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Carcinosarcoma of the Breast: An Aggressive Subtype of Metaplastic Cancer. Report of a Rare Case in a Young BRCA-1 Mutated Woman

Clinical breast cancer, 2017-02, Vol.17 (1), p.e31-e35

2017

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Haplotype and Phenotype Analysis of Nine Recurrent BRCA2 Mutations in 111 Families: Results of an International Study

American journal of human genetics, 1998-06, Vol.62 (6), p.1381-1388

1998

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Genetic instability, p53 and nm23 mutation and clinicopathological features in rectal carcinoma

Anticancer research, 1998-03, Vol.18 (2A), p.989

1998

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Increased rate of base substitution in a hamster mutator strain obtained during serial selection for gene amplification

Molecular and Cellular Biology, 1990-12, Vol.10 (12), p.6805-6808

1990

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Impact of TAS2R38 polymorphisms on nasal nitric oxide and Pseudomonas infections in primary ciliary dyskinesia: relation to genotype

Thorax, 2024-10, Vol.79 (11), p.1069-1076

2024

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Aberrant expression of BARD1 in breast and ovarian cancers with poor prognosis

International journal of cancer, 2006-03, Vol.118 (5), p.1215-1226

2006

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Effect of the expression of BRCA2 on spontaneous homologous recombination and DNA damage-induced nuclear foci in Saccharomyces cerevisiae

Mutagenesis, 2013-03, Vol.28 (2), p.187-195

2013

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The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers

Breast cancer research and treatment, 2012-04, Vol.132 (3), p.1119-1126

2012

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Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families : Results of an international study

American journal of human genetics, 1996-02, Vol.58 (2), p.271-280

1996

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Genetic Testing and Clinical Management Practices for Variants in Non- BRCA1 / 2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group

JCO precision oncology, 2018 (2), p.1-42

2018

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PIK3CA in breast carcinoma: a mutational analysis of sporadic and hereditary cases

Diagnostic molecular pathology, 2009-12, Vol.18 (4), p.200-205

2009

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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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Consortium study on 1280 breast carcinomas : Allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters

Cancer research (Chicago, Ill.), 1998-03, Vol.58 (5), p.1004-1012

1998

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FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

Human molecular genetics, 2015, Vol.24 (18), p.5345

2015

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The CHEK2 c.1100delC mutation plays an irrelevant role in breast cancer predisposition in Italy

Human mutation, 2004-07, Vol.24 (1), p.100-101

2004

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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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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2mutation carriers

Breast cancer research : BCR, 2010-11, Vol.12 (6), Article R102

2010

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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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Down regulation of NM23.H1, NM23.H2 and c-myc genes during differentiation induced by 1,25 dihydroxyvitamin D3

Leukemia research, 1996-02, Vol.20 (2), p.161-167

1996

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A region on the long arm of chromosome 16 is frequently deleted in metastatic node-negative breast cancer

International journal of oncology, 1998-07, Vol.13 (1), p.177

1998

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Microsatellite instability is co-selectable with gene amplification in a mammalian mutator phenotype

Anticancer research, 1999-03, Vol.19 (2A), p.1271

1999

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Down regulation of NM23.H1, NM23.H2 and c-myc genes during differentiation induced by 1,25 dihydroxyvitamin D 3

Leukemia research, 1996-02, Vol.20 (2), p.161-167

1996

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Lactoferrin expression in human breast cancer

Cancer biochemistry biophysics, 1999-07, Vol.17 (1-2), p.163

1999

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The progestin ORG2058 but not retinoic acid stimulates BRCA1 mRNA expression in MCF-7 human breast cancer cells

International journal of oncology, 1997-02

1997

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Stimulation of carrot somatic embryogenesis by proline and serine

Plant cell reports, 1984-10, Vol.3 (5), p.210-214

1984

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Carcinosarcoma of the Breast: An Aggressive Subtype of Metaplastic Cancer. Report of a Rare Case in a Young BRCA-1 Mutated Woman

Haplotype and Phenotype Analysis of Nine Recurrent BRCA2 Mutations in 111 Families: Results of an International Study

Genetic instability, p53 and nm23 mutation and clinicopathological features in rectal carcinoma

Increased rate of base substitution in a hamster mutator strain obtained during serial selection for gene amplification

Impact of TAS2R38 polymorphisms on nasal nitric oxide and Pseudomonas infections in primary ciliary dyskinesia: relation to genotype

Aberrant expression of BARD1 in breast and ovarian cancers with poor prognosis

Effect of the expression of BRCA2 on spontaneous homologous recombination and DNA damage-induced nuclear foci in Saccharomyces cerevisiae

The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families : Results of an international study

Genetic Testing and Clinical Management Practices for Variants in Non- BRCA1 / 2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group

PIK3CA in breast carcinoma: a mutational analysis of sporadic and hereditary cases

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

Consortium study on 1280 breast carcinomas : Allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

The CHEK2 c.1100delC mutation plays an irrelevant role in breast cancer predisposition in Italy

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

Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2mutation carriers

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

Down regulation of NM23.H1, NM23.H2 and c-myc genes during differentiation induced by 1,25 dihydroxyvitamin D3

A region on the long arm of chromosome 16 is frequently deleted in metastatic node-negative breast cancer

Microsatellite instability is co-selectable with gene amplification in a mammalian mutator phenotype

Down regulation of NM23.H1, NM23.H2 and c-myc genes during differentiation induced by 1,25 dihydroxyvitamin D 3

Lactoferrin expression in human breast cancer

The progestin ORG2058 but not retinoic acid stimulates BRCA1 mRNA expression in MCF-7 human breast cancer cells

Stimulation of carrot somatic embryogenesis by proline and serine

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