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Whole mitochondrial DNA sequencing in Alpine populations and the genetic history of the Neolithic Tyrolean Iceman

Scientific reports, 2016-01, Vol.6 (1), p.18932-18932, Article 18932

2016

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P04.11 GENETIC POLYMORPHISMS OF EGF 5'-UTR IN PATIENTS WITH GLIOMA: A POSSIBLE PREDICTIVE MARKER OF OUTCOME

Neuro-oncology (Charlottesville, Va.), 2014-09, Vol.16 (suppl 2), p.ii39-ii39

2014

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The 5300-year-old Helicobacter pylori genome of the Iceman

Science (American Association for the Advancement of Science), 2016-01, Vol.351 (6269), p.162-165

2016

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New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing

Nature communications, 2012-02, Vol.3 (1), p.698-698, Article 698

2012

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Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations

Journal of medical genetics, 2004-04, Vol.41 (4), p.278-285

2004

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Genetic alterations in hereditary breast cancer

Annals of oncology, 2004-01, Vol.15 (suppl-1), p.i7-i13

2004

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Reconstructing the Genealogy of a BRCA1 Founder Mutation by Phylogenetic Analysis

Annals of human genetics, 2008-05, Vol.72 (3), p.310-318

2008

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P04.11GENETIC POLYMORPHISMS OF EGF 5'-UTR IN PATIENTS WITH GLIOMA: A POSSIBLE PREDICTIVE MARKER OF OUTCOME

Neuro-oncology (Charlottesville, Va.), 2014-09, Vol.16 (Suppl 2), p.ii39-ii39

2014

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Bcl-2, p53 and MIB-1 expression in normal and neoplastic parathyroid tissues

Journal of endocrinological investigation, 1998-03, Vol.21 (3), p.136-141

1998

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Papillary lesions of the breast: a molecular progression?

Breast cancer research and treatment, 2005-03, Vol.90 (1), p.71-76

2005

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Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1 2 mutations

European journal of human genetics : EJHG, 2004-11, Vol.12 (11), p.899-906

2004

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Breast MR imaging screening in eight women proved or suspected to be carriers of BRCA1&2 gene mutations

Journal of experimental & clinical cancer research, 2002-09, Vol.21 (3 Suppl), p.137-140

2002

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PCR: potential and problems

Pathologica, 2005-08, Vol.97 (4), p.203

2005

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A low NM23.H1 gene expression identifying high malignancy human melanomas

Melanoma research, 1994-06, Vol.4 (3), p.179-184

1994

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Haplotype analysis of BRCA1 gene reveals a new gene rearrangement: characterization of a 19.9 KBP deletion

European journal of human genetics : EJHG, 2004-09, Vol.12 (9), p.775-777

2004

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Mutation Analysis of BRCA1 and BRCA2 in Italian Hereditary and Sporadic Forms of Breast and Ovarian Cancers: Tumor Genotype‐Phenotype Correlation in Breast Cancer BRCA‐Mutation Carriers

Disease markers, 1999-01, Vol.15 (1-3), p.101-102

1999

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Decreasing expression of NM23 gene in metastatic murine mammary tumors of viral etiology (MMTV)

Anticancer research, 1992-05, Vol.12 (3), p.969

1992

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p53 inactivation is a rare event in familial breast tumors negative for BRCA1 and BRCA2 mutations

Breast cancer research and treatment, 2003-11, Vol.82 (1), p.1-9

2003

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Down‐regulation of the nm23.h1 gene inhibits cell proliferation

International journal of cancer, 1997-10, Vol.73 (2), p.297-302

1997

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Clinicopathological significance of GADD45 gene alterations in human familial breast carcinoma

Breast cancer research and treatment, 2004-09, Vol.87 (2), p.197-201

2004

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Different expressivity of BRCA1 and BRCA2: analysis of 179 Italian pedigrees with identified mutation

Breast cancer research and treatment, 2003-09, Vol.81 (1), p.71-79

2003

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NM23 gene expression correlates with cell growth rate and S‐phase

International journal of cancer, 1995-03, Vol.60 (6), p.837-842

1995

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Genetic alterations in hereditary breast cancer: Familial breast cancer screening: ethical and social implications

Annals of oncology, 2004, Vol.15, p.i7-i13

2004

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BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations

Oncogene, 1996-10, Vol.13 (7), p.1483-1488

1996

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Whole mitochondrial DNA sequencing in Alpine populations and the genetic history of the Neolithic Tyrolean Iceman

P04.11 GENETIC POLYMORPHISMS OF EGF 5'-UTR IN PATIENTS WITH GLIOMA: A POSSIBLE PREDICTIVE MARKER OF OUTCOME

The 5300-year-old Helicobacter pylori genome of the Iceman

New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing

Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations

Genetic alterations in hereditary breast cancer

Reconstructing the Genealogy of a BRCA1 Founder Mutation by Phylogenetic Analysis

The Iceman’s Last Meal Consisted of Fat, Wild Meat, and Cereals

P04.11GENETIC POLYMORPHISMS OF EGF 5'-UTR IN PATIENTS WITH GLIOMA: A POSSIBLE PREDICTIVE MARKER OF OUTCOME

Bcl-2, p53 and MIB-1 expression in normal and neoplastic parathyroid tissues

Papillary lesions of the breast: a molecular progression?

Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1 2 mutations

Breast MR imaging screening in eight women proved or suspected to be carriers of BRCA1&2 gene mutations

PCR: potential and problems

A low NM23.H1 gene expression identifying high malignancy human melanomas

Haplotype analysis of BRCA1 gene reveals a new gene rearrangement: characterization of a 19.9 KBP deletion

Mutation Analysis of BRCA1 and BRCA2 in Italian Hereditary and Sporadic Forms of Breast and Ovarian Cancers: Tumor Genotype‐Phenotype Correlation in Breast Cancer BRCA‐Mutation Carriers

Decreasing expression of NM23 gene in metastatic murine mammary tumors of viral etiology (MMTV)

p53 inactivation is a rare event in familial breast tumors negative for BRCA1 and BRCA2 mutations

Down‐regulation of the nm23.h1 gene inhibits cell proliferation

Clinicopathological significance of GADD45 gene alterations in human familial breast carcinoma

Different expressivity of BRCA1 and BRCA2: analysis of 179 Italian pedigrees with identified mutation

NM23 gene expression correlates with cell growth rate and S‐phase

Genetic alterations in hereditary breast cancer: Familial breast cancer screening: ethical and social implications

BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations

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