Sfoglia per SSD
VESSEL ASSOCIATED PROGENITOR CELLS AS A PROMISING CELL-BASED APPROACH TO TREAT CYSTIC FIBROSIS DISEASE
2016 C. Vezzali
Viable hypomorphic signaling mutant of the Met receptor reveals a role for hepatocyte growth factor in postnatal cerebellar development
2002 A. Ieraci, P.E. Forni, C. Ponzetto
VID22 counteracts G-quadruplex-induced genome instability
2021 E. Galati, M.C. Bosio, D. Novarina, M. Chiara, G.M. Bernini, A.M. Mozzarelli, M.L. Garcia-Rubio, B. Gomez-Gonzalez, A. Aguilera, T. Carzaniga, M. Todisco, T. Bellini, G.M. Nava, G. Frige, S. Sertic, D.S. Horner, A. Baryshnikova, C. Manzari, A.M. D'Erchia, G. Pesole, G.W. Brown, M. Muzi-Falconi, F. Lazzaro
VINYL : Variant prIoritizatioN bY survivaL analysis
2020 P. Mandreoli, M.A. Tangaro, D.S. Horner, F. Zambelli, G. Pesole, M. Chiara
VINYL : Variant prIoritizatioN by survivaL analysis
2020 M. Chiara, P. Mandreoli, M.A. Tangaro, A.M. D'Erchia, S. Sorrentino, C. Forleo, D.S. Horner, F. Zambelli, G. Pesole
VINYL: Variant prIoritizatioN bY survivaL analysis
2020 M. Chiara, P. Mandreoli, M.A. Tangaro, A.M. D’Erchia, S. Sorrentino, C. Forleo, D.S. Horner, F. Zambelli, G. Pesole
Visualization of recombination-mediated damage bypass by template switching
2014 M. Giannattasio, K. Zwicky, C. Follonier, M. Foiani, M. Lopes, D. Branzei
Vitamin D, parathyroid hormone and muscle impairment in myotonic dystrophies
2013 E. Passeri, E. Bugiardini, V. Sansone, R. Valaperta, E. Costa, B. Ambrosi, G. Meola, S. Corbetta
Volume growth in animal cells is cell cycle dependent and shows additive fluctuations
2022 C. Cadart, L. Venkova, M. Piel, M. Cosentino Lagomarsino
WDR5 inhibition halts metastasis dissemination by repressing the mesenchymal phenotype of breast cancer cells
2019 S. Punzi, C. Balestrieri, C. D'Alesio, D. Bossi, G.I. Dellino, E. Gatti, G. Pruneri, C. Criscitiello, G. Lovati, M. Meliksetyan, A. Carugo, G. Curigliano, G. Natoli, P.G. Pelicci, L. Lanfrancone
WEAPONIZING CRISPR/CAS9
2022 S. Tavella
Weeder Web: discovery of transcription factor binding sites in a set of sequences from co-regulated genes
2004 G. Pavesi, P. Mereghetti, G. Mauri, G. Pesole
WeederH : an algorithm for finding conserved regulatory motifs and regions in homologous sequences
2007 G. Pavesi, F. Zambelli, G. Pesole
What to Do with the Grail Now that We Have It? iPSCs, Potentiality, and Public Policy
2009 G. Testa
What we know and would like to know about CDKL5 and its involvement in epileptic encephalopathy
2012 C. Kilstrup-Nielsen, L. Rusconi, P.L. Montanara, D. Ciceri, A. Bergo, F. Bedogni, N. Landsberger
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism
2013 M.C. Proverbio, E. Mangano, A. Gessi, R. Bordoni, R. Spinelli, R. Asselta, P. Sogno Valin, S. Di Candia, I. Zamproni, C. Diceglie, S. Mora, M. Caruso-Nicoletti, A. Salvatoni, G. De Bellis, C. Battaglia
Whole transcriptome profiling of Late-Onset Alzheimer's Disease patients provides insights into the molecular changes involved in the disease
2018 A. Annese, C. Manzari, C. Lionetti, E. Picardi, D.S. Horner, M. Chiara, M.F. Caratozzolo, A. Tullo, B. Fosso, G. Pesole, A.M. D'Erchia
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease
2016 D. Smedley, M. Schubach, J.O.B. Jacobsen, S. Köhler, T. Zemojtel, M. Spielmann, M. Jäger, H. Hochheiser, N.L. Washington, J.A. Mcmurry, M.A. Haendel, C.J. Mungall, S.E. Lewis, T. Groza, G. Valentini, P.N. Robinson
A WHOLE-GENOME APPROACH TO IDENTIFY MICRORNA 'MODIFIERS' OF BREAST CANCER STEM CELL SELF-RENEWAL
2015 M.E. Bicchieri
Widespread generation of alternative UTRs contributes to sex-specific RNA binding by UNR
2012 M. Mihailovich, L. Wurth, F. Zambelli, I. Abaza, C. Militti, F.M. Mancuso, G. Roma, G. Pavesi, F. Gebauer
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