Sfoglia per SSD
La valutazione del rischio ambientale dell'emissione deliberata nell'ambiente di organismi geneticamente modificati
2005 C. Sorlini, M. Buiatti, G. Burgio, F. Cellini, V. Giovannelli, M. Lerner, G. Massari, P. Perrino, E. Selva, A. Spagnoletti, G. Staiano
The variability of SMCHD1 gene in FSHD patients: evidence of new mutations
2019 C. Strafella, V. Caputo, R.M. Galota, G. Campoli, C. Bax, L. Colantoni, G. Minozzi, C. Orsini, L. Politano, G. Tasca, G. Novelli, E. Ricci, E. Giardina, R. Cascella
Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy
2021 N. Voisin, R.E. Schnur, S. Douzgou, S.M. Hiatt, C.F. Rustad, N.J. Brown, D.L. Earl, B. Keren, O. Levchenko, S. Geuer, S. Verheyen, D. Johnson, Y.A. Zarate, M. Hancarova, D.J. Amor, E.M. Bebin, J. Blatterer, A. Brusco, G. Cappuccio, J. Charrow, N. Chatron, G.M. Cooper, T. Courtin, E. Dadali, J. Delafontaine, E. Del Giudice, M. Doco, G. Douglas, A. Eisenkolbl, T. Funari, G. Giannuzzi, U. Gruber-Sedlmayr, N. Guex, D. Heron, O.L. Holla, A.C.E. Hurst, J. Juusola, D. Kronn, A. Lavrov, C. Lee, S. Lorrain, E. Merckoll, A. Mikhaleva, J. Norman, S. Pradervand, D. Prchalova, L. Rhodes, V.R. Sanders, Z. Sedlacek, H.A. Seebacher, E.A. Sellars, F. Sirchia, T. Takenouchi, A.J. Tanaka, H. Taska-Tench, E. Tonne, K. Tveten, G. Vitiello, M. Vlckova, T. Uehara, C. Nava, B. Yalcin, K. Kosaki, D. Donnai, S. Mundlos, N. Brunetti-Pierri, W.K. Chung, A. Reymond
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
2021 S. Bassani, E. van Beelen, M. Rossel, N. Voisin, A. Morgan, Y. Arribat, N. Chatron, J. Chrast, M. Cocca, B. Delprat, F. Faletra, G. Giannuzzi, N. Guex, R. Machavoine, S. Pradervand, J.J. Smits, J.M. van de Kamp, A. Ziegler, F. Amati, S. Marlin, H. Kremer, H. Locher, T. Maurice, P. Gasparini, G. Girotto, A. Reymond
Variants of endothelial nitric oxide synthase gene are associated with components of metabolic syndrome in an Arab population
2012 K.M. Alkharfy, N.M. Al-Daghri, O.S. Al-Attas, M.S. Alokail, A.K. Mohammed, B. Vonodson, M. Clerici, U. Kazmi, T. Hussain, H.M. Draz
Ve-ptp modulates vascular integrity by promoting adherens junction maturation
2012 S. Carra, E. Foglia, S. Cermenati, E. Bresciani, C. Giampietro, C. Lora Lamia Donin, E. Dejana, M. Beltrame, F. Cotelli
Venturia inaequalis resistance in apple
2006 C. Gessler, A. Patocchi, S. Sansavini, S. Tartarini, L. Gianfranceschi
VERDANDI is a direct target of the MADS domain ovule identity complex and affects embryo sac differentiation in Arabidopsis
2010 L. Matias-Hernandez, R. Battaglia, F. Galbiati, M. Rubes, C. Eichenberger, U. Grossniklaus, M. Kater, L. Colombo
Versatile roles of Arabidopsis plastid ribosomal proteins in plant growth and development
2012 I. Romani, L. Tadini, F. Rossi, S. Masiero, M. Pribil, P. Jahns, M. Kater, D. Leister, P. Pesaresi
Vitamin D and VDR in cancer cachexia and muscle regeneration
2017 A. Camperi, F. Pin, D. Costamagna, F. Penna, M.L. Menduina, Z. Aversa, T. Zimmers, R. Verzaro, R. Fittipaldi, G. Caretti, F.M. Baccino, M. Muscaritoli, C. Paola
Vitamin D receptor gene polymorphisms and HLA DRB1*04 cosegregation in Saudi type 2 diabetes patients
2012 N.M. Al Daghri, O. Al Attas, M.S. Alokail, K.M. Alkharfy, H.M. Draz, C. Agliardi, A.K. Mohammed, F.R. Guerini, M. Clerici
VPS54 genetic analysis in ALS Italian Cohort
2011 L. Corrado, S. Gagliardi, Y. Carlomagno, T. Mennini, N. Ticozzi, L. Mazzini, V. Silani, C. Cereda, S. D'Alfonso
VvMYB60 expression is restricted to guard cells and correlates with stomatal conductance in the grape leaf
2019 L. Simoni, M. Zottini, C. Tonelli, M. Galbiati
Water: the invisible problem. Access to fresh water is considered to be a universal and free human right, but dwindling resources and a burgeoning population are increasing its economic value
2009 E. Cominelli, M. Galbiati, C. Tonelli, C. Bowler
What ENCODE is teaching us on the genomic sites of transcription factors
2013 R. Mantovani
Wheat with greatly reduced accumulation of free asparagine in the grain, produced by CRISPR/Cas9 editing of asparagine synthetase gene TaASN2
2021 S. Raffan, C. Sparks, A. Huttly, L. Hyde, D. Martignago, A. Mead, S.J. Hanley, P.A. Wilkinson, G. Barker, K.J. Edwards, T.Y. Curtis, S. Usher, O. Kosik, N.G. Halford
WhiB5, a Transcriptional Regulator That Contributes to Mycobacterium tuberculosis Virulence and Reactivation
2012 S. Casonato, A. Cervantes Sánchez, H. Haruki, M. Rengifo González, R. Provvedi, E. Dainese, T. Jaouen, S. Gola, E. Bini, M. Vicente, K. Johnsson, D. Ghisotti, G. Palù, R. Hernández Pando, R. Manganelli
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-cell assay for specific inhibitors of translation initiation in bacteria
2015 M. Raneri, B. Sciandrone, F. Briani
X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene
2017 A. Ciammola, P. Carrera, A..B. Di Fonzo, J. Sassone, R. Villa, B. Poletti, M. Ferrari, F. Girotti, E. Monfrini, G. Buongarzone, V. Silani, C..M. Cinnante, M.L. Mignona, P. D'Adamo, M.T. Bonati
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