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Mostrati risultati da 30.713 a 30.732 di 123.294
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Disruption of the ASTN2/tTRIM32 locus at 9p33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. 1-gen-2014 Lionel, Ac; Tammimies, K; Vaags, Ak; Rosenfeld, Ja; Ahn, Jw; Merico, D; Noor, A; Runke, Ck; Pillalamarri, Vk; Carter, Mt; Gazzellone, Mj; Thiruvahindrapuram, B; Fagerberg, C; Laulund, Lw; Pellecchia, G; Lamoureux, S; Deshpande, C; Clayton Smith, J; White, Ac; Leather, S; Trounce, J; Melanie Bedford, H; Hatchwell, E; Eis, Ps; Yuen, Rk; Walker, S; Uddin, M; Geraghty, Mt; Nikkel, Sm; Tomiak, Em; Fernandez, Ba; Soreni, N; Crosbie, J; Arnold, Pd; Schachar, Rj; Roberts, W; Paterson, Ad; So, J; Szatmari, P; Chrysler, C; Woodbury Smith, M; Brian Lowry, R; Zwaigenbaum, L; Mandyam, D; Wei, J; Macdonald, Jr; Howe, Jl; Nalpathamkalam, T; Wang, Z; Tolson, D; Cobb, Ds; Wilks, Tm; Sorensen, Mj; Bader, Pi; An, Y; Wu, Bl; Musumeci, Sa; Romano, C; Postorivo, D; Nardone, Am; Monica, Md; Scarano, G; Zoccante, L; Novara, F; Zuffardi, Orsetta; Ciccone, Roberto; Antona, V; Carella, M; Zelante, L; Cavalli, P; Poggiani, C; Cavallari, U; Argiropoulos, B; Chernos, J; Brasch Andersen, C; Speevak, M; Fichera, M; Ogilvie, Cm; Shen, Y; Hodge, Jc; Talkowski, Me; Stavropoulos, Dj; Marshall, Cr; Scherer, Sw
Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome 1-gen-2001 Bonaglia, Mc; Giorda, R; Borgatti, R; Felisari, G; Gagliardi, C; Selicorni, A; Zuffardi, O
Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the èèq13.3 deletion syndrome 1-gen-2001 Bonaglia, Mc; Giorda, R; Borgatti, R; Felisari, G; Gagliardi, C; Selicorni, A; Zuffardi, Orsetta
Dissecazione Aortica: cosa c'è di nuovo? 1-gen-2010 Gambarin, Fabiana; Massetti, ; Serio, Alessandra; Pasotti, Michele; Bozzani, Antonio; Dore, Roberto; Disabella, Eliana; De, Giorgio; Odero, ATTILIO NICOLO'; Arbustini, Eloisa
La dissecazione spontanea dell'aorta toracica: risorse diagnostiche e terapeutiche tra chances di successo e alee di insuccesso 1-gen-2004 Buzzi, Fabio; Bovio, C.
Dissecting clinical findings: platelet defects segregate independently of deafness and cataract in a family affected by an apparent syndromic form of macrothrombocytopenia. 1-gen-2005 Gangarossa, S.; Seri, M.; Pecci, Alessandro; Di Bari, F.; Cusano, R.; Balduini, Carlo; Gasparini, P.; Savoia, A.
Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains 1-gen-1999 Adinolfi, S; Bagni, C; Musco, G; Gibson, T; Mazzarella, L; Pastore, Annalisa
DISSECTING METABOLIC SYNDROME COMPONENTS: DATA FROM A POPULATION-BASED EPIDEMIOLOGICAL SURVEY IN A GENETIC ISOLATE 1-gen-2015 Ginevra, Biino; Maria Pina, Concas; Cena, Hellas; Debora, Parracciani; Simona, Vaccargiu; Massimiliano, Cosso; Francesca, Marras; Vittoria, D'Esposito; Francesco, Beguinot; Mario, Pirastu
Dissecting metabolic syndrome components: data from an epidemiologic survey in a genetic isolate. 1-gen-2015 Biino, Ginevra; Concas, corresponding author Maria Pina; Cena, Hellas; Parracciani, Debora; Vaccargiu, Simona; Cosso, Massimiliano; Marras, Francesca; D’Esposito, Vittoria; Beguinot, Francesco; Pirastu, Mario
Dissecting out migraine complexity through comprehensive analysis of allodynia 1-gen-2019 De Icco, R.; Tassorelli, C.
Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein 1-gen-2023 Kretz, Perrine F.; Wagner, Christel; Mikhaleva, Anna; Montillot, Charlotte; Hugel, Sylvain; Morella, Ilaria; Kannan, Meghna; Fischer, Marie-Christine; Milhau, Maxence; Yalcin, Ipek; Brambilla, Riccardo; Selloum, Mohammed; Herault, Yann; Reymond, Alexandre; Collins, Stephan C.; Yalcin, Binnaz
Dissecting the calcium-induced differentiation of human primary keratinocytes stem cells by integrative and structural network analyses 1-gen-2015 Toufighi, Kiana; Yang, Jae-Seong; Luis, Nuno Miguel; Aznar Benitah, Salvador; Lehner, Ben; Serrano, Luis; Kiel, Christina
Dissecting the Extracellular Complexity of Neuromuscular Junction Organizers 1-gen-2020 Guarino, S. R.; Canciani, A.; Forneris, F.
Dissecting the genetic bases of Amyotrophic lateral sclerosis and Late-onset Pompe disease through Next-generation sequencing 23-mag-2021 Palmieri, Ilaria
Dissecting the molecular features of systemic light chain (Al) amyloidosis: Contributions from proteomics 1-gen-2021 Rognoni, P.; Mazzini, G.; Caminito, S.; Palladini, G.; Lavatelli, F.
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder 1-gen-2022 Caporali, Leonardo; Fiorini, Claudio; Palombo, Flavia; Romagnoli, Martina; Baccari, Flavia; Zenesini, Corrado; Visconti, Paola; Posar, Annio; Scaduto, Maria Cristina; Ormanbekova, Danara; Battaglia, Agatino; Tancredi, Raffaella; Cameli, Cinzia; Viggiano, Marta; Olivieri, Anna; Torroni, Antonio; Maestrini, Elena; Rochat, Magali Jane; Bacchelli, Elena; Carelli, Valerio; Maresca, Alessandra
Dissecting the phenotypic variability of osteogenesis imperfecta 1-gen-2022 Garibaldi, N; Besio, R; Dalgleish, R; Villani, S; Barnes, Am; Marini, Jc; Forlino, A
Dissecting the Pre-Columbian genomic ancestry of Native Americans along the Andes-Amazonia divide 1-gen-2019 Gnecchi-Ruscone, Guido Alberto; Sarno, Stefania; De Fanti, Sara; Gianvincenzo, Laura; Giuliani, Cristina; Boattini, Alessio; Bortolini, Eugenio; Di Corcia, Tullia; Sanchez Mellado, Cesar; Dàvila Francia, Taylor Jesus; Gentilini, Davide; Di Blasio, Anna Maria; Di Cosimo, Patrizia; Cilli, Elisabetta; Gonzalez-Martin, Antonio; Franceschi, Claudio; Franceschi, Zelda Alice; Rickards, Olga; Sazzini, Marco; Luiselli, Donata; Pettener, Davide
Dissecting the role of calcium in Osteogenesis Imperfecta: an in vitro and in vivo study 18-dic-2023 Contento, BARBARA MARIA
DISSECTING TITIN INTO ITS STRUCTURAL MOTIFS - IDENTIFICATION OF AN ALPHA-HELIX MOTIF NEAR THE TITIN N-TERMINUS 1-gen-1995 Musco, G; Tziatzios, C; Schuck, P; Pastore, Annalisa
Mostrati risultati da 30.713 a 30.732 di 123.294
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