Sfoglia per SSD
KNOCKOUT OF FRATAXIN GENE CAUSES EMBRYO LETHALITY IN ARABIDOPSIS
2007 I. Murgia, V. Vazzola, A. Losa, C. Soave
KSRP ablation enhances brown fat gene program in white adipose tissue through reduced miR-150 expression
2014 C. Chou, Y. Lin, H. Wang, X. Zhu, M. Giovarelli, P. Briata, R. Gherzi, W.T. Garvey, C. Chen
KSRP silencing favors neural differentiation of P19 teratocarcinoma cells
2013 M. Giovarelli, G. Bucci, M. Pasero, R. Gherzi, P. Briata
KSRP, many functions for a single protein
2011 P. Briata, C. Chen, M. Giovarelli, M. Pasero, M. Trabucchi, A. Ramos, R. Gherzi
Kynurenine pathway is altered in BDNF Val66Met knock-in mice: Effect of physical exercise
2020 A. Ieraci, S. Beggiato, L. Ferraro, S.S. Barbieri, M. Popoli
L-aspartate oxidase from Escherichia coli. I. Characterization of coenzyme binding and product inhibition
1996 M. Mortarino, A. Negri, G. Tedeschi, T. Simonic, S. Duga, H.G. Gassen, S. Ronchi
La DNA elicasi Sgs 1 di lievito previene l’accumulo di intermedi ricombinanti durante la replicazione del DNA danneggiato
2004 G.L. Maffioletti
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA
2005 G. Soldà, R. Asselta, R. Ghiotto, M. Malcovati, M.L. Tenchini, G. Castaman, S. Duga
La proteina di checkpoint Ddc1 svolge un ruolo nel processo di adattamento ai danni al DNA
2005 L.L. DI NOLA
La qualità ‘possibile’ nella formazione degli operatori sanitari : riflessioni a partire dalla riforma dell’autonomia universitaria
2001 M. Malcovati, L. Zannini
Label-free characterization of extracellular vesicles from human Mesenchymal Stem Cells by Raman spectroscopy
2015 A. Gualerzi, R. Vanna, M.E. Bernardo, A. Milani, S. Niada, A.T. Brini, C. Morasso, S. Picciolini, M. Bedoni, F. Ciceri, F. Gramatica
Label-free mass spectrometry-based quantification of linker histone h1 variants in clinical samples
2020 R. Noberini, C.M. Torres, E.O. Savoia, S. Brandini, M.G. Jodice, G. Bertalot, G. Bonizzi, M. Capra, G. Diaferia, P. Scaffidi, T. Bonaldi
Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies
2010 T.L. Assimes, H. Hólm, S. Kathiresan, M.P. Reilly, G. Thorleifsson, B.F. Voight, J. Erdmann, C. Willenborg, D. Vaidya, C. Xie, C.C. Patterson, T.M. Morgan, M.S. Burnett, M. Li, M.A. Hlatky, J.W. Knowles, J.R. Thompson, D. Absher, C. Iribarren, A. Go, S.P. Fortmann, S. Sidney, N. Risch, H. Tang, R.M. Myers, K. Berger, M. Stoll, S.H. Shah, G. Thorgeirsson, K. Andersen, A.S. Havulinna, J.E. Herrera, N. Faraday, Y. Kim, B.G. Kral, R.A. Mathias, I. Ruczinski, B. Suktitipat, A.F. Wilson, L.R. Yanek, L.C. Becker, P. Linsel Nitschke, W. Lieb, I.R. König, C. Hengstenberg, M. Fischer, K. Stark, W. Reinhard, J. Winogradow, M. Grassl, A. Grosshennig, M. Preuss, S. Schreiber, H.E. Wichmann, C. Meisinger, J. Yee, Y. Friedlander, R. Do, J.B. Meigs, G. Williams, D.M. Nathan, C.A. Macrae, L. Qu, R.L. Wilensky, W.H.J. Matthai, A.N. Qasim, H. Hakonarson, A.D. Pichard, K.M. Kent, L. Satler, J.M. Lindsay, R. Waksman, C.W. Knouff, D.M. Waterworth, M.C. Walker, V.E. Mooser, J. Marrugat, G. Lucas, I. Subirana, J. Sala, R. Ramos, N. Martinelli, O. Olivieri, E. Trabetti, G. Malerba, P.F. Pignatti, C. Guiducci, D. Mirel, M. Parkin, J.N. Hirschhorn, R. Asselta, S. Duga, K. Musunuru, M.J. Daly, S. Purcell, S. Eifert, P.S. Braund, B.J. Wright, A.J. Balmforth, S.G. Ball, M. Infarction Genetics Consortium, W. Trust Case Control Consortium, Cardiogenics, W.H. Ouwehand, P. Delouka, M. Scholz, F. Cambien, A. Huge, T. Scheffold, V. Salomaa, D. Girelli, C.B. Granger, L. Peltonen, P.P. Mckeown, D. Altshuler, O. Melander, J.M. Devaney, S.E. Epstein, D.J. Rader, R. Elosua, J.C. Engert, S.S. Anand, A.S. Hall, A. Ziegler, C.J. O'Donnell, J.A. Spertus, D. Siscovick, S.M. Schwartz, D. Becker, U. Thorsteinsdottir, K. Stefansson, H. Schunkert, N.J. Samani, T. Quertermous
Lack of evidence for association of meiotic nondisjunction with particular DNA haplotypes on chromosome 21
1988 N. Sacchi, J.F. Gusella, L. Perroni, F.D. Bricarelli, T.S. Papas
Lack of evidence for post-vaccine onset of autoimmune/lymphoproliferative disorders, during a nine-month follow-up in multiply vaccinated Italian military
2017 C. Ferlito, V. Barnaba, S. Abrignani, M. Bombaci, A. Sette, J. Sidney, R. Biselli, E. Tomao, M.S. Cattaruzza, V. Germano, M.I. Biondo, G. Salerno, P. Lulli, S. Caporuscio, A.P. Diamanti, M. Falco, V. Biselli, P. Cardelli, A. Autore, E. Lucertini, D.P. De Cesare, M.S. Peragallo, F. Lista, C. Martire, S. Salemi, R. Nisini, R. D'Amelio
Lack of functional pnp gene results in increased cell aggregation and poly-N-acetylglucosamine (PNAG) production in Escherichia coli C
2011 D. Antoniani, T. Carzaniga, G. Dehò, F. Briani, P. Landini
Lack of Methyl-CpG Binding Protein 2 (MeCP2) Affects Cell Fate Refinement During Embryonic Cortical Development
2018 C.G. Clementina, S. Linda, D.S. Marco, R. Riccardo L, P. Davide, M. Pagani, N. Landsberger, F. Bedogni
Lack of movement in neurological diseases : effects on neurogenesis and muscle-nerve interaction
2016 D. Bottai, R. Adami, J. Pagano, M. Colombo, N. Platonova, R. Chiaramonte, R. Ghidoni, R.B.A.M.C. Bottinelli, M. Canepari
Lactic acid bacteria as potential probiotics for the pharyngeal mucosa
2011 V. Taverniti, M. Minuzzo, S. Arioli, M. Stuknytė, I. Zanoni, F. Granucci, M. Karp, D. Mora, S. Guglielmetti
Lactobacillus helveticus MIMLh5-Specific Antibodies for Detection of S-Layer Protein in Grana Padano Protected-Designation-of-Origin Cheese
2014 M. Stuknyte, E. Brockmann, T. Huovinen, S. Guglielmetti, D. Mora, V. Taverniti, S. Arioli, I. De Noni, U. Lamminmäki
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