Sfoglia per Tipologia Article (author)
Mutants, overexpressors and interactors of Arabidopsis plastocyanin isoforms: revised roles of plastocyanin in photosynthetic electron flow and thylakoid redox state
2009 P. Pesaresi, M. Schrfenberg, M. Weigel, I. Granlund, W.P. Schröder, G. Finazzi, F. Rappaport, S. Masiero, A. Furini, P. Jahns, D. Leister
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction
2008 R. Del Bo, M. Moggio, M. Rango, S. Bonato, M.G. D'Angelo, S. Ghezzi, G. Airoldi, M.T. Bassi, M. Guglieri, L. Napoli, C. Lamperti, S. Corti, A. Federico, N. Bresolin, G.P. Comi
Mutated nucleophosmin detects clonal multilineage involvement in acute myeloid leukemia : impact on WHO classification
2006 L. Pasqualucci, A. Liso, M.P. Martelli, N. Bolli, R. Pacini, A. Tabarrini, M. Carini, B. Bigerna, A. Pucciarini, R. Mannucci, I. Nicoletti, E. Tiacci, G. Meloni, G. Specchia, N. Cantore, F. Di Raimondo, S. Pileri, C. Mecucci, F. Mandelli, M.F. Martelli, B. Falini
Mutatio libelli nelle domande di nullità brevettuale : le ragioni di una possibile lettura alternativa
2018 S.M. Vanzetti
Mutation analysis of CHCHD10 in different neurodegenerative diseases
2015 M. Zhang, Z. Xi, L. Zinman, A.C. Bruni, R.G. Maletta, S.A..M. Curcio, I. Rainero, E. Rubino, L. Pinessi, B. Nacmias, S. Sorbi, D. Galimberti, A.E. Lang, S. Fox, E.I. Surace, M. Ghani, J. Guo, C. Sato, D. Moreno, Y. Liang, J. Keith, B.J. Traynor, P. St George Hyslop, E. Rogaeva
Mutation analysis of hepcidin and ferroportin genes : possible relationship with iron overload in italian prospective blood-donors
2008 L. Duca, P. Delbini, I. Nava, V. Vaja, G. Fiorelli, M.D. Cappellini
Mutation analysis of hepcidin and ferroportin genes in Italian prospective blood donors with iron overload
2009 L. Duca, P. Delbini, I. Nava, V. Vaja, G. Fiorelli, M.D. Cappellini
Mutation analysis of the BRCA1 gene in Malaysian breast cancer patients
2002 P. Balraj, A.S.B. Khoo, L. Volpi, J.A.M.A. Tan, S. Nair, H. Abdullah
Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure
2002 A. Marozzi, C. Porta, W. Vegetti, P.G. Crosignani, M.G. Tibiletti, L. Dalpra, E. Ginelli
Mutation analysis of the VPS54 gene in ALS patients
2008 C. Cereda, L. Corrado, Y. Carlomagno, S. Gagliardi, L. Testa, L. Mazzini, A. Ratti, N. Ticozzi, D. D'Alfonso, V. Silani, M. Ceroni
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B
2004 S. Bione, F. Rizzolio, C. Sala, R. Ricotti, M. Goegan, M.C. Manzini, R. Battaglia, A. Marozzi, W. Vegetti, L. Dalpra, P.G. Crosignani, E. Ginelli, R. Nappi, S. Bernabini, V. Bruni, F. Torricelli, O. Zuffardi, D. Toniolo
A mutation and expression analysis of the oncogene BRAF in pituitary adenomas
2007 I. Ewing, S. Pedder-Smith, G. Franchi, M. Ruscica, M. Emery, V. Vax, E. Garcia, S. Czirják, Z. Hanzély, B. Kola, M. Korbonits, A.B. Grossman
Mutation and loss of expression of ARID1A in uterine low-grade endometrioid carcinoma
2011 B. Guan, T.-. Mao, P.K. Panuganti, E. Kuhn, R.J. Kurman, D. Maeda, E. Chen, Y.-. Jeng, T.-. Wang, I.-. Shih
Mutation and suppressor analysis of the essential lipopolysaccharide transport protein LptA reveals strategies to overcome severe outer membrane permeability defects in Escherichia coli
2018 F.A. Falchi, E.A. Maccagni, S. Puccio, C. Peano, C. De Castro, A. Palmigiano, D. Garozzo, A.M. Martorana, A. Polissi, G. Dehò, P. Sperandeo
Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel 'hot spot' in codon 47
2000 A. Ferlini, L. Obici, E. Manzati, O. Biadi, E. Tarantino, P. Conigli, G. Merlini, M. D'Alessandro, V. Mazzaferro, C. Tassinari, F. Salvi
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies
2005 R. Cagliani, F. Magri, A. Toscano, L. Merlini, F. Fortunato, C. Lamperti, C. Rodolico, A. Prelle, M. Sironi, M. Aguennouz, P. Ciscato, A. Uncini, M. Moggio, N. Bresolin, G.P. Comi
A mutation in polynucleotide phosphorylase from Escherichia coli impairing RNA binding and degradosome stability
2004 M.E. Regonesi, F. Briani, A. Ghetta, S. Zangrossi, D. Ghisotti, P. Tortora, G. Dehò
Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function
2016 S. Biel, M. Aquila, B. Hertel, A. Berthold, T. Neumann, D. Difrancesco, A. Moroni, G. Thiel, S. Kauferstein
Mutation in Serratia marcescens AmpC beta-lactamase producing high-level resistance to ceftazidime and cefpirome
2001 A. Raimondi, F. Sisto, H. Nikaido
Mutation in the ATP-binding pocket of the ABL kinase domain in an STI571-resistant BCR/ABL-positive cell line
2002 C. Ricci, B. Scarpini, V. Divoky, S. Gatto, F. Onida, S. Verstovsek, H.M. Kantarjian, M. Beran
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