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DNA damage and repair in human cancer: molecular mechanisms and contribution to therapy-related leukemias

International journal of environmental research and public health, 2012-08, Vol.9 (8), p.2636-2657

2012

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The Risk of Recurrent Deep Venous Thrombosis among Heterozygous Carriers of Both Factor V Leiden and the G20210A Prothrombin Mutation

The New England journal of medicine, 1999-09, Vol.341 (11), p.801-806

1999

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Role of mismatch repair and MGMT in response to anticancer therapies

Anti-cancer agents in medicinal chemistry, 2008-05, Vol.8 (4), p.368-380

2008

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Intratumoral injection of IFN-alpha dendritic cells after dacarbazine activates anti-tumor immunity: results from a phase I trial in advanced melanoma

Journal of translational medicine, 2015-05, Vol.13 (1), p.139, Article 139

2015

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Role of MUTYH and MSH2 in the Control of Oxidative DNA Damage, Genetic Instability, and Tumorigenesis

Cancer research (Chicago, Ill.), 2009-05, Vol.69 (10), p.4372-4379

2009

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The Mutyh base excision repair gene influences the inflammatory response in a mouse model of ulcerative colitis

PloS one, 2010-08, Vol.5 (8), p.e12070

2010

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Repeated Sequences in CASPASE-5 and FANCD2 but not NF1 Are Targets for Mutation in Microsatellite-Unstable Acute Leukemia/Myelodysplastic Syndrome

Molecular cancer research, 2005-05, Vol.3 (5), p.251-260

2005

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Cholesterol Granuloma of the Frontal Sinus : A Case Report

Case reports in otolaryngology, 2012-01, Vol.2012 (2012), p.1-3

2012

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MUTYH mediates the toxicity of combined DNA 6-thioguanine and UVA radiation

Oncotarget, 2015-04, Vol.6 (10), p.7481-7492

2015

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Prevalence of the factor II G20210A mutation in symptomatic patients with inherited thrombophilia

Thrombosis and haemostasis, 1998-08, Vol.80 (2), p.342-343

1998

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G20210A prothrombin gene polymorphism and extent of coronary disease

Thrombosis and haemostasis, 2000-07, Vol.84 (1), p.142-143

2000

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Prevalence of the 677C to T mutation in the methylenetetrahydrofolate reductase gene in Italian patients with venous thrombotic disease

Thrombosis and haemostasis, 1998-03, Vol.79 (3), p.686-687

1998

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Prothrombin G20210A Mutant Genotype Is a Risk Factor for Cerebrovascular Ischemic Disease in Young Patients

Blood, 1998-05, Vol.91 (10), p.3562-3565

1998

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Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients

Blood, 1998-05, Vol.91 (10), p.3562-3565

1998

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Hepatic vein thrombosis in a patient with mutant prothrombin 20210A allele

Thrombosis and haemostasis, 1998-09, Vol.80 (3), p.519-519

1998

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The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation

British journal of haematology, 2001-06, Vol.113 (3), p.630-635

2001

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Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease

The American journal of gastroenterology, 2001-09, Vol.96 (9), p.2677-2682

2001

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Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease

The American journal of gastroenterology, 2001, Vol.96 (9), p.2677-2682

2001

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Drug treatment in the development of mismatch repair defective acute leukemia and myelodysplastic syndrome

DNA repair, 2003-05, Vol.2 (5), p.547-559

2003

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Methylation damage response in hematopoietic progenitor cells

DNA repair, 2007-08, Vol.6 (8), p.1170-1178

2007

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Interaction between Hyperhomocysteinemia and Inherited Thrombophilic Factors in Venous Thromboembolism

Seminars in thrombosis and hemostasis, 2000, Vol.26 (3), p.305-312

2000

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Prevalence of mild hyperhomocysteinaemia and association with thrombophilic genotypes (factor V Leiden and prothrombin G20210A) in Italian patients with venous thromboembolic disease

British journal of haematology, 1999-08, Vol.106 (2), p.564-568

1999

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A recursive network approach can identify constitutive regulatory circuits in gene expression data

Physica A, 2005-03, Vol.348, p.349-370

2005

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Methylation damage response in hematopoietic progenitor cells: MGMT: REVERSAL OF FORTUNE. From basic biochemistry to clinical exploitation of the DNA damage reversal protein, O6-methylguanine-DNA methyltransferase

DNA repair, 2007, Vol.6 (8), p.1170-1178

2007

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T2079 Frequency of Microsatellite Instability and Alterations of DNA Repair Systems in Non-Dysplastic Mucosa of Inflammatory Bowel Disease Patients

Gastroenterology (New York, N.Y. 1943), 2008, Vol.134 (4), p.A-614-A-614

2008

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DNA damage and repair in human cancer: molecular mechanisms and contribution to therapy-related leukemias

The Risk of Recurrent Deep Venous Thrombosis among Heterozygous Carriers of Both Factor V Leiden and the G20210A Prothrombin Mutation

Role of mismatch repair and MGMT in response to anticancer therapies

Intratumoral injection of IFN-alpha dendritic cells after dacarbazine activates anti-tumor immunity: results from a phase I trial in advanced melanoma

Role of MUTYH and MSH2 in the Control of Oxidative DNA Damage, Genetic Instability, and Tumorigenesis

The Mutyh base excision repair gene influences the inflammatory response in a mouse model of ulcerative colitis

Repeated Sequences in CASPASE-5 and FANCD2 but not NF1 Are Targets for Mutation in Microsatellite-Unstable Acute Leukemia/Myelodysplastic Syndrome

Cholesterol Granuloma of the Frontal Sinus : A Case Report

MUTYH mediates the toxicity of combined DNA 6-thioguanine and UVA radiation

Prevalence of the factor II G20210A mutation in symptomatic patients with inherited thrombophilia

G20210A prothrombin gene polymorphism and extent of coronary disease

Prevalence of the 677C to T mutation in the methylenetetrahydrofolate reductase gene in Italian patients with venous thrombotic disease

Prothrombin G20210A Mutant Genotype Is a Risk Factor for Cerebrovascular Ischemic Disease in Young Patients

Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients

Hepatic vein thrombosis in a patient with mutant prothrombin 20210A allele

The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation

Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease

Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease

Drug treatment in the development of mismatch repair defective acute leukemia and myelodysplastic syndrome

Methylation damage response in hematopoietic progenitor cells

Interaction between Hyperhomocysteinemia and Inherited Thrombophilic Factors in Venous Thromboembolism

Prevalence of mild hyperhomocysteinaemia and association with thrombophilic genotypes (factor V Leiden and prothrombin G20210A) in Italian patients with venous thromboembolic disease

A recursive network approach can identify constitutive regulatory circuits in gene expression data

Methylation damage response in hematopoietic progenitor cells: MGMT: REVERSAL OF FORTUNE. From basic biochemistry to clinical exploitation of the DNA damage reversal protein, O6-methylguanine-DNA methyltransferase

T2079 Frequency of Microsatellite Instability and Alterations of DNA Repair Systems in Non-Dysplastic Mucosa of Inflammatory Bowel Disease Patients

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