolar- and chromocenter-localized proteins that undergo stress-mediated relocalization and are involved in epigenetic gene silencing.

G. Maga, Asif Khan, S. Barak, 2014, The Plant journal : for cell and molecular biology.

RFLP-based genetic relationships of Einkorn wheats

G. Maga, F. Salamini, M. Heun, 1994, Theoretical and Applied Genetics.

DDX3X inhibitors, an effective way to overcome HIV-1 resistance targeting host proteins.

C. Zamperini, E. Dreassi, G. Maga, 2020, European journal of medicinal chemistry.

Novel pyrazolo[3,4-d]pyrimidines as dual Src-Abl inhibitors active against mutant form of Abl and the leukemia K-562 cell line.

Riham F. George, E. Crespan, G. Maga, 2016, European journal of medicinal chemistry.

Inhibition of Bcr‐Abl Phosphorylation and Induction of Apoptosis by Pyrazolo[3,4‐d]pyrimidines in Human Leukemia Cells

C. Brullo, G. Maga, S. Schenone, 2007, ChemMedChem.

A unique domain for a unique target: selective inhibitors of host cell DDX3X to fight emerging viruses.

E. Dreassi, G. Maga, M. Botta, 2020, Journal of medicinal chemistry.

Exploring the Implication of DDX3X in DENV Infection: Discovery of the First-in-Class DDX3X Fluorescent Inhibitor.

E. Dreassi, G. Maga, M. Botta, 2020, ACS medicinal chemistry letters.

Pharmacophore modeling and molecular docking led to the discovery of inhibitors of human immunodeficiency virus-1 replication targeting the human cellular aspartic acid-glutamic acid-alanine-aspartic acid box polypeptide 3.

G. Maga, M. Botta, M. Witvrouw, 2008, Journal of medicinal chemistry.

What makes y family pols potential candidates for molecular targeted therapies and novel biotechnological applications.

G. Maga, G. Casari, Antonio Tomasso, 2014, Current molecular medicine.

Determination of permeability and lipophilicity of pyrazolo-pyrimidine tyrosine kinase inhibitors and correlation with biological data.

E. Dreassi, G. Maga, S. Schenone, 2009, European journal of medicinal chemistry.

Exploring the role of 2-chloro-6-fluoro substitution in 2-alkylthio-6-benzyl-5-alkylpyrimidin-4(3H)-ones: effects in HIV-1-infected cells and in HIV-1 reverse transcriptase enzymes.

Rino Ragno, Flavio Ballante, Roberto Cirilli, 2014, Journal of medicinal chemistry.

Substrate‐Induced Stable Enzyme–Inhibitor Complex Formation Allows Tight Binding of Novel 2‐Aminopyrimidin‐4(3H)‐ones to Drug‐Resistant HIV‐1 Reverse Transcriptase Mutants

Antonello Mai, Mercedes Armand-Ugón, José A. Esté, 2008, ChemMedChem.

Slow‐, Tight‐Binding HIV‐1 Reverse Transcriptase Non‐Nucleoside Inhibitors Highly Active against Drug‐Resistant Mutants

Gianluca Sbardella, Antonello Mai, Imma Clotet-Codina, 2007, ChemMedChem.

Human terminal deoxynucleotidyl transferases as novel targets for anticancer chemotherapy.

G. Maga, R. Di Santo, 2006, Current medicinal chemistry.

Human DNA polymerases lambda and beta show different efficiencies of translesion DNA synthesis past abasic sites and alternative mechanisms for frameshift generation.

G. Maga, U. Hübscher, Kristijan Ramadan, 2004, Biochemistry.

DNA polymerase lambda from calf thymus preferentially replicates damaged DNA.

G. Maga, U. Hübscher, Kristijan Ramadan, 2002, Journal of Biological Chemistry.

Structure‐Based Pharmacophore Identification of New Chemical Scaffolds as Non‐Nucleoside Reverse Transcriptase Inhibitors.

Angela Rao, Alba Chimirri, Nunzio Iraci, 2007 .

The 2009 influenza pandemic: promising lessons for antiviral therapy for future outbreaks.

G. Maga, L. Bavagnoli, 2011, Current Medicinal Chemistry.

Identification of a novel antiviral micro-RNA targeting the NS1 protein of the H1N1 pandemic human influenza virus and a corresponding viral escape mutation.

S. Bione, F. Baldanti, G. Maga, 2019, Antiviral research.

HIV‐1 reverse transcriptase and integrase enzymes physically interact and inhibit each other

G. Maga, U. Hübscher, M. Hottiger, 2001, FEBS letters.

Tyrosine Kinase Inhibitor Si409 Has In Vitro and In Vivo Anti-Tumor Activity Against Diffuse Large B-Cell Lymphoma

C. Zamperini, E. Dreassi, E. Crespan, 2023, Pharmaceutical Chemistry Journal.

High Flexibility of RNaseH2 Catalytic Activity with Respect to Non-Canonical DNA Structures

E. Crespan, G. Maga, V. Pirota, 2021, International journal of molecular sciences.

Enantioselective binding of second generation pyrrolobenzoxazepinones to the catalytic ternary complex of HIV-1 RT wild-type and L100I and K103N drug resistant mutants.

E. Novellino, S. Zanoli, G. Maga, 2011, Bioorganic & medicinal chemistry letters.

Specific targeting of highly conserved residues in the HIV-1 reverse transcriptase primer grip region. 2. Stereoselective interaction to overcome the effects of drug resistant mutations.

A. Bergamini, E. Novellino, S. Zanoli, 2009, Journal of medicinal chemistry.

Human Immunodeficiency Virus (HIV-1) Auxiliary Protein Vif and Cellular APOBEC Deaminases: Their Roles Unveiled?

G. Maga, S. Spadari, R. Franca, 2005 .

Nevirapine-selected mutations Y181I/C of HIV-1 reverse transcriptase confer cross-resistance to stavudine

F. Baldanti, G. Maga, G. Gerna, 2003, AIDS.

Detection of a new HIV-1 reverse transcriptase mutation (Q145M) conferring resistance to nucleoside and non-nucleoside inhibitors in a patient failing highly active antiretroviral therapy.

F. Baldanti, G. Maga, G. Gerna, 2003, AIDS.

Biological Evaluation and In Vitro Characterization of ADME Profile of In-House Pyrazolo[3,4-d]pyrimidines as Dual Tyrosine Kinase Inhibitors Active against Glioblastoma Multiforme

F. Musumeci, E. Dreassi, E. Crespan, 2023, Pharmaceutics.

New nitrogen containing substituents at the indole-2-carboxamide yield high potent and broad spectrum indolylarylsulfone HIV-1 non-nucleoside reverse transcriptase inhibitors.

E. Novellino, B. Clotet, A. Coluccia, 2012, Journal of medicinal chemistry.

Structure-Based Pharmacophore Identification of New Chemical Scaffolds as Non-Nucleoside Reverse Transcriptase Inhibitors

M. Letizia Barreca, Angela Rao, Laura De Luca, 2007, J. Chem. Inf. Model..

NNRTI-selected mutations at codon 190 of human immunodeficiency virus type 1 reverse transcriptase decrease susceptibility to stavudine and zidovudine.

F. Baldanti, G. Maga, G. Gerna, 2007, Antiviral research.

Gln145Met/Leu Changes in Human Immunodeficiency Virus Type 1 Reverse Transcriptase Confer Resistance to Nucleoside and Nonnucleoside Analogs and Impair Virus Replication

Maurizio Zazzi, Fausto Baldanti, F. Baldanti, 2004, Antimicrobial Agents and Chemotherapy.

3D QSAR Models Built on Structure‐Based Alignments of Abl Tyrosine Kinase Inhibitors

Fabrizio Manetti, Maurizio Botta, Silvia Schenone, 2009, ChemMedChem.

DNA polymerase theta purified from human cells is a high-fidelity enzyme.

G. Maga, U. Hübscher, Kristijan Ramadan, 2002, Journal of molecular biology.

Pyrazolo[3,4-d]pyrimidine Prodrugs: Strategic Optimization of the Aqueous Solubility of Dual Src/Abl Inhibitors.

M. Radi, F. Musumeci, C. Zamperini, 2013, ACS medicinal chemistry letters.

Human DNA Polymerase Functionally and Physically Interacts with Proliferating Cell Nuclear Antigen in Normal and

Consejo Superior de Investigaciones, G. Maga, L. Blanco, 2002 .

Hepatitis C virus NS3 ATPase/helicase: an ATP switch regulates the cooperativity among the different substrate binding sites.

G. Maga, S. Spadari, G. Locatelli, 2002, Biochemistry.

Identification of Broad‐Spectrum Dengue/Zika Virus Replication Inhibitors by Functionalization of Quinoline and 2,6‐Diaminopurine Scaffolds

M. Radi, E. Crespan, G. Maga, 2018, ChemMedChem.

Interaction of SARS-CoV-2 Nucleocapsid Protein and Human RNA Helicases DDX1 and DDX3X Modulates Their Activities on Double-Stranded RNA

G. Maga, A. De Palma, P. Mauri, 2023, International journal of molecular sciences.

DNA Polymerases

G. Maga, 2019, Reference Module in Biomedical Sciences.

Indolylarylsulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: new cyclic substituents at the indole-2-carboxamide

E. Novellino, A. Coluccia, A. Brancale, 2011 .

N2‐Benzyloxycarbonylguan‐9‐yl Acetic Acid Derivatives as HIV‐1 Reverse Transcriptase Non‐Nucleoside Inhibitors with Decreased Loss of Potency Against Common Drug‐Resistance Mutations.

S. Zanoli, G. Maga, N. Howarth, 2007, ChemMedChem.

Identification and Biological Characterization of the Pyrazolo[3,4-d]pyrimidine Derivative SI388 Active as Src Inhibitor

F. Musumeci, E. Crespan, G. Maga, 2023, Pharmaceuticals.

AKAP149 binds to HIV-1 reverse transcriptase and is involved in the reverse transcription.

J. Rain, G. Maga, R. Benarous, 2008, Journal of molecular biology.

Chiral Indolylarylsulfone Non-Nucleoside Reverse Transcriptase Inhibitors as New Potent and Broad Spectrum Anti-HIV-1 Agents.

C. Limatola, E. Novellino, A. Coluccia, 2017, Journal of medicinal chemistry.

Cell cycle‐dependent dynamic association of cyclin/Cdk complexes with human DNA replication proteins

G. Biamonti, G. Maga, U. Hübscher, 2002, The EMBO journal.

Eukaryotic DNA polymerases.

G. Maga, U. Hubscher, S. Spadari, 2002, Annual review of biochemistry.

A cascade screening approach for the identification of Bcr-Abl myristate pocket binders active against wild type and T315I mutant.

M. Radi, C. Tintori, A. L. Fallacara, 2016, Bioorganic & medicinal chemistry letters.

Oxidative DNA Damage Bypass in Arabidopsis thaliana Requires DNA Polymerase λ and Proliferating Cell Nuclear Antigen 2[W]

C. Bergounioux, E. Crespan, G. Maga, 2011, Plant Cell.

Replication protein A and proliferating cell nuclear antigen coordinate DNA polymerase selection in 8-oxo-guanine repair

E. Crespan, G. Maga, U. Hübscher, 2008, Proceedings of the National Academy of Sciences.

A Combination Strategy to Inhibit Pim‐1: Synergism between Noncompetitive and ATP‐Competitive Inhibitors

M. Radi, C. Tintori, F. Musumeci, 2013, ChemMedChem.

DNA replication and repair bypass machines.

G. Maga, U. Hübscher, 2011, Current opinion in chemical biology.

Proliferating cell nuclear antigen (PCNA): a dancer with many partners

G. Maga, U. Hübscher, 2003, Journal of Cell Science.

Human DNA Polymerases: Biology, Medicine and Biotechnology

G. Maga, U. Hübscher, S. Spadari, 2017 .

Mutant DNA polymerase delta from thermosensitive Schizosaccharomyces pombe strains display reduced stimulation by proliferating cell nuclear antigen.

G. Maga, U. Hübscher, S. Francesconi, 1998, The Biochemical journal.