F. Fabiani

发表

Identification of a new mutation in the gene coding for hairless protein responsible for alopecia universalis: The importance of direct gene sequencing.

T. Longo, F. Baudi, F. Trapasso, 2011, Dermatology online journal.

Real‐life 3D therapy failure: Analysis of NS5A 93H RAS plus 108 K polymorphism in complex with ombitasvir by molecular modeling

A. Focà, M. Liberto, N. Marascio, 2018, Journal of medical virology.

Epigenetic Regulation of Mitochondrial Quality Control Genes in Multiple Myeloma: A Sequenom MassARRAY Pilot Investigation on HMCLs

G. Viglietto, A. Neri, P. D’Aquila, 2021, Journal of clinical medicine.

Germline Testing in a Cohort of Patients at High Risk of Hereditary Cancer Predisposition Syndromes: First Two-Year Results from South Italy

F. Baudi, F. Paduano, F. Trapasso, 2022, Genes.

Loss of the tumor suppressor gene PTEN marks the transition from intratubular germ cell neoplasias (ITGCN) to invasive germ cell tumors

G. Viglietto, P. Chieffi, A. Fusco, 2005, Oncogene.

The sodium-phosphate co-transporter SLC34A2, and pulmonary alveolar microlithiasis: Presentation of an inbred family and a novel truncating mutation in exon 3

M. Vismara, R. Iuliano, O. Tamburrini, 2015, Respiratory medicine case reports.

Loss of p27 Expression Through RAS->BRAF->MAP Kinase-Dependent Pathway in Human Thyroid Carcinomas

G. Viglietto, M. Santoro, A. Fusco, 2007, Cell cycle.

Clinical and Molecular Evaluation of a Case of Male Infertility and Azoospermia

F. Trapasso, D. Taverna, A. Primerano, 2015 .

DNA-demethylating and anti-tumor activity of synthetic miR-29b mimics in multiple myeloma

M. Negrini, P. Tassone, P. Tagliaferri, 2012, Oncotarget.

Signaling Networks Associated with AKT Activation in Non-Small Cell Lung Cancer (NSCLC): New Insights on the Role of Phosphatydil-Inositol-3 kinase

M. Ceccarelli, P. Zoppoli, G. Viglietto, 2012, PloS one.

Polymorphic Variants in NR1I3 and UGT2B7 Predict Taxane Neurotoxicity and Have Prognostic Relevance in Patients With Breast Cancer: A Case‐Control Study

Mario Cannataro, Giuseppe Agapito, Mariamena Arbitrio, 2019, Clinical pharmacology and therapeutics.

Single nucleotide polymorphisms of ABCC5 and ABCG1 transporter genes correlate to irinotecan-associated gastrointestinal toxicity in colorectal cancer patients: A DMET microarray profiling study

Mario Cannataro, Pietro Hiram Guzzi, Mariamena Arbitrio, 2011, Cancer biology & therapy.

Activating E17K mutation in the gene encoding the protein kinase AKT1 in a subset of squamous cell carcinoma of the lung.

G. Viglietto, R. Franco, R. Savino, 2008, Cell cycle.

Multiple Genetic Alterations within the PI3K Pathway Are Responsible for AKT Activation in Patients with Ovarian Carcinoma

G. Viglietto, R. Franco, C. de Marco, 2013, PloS one.

The nonreceptor-type tyrosine phosphatase PTPN13 is a tumor suppressor gene in non-small cell lung cancer.

G. Viglietto, R. Franco, C. de Marco, 2012, The American journal of pathology.

Case Report: Identification of a Novel Pathogenic Germline TP53 Variant in a Family With Li–Fraumeni Syndrome

F. Baudi, V. Barbieri, F. Paduano, 2021, Frontiers in Genetics.

A novel ABCC6 variant causative of pseudoxanthoma elasticum

Rossana Tallerico, M. Enzo, S. Nisticò, 2019, Human Genome Variation.

New SLC12A3 disease causative mutation of Gitelman’s syndrome

M. Vismara, R. Iuliano, E. Colao, 2016, World journal of nephrology.

Interleukin 27 polymorphisms in HCV RNA positive patients: is there an impact on response to interferon therapy?

F. Trapasso, A. Focà, M. Liberto, 2014, BMC Infectious Diseases.

Activating E17K mutation in the gene encoding the protein kinase AKT in a subset of squamous cell carcinoma of the lung

Gaetano Rocco, Natalia Malara, Virginia Tirino, 2008, Cell cycle.

A Familial Form of Epidermolysis Bullosa Simplex Associated with a Pathogenic Variant in KRT5

C. Mignogna, F. Paduano, F. Trapasso, 2021, Genes.