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Assessment of EGFR Mutations in Circulating Tumor Cell Preparations from NSCLC Patients by Next Generation Sequencing: Toward a Real-Time Liquid Biopsy for Treatment.
Published in:
PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0103883
By:
- Marchetti, Antonio;
- Del Grammastro, Maela;
- Felicioni, Lara;
- Malatesta, Sara;
- Filice, Giampaolo;
- Centi, Irene;
- De Pas, Tommaso;
- Santoro, Armando;
- Chella, Antonio;
- Brandes, Alba Ariela;
- Venturino, Paola;
- Cuccurullo, Franco;
- Crinò, Lucio;
- Buttitta, Fiamma
Publication type:
Article
Complex Mutations & Subpopulations of Deletions at Exon 19 of EGFR in NSCLC Revealed by Next Generation Sequencing: Potential Clinical Implications.
Published in:
PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0042164
By:
- Marchetti, Antonio;
- Grammastro, Maela Del;
- Filice, Giampaolo;
- Felicioni, Lara;
- Rossi, Giulio;
- Graziano, Paolo;
- Sartori, Giuliana;
- Leone, Alvaro;
- Malatesta, Sara;
- Iacono, Michele;
- Guetti, Luigi;
- Viola, Patrizia;
- Mucilli, Felice;
- Cuccurullo, Franco;
- Buttitta, Fiamma
Publication type:
Article
Mutational Profile of GNAQQ209 in Human Tumors.
Published in:
PLoS ONE, 2009, v. 4, n. 8, p. 1, doi. 10.1371/journal.pone.0006833
By:
- Lamba, Simona;
- Felicioni, Lara;
- Buttitta, Fiamma;
- Bleeker, Fonnet E.;
- Malatesta, Sara;
- Corbo, Vincenzo;
- Scarpa, Aldo;
- Rodolfo, Monica;
- Knowles, Margaret;
- Frattini, Milo;
- Marchetti, Antonio;
- Bardelli, Alberto
Publication type:
Article
Role of the Molecular Tumor Board for the Personalized Treatment of Patients with Metastatic Breast Cancer: A Focus on the State of the Art in Italy.
Published in:
Cancers, 2023, v. 15, n. 6, p. 1727, doi. 10.3390/cancers15061727
By:
- Irelli, Azzurra;
- Chiatamone Ranieri, Sofia;
- Di Giacomo, Daniela;
- Malatesta, Sara;
- Patruno, Leonardo Valerio;
- Tessitore, Alessandra;
- Alesse, Edoardo;
- Cannita, Katia
Publication type:
Article
High-risk human papilloma virus infection, tumor pathophenotypes, and BRCA1/2 and TP53 status in juvenile breast cancer.
Published in:
Breast Cancer Research & Treatment, 2010, v. 122, n. 3, p. 671, doi. 10.1007/s10549-009-0596-6
By:
- Aceto, Gitana;
- Solano, Angela;
- Neuman, Maria;
- Veschi, Serena;
- Morgano, Annalisa;
- Malatesta, Sara;
- Chacon, Reinaldo;
- Pupareli, Carmen;
- Lombardi, Mercedes;
- Battista, Pasquale;
- Marchetti, Antonio;
- Mariani-Costantini, Renato;
- Podestà, Ernesto
Publication type:
Article
Role of Breast Cancer Risk Estimation Models to Identify Women Eligible for Genetic Testing and Risk-Reducing Surgery.
Published in:
Biomedicines, 2024, v. 12, n. 4, p. 714, doi. 10.3390/biomedicines12040714
By:
- Irelli, Azzurra;
- Patruno, Leonardo Valerio;
- Chiatamone Ranieri, Sofia;
- Di Giacomo, Daniela;
- Malatesta, Sara;
- Alesse, Edoardo;
- Tessitore, Alessandra;
- Cannita, Katia
Publication type:
Article
Reduction of atherothrombotic burden before stent deployment in non- ST elevation acute coronary syndromes: Reduction of myocardial necrosis achieved with nose-dive manual thrombus aspiration ( REMNANT) trial. A volumetric intravascular ultrasound study.
Published in:
Catheterization & Cardiovascular Interventions, 2016, v. 88, n. 5, p. 716, doi. 10.1002/ccd.26301
By:
- Zimarino, Marco;
- Angeramo, Francesca;
- Prasad, Abhiram;
- Ruggieri, Benedetta;
- Malatesta, Sara;
- Prati, Francesco;
- Buttitta, Fiamma;
- De Caterina, Raffaele
Publication type:
Article
IDH1 mutations at residue p.R132 ( IDH1R132) occur frequently in high-grade gliomas but not in other solid tumors.
Published in:
Human Mutation, 2009, v. 30, n. 1, p. 7, doi. 10.1002/humu.20937
By:
- Bleeker, Fonnet E.;
- Lamba, Simona;
- Leenstra, Sieger;
- Troost, Dirk;
- Hulsebos, Theo;
- Vandertop, W. Peter;
- Frattini, Milo;
- Molinari, Francesca;
- Knowles, Margaret;
- Cerrato, Aniello;
- Rodolfo, Monica;
- Scarpa, Aldo;
- Felicioni, Lara;
- Buttitta, Fiamma;
- Malatesta, Sara;
- Marchetti, Antonio;
- Bardelli, Alberto
Publication type:
Article
Frequent mutations in the neurotrophic tyrosine receptor kinase gene family in large cell neuroendocrine carcinoma of the lung.
Published in:
Human Mutation, 2008, v. 29, n. 5, p. 609, doi. 10.1002/humu.20707
By:
- Marchetti, Antonio;
- Felicioni, Lara;
- Pelosi, Giuseppe;
- Del Grammastro, Maela;
- Fumagalli, Caterina;
- Sciarrotta, Mariagrazia;
- Malatesta, Sara;
- Chella, Antonio;
- Barassi, Fabio;
- Mucilli, Felice;
- Camplese, Pierpaolo;
- D'Antuono, Tommaso;
- Sacco, Rocco;
- Buttitta, Fiamma
Publication type:
Article

Found: 9

Assessment of <i>EGFR</i> Mutations in Circulating Tumor Cell Preparations from NSCLC Patients by Next Generation Sequencing: Toward a Real-Time Liquid Biopsy for Treatment.

Complex Mutations & Subpopulations of Deletions at Exon 19 of EGFR in NSCLC Revealed by Next Generation Sequencing: Potential Clinical Implications.

Mutational Profile of GNAQ<sup>Q209</sup> in Human Tumors.

Role of the Molecular Tumor Board for the Personalized Treatment of Patients with Metastatic Breast Cancer: A Focus on the State of the Art in Italy.

High-risk human papilloma virus infection, tumor pathophenotypes, and BRCA1/2 and TP53 status in juvenile breast cancer.

Role of Breast Cancer Risk Estimation Models to Identify Women Eligible for Genetic Testing and Risk-Reducing Surgery.

Reduction of atherothrombotic burden before stent deployment in non- ST elevation acute coronary syndromes: Reduction of myocardial necrosis achieved with nose-dive manual thrombus aspiration ( REMNANT) trial. A volumetric intravascular ultrasound study.

IDH1 mutations at residue p.R132 ( IDH1<sup>R132</sup>) occur frequently in high-grade gliomas but not in other solid tumors.

Frequent mutations in the neurotrophic tyrosine receptor kinase gene family in large cell neuroendocrine carcinoma of the lung.