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Data di pubblicazione Titolo Autore(i) File
1-gen-2009 A multi-perspective view of genetic variation in Cameroon. Coia, Valentina; Brisighelli, Francesca; Donati, F; Pascali, Vincenzo Lorenzo; Boschi, Ilaria; Luiselli, D; Battaggia, C; Batini, C; Taglioli, L; Cruciani, F; Paoli, G; Capelli, Cristian; Spedini, G; Destro Bisol, Giovanni
1-gen-2012 A National project for in vivo dosimetry procedures in radiotherapy: First results Piermattei, Angelo; Greco, Francesca; Azario, Luigi; Porcelli, Andrea; Cilla, Savino; Zucca, S; Russo, A; Castro, E. D; Russo, Michele; Caivano, Rocchina; Fusco, V; Morganti, Alessio Giuseppe; Fidanzio, Andrea
1-gen-2012 A National project for in vivo dosimetry procedures in radiotherapy: First results Piermattei, Angelo; Greco, Francesca; Azario, Luigi; Porcelli, Andrea; Cilla, Savino; Zucca, S; Russo, A; Castro, Ed; Russo, M; Caivano, Rocchina; Fusco, Vincenzo; Morganti, Alessio Giuseppe; Fidanzio, Andrea
1-gen-2009 A new beta-chain haemoglobin variant with increased oxygen affinity: Hb Roma [beta115(g17)Ala-->Val] Manconi, B; De Rosa, Mc; Cappabianca, Mp; Olianas, A; Carelli Alinovi, Cristiana; Mastropietro, F; Ponzini, D; Amato, A; Pellegrini, M.
1-gen-2000 A new method for the evaluation of matches in non-recombining genomes: application to Y-chromosomal short tandem repeat (STR) haplotypes in European males Roewer, L.; Kayser, M.; De Knijff, P.; Anslinger, K.; Betz, A.; Caglià, A.; Corach, D.; Füredi, S.; Henke, L.; Hidding, M.; Kärgel, H. j.; Lessig, R.; Nagy, M.; Pascali, Vincenzo Lorenzo; Parson, W.; Rolf, B.; Schmitt, C.; Szibor, R.; Teifel Greding, J.; Krawczak, M.
1-gen-2008 A new T677C mutation of the aspartoacylase gene encodes for a protein with no enzymatic activity Tavazzi, Barbara; Di Pietro, Valentina; Amorini, Angela Maria; Giardina, Bruno; Lazzarino, Giuseppe
1-gen-2010 A nickel ABC-transporter of Staphylococcus aureus is involved in urinary tract infection Hiron, Aurelia; Posteraro, Brunella; Carriere, Marie; Remy, Laetitia; Delporte, Cecile; La Sorda, Marilena; Sanguinetti, Maurizio; Juilliard, Vincent; Borezee Durant, Elise
1-gen-2010 A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome Steindl, K; Alazami, Am; Bhatia, Kp; Wuerfel, Jt; Petersen, D; Cartolari, R; Neri, Giovanni; Klein, C; Mongiardo, B; Alkuraya, Fs; Scheider, Sa
1-gen-2011 A novel L67P SOD1 mutation in an Italian ALS patient. Del Grande, Alessandra; Luigetti, Marco; Conte, Amelia; Mancuso, Irene; Lattante, Serena; Marangi, Giuseppe; Zollino, Marcella; Sabatelli, Mario; Stipa, G.
1-gen-2003 A Novel Route of Transplantation of Human Cord Blood Stem Cells in Preimmune Fetal Sheep: The Intracelomic Cavity Noia, Giuseppe; Pierelli, Luca; Bonanno, Giuseppina; Monego, Giovanni; Perillo, Alessandro; Rutella, Sergio; Cavaliere, Anna Franca; De Santis, Marco; Ligato, Maria Serena; Fortunato, Giuseppe; Scambia, Giovanni; Terzano, Marinella; Iannace, Enrico; Zelano, Giovanni; Michetti, Fabrizio; Leone, Giuseppe; Mancuso, Salvatore
1-gen-2009 A pivotal role for NAADP in histamine H1 receptor-induced calcium signaling Esposito, Bianca; Gambara, Guido; Lewis M, Alexander; Churchill, Grant C; Palombi, Fioretta; D'Alessio, Alessio; Genazzani, Armando; Galione, Antony; Filippini, Antonio
1-gen-2004 A pRb-independent mechanism preserves the postmitotic state in terminally differentiated skeletal muscle cells Camarda, G; Siepi, F; Pajalunga, D; Bernardini, Camilla; Rossi, R; Montecucco, A; Meccia, E; Crescenzi, M.
1-gen-2001 A predominantly indigenous paternal heritage for the Austronesian-speaking peoples of insular Southeast Asia and Oceania Capelli, Cristian; Wilson, Jf; Richards, M; Stumpf, Mph; Gratrix, F; Oppenheimer, S; Underhill, P; Pascali, Vincenzo Lorenzo; Ko, Tm; Goldstein, Db
1-gen-2004 A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa Arredi, Barbara; Poloni, Es; Paracchini, S; Zerjal, Tatiana; Fathallah, Dm; Makrelouf, M; Pascali, Vincenzo Lorenzo; Novelletto, A; Tyler Smith, C.
1-gen-2009 A premature infant with Costello syndrome due to a rare G13C HRAS mutation Piccione, Maria; Pomponi, Maria Grazia; Pietrobono, Roberta; Neri, Giovanni
1-gen-2009 A premature infant with Costello syndrome due to a rare G13C HRAS mutation. Neri, Giovanni; Piccione, M; Piro, Maddalena; Pomponi, Maria Grazia; Pietrobono, Roberta; Candela, E; Gabriele, B; Corsello, Giovanni
1-gen-2009 A Prolonged Neonatal Jaundice Associated With a Rare G6PD Mutation Minucci, Angelo; Concolino, Paola; De Luca, Daniele; Giardina, Bruno; Zuppi, Cecilia; Capoluongo, Ettore Domenico
1-gen-2009 A proteomic approach to characterizing ciglitazone-induced cancer cell differentiation in Hep-G2 cell line Bottoni, Patrizia; Giardina, Bruno; Vitali, Alberto; Boninsegna Lucarelli, Alma; Scatena, Roberto
1-gen-2012 A radial glia-specific role of RhoA in double cortex formation Cappello, S; Böhringer, Crj; Bergami, M; Conzelmann, K; Ghanem, A; Tomassy, Gs; Arlotta, P; Mainardi, Marco; Allegra, M; Caleo, M; Van Hengel, J; Brakebusch, C; Götz, M.
1-gen-2011 A Reversed-Phase HPLC Fluorimetric Method for Simultaneous Determination of Homocysteine-Related Thiols in Different Body Fluids Persichilli, Silvia; Gervasoni, Jacopo; Castagnola, Massimo; Zuppi, Cecilia; Zappacosta, Bruno
Mostrati risultati da 50 a 69 di 4.440
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