Хайлтын үр дүнгүүд - Roberto Giorda

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  1. 1
    Mouse NKR-P1. A family of genes selectively coexpressed in adherent lymphokine-activated killer cells.

    Mouse NKR-P1. A family of genes selectively coexpressed in adherent lymphokine-activated killer cells. -н Roberto Giorda, Massimo Trucco

    Хэвлэсэн 1991
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    Artigo
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  2. 2
    Inverted duplications deletions: underdiagnosed rearrangements??

    Inverted duplications deletions: underdiagnosed rearrangements?? -н Orsetta Zuffardi, María Clara Bonaglia, Roberto Ciccone, Roberto Giorda

    Хэвлэсэн 2009
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    Revisão
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  3. 3
    Constitutive Expression and Role of the TNF Family Ligands in Apoptotic Killing of Tumor Cells by Human NK Cells

    Constitutive Expression and Role of the TNF Family Ligands in Apoptotic Killing of Tumor Cells by Human NK Cells -н Yoshiro Kashii, Roberto Giorda, Ronald B. Herberman, Theresa L. Whiteside, Nikola L. Vujanović

    Хэвлэсэн 1999
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    Artigo
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  4. 4
    Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome

    Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome -н María Clara Bonaglia, Roberto Giorda, Renato Borgatti, G. Felisari, Chiara Gagliardi, Angelo Selicorni, Orsetta Zuffardi

    Хэвлэсэн 2001
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    Artigo
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  5. 5
    XX males SRY negative: a confirmed cause of infertility

    XX males SRY negative: a confirmed cause of infertility -н Annalisa Vetro, Roberto Ciccone, Roberto Giorda, Maria Grazia Patricelli, Erika Della Mina, Antonella Forlino, Orsetta Zuffardi

    Хэвлэсэн 2011
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    Artigo
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  6. 6
    KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia

    KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia -н Sara Mascheretti, Valentina Riva, Roberto Giorda, Silvana Beri, Lara Francesca Emilia Lanzoni, Maria Rosaria Cellino, Cecilia Marino

    Хэвлэсэн 2014
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    Artigo
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  7. 7
    DCDC2 genetic variants and susceptibility to developmental dyslexia

    DCDC2 genetic variants and susceptibility to developmental dyslexia -н Cecilia Marino, Haiying Meng, Sara Mascheretti, Marianna Rusconi, Natalie Cope, Roberto Giorda, Massimo Molteni, Jeffrey R. Gruen

    Хэвлэсэн 2011
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    Artigo
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  8. 8
    Silencer elements as possible inhibitors of pseudoexon splicing

    Silencer elements as possible inhibitors of pseudoexon splicing -н Manuela Sironi, Giorgia Menozzi, Laura Riva, Rachele Cagliani, Giacomo P. Comi, Nereo Bresolin, Roberto Giorda, Uberto Pozzoli

    Хэвлэсэн 2004
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    Artigo
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  9. 9
    Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome

    Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome -н María Clara Bonaglia, Roberto Giorda, Elisa Mani, Giammarco Aceti, B-M Anderlid, Anna Baroncini, Tiziano Pramparo, Orsetta Zuffardi

    Хэвлэсэн 2005
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    Carta
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  10. 10
    Rat natural killer cell antigen, NKR-P1, related to C-type animal lectins is a carbohydrate-binding protein

    Rat natural killer cell antigen, NKR-P1, related to C-type animal lectins is a carbohydrate-binding protein -н Karel Bezouška, G. Vlahas, Ondřej Horváth, G. Jinochová, Anna Fišerová, Roberto Giorda, William H. Chambers, Ten Feizi, Milan Pospı́šil

    Хэвлэсэн 1994
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    Artigo
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  11. 11
    Analysis of the Structure and Expression of the Augmenter of Liver Regeneration (ALR) Gene

    Analysis of the Structure and Expression of the Augmenter of Liver Regeneration (ALR) Gene -н Roberto Giorda, Michio Hagiya, Tatsuya Seki, Manabu Shimonishi, Harumi Sakai, James Michaelson, A. Francavilla, Thomas E. Starzl, Massimo Trucco

    Хэвлэсэн 1996
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    Artigo
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  12. 12
    Association of short‐term memory with a variant within<i> DYX1C1 </i>in developmental dyslexia

    Association of short‐term memory with a variant within<i> DYX1C1 </i>in developmental dyslexia -н Cecilia Marino, Andrea Citterio, Roberto Giorda, Andrea Facoetti, Giorgia Menozzi, Laura Vanzin, Maria Luisa Lorusso, Maria Nobile, Massimo Molteni

    Хэвлэсэн 2006
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    Artigo
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  13. 13
    Pain-related stress during the Neonatal Intensive Care Unit stay and SLC6A4 methylation in very preterm infants

    Pain-related stress during the Neonatal Intensive Care Unit stay and SLC6A4 methylation in very preterm infants -н Livio Provenzi, Monica Fumagalli, Ida Sirgiovanni, Roberto Giorda, Uberto Pozzoli, Francesco Morandi, Silvana Beri, Giorgia Menozzi, Fabio Mosca, Renato Borgatti, Rosario Montirosso

    Хэвлэсэн 2015
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    Artigo
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  14. 14
    An assessment of gene‐by‐environment interactions in developmental dyslexia‐related phenotypes

    An assessment of gene‐by‐environment interactions in developmental dyslexia‐related phenotypes -н Sara Mascheretti, Alexandre Bureau, Marco Battaglia, D. Simone, Ermanno Quadrelli, Jordie Croteau, Maria Rosaria Cellino, Roberto Giorda, Silvana Beri, Michel Maziade, Cecilia Marino

    Хэвлэсэн 2012
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    Artigo
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  15. 15
    A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia

    A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia -н Cecilia Marino, Roberto Giorda, Maria Luisa Lorusso, Laura Vanzin, Nello Salandi, Maria Nobile, Alessandra Citterio, Silvana Beri, Valentina Crespi, Marco Battaglia, Massimo Molteni

    Хэвлэсэн 2005
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    Artigo
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  16. 16
    Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation

    Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation -н Renata Bocciardi, Roberto Giorda, Jens Buttgereit, Stefania Gimelli, Maria Teresa Divizia, Silvana Beri, Silvio Garofalo, Sara Tavella, Margherita Lerone, Orsetta Zuffardi, Michael Bäder, Roberto Ravazzolo, Giorgio Gimelli

    Хэвлэсэн 2007
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    Artigo
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  17. 17
    The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia

    The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia -н Cecilia Marino, Paola Scifo, Pasquale Anthony Della Rosa, Sara Mascheretti, Andrea Facoetti, Maria Luisa Lorusso, Roberto Giorda, Monica Consonni, Andrea Falini, Massimo Molteni, Jeffrey R. Gruen, Daniela Perani

    Хэвлэсэн 2014
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    Artigo
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  18. 18
    Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements

    Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements -н Sabrina Giglio, Karl W. Broman, Naomichi Matsumoto, Vladimiro Calvari, Giorgio Gimelli, Thomas Neumann, Hirofumi Ohashi, Lucille Voullaire, Daniela Larizza, Roberto Giorda, Jim L. Weber, David H. Ledbetter, Orsetta Zuffardi

    Хэвлэсэн 2001
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    Artigo
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  19. 19
    From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth

    From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth -н Monica Fumagalli, Livio Provenzi, Pietro De Carli, Francesca Dessimone, Ida Sirgiovanni, Roberto Giorda, Claudia Cinnante, Letizia Squarcina, Uberto Pozzoli, Fabio Triulzi, Paolo Brambilla, Renato Borgatti, Fabio Mosca, Rosario Montirosso

    Хэвлэсэн 2018
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    Artigo
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  20. 20
    A novel<i>CLN8</i>mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function

    A novel<i>CLN8</i>mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function -н Chiara Vantaggiato, Francesca Redaelli, Sestina Falcone, Cristiana Perrotta, Alessandra Tonelli, Sara Bondioni, Michela Morbin, Daria Riva, Veronica Saletti, María Clara Bonaglia, Roberto Giorda, Nereo Bresolin, Emilio Clementi, Maria Teresa Bassi

    Хэвлэсэн 2009
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    Artigo
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