Resultats de la cerca - Nicola Migone

  • Mostrar 1 - 16 resultats de 16
Refinar resultats
  1. 1
    Molecular analysis of human gamma/delta+ clones from thymus and peripheral blood.

    Molecular analysis of human gamma/delta+ clones from thymus and peripheral blood. per Giulia Casorati, Gennaro De Libero, Antonio Lanzavecchia, Nicola Migone

    Publicat 1989
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  2. 2
    Heteroduplex analysis of T-cell receptor gamma gene rearrangements for diagnosis and monitoring of cutaneous T-cell lymphomas

    Heteroduplex analysis of T-cell receptor gamma gene rearrangements for diagnosis and monitoring of cutaneous T-cell lymphomas per Martim Bottaro, Emilio Berti, Andrea Biondi, Nicola Migone, Lucia Crosti

    Publicat 1994
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  3. 3
    Selection by two powerful antigens may account for the presence of the major population of human peripheral gamma/delta T cells.

    Selection by two powerful antigens may account for the presence of the major population of human peripheral gamma/delta T cells. per Gennaro De Libero, Giulia Casorati, Claudia Giachino, Caterina Carbonara, Nicola Migone, Polly Matzinger, Antonio Lanzavecchia

    Publicat 1991
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  4. 4
    Antigen recognition by human T cell receptor gamma-positive lymphocytes. Specific lysis of allogeneic cells after activation in mixed lymphocyte culture.

    Antigen recognition by human T cell receptor gamma-positive lymphocytes. Specific lysis of allogeneic cells after activation in mixed lymphocyte culture. per Ermanno Ciccone, O Viale, Cristina Bottino, Daniela Pende, Nicola Migone, Giulia Casorati, Giuseppe Tambussi, Alessandro Moretta, Lorenzo Moretta

    Publicat 1988
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  5. 5
    An Enhanced Polymerase Chain Reaction Assay to Detect Pre- and Full Mutation Alleles of the Fragile X Mental Retardation 1 Gene

    An Enhanced Polymerase Chain Reaction Assay to Detect Pre- and Full Mutation Alleles of the Fragile X Mental Retardation 1 Gene per Alessandro Saluto, Alessandro Brussino, Flora Tassone, Carlo Arduino, Claudia Cagnoli, Patrizia Pappi, Paul J. Hagerman, Nicola Migone, Alfredo Brusco

    Publicat 2005
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  6. 6
    The SH3 Domains of Endophilin and Amphiphysin Bind to the Proline-rich Region of Synaptojanin 1 at Distinct Sites That Display an Unconventional Binding Specificity

    The SH3 Domains of Endophilin and Amphiphysin Bind to the Proline-rich Region of Synaptojanin 1 at Distinct Sites That Display an Unconventional Binding Specificity per Gianluca Cestra, Luisa Castagnoli, Luciana Dente, Olga Minenkova, Annalisa Petrelli, Nicola Migone, Ulrich Hoffmüller, Jens Schneider‐Mergener, Gianni Cesareni

    Publicat 1999
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  7. 7
    Mechanisms accounting for lymphocytic alveolitis in hypersensitivity pneumonitis.

    Mechanisms accounting for lymphocytic alveolitis in hypersensitivity pneumonitis. per Livio Trentin, Nicola Migone, Renato Zambello, Paola Francia di Celle, F. Aina, Cristina Feruglio, Pietro Bulian, M Masciarelli, Carlo Agostini, A Cipriani

    Publicat 1990
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  8. 8
    Different stages of B cell differentiation in non-T acute lymphoblastic leukemia.

    Different stages of B cell differentiation in non-T acute lymphoblastic leukemia. per Robin Foà, Nicola Migone, M Saitta, Maria Teresa Fierro, M. C. Giubellino, Paolo Lusso, Luca Cordero di Montezemolo, R. Miniero, F. Lauria

    Publicat 1984
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  9. 9
    Polycystin-1 expression in PKD1, early-onset PKD1, and TSC2/PKD1 cystic tissue

    Polycystin-1 expression in PKD1, early-onset PKD1, and TSC2/PKD1 cystic tissue per Albert Ong, Peter C. Harris, David R. Davies, L Pritchard, Sandro Rossetti, Simon Biddolph, David J. Vaux, Nicola Migone, Christopher J. Ward

    Publicat 1999
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  10. 10
    Multiple gene deletions within the human immunoglobulin heavy-chain cluster.

    Multiple gene deletions within the human immunoglobulin heavy-chain cluster. per Nicola Migone, Salvatore Oliviero, G. de Lange, Dominique L. Delacroix, D Boschis, Fiorella Altruda, Lorenzo Silengo, M. DeMarchi, A. O. Carbonara

    Publicat 1984
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  11. 11
    Rearrangements of immunoglobulin and T cell receptor beta and gamma genes are associated with terminal deoxynucleotidyl transferase expression in acute myeloid leukemia.

    Rearrangements of immunoglobulin and T cell receptor beta and gamma genes are associated with terminal deoxynucleotidyl transferase expression in acute myeloid leukemia. per Robin Foà, Giulia Casorati, M. C. Giubellino, Giuseppe Basso, R Schirò, Giovanni Pizzolo, F. Lauria, Marie‐Paule Lefranc, Terence H. Rabbitts, Nicola Migone

    Publicat 1987
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  12. 12
    Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man.

    Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man. per Nicola Migone, John N. Feder, Howard M. Cann, B. Van West, Jason Y. Hwang, Naoki Takahashi, Tasuku Honjo, Alberto Piazza, Luigi Luca Cavalli-Sforza

    Publicat 1983
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  13. 13
    SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22–q11.2

    SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22–q11.2 per Claudia Cagnoli, Caterina Mariotti, Franco Taroni, Marco Seri, Alessandro Brussino, Chiara Michielotto, Marina Grisoli, Daniela Di Bella, Nicola Migone, Cinzia Gellera, Stefano Di Donato, Alfredo Brusco

    Publicat 2005
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  14. 14
    Comparison of the functional and structural characteristics of rare <i>TSC2</i> variants with clinical and genetic findings

    Comparison of the functional and structural characteristics of rare <i>TSC2</i> variants with clinical and genetic findings per Luiz Gustavo Dufner‐Almeida, Santoesha Nanhoe, Andrea Zonta, Mitra Hosseinzadeh, Regina Kom‐Gortat, Peter Elfferich, Gerben Schaaf, Annegien Kenter, Daniel Kümmel, Nicola Migone, Sue Povey, Rosemary Ekong, Mark Nellist

    Publicat 2019
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  15. 15
    Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment

    Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment per Katrien Janssens, Filip Vanhoenacker, M Bonduelle, Leon Verbruggen, Lionel Van Maldergem, Stuart H. Ralston, Núria Guañabens, Nicola Migone, Shlomo Wientroub, Maria Teresa Divizia, Carsten Bergmann, Craig R. Bennett, Suat Şimşek, S. Melançon, Tim Cundy, Wim Van Hul

    Publicat 2005
    Obtenir text complet Obtenir text complet
    Revisão
    Afegir a favorits
    Guardat en:
  16. 16
    Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias

    Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias per Claudia Cagnoli, Giovanni Stévanin, Alessandro Brussino, Marco Barberis, Cecilia Mancini, Russell L. Margolis, Susan E. Holmes, Marcello Nobili, Sylvie Forlani, Sergio Padovan, Patrizia Pappi, Cécile Zaros, Isabelle Leber, Pascale Ribaı̈, Luisa Pugliese, Corrado Assalto, Alexis Brice, Nicola Migone, Alexandra Dürr, Alfredo Brusco

    Publicat 2010
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:

Eines de cerca: