Lista de obras - Lucia Anna Muscarella - Dominio Público Uruguay

<i>NRG</i> fusions in tumors: moving from the past to future knowledge

scientific article published on 05 January 2021

A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohort

article

Aberrant genes promoter methylation in neural crest-derived tumors

article

Alteration of hypothalamic-pituitary-thyroid axis function in non-small-cell lung cancer patients.

artículo científico publicado en 2011

An 11-bp duplication in the promoter region of the VHL gene in a patient with cerebellar hemangioblastoma and renal oncocytoma

article

Antiphase signalling in the neuroendocrine-immune system in healthy humans

artículo científico publicado en 2011

Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

artículo científico publicado en 2004

CD74-NRG1 fusions in lung adenocarcinoma

artículo científico publicado en 2014

CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort

article by Vito Guarnieri et al published 18 September 2012 in Cellular Oncology

Candidate gene study of HOXB1 in autism spectrum disorder

artículo científico publicado el 25 de mayo de 2010

Circadian aspects of growth hormone-insulin-like growth factor axis function in patients with lung cancer.

artículo científico publicado en 2011

Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family.

artículo científico publicado en 2011

Comprehensive genomic profiles of small cell lung cancer

artículo científico publicado en 2015

Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillance.

artículo científico publicado en 2006

Diagnostic and Prognostic Value of B4GALT1 Hypermethylation and Its Clinical Significance as a Novel Circulating Cell-Free DNA Biomarker in Colorectal Cancer

artículo científico publicado en 2019

EZH2 and ZFX oncogenes in malignant behaviour of parathyroid neoplasms.

artículo científico publicado en 2016

Effects of KEAP1 Silencing on the Regulation of NRF2 Activity in Neuroendocrine Lung Tumors.

artículo científico publicado en 2019

Epigenetic Scanning of KEAP1 CpG Sites Uncovers New Molecular-Driven Patterns in Lung Adeno and Squamous Cell Carcinomas

scientific article published on 22 September 2020

Epigenetic versus Genetic Deregulation of the KEAP1/NRF2 Axis in Solid Tumors: Focus on Methylation and Noncoding RNAs.

artículo científico publicado en 2018

Establishment and genetic characterization of ANGM-CSS, a novel, immortal cell line derived from a human glioblastoma multiforme

artículo científico publicado en 2013

FOXP1 and TP63 involvement in the progression of myelodysplastic syndrome with 5q- and additional cytogenetic abnormalities

artículo científico publicado en 2014

Frequent epigenetics inactivation of KEAP1 gene in non-small cell lung cancer

artículo científico publicado en 2011

Gene expression of muscular and neuronal pathways is cooperatively dysregulated in patients with idiopathic achalasia

artículo científico publicado en 2016

Gene expression of somatostatin receptor subtypes SSTR2a, SSTR3 and SSTR5 in peripheral blood of neuroendocrine lung cancer affected patients.

artículo científico publicado en 2011

Genomic and evolutionary classification of lung cancer in never smokers

artículo científico publicado en 2021

Hemangioblastomas of central nervous system: molecular genetic analysis and clinical management.

artículo científico publicado en 2005

High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient's outcome

artículo científico publicado en 2011

Identification and functional characterization of three NoLS (nucleolar localisation signals) mutations of the CDC73 gene

artículo científico publicado en 2013

Identification of a novel RUNX2 gene mutation in an Italian family with cleidocranial dysplasia

artículo científico publicado en 2010

Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer

artículo científico publicado en 2012

Liquid biopsy and NSCLC

artículo científico publicado en 2016

Molecular Analysis of NPHS2 and ACTN4 Genes in a Series of 33 Italian Patients Affected by Adult-Onset Nonfamilial Focal Segmental Glomerulosclerosis

article

Molecular analysis of the HuD gene in neuroendocrine lung cancers.

artículo científico publicado en 2010

Molecular dissection of the VHL gene in solitary capillary hemangioblastoma of the central nervous system.

artículo científico publicado en 2014

NRF2 Regulation by Noncoding RNAs in Cancers: The Present Knowledge and the Way Forward

artículo científico publicado en 2020

Novel mutations of dystrophin gene in DMD patients detected by rapid scanning in biplex exons DHPLC analysis

article

Nrf2 and Notch Signaling in Lung Cancer: Near the Crossroad

artículo científico publicado en 2016

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.

artículo científico publicado en 2005

Potential Prognostic Role of SPARC Methylation in Non-Small-Cell Lung Cancer

artículo científico publicado en 2020

Regulation of KEAP1 expression by promoter methylation in malignant gliomas and association with patient's outcome

artículo científico publicado en 2011

Small deletion at the 7q21.2 locus in a CCM family detected by real-time quantitative PCR

artículo científico publicado en 2010

Stage dependent destructuration of neuro-endocrine-immune system components in lung cancer patients

artículo científico publicado en 2010

The Post-Surgical Long-Term Behaviour of Lung Carcinoid Tumours

artículo científico publicado en 2015

VHL frameshift mutation as target of nonsense-mediated mRNA decay in Drosophila melanogaster and human HEK293 cell line.

artículo científico publicado en 2009

VHL gene alterations in Italian patients with isolated renal cell carcinomas

artículo científico publicado en 2013

WITHDRAWN: Neuroendocrine axes function in healthy aging: Evaluation of predictive and manipulable blood serum indexes

retracted scientific article published on 25 September 2010

Lista de obras de Lucia Anna Muscarella

<i>NRG</i> fusions in tumors: moving from the past to future knowledge

A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohort

Aberrant genes promoter methylation in neural crest-derived tumors

Alteration of hypothalamic-pituitary-thyroid axis function in non-small-cell lung cancer patients.

An 11-bp duplication in the promoter region of the VHL gene in a patient with cerebellar hemangioblastoma and renal oncocytoma

Antiphase signalling in the neuroendocrine-immune system in healthy humans

Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

CD74-NRG1 fusions in lung adenocarcinoma

CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort

Candidate gene study of HOXB1 in autism spectrum disorder

Circadian aspects of growth hormone-insulin-like growth factor axis function in patients with lung cancer.

Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family.

Comprehensive genomic profiles of small cell lung cancer

Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillance.

Diagnostic and Prognostic Value of B4GALT1 Hypermethylation and Its Clinical Significance as a Novel Circulating Cell-Free DNA Biomarker in Colorectal Cancer

EZH2 and ZFX oncogenes in malignant behaviour of parathyroid neoplasms.

Effects of KEAP1 Silencing on the Regulation of NRF2 Activity in Neuroendocrine Lung Tumors.

Epigenetic Scanning of KEAP1 CpG Sites Uncovers New Molecular-Driven Patterns in Lung Adeno and Squamous Cell Carcinomas

Epigenetic versus Genetic Deregulation of the KEAP1/NRF2 Axis in Solid Tumors: Focus on Methylation and Noncoding RNAs.

Establishment and genetic characterization of ANGM-CSS, a novel, immortal cell line derived from a human glioblastoma multiforme

FOXP1 and TP63 involvement in the progression of myelodysplastic syndrome with 5q- and additional cytogenetic abnormalities

Frequent epigenetics inactivation of KEAP1 gene in non-small cell lung cancer

Gene expression of muscular and neuronal pathways is cooperatively dysregulated in patients with idiopathic achalasia

Gene expression of somatostatin receptor subtypes SSTR2a, SSTR3 and SSTR5 in peripheral blood of neuroendocrine lung cancer affected patients.

Genomic and evolutionary classification of lung cancer in never smokers

Hemangioblastomas of central nervous system: molecular genetic analysis and clinical management.

High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient's outcome

Identification and functional characterization of three NoLS (nucleolar localisation signals) mutations of the CDC73 gene

Identification of a novel RUNX2 gene mutation in an Italian family with cleidocranial dysplasia

Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer

Liquid biopsy and NSCLC

Molecular Analysis of NPHS2 and ACTN4 Genes in a Series of 33 Italian Patients Affected by Adult-Onset Nonfamilial Focal Segmental Glomerulosclerosis

Molecular analysis of the HuD gene in neuroendocrine lung cancers.

Molecular dissection of the VHL gene in solitary capillary hemangioblastoma of the central nervous system.

NRF2 Regulation by Noncoding RNAs in Cancers: The Present Knowledge and the Way Forward

Novel mutations of dystrophin gene in DMD patients detected by rapid scanning in biplex exons DHPLC analysis

Nrf2 and Notch Signaling in Lung Cancer: Near the Crossroad

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.

Potential Prognostic Role of SPARC Methylation in Non-Small-Cell Lung Cancer

Regulation of KEAP1 expression by promoter methylation in malignant gliomas and association with patient's outcome

Small deletion at the 7q21.2 locus in a CCM family detected by real-time quantitative PCR

Stage dependent destructuration of neuro-endocrine-immune system components in lung cancer patients

The Post-Surgical Long-Term Behaviour of Lung Carcinoid Tumours

VHL frameshift mutation as target of nonsense-mediated mRNA decay in Drosophila melanogaster and human HEK293 cell line.

VHL gene alterations in Italian patients with isolated renal cell carcinomas

WITHDRAWN: Neuroendocrine axes function in healthy aging: Evaluation of predictive and manipulable blood serum indexes