BORTOLUZZI, STEFANIA

BORTOLUZZI, STEFANIA  

Dipartimento di Medicina Molecolare - DMM  

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Risultati 1 - 20 di 114 (tempo di esecuzione: 0.039 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A Comprehensive, high-resolution genomic transcript map of human skeletal muscle. 1998 BORTOLUZZI, STEFANIATISO, NATASCIATOPPO, STEFANOVALLE, GIORGIOLANFRANCHI, GEROLAMODANIELI, GIAN ANTONIO + GENOME RESEARCH - -
A computational reconstruction of the adult human heart transcriptional profile 2000 BORTOLUZZI, STEFANIADANIELI, GIAN ANTONIO + JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY - -
A constitutive active MAPK/ERK pathway due to BRAFV600E positively regulates AHR pathway in PTC 2015 OCCHI, GIANLUCABAROLLO, SUSIREGAZZO, DANIELABERTAZZA, LORISGALUPPINI, FRANCESCAGUZZARDO, VINCENZACIATO, DENISCECCATO, FILIPPOWATUTANTRIGE FERNANDO, SARABISOGNIN, ANDREABORTOLUZZI, STEFANIAPENNELLI, GIANMARIABOSCARO, MARCOSCARONI, CARLAMIAN, CATERINA + ONCOTARGET - -
A data-driven network model of primary myelofibrosis: transcriptional and post-transcriptional alterations in CD34+ cells 2016 CALURA, ENRICAPIZZINI, SILVIABISOGNIN, ANDREACOPPE, ALESSANDROSALES, GABRIELEGAFFO, ENRICOROMUALDI, CHIARABORTOLUZZI, STEFANIA + BLOOD CANCER JOURNAL - -
A guilt-by-association mutation network in LGL leukemia 2017 Coppe AlessandroBortoluzzi, Stefania + ONCOTARGET - -
A high definition picture of key genes and pathways mutated in pediatric follicular lymphoma 2019 Lovisa, FedericaBinatti, AndreaCoppe, AlessandroPizzi, MarcoGuzzardo, VincenzaBasso, GiuseppeBortoluzzi, StefaniaMussolin, Lara + HAEMATOLOGICA - -
A high definition picture of somatic mutations in chronic lymphoproliferative disorder of natural killer cells 2020 Gasparini V. R.Binatti A.Coppe A.Teramo A.Vicenzetto C.Calabretto G.Barila G.Barizza A.Giussani E.Facco M.Semenzato G.Zambello R.Bortoluzzi S. + BLOOD CANCER JOURNAL - -
A multi-step bioinformatic approach detects putative regulatory elements in gene promoter 2005 BORTOLUZZI, STEFANIACOPPE, ALESSANDROBISOGNIN, ANDREAPIZZI, CINZIADANIELI, GIAN ANTONIO BMC BIOINFORMATICS - -
A multistep bioinformatic approach detects putative regulatory elements in gene promoters 2005 Bortoluzzi S.Coppe A.Bisognin A.Pizzi C. + BMC BIOINFORMATICS - -
A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T-cell Acute Lymphoblastic Leukemia 2020 Antonio MarzolloCaterina TrettiAlessandro CoppeStefania BortoluzziAlessandra BiffiSilvia Bresolin + AMERICAN JOURNAL OF HEMATOLOGY - -
A novel resource for the study of genes expressed in the adult human retina 2000 BORTOLUZZI, STEFANIADANIELI, GIAN ANTONIO + INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE - -
A survey of software tools for microRNA discovery and characterization using RNA-seq 2019 BORTOLOMEAZZI, MICHELEGaffo EBortoluzzi S. BRIEFINGS IN BIOINFORMATICS - -
A-MADMAN: annotation-based microarray data meta-analysis tool. 2009 BISOGNIN, ANDREACOPPE, ALESSANDRORISSO, DAVIDEROMUALDI, CHIARABICCIATO SBORTOLUZZI, STEFANIA + BMC BIOINFORMATICS - -
Abnormal expression patterns of WT1-as, MEG3 and ANRIL long non-coding RNAs in CD34+ cells from patients with primary myelofibrosis and their clinical correlations. 2014 BISOGNIN, ANDREABORTOLUZZI, STEFANIACOPPE, ALESSANDROSACCOMAN, CLAUDIA + LEUKEMIA & LYMPHOMA - -
Abstracts of the XXIII rd World Congress of Psychiatric Genetics (WCPG): Poster abstracts 2017 Cecilia SalvoroCAMPANELLI, CARLOLivio FinosGiorgio ValleLuisa MostacciuoloStefania BortoluzziGiovanni Vazza EUROPEAN NEUROPSYCHOPHARMACOLOGY - -
An integrative approach for the identification of prognostic and predictive biomarkers in rectal cancer. 2015 Agostini, MarcoD'ANGELO, EDOARDOZANGRANDO, ANDREADIGITO, MAURABORTOLUZZI, STEFANIANITTI, DONATOPUCCIARELLI, SALVATORE + ONCOTARGET - -
An integrative framework identifies alternative splicing events in colorectal cancer development. 2014 BISOGNIN, ANDREAPIZZINI, SILVIAPERILLI, LISANITTI, DONATOMOCELLIN, SIMONEZANOVELLO, PAOLABORTOLUZZI, STEFANIAMANDRUZZATO, SUSANNA + MOLECULAR ONCOLOGY - -
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy 2008 BORTOLUZZI, STEFANIAVETTORI, ANDREA + NEUROSCIENCE LETTERS - -
Characterisation and discovery of novel miRNAs and moRNAs in JAK2V617F mutated SET2 cells. 2012 BORTOLUZZI, STEFANIABISOGNIN, ANDREA + BLOOD - -
Characterization of C14orf4, a novel intronless human gene containing a polyglutamine repeat, mapped to the ARVD1 critical region 2000 RAMPAZZO, ALESSANDRAOCCHI, GIANLUCATISO, NATASCIABORTOLUZZI, STEFANIANAVA, ANDREADANIELI, GIAN ANTONIO + BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS - -