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Sfoglia per Autore  LINTAS, CARLA

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Mostrati risultati da 1 a 20 di 55
Titolo Data di pubblicazione Autore(i) File
Genetic variation of the european eel (Anguilla anguilla) 1-gen-1998 Lintas, C; Hirano, J; Archer, S
Mutations that affect the ability of the vnd/NK-2 homeoprotein to regulate gene expression: transgenic alterations and tertiary structure 1-gen-2003 Koizumi, Keita; Lintas, Carla; Nirenberg, Marshall; Maeng, Jin-Soo; Ju, Jeong-Ho; Mack, James W; Gruschus, James M; Odenwald, Ward F; Ferretti, James A
Do mutations of RAG genes have a role in human autoimmunity? The Notarangelo's hypothesis revisited 1-gen-2006 Fierabracci, Alessandra; Lintas, Carla; Altieri, Laura; Saura, Francesca; Crino', Antonio; Ugazio, Alberto G; Bottazzo, Gian Franco
Methylation profile in tumor and sputum samples of lung cancer patients detected by spiral computed tomography: a nested case-control study 1-gen-2006 Cirincione, Rosalia; Lintas, Carla; Conte, Davide; Mariani, Luigi; Roz, Luca; Vignola, Antonio Maurizio; Pastorino, Ugo; Sozzi, Gabriella
Immune transcriptome alterations in the temporal cortex of subjects with autism 1-gen-2008 Garbett, Krassimira; Ebert, Philip J; Mitchell, Amanda; Lintas, Carla; Manzi, Barbara; Mirnics, Károly; Persico, Antonio M
An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (AIRE) 1-gen-2008 Lintas, Carla; Cappa, Marco; Comparcola, Donatella; Nobili, Valerio; Fierabracci, Alessandra
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism 1-gen-2009 Gregory, Simon G; Connelly, Jessica J; Towers, Aaron J; Johnson, Jessica; Biscocho, Dhani; Markunas, Christina A; Lintas, Carla; Abramson, Ruth K; Wright, Harry H; Ellis, Peter; Langford, Cordelia F; Worley, Gordon; Delong, G Robert; Murphy, Susan K; Cuccaro, Michael L; Persico, Antonello; Pericak-Vance, Margaret A
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression 1-gen-2009 Lintas, C; Sacco, R; Garbett, K; Mirnics, K; Militerni, R; Bravaccio, C; Curatolo, P; Manzi, B; Schneider, C; Melmed, R; Elia, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, K-L; Persico, A M
Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist 1-gen-2009 Lintas, C; Persico, A M
Neocortical RELN promoter methylation increases significantly after puberty 1-gen-2010 Lintas, Carla; Persico, Antonio M
Association of autism with polyomavirus infection in postmortem brains 1-gen-2010 Lintas, Carla; Altieri, Laura; Lombardi, Federica; Sacco, Roberto; Persico, Antonio M
Decreased serum arylesterase activity in autism spectrum disorders 1-gen-2010 Gaita, Laura; Manzi, Barbara; Sacco, Roberto; Lintas, Carla; Altieri, Laura; Lombardi, Federica; Pawlowski, Tracy L; Redman, Margot; Craig, David W; Huentelman, Matthew J; Ober-Reynolds, Sharman; Brautigam, Sarah; Melmed, Raun; Smith, Christopher J; Marsillach, Judith; Camps, Jordi; Curatolo, Paolo; Persico, Antonio M
Lack of infection with XMRV or other MLV-related viruses in blood, post-mortem brains and paternal gametes of autistic individuals 1-gen-2011 Lintas, Carla; Guidi, Francesco; Manzi, Barbara; Mancini, Antonio; Curatolo, Paolo; Persico, Antonio M
Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome 1-gen-2012 Lintas, Carla; Sacco, Roberto; Persico, Antonio M
Autism genetics: Methodological issues and experimental design 1-gen-2015 Sacco, Roberto; Lintas, Carla; Persico, Antonio M
Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders 1-gen-2016 Picinelli, Chiara; Lintas, Carla; Piras, Ignazio Stefano; Gabriele, Stefano; Sacco, Roberto; Brogna, Claudia; Persico, Antonio Maria
Differential methylation at the RELN gene promoter in temporal cortex from autistic and typically developing post-puberal subjects 1-gen-2016 Lintas, Carla; Sacco, Roberto; Persico, Antonio M
Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features 1-gen-2016 Lintas, Carla; Picinelli, Chiara; Piras, Ignazio S; Sacco, Roberto; Gabriele, Stefano; Verdecchia, Magda; Persico, Antonio M
Copy number variation in 19 Italian multiplex families with autism spectrum disorder: Importance of synaptic and neurite elongation genes 1-gen-2017 Lintas, Carla; Picinelli, Chiara; Piras, Ignazio Stefano; Sacco, Roberto; Brogna, Claudia; Persico, Antonio M
Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes 1-gen-2018 Lintas, C; Persico, A M
Mostrati risultati da 1 a 20 di 55
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