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Hereditary Breast Cancer: The Era of New Susceptibility Genes

BioMed research international, 2013-01, Vol.2013, p.747318-11

2013

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The Case of Medication-Related Osteonecrosis of the Jaw Addressed from a Pathogenic Point of View. Innovative Therapeutic Strategies: Focus on the Most Recent Discoveries on Oral Mesenchymal Stem Cell-Derived Exosomes

Pharmaceuticals (Basel, Switzerland), 2020-11, Vol.13 (12), p.423

2020

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Novel insights into the pharmacological modulation of human periodontal ligament stem cells by the amino-bisphosphonate Alendronate

European journal of cell biology, 2023-12, Vol.102 (4), p.151354-151354, Article 151354

2023

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From Notochord Formation to Hereditary Chordoma: The Many Roles of Brachyury

BioMed research international, 2013-01, Vol.2013, p.826435-14

2013

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Case Report: Identification of a Novel Pathogenic Germline TP53 Variant in a Family With Li–Fraumeni Syndrome

Frontiers in genetics, 2021-09, Vol.12

2021

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Germline Testing in a Cohort of Patients at High Risk of Hereditary Cancer Predisposition Syndromes: First Two-Year Results from South Italy

Genes, 2022-07, Vol.13 (7), p.1286

2022

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The Role of MicroRNAs in Cancer Susceptibility

BioMed research international, 2013-01, Vol.2013, p.591931-9

2013

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Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion

BioMed research international, 2013-01, Vol.2013, p.219897-7

2013

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The tyrosine phosphatase PTPRJ/DEP-1 genotype affects thyroid carcinogenesis

Oncogene, 2004-11, Vol.23 (52), p.8432-8438

2004

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p53-Mediated downregulation of H ferritin promoter transcriptional efficiency via NF-Y

The international journal of biochemistry & cell biology, 2008, Vol.40 (10), p.2110-2119

2008

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Hereditary Tumours

BioMed research international, 2013-01, Vol.2013, p.490357-2

Baudi, Francesco

2013

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BRCA1 5083del19 Mutant Allele Selectively Up-Regulates Periostin Expression In vitro and In vivo

Clinical cancer research, 2008-11, Vol.14 (21), p.6797-6803

2008

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Specific changes in the proteomic pattern produced by the BRCA1-Ser1841Asn missense mutation

The international journal of biochemistry & cell biology, 2007, Vol.39 (1), p.220-226

2007

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BRCA1/2 genetic background-based therapeutic tailoring of human ovarian cancer: hope or reality?

Journal of ovarian research, 2009-10, Vol.2 (1), p.14-14

2009

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Corrigendum to ‘specific changes in the proteomic pattern produced by the BRCA1-Ser1841Asn missense mutation’ [International Journal of Biochemistry and Cell Biology (2007) 220–226]

The international journal of biochemistry & cell biology, 2017-07, Vol.88, p.236-237

2017

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A peroxisome proliferator‐activated receptor gamma (PPARG) polymorphism is associated with zoledronic acid‐related osteonecrosis of the jaw in multiple myeloma patients: analysis by DMET microarray profiling

British journal of haematology, 2011-08, Vol.154 (4), p.529-533

2011

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A polymorphism of HMGA1 is associated with increased risk of metabolic syndrome and related components

Scientific reports, 2013, Vol.3 (1), p.1491-1491, Article 1491

2013

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Diagnosis and follow-up of Bartonella henselae infection in the spleen of an immunocompetent patient by real-time quantitative PCR

Journal of medical microbiology, 2013-07, Vol.62 (7), p.1081-1085

2013

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A proteomics approach to identify changes in protein profiles in serum of Familial Adenomatous Polyposis patients

Cancer letters, 2008-12, Vol.272 (1), p.40-52

2008

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Molecular identification of Bartonella quintana infection using species-specific real-time PCR targeting transcriptional regulatory protein ( bqtR) gene

Molecular and cellular probes, 2011-10, Vol.25 (5), p.238-242

2011

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In vitro analysis of genomic instability triggered by BRCA1 missense mutations

Human mutation, 2006-07, Vol.27 (7), p.715-715

2006

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Evidence of a founder mutation of BRCA1 in a highly homogeneous population from southern Italy with breast/ovarian cancer

Human mutation, 2001-08, Vol.18 (2), p.163-164

2001

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Missense mutations of BRCA1 gene affect the binding with p53 both in vitro and in vivo

Oncology reports, 2006-10, Vol.16 (4), p.811-815

2006

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In vitro analysis of genomic instability triggered by BRCA1 missense mutations

Human mutation, 2006-01, Vol.27 (7), p.715-715

2006

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Detection and functional analysis of an SNP in the promoter of the human ferritin H gene that modulates the gene expression

Gene, 2006-08, Vol.377, p.1-5

2006

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Hereditary Breast Cancer: The Era of New Susceptibility Genes

The Case of Medication-Related Osteonecrosis of the Jaw Addressed from a Pathogenic Point of View. Innovative Therapeutic Strategies: Focus on the Most Recent Discoveries on Oral Mesenchymal Stem Cell-Derived Exosomes

Novel insights into the pharmacological modulation of human periodontal ligament stem cells by the amino-bisphosphonate Alendronate

From Notochord Formation to Hereditary Chordoma: The Many Roles of Brachyury

Case Report: Identification of a Novel Pathogenic Germline TP53 Variant in a Family With Li–Fraumeni Syndrome

Germline Testing in a Cohort of Patients at High Risk of Hereditary Cancer Predisposition Syndromes: First Two-Year Results from South Italy

The Role of MicroRNAs in Cancer Susceptibility

Contribution of Large Genomic Rearrangements in Italian Lynch Syndrome Patients: Characterization of a Novel Alu-Mediated Deletion

The tyrosine phosphatase PTPRJ/DEP-1 genotype affects thyroid carcinogenesis

p53-Mediated downregulation of H ferritin promoter transcriptional efficiency via NF-Y

Hereditary Tumours

BRCA1 5083del19 Mutant Allele Selectively Up-Regulates Periostin Expression In vitro and In vivo

Specific changes in the proteomic pattern produced by the BRCA1-Ser1841Asn missense mutation

BRCA1/2 genetic background-based therapeutic tailoring of human ovarian cancer: hope or reality?

Corrigendum to ‘specific changes in the proteomic pattern produced by the BRCA1-Ser1841Asn missense mutation’ [International Journal of Biochemistry and Cell Biology (2007) 220–226]

A peroxisome proliferator‐activated receptor gamma (PPARG) polymorphism is associated with zoledronic acid‐related osteonecrosis of the jaw in multiple myeloma patients: analysis by DMET microarray profiling

A polymorphism of HMGA1 is associated with increased risk of metabolic syndrome and related components

Diagnosis and follow-up of Bartonella henselae infection in the spleen of an immunocompetent patient by real-time quantitative PCR

A proteomics approach to identify changes in protein profiles in serum of Familial Adenomatous Polyposis patients

Molecular identification of Bartonella quintana infection using species-specific real-time PCR targeting transcriptional regulatory protein ( bqtR) gene

In vitro analysis of genomic instability triggered by BRCA1 missense mutations

Evidence of a founder mutation of BRCA1 in a highly homogeneous population from southern Italy with breast/ovarian cancer

Missense mutations of BRCA1 gene affect the binding with p53 both in vitro and in vivo

In vitro analysis of genomic instability triggered by BRCA1 missense mutations

Detection and functional analysis of an SNP in the promoter of the human ferritin H gene that modulates the gene expression

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