Lista de obras - Chiara Menin - Dominio Público Uruguay

Altered tumor formation and evolutionary selection of genetic variants in the human MDM4 oncogene.

scholarly article

Analysis of Epstein-Barr virus (EBV) type and variant in spontaneous lymphoblastoid cells and Hu-SCID mouse tumours.

artículo científico publicado en 1996

Association between MDM2-SNP309 and age at colorectal cancer diagnosis according to p53 mutation status.

artículo científico publicado en 2006

Association of CDK4 germline and BRAF somatic mutations in a patient with multiple primary melanomas and BRAF inhibitor resistance.

artículo científico publicado en 2015

BRCA1p.Val1688del Is a Deleterious Mutation That Recurs in Breast and Ovarian Cancer Families From Northeast Italy

artículo científico publicado en 2008

CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessment.

artículo científico publicado en 2014

Clinical genetic testing for familial melanoma in Italy: A cooperative study

article

Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies

scientific article published on 15 November 2019

Contribution of susceptibility gene variants to melanoma risk in families from the Veneto region of Italy

article

Differences in telomere length between sporadic and familial cutaneous melanoma.

artículo científico publicado en 2016

Different Expressivity of BRCA1 and BRCA2: Analysis of 179 Italian Pedigrees with Identified Mutation

article

Dominance of a single Epstein-Barr virus strain in SCID-mouse tumors induced by injection of peripheral blood mononuclear cells from healthy human donors.

artículo científico publicado en 1995

Dried blood spot sampling for detection of monoclonal immunoglobulin gene rearrangement

artículo científico publicado en 2013

Dynamics of Epstein-Barr virus in HIV-1-infected subjects on highly active antiretroviral therapy

artículo científico publicado en 2002

Functional impairment of p16(INK4A) due to CDKN2A p.Gly23Asp missense mutation.

artículo científico publicado en 2009

Genetic Variants of the TERT Gene, Telomere Length, and Circulating TERT as Prognostic Markers in Rectal Cancer Patients

artículo científico publicado en 2020

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

artículo científico publicado en 2020

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families

artículo científico publicado en 2003

Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations.

artículo científico publicado en 2008

Germline variation of circadian pathway genes and prognosis of gastric cancer patients.

artículo científico publicado en 2017

Histopathological characteristics of subsequent melanomas in patients with multiple primary melanomas

artículo científico publicado en 2012

Human IgGs induce synthesis and secretion of IgGs and neonatal Fc receptor in human umbilical vein endothelial cells.

artículo científico publicado en 2016

Identification of BRCA1 and BRCA2 carriers by allele-specific gene expression (AGE) analysis

scientific article published on 01 April 2002

Identification of a 3 kb Alu-mediated BRCA1 gene rearrangement in two breast/ovarian cancer families

artículo científico publicado en 1999

Identification of a human endogenous LTR-like sequence using HIV-1 LTR specific primers.

artículo científico publicado en 1996

Infection of simian B lymphoblastoid cells with simian immunodeficiency virus is associated with upregulation of CD23 and CD40 cell surface markers

artículo científico publicado en 2002

Lack of association between androgen receptor CAG polymorphism and familial breast/ovarian cancer

scientific article published on 01 July 2001

Lymphoproliferative disease in human peripheral blood mononuclear cell-injected SCID mice. I. T lymphocyte requirement for B cell tumor generation

artículo científico publicado en 1992

MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort

scientific article published on 12 March 2019

MDM2 SNP309 accelerates colorectal tumour formation in women.

artículo científico publicado en 2006

Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup.

artículo científico publicado en 2016

Myasthenic syndrome and oligoclonal lymphocytosis: evolution into chronic lymphocytic leukemia

scientific article published on 01 January 1998

No Evidence for Linkage with Melanoma in Italian Melanoma-Prone Families

artículo científico publicado en 2008

Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma.

artículo científico publicado en 1994

Occurrence of post-transplant lymphoproliferative disorders among over thousand adult recipients: any role for hepatitis C infection?

scientific article published on 01 October 2006

Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI.

artículo científico publicado en 2017

Sequential development of large B cell lymphoma in a patient with peripheral T-cell lymphoma

scientific article published on 01 January 2008

Survivin expression impacts prognostically on NSCLC but not SCLC

artículo científico publicado en 2013

TERT Promoter Mutations Differently Correlate with the Clinical Outcome of MAPK Inhibitor-Treated Melanoma Patients

scientific article published on 11 April 2020

TLR7 Gln11Leu single nucleotide polymorphism and susceptibility to cutaneous melanoma

artículo científico publicado en 2016

TP53 gene mutations in gastric carcinoma detected by polymerase chain reaction/single-strand conformation polymorphism analysis of archival material.

artículo científico

The BRCA2 sequence variant IVS19+1G-->A leads to an aberrant transcript lacking exon 19

scientific article published on 01 March 2003

The CDKN2A/p16(INK) (4a) 5'UTR sequence and translational regulation: impact of novel variants predisposing to melanoma

artículo científico publicado en 2015

The p53 codon 72 Pro/Pro genotype identifies poor-prognosis neuroblastoma patients: correlation with reduced apoptosis and enhanced senescence by the p53-72P isoform.

artículo científico publicado en 2012

Tumours induced by Moloney murine sarcoma virus are clonal in rats, not clonal in mice ⬇️

artículo científico publicado el 1 de enero de 1992

Lista de obras de Chiara Menin

Altered tumor formation and evolutionary selection of genetic variants in the human MDM4 oncogene.

Analysis of Epstein-Barr virus (EBV) type and variant in spontaneous lymphoblastoid cells and Hu-SCID mouse tumours.

Association between MDM2-SNP309 and age at colorectal cancer diagnosis according to p53 mutation status.

Association of CDK4 germline and BRAF somatic mutations in a patient with multiple primary melanomas and BRAF inhibitor resistance.

BRCA1p.Val1688del Is a Deleterious Mutation That Recurs in Breast and Ovarian Cancer Families From Northeast Italy

CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessment.

Clinical genetic testing for familial melanoma in Italy: A cooperative study

Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies

Contribution of susceptibility gene variants to melanoma risk in families from the Veneto region of Italy

Differences in telomere length between sporadic and familial cutaneous melanoma.

Different Expressivity of BRCA1 and BRCA2: Analysis of 179 Italian Pedigrees with Identified Mutation

Dominance of a single Epstein-Barr virus strain in SCID-mouse tumors induced by injection of peripheral blood mononuclear cells from healthy human donors.

Dried blood spot sampling for detection of monoclonal immunoglobulin gene rearrangement

Dynamics of Epstein-Barr virus in HIV-1-infected subjects on highly active antiretroviral therapy

Functional impairment of p16(INK4A) due to CDKN2A p.Gly23Asp missense mutation.

Genetic Variants of the TERT Gene, Telomere Length, and Circulating TERT as Prognostic Markers in Rectal Cancer Patients

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families

Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations.

Germline variation of circadian pathway genes and prognosis of gastric cancer patients.

Histopathological characteristics of subsequent melanomas in patients with multiple primary melanomas

Human IgGs induce synthesis and secretion of IgGs and neonatal Fc receptor in human umbilical vein endothelial cells.

Identification of BRCA1 and BRCA2 carriers by allele-specific gene expression (AGE) analysis

Identification of a 3 kb Alu-mediated BRCA1 gene rearrangement in two breast/ovarian cancer families

Identification of a human endogenous LTR-like sequence using HIV-1 LTR specific primers.

Infection of simian B lymphoblastoid cells with simian immunodeficiency virus is associated with upregulation of CD23 and CD40 cell surface markers

Lack of association between androgen receptor CAG polymorphism and familial breast/ovarian cancer

Lymphoproliferative disease in human peripheral blood mononuclear cell-injected SCID mice. I. T lymphocyte requirement for B cell tumor generation

MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort

MDM2 SNP309 accelerates colorectal tumour formation in women.

Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup.

Myasthenic syndrome and oligoclonal lymphocytosis: evolution into chronic lymphocytic leukemia

No Evidence for Linkage with Melanoma in Italian Melanoma-Prone Families

Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma.

Occurrence of post-transplant lymphoproliferative disorders among over thousand adult recipients: any role for hepatitis C infection?

Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI.

Sequential development of large B cell lymphoma in a patient with peripheral T-cell lymphoma

Survivin expression impacts prognostically on NSCLC but not SCLC

TERT Promoter Mutations Differently Correlate with the Clinical Outcome of MAPK Inhibitor-Treated Melanoma Patients

TLR7 Gln11Leu single nucleotide polymorphism and susceptibility to cutaneous melanoma

TP53 gene mutations in gastric carcinoma detected by polymerase chain reaction/single-strand conformation polymorphism analysis of archival material.

The BRCA2 sequence variant IVS19+1G-->A leads to an aberrant transcript lacking exon 19

The CDKN2A/p16(INK) (4a) 5'UTR sequence and translational regulation: impact of novel variants predisposing to melanoma

The p53 codon 72 Pro/Pro genotype identifies poor-prognosis neuroblastoma patients: correlation with reduced apoptosis and enhanced senescence by the p53-72P isoform.

Tumours induced by Moloney murine sarcoma virus are clonal in rats, not clonal in mice ⬇️