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Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria 1-gen-2018 Gagliardi, M; Arabia, G; Nisticò, R; Iannello, G; Procopio, R; Manfredini, L; Annesi, G; Quattrone, A.
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria 1-gen-2018 Gagliardi, M.; Arabia, G.; Nistico, R.; Iannello, G.; Procopio, R.; Manfredini, L.; Annesi, G.; Quattrone, A.
Mutational Analysis of the AVP Gene in a Calabrian Family Affected by adFNDI 1-gen-2021 Mirabelli, Maria; Tocci, Vera; Kvistgaard, Helene; Corigliano, DOMENICA MARIA; Arcidiacono, Biagio; Knudsen Jane, Hagelskjær; Chiefari, Eusebio; Foti, Daniela Patrizia Francesca; Christensen Jane, Hvarregaard; Brunetti, Antonio.
Mutational oncology of lung cancer: Molecular markers, drugs, negotiation conditions and experiences in national reference centers 1-gen-2021 Esposito, I.; Calabria, S.; Piccinni, C.; Addesi, A.; Dondi, L.; Ronconi, G.; Pedrini, A.; Maggioni, A. P.; Curigliano, G.; Listi, A.; Righi, L.; Novello, S.; Buglioni, S.; Ciliberto, G.; Pruneri, G.; Martini, N.
Mutations and polymorphisms in mitochondrial DNA in head and neck cancer cell lines 1-gen-2006 Garozzo, A; Lombardo, N; De Clemente, M; Carey, Te.; Allegra, E
Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy 1-gen-2004 D'Agostino, D; Bertelli, M; Gallo, S; Cecchin, S; Albiero, E; Garofalo, Pg; Gambardella, A; ST HILAIRE, Jm; Kwiecinski, H; Andermann, E; Pandolfo, M.
Mutations and prognosis in primary myelofibrosis 1-gen-2013 Vannucchi, ALESSANDRO MARIA; Lasho, Tl; Guglielmelli, Paola; Biamonte, Flavia; Pardanani, A; Pereira, A; Finke, C; Score, J; Gangat, N; Mannarelli, Carmela; Ketterling, Rp; Rotunno, Giada; Knudson, Ra; Susini, Mc; Laborde, Rr; Spolverini, Ambra; Pancrazzi, Alessandro; Pieri, Lisa; Manfredini, R; Tagliafico, E; Zini, R; Jones, A; Zoi, K; Reiter, A; Duncombe, A; Pietra, D; Rumi, E; Cervantes, F; Barosi, G; Cazzola, M; Cross, Nc; Tefferi, A.
Mutations at coding mononucleotide repeats in gastric cancer with the microsatellite mutator phenotype 1-gen-1998 Ottini, L; Falchetti, M; D'Amico, C; Amorosi, A; Saieva, C; Masala, G; Frati, L; Cama, A; Palli, D; MARIANI-COSTANTINI, R
Mutations in Box B of the promoter of a eucaryotic tRNAPro gene affect rate of transcription, processing, and stability of the transcripts 1-gen-1984 Traboni, C.; Ciliberto, G; Cortese, R.
Mutations in Col4a1 Cause Perinatal Cerebral Hemorrhage and Porencephaly 1-gen-2005 Gould, Db; Phalan, C; VAN DER KNAAP, Ms; VAN MIL, Se; Smith, Rs; Schimenti, Jc; Aguglia, U; Breedveld, Gj; HEUTINK P., AND JOHN SWM
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP 1-gen-2013 Labate, A; Tarantino, P; Palamara, G; Gagliardi, M; Cavalcanti, F; Ferlazzo, E; Sturniolo, M; Incorpora, G; Annesi, G; Aguglia, U; Gambardella, A
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP 1-gen-2013 Labate, A.; Tarantino, P.; Palamara, G.; Gagliardi, M.; Cavalcanti, F.; Ferlazzo, E.; Sturniolo, M.; Incorpora, G.; Annesi, G.; Aguglia, U.; Gambardella, A.
Mutations in the insulin receptor gene in genetic forms of insulin resistance 1-gen-1990 S. I., Taylor; T., Kadowaki; D., Accili; A., Cama; H., Kadowaki; C., MC KEON; V., Moncada; B., MARCUS SAMUELS; C., Bevins; K., Ojama; C., Frapier; L., Beitz; Perrotti, N; R., REES-JONES; R., Margolis; E., Imano; S., Najjar; F., Courtney; R., Arakaki; P., Gorden; J., Roth
Mutations in the KEAP1-NFE2L2 Pathway Define a Molecular Subset of Rapidly Progressing Lung Adenocarcinoma 1-gen-2019 Goeman, Frauke; De Nicola, Francesca; Scalera, Stefano; Sperati, Francesca; Gallo, Enzo; Ciuffreda, Ludovica; Pallocca, Matteo; Pizzuti, Laura; Krasniqi, Eriseld; Barchiesi, Giacomo; Vici, Patrizia; Barba, Maddalena; Buglioni, Simonetta; Casini, Beatrice; Visca, Paolo; Pescarmona, Edoardo; Mazzotta, Marco; De Maria, Ruggero; Fanciulli, Maurizio; Ciliberto, Gennaro; Maugeri-Saccà, Marcello
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 1-gen-2014 Johnson, Jo; Pioro, Ep; Boehringer, A; Chia, R; Feit, H; Renton, Ae; Pliner, Ha; Abramzon, Y; Marangi, G; Winborn, Bj; Gibbs, Jr; Nalls, Ma; Morgan, S; Shoai, M; Hardy, J; Pittman, A; Orrell, Rw; Malaspina, A; Sidle, Kc; Fratta, P; Harms, Mb; Baloh, Rh; Pestronk, A; Weihl, Cc; Rogaeva, E; Zinman, L; Drory, Ve; Borghero, G; Mora, G; Calvo, A; Rothstein, Jd; Italsgen, Consortium; Drepper, C; Sendtner, M; Singleton, Ab10; Taylor, Jp8; Cookson, Mr; Restagno, G; Sabatelli, M; Bowser, R; Chiò, A; Traynor, Bj; Moglia, C; Cammarosano, S; Canosa, A; Gallo, S; Brunetti, M; Ossola, I; Marinou, K; Papetti, L; Pisano, F; Pinter, Gl; Conte, A; Luigetti, M; Zollino, M; Lattante, S; Marangi, G; La Bella, V; Spataro, R; Colletti, T; Giannini, F; Battistini, S; Ricci, C; Caponnetto, C; Mancardi, G; Mandich, P; Salvi, F; Bartolomei, I; Mandrioli, J; Sola, P; Lunetta, C; Penco, S; Monsurrò, Mr; Tedeschi, G; Conforti, Fl; Gambardella, A; Quattrone, A; Volanti, P; Floris, G; Cannas, A; Piras, V; Marrosu, F; Marrosu, Mg; Murru, Mr; Pugliatti, M; Parish, Ld; Sotgiu, A; Solinas, G; Ulgheri, L; Ticca, A; Simone, I; Logroscino, G; Pirisi, A.
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 1-gen-2010 Amorini, Maria; Rigoli, Luciana Concetta; C., Fede; Chimenz, Roberto; Romeo, Petronilla; Gallizzi, Romina; Briuglia, Silvana; SALPIETRO DAMIANO, Carmelo; E. M., Valente
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 1-gen-2010 Amorini, M.; Rigoli, L.; Fede, C.; Chimenz, R.; Romeo, P.; Gallizzi, R.; Briuglia, S.; Salpietro, C.; Valente, E. M.
Mutations in TMEM230 are not a common cause of Parkinson’s disease in southern Italy 1-gen-2017 Annesi, G; Gagliardi, M; Iannello, G; Procopio, R; Nicoletti, G; Morelli, M; Quattrone, A.
Mutations of the K-ras and p53 Genes in Gastric Adenocarcinomas from a High-Incidence Region around Florence, Italy 1-gen-1995 Hongyo, T.; Buzard, G. S.; Palli, D.; Weghorst, C. M.; Amorosi, A.; Galli, M.; Caporaso, N. E.; Fraumeni, J. F.; Rice, J. M.
Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE 1-gen-2011 Bouchardy, I; Steinlein, O; Combi, R; Ferini-Strambi, L; Gambardella, A; Rudolf, G; Morris, Ma; Picard, F
Mostrati risultati da 17.532 a 17.551 di 28.980
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