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P2X7 receptor restrains pathogenic Tfh cell generation in systemic lupus erythematosus
2019 C.E. Faliti, R. Gualtierotti, E. Rottoli, M. Gerosa, L. Perruzza, A. Romagnani, G. Pellegrini, B. De Ponte Conti, R.L. Rossi, M. Idzko, E.M.C. Mazza, S. Bicciato, E. Traggiai, P.L. Meroni, F. Grassi
A p38-dependent pathway regulates DeltaNp63 DNA binding to p53-dependent promoters in UV-induced apoptosis of keratinocytes
2005 M. Papoutsaki, F. Moretti, M. Lanza, B. Marinari, V. Sartorelli, L. Guerrini, S. Chimenti, M. Levrero, A. Costanzo
p63 is a cereblon substrate involved in thalidomide teratogenicity
2019 T. Asatsuma-Okumura, H. Ando, M. De Simone, J. Yamamoto, T. Sato, N. Shimizu, K. Asakawa, Y. Yamaguchi, T. Ito, L. Guerrini, H. Handa
Paenibacillus tylopili sp.nov., a chitinolytic bacterium isolated from the mycorhizosphere of Tylopilus felleus
2008 N. Kuisiene, J. Raugalas, C. Sproer, R. M. Kroppenstedt, M. Stuknyte, D. Chitavichius
A pair of partially overlapping arabidopsis genes with antagonistic circadian expression
2012 A. Kunova, E. Zubko, P. Meyer
Palmdelphin Regulates Nuclear Resilience to Mechanical Stress in the Endothelium
2021 M. Sainz-Jaspeado, R.O. Smith, O. Plunde, S.-. Pawelzik, Y. Jin, S. Nordling, Y. Ding, P. Aspenstrom, M. Hedlund, G. Bastianello, F. Ascione, Q. Li, C.S. Demir, D. Fernando, G. Daniel, A. Franco-Cereceda, J. Kroon, M. Foiani, T.V. Petrova, M.W. Kilimann, M. Back, L. Claesson-Welsh
Pangenomics provides insights into the role of synanthropy in barn swallow evolution
2022 S. Secomandi, G. Gallo, M. Sozzoni, A. Iannucci, E. Galati, L. Abueg, J. Balacco, M. Caprioli, W. Chow, C. Ciofi, J. Collins, O. Fedrigo, L. Ferretti, A. Fungtammasan, B. Haase, K. Howe, W. Kwak, G. Lombardo, P. Masterson, G. Messina, A. Møller, J. Mountcastle, T. Mousseau, J. Ferrer-Obiol, A. Olivieri, A. Rhie, D. Rubolini, M. Saclier, R. Stanyon, D. Stucki, F. Thibaud-Nissen, J. Torrance, A. Torroni, K. Weber, R. Ambrosini, A. Bonisoli-Alquati, E. Jarvis, L. Gianfranceschi, G. Formenti
Parental histone deposition on the replicated strands promotes error-free DNA damage tolerance and regulates drug resistance
2022 V. Dolce, S. Dusi, M. Giannattasio, C. Joseph, M. Fumasoni, D. Branzei
Paroxysmal non-kinesigenic dyskinesia is caused by mutations of the MR-1 mitochondrial targeting sequence
2009 D. Ghezzi, C. Viscomi, A. Ferlini, F. Gualandi, P. Mereghetti, D. Degrandis, M. Zeviani
PARP14 controls the nuclear accumulation of a subset of type i IFN-inducible proteins
2018 G. Caprara, E. Prosperini, V. Piccolo, G. Sigismondo, A. Melacarne, A. Cuomo, M. Boothby, M. Rescigno, T. Bonaldi, G. Natoli
Partial characterization of plasmids from Geobacillus stearothermophilus strain 3 and the other related strains
2003 M. Stuknyte, N. Kuisiene, K. Pokusajeva, D. Chitavichius
PARylation of BRCA1 limits DNA break resection through BRCA2 and EXO1
2023 S. Lodovichi, R. Quadri, S. Sertic, A. Pellicioli
PAT-H-MS coupled with laser microdissection to study histone post-translational modifications in selected cell populations from pathology samples
2017 R. Noberini, R. Longuespee, C. Richichi, G. Pruneri, M. Kriegsmann, G. Pelicci, T. Bonaldi
Pathophysiology of hereditary angioedema
2014 S. Caccia, C. Suffritti, M. Cicardi
Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair
2011 L. Colnaghi, J. M. J. K., C.R. X. M., S. D., H. H., H. T. T.
Patient-specific cancer genes contribute to recurrently perturbed pathways and establish therapeutic vulnerabilities in esophageal adenocarcinoma
2019 T.P. Mourikis, L. Benedetti, E. Foxall, D. Temelkovski, J. Nulsen, J. Perner, M. Cereda, J. Lagergren, M. Howell, C. Yau, R.C. Fitzgerald, P. Scaffidi, A. Noorani, P.A.W. Edwards, R.F. Elliott, N. Grehan, B. Nutzinger, C. Hughes, E. Fidziukiewicz, J. Bornschein, S. Macrae, J. Crawte, A. Northrop, G. Contino, X. Li, R. de la Rue, A. Katz-Summercorn, S. Abbas, D. Loureda, M. O'Donovan, A. Miremadi, S. Malhotra, M. Tripathi, S. Tavare, A.G. Lynch, M. Eldridge, M. Secrier, L. Bower, G. Devonshire, S. Jammula, J. Davies, C. Crichton, N. Carroll, P. Safranek, A. Hindmarsh, V. Sujendran, S.J. Hayes, Y. Ang, A. Sharrocks, S.R. Preston, S. Oakes, I. Bagwan, V. Save, R.J.E. Skipworth, T.R. Hupp, J. Robert O'Neill, O. Tucker, A. Beggs, P. Taniere, S. Puig, T.J. Underwood, R.C. Walker, B.L. Grace, H. Barr, N. Shepherd, O. Old, J. Gossage, A. Davies, F. Chang, J. Zylstra, U. Mahadeva, V. Goh, G. Sanders, R. Berrisford, C. Harden, M. Lewis, E. Cheong, B. Kumar, S.L. Parsons, I. Soomro, P. Kaye, J. Saunders, L. Lovat, R. Haidry, L. Igali, M. Scott, S. Sothi, S. Suortamo, S. Lishman, G.B. Hanna, C.J. Peters, K. Moorthy, A. Grabowska, R. Turkington, D. Mcmanus, D. Khoo, W. Fickling, F.D. Ciccarelli
Patients with genetically heterogeneous synchronous colorectal cancer carry rare damaging germline mutations in immune-related genes
2016 M. Cereda, G. Gambardella, L. Benedetti, F. Iannelli, D. Patel, G. Basso, R.F. Guerra, T.P. Mourikis, I. Puccio, S. Sinha, L. Laghi, J. Spencer, M. Rodriguez-Justo, F.D. Ciccarelli
PCNA ubiquitylation as the wet readout of a Post-Replication Repair computational model
2011 F. Amara, R. Colombo, F. Spadaro, D. Besozzi, M. Muzi-Falconi, P. Plevani
PCSK9 (PROPROTEIN CONVERTASE SUBTILISIN/KEXIN TYPE 9)AND GLUCOSE METABOLISM: WHICH CONNECTION?
2018 G. Balzarotti
PEGylated liposomes associate with Wnt3A protein and expand putative stem cells in human bone marrow populations
2017 A.A. Janeczek, E. Scarpa, M.H. Horrocks, R.S. Tare, C.A. Rowland, D. Jenner, T.A. Newman, R.O.C. Oreffo, S.F. Lee, N.D. Evans
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