List of works - Concetta Maria Faniello

A Common Mechanism Underlying the E1A Repression and the cAMP Stimulation of the H Ferritin Transcription ⬇️

scientific article published in Journal of Biological Chemistry

A novel Q3034R BRCA2 germline mutation identified in a fallopian tube cancer patient.

scientific article

A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy

article

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

scientific article published on 29 July 2008

An alternative model of H ferritin promoter transactivation by c-Jun

scientific article

BRCA1 5083del19 mutant allele selectively up-regulates periostin expression in vitro and in vivo.

scientific article

BRCA1 is required for hMLH1 stabilization following doxorubicin-induced DNA damage

scientific article published on 16 August 2011

Bilateral cataract in a subject carrying a C to A transition in the L ferritin promoter region.

scientific article published on 27 February 2009

DJ-1 in Endometrial Cancer

scientific article published on 01 May 2014

H ferritin gene silencing in a human metastatic melanoma cell line: a proteomic analysis.

scientific article

H-ferritin-regulated microRNAs modulate gene expression in K562 cells

scientific article published on 27 March 2015

Identification of H ferritin-dependent and independent genes in K562 differentiating cells by targeted gene silencing and expression profiling.

scientific article published on 14 November 2013

Negative transcriptional regulation of the human periostin gene by YingYang-1 transcription factor

article

Okadaic Acid Stimulates H Ferritin Transcription in HeLa Cells by Increasing the Interaction between the p300 CO-Activator Molecule and the Transcription Factor Bbf

scientific article published on 01 November 1997

Plasma Proteomic Profiling in Hereditary Breast Cancer Reveals a BRCA1-Specific Signature: Diagnostic and Functional Implications

scientific article published on 10 June 2015

Polymorphic repeat length in the AIB1 gene and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a meta-analysis of observational studies.

scientific article

Proteomics in Ménière disease

scientific article published in January 2012

Transcriptional regulation of the mismatch repair gene hMLH1

article

List of works by Concetta Maria Faniello

A Common Mechanism Underlying the E1A Repression and the cAMP Stimulation of the H Ferritin Transcription ⬇️

A novel Q3034R BRCA2 germline mutation identified in a fallopian tube cancer patient.

A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy

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

An alternative model of H ferritin promoter transactivation by c-Jun

BRCA1 5083del19 mutant allele selectively up-regulates periostin expression in vitro and in vivo.

BRCA1 is required for hMLH1 stabilization following doxorubicin-induced DNA damage

Bilateral cataract in a subject carrying a C to A transition in the L ferritin promoter region.

DJ-1 in Endometrial Cancer

H ferritin gene silencing in a human metastatic melanoma cell line: a proteomic analysis.

H-ferritin-regulated microRNAs modulate gene expression in K562 cells

Identification of H ferritin-dependent and independent genes in K562 differentiating cells by targeted gene silencing and expression profiling.

Negative transcriptional regulation of the human periostin gene by YingYang-1 transcription factor

Okadaic Acid Stimulates H Ferritin Transcription in HeLa Cells by Increasing the Interaction between the p300 CO-Activator Molecule and the Transcription Factor Bbf

Plasma Proteomic Profiling in Hereditary Breast Cancer Reveals a BRCA1-Specific Signature: Diagnostic and Functional Implications

Polymorphic repeat length in the AIB1 gene and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a meta-analysis of observational studies.

Proteomics in Ménière disease

Transcriptional regulation of the mismatch repair gene hMLH1