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La ricerca find articoli where authors phrase all words ' Basile, GD' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 12 riferimenti
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    1. Stepp, S; Mathew, P; Bennett, M; Basile, GD; Kumar, V
      On the pathogenesis of perforin defects and related immunodeficiencies - Response to Moretta et al. and Arnaout

      IMMUNOLOGY TODAY
    2. Fischer, A; Hacein-Bey, S; Le Deist, F; Soudais, C; Di Santo, JP; Basile, GD; Cavazzana-Calvo, M
      Gene therapy of severe combined immunodeficiencies

      IMMUNOLOGICAL REVIEWS
    3. Dufourcq-Lagelouse, R; Pastural, E; Barrat, FJ; Feldmann, J; le Deist, F; Fischer, A; Basile, GD
      Genetic basis of hemophagocytic lymphohistiocytosis syndrome (Review)

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    4. Stepp, SE; Dufourcq-Lagelouse, R; Le Deist, F; Bhawan, S; Certain, S; Mathew, PA; Henter, JI; Bennett, M; Fischer, A; Saint Basile, GD; Kumar, V
      Perforin gene defects in familiar hemophagocytic lymphohistiocytosis

      SCIENCE
    5. Dufourcq-Lagelouse, R; Jabado, N; Le Deist, F; Stephan, JL; Souillet, G; Bruin, M; Vilmer, E; Schneider, M; Janka, G; Fischer, A; Basile, GD
      Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneity

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. HACEINBEY S; BASILE GD; LEMERLE J; FISCHER A; CAVAZZANACALVO M
      GAMMA-C GENE-TRANSFER IN THE PRESENCE OF STEM-CELL FACTOR, FLT-3L, INTERLEUKIN-7 (IL-7), IL-1-ALPHA, AND IL-15 CYTOKINES RESTORES T-CELL DIFFERENTIATION FROM GAMMA-C(-) X-LINKED SEVERE COMBINED IMMUNODEFICIENCY HEMATOPOIETIC PROGENITOR CELLS IN MURINE FETAL THYMIC ORGAN-CULTURES

      Blood
    7. Fischer, A; Basile, GD; Disanto, JP; Cavazzana-Calvo, M
      Gene therapy of primary immunodeficiencies

      BIOTHERAPY OF CANCERS
    8. STEPHAN V; WAHN V; LEDEIST F; DIRKSEN U; BROKER B; MULLERFLECKENSTEIN I; HORNEFF G; SCHROTEN H; FISCHER A; BASILE GD
      ATYPICAL X-LINKED SEVERE COMBINED IMMUNODEFICIENCY DUE TO POSSIBLE SPONTANEOUS REVERSION OF THE GENETIC-DEFECT IN T-CELLS

      The New England journal of medicine
    9. BASILE GD; LAGELOUSE RD; LAMBERT N; SCHWARZ K; LEMARECK B; ODENT S; SCHLEGEL N; FISCHER A
      ISOLATED X-LINKED THROMBOCYTOPENIA IN 2 UNRELATED FAMILIES IS ASSOCIATED WITH POINT MUTATIONS IN THE WISKOTT-ALDRICH SYNDROME PROTEIN GENE

      The Journal of pediatrics
    10. CAVAZZANACALVO M; HACEINBEY S; BASILE GD; DECOENE C; SELZ F; LEDEIST F; FISCHER A
      ROLE OF INTERLEUKIN-2 (IL-2), IL-7, AND IL-15 IN NATURAL-KILLER-CELL DIFFERENTIATION FROM CORD-BLOOD HEMATOPOIETIC PROGENITOR CELLS AND FROM GAMMA-C TRANSDUCED SEVERE COMBINED IMMUNODEFICIENCY-XI BONE-MARROW CELLS

      Blood
    11. HACEINBEY S; CAVAZZANACALVO M; LEDEIST F; DAUTRYVARSAT A; HIVROZ C; RIVIERE J; DANOS O; HEARD JM; SUGAMURA K; FISCHER A; BASILE GD
      GAMMA-C GENE-TRANSFER INTO SCID X1 PATIENTS B-CELL LINES RESTORES NORMAL HIGH-AFFINITY INTERLEUKIN-2 RECEPTOR EXPRESSION AND FUNCTION

      Blood
    12. CAVAZZANACALVO M; BASILE GD; LEDEIST F; DISANTO J; CERTAIN S; DECOENE C; DANOS O; HEARD JM; FISCHER A
      RETROVIRAL IL-2 RECEPTOR-GAMMA-CHAIN GENE-TRANSFER INTO NORMAL AND SCIDX1 HUMAN BONE-MARROW CELLS

      Blood


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/08/20 alle ore 02:24:29