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La ricerca find articoli where soggetti phrase all words 'CLASS-II DEFICIENCY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 36 riferimenti
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    1. Fischer, A
      Primary T-lymphocyte immunodeficiencies

      CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
    2. Reith, W; Mach, B
      The bare lymphocyte syndrome and the regulation of MHC expression

      ANNUAL REVIEW OF IMMUNOLOGY
    3. Fischer, A
      Primary immunodeficiency diseases: an experimental model for molecular medicine

      LANCET
    4. Kern, A; Liu, K; Mansbridge, J
      Modification of fibroblast gamma-interferon responses by extracellular matrix

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    5. Gennery, AR; Cant, AJ
      Diagnosis of severe combined immunodeficiency

      JOURNAL OF CLINICAL PATHOLOGY
    6. Wolf, HM; Thon, V; Gulle, H; Lechleitner, S; Eibl, MM; Petzelbauer, P
      Residual expression of functional MHC class II molecules in twin brothers with MHC class II deficiency is cell type specific

      BRITISH JOURNAL OF HAEMATOLOGY
    7. Gaspar, HB; Gilmour, KC; Jones, AM
      Severe combined immunodeficiency - molecular pathogenesis and diagnosis

      ARCHIVES OF DISEASE IN CHILDHOOD
    8. Fischer, A
      Gene therapy of lymphoid primary immunodeficiencies

      CURRENT OPINION IN PEDIATRICS
    9. Durand, B; Vandaele, C; Spencer, D; Pantalacci, S; Couble, P
      Cloning and characterization of dRFX, the Drosophila member of the RFX family of transcription factors

      GENE
    10. Nekrep, N; Jabrane-Ferrat, N; Peterlin, BM
      Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex

      MOLECULAR AND CELLULAR BIOLOGY
    11. Godthelp, BC; Van Eggermond, MCJA; Van Tol, MJD; Vossen, JM; van den Elsen, PJ
      T cell immune reconstitution after allogeneic bone marrow transplantation in bare lymphocyte syndrome

      HUMAN IMMUNOLOGY
    12. 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
    13. Wiszniewski, W; Fondaneche, MC; Lambert, N; Masternak, K; Picard, C; Notarangelo, L; Schwartz, K; Bal, J; Reith, W; Alcaide, C; de saint Basile, G; Fischer, A; Lisowska-Grospierre, B
      Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B

      IMMUNOGENETICS
    14. Peijnenburg, A; Van den Berg, R; Van Eggermond, MJCA; Sanal, O; Vossen, JMJJ; Lennon, AM; Alcaide-Loridan, C; Van den Elsen, PJ
      Defective MHC class II expression in an MHC class II deficiency patient iscaused by a novel deletion of a splice donor site in the MHC class II transactivator gene

      IMMUNOGENETICS
    15. Buckley, RH
      Primary immunodeficiency diseases due to defects in lymphocytes.

      NEW ENGLAND JOURNAL OF MEDICINE
    16. Tierney, R; Kirby, H; Nagra, J; Rickinson, A; Bell, A
      The Epstein-Barr virus promoter initiating B-cell transformation is activated by RFX proteins and the B-cell-specific activator protein BSAP/Pax5

      JOURNAL OF VIROLOGY
    17. Atkinson, JC; O'Connell, A; Aframian, D
      Oral manisfestations of primary immunological diseases

      JOURNAL OF THE AMERICAN DENTAL ASSOCIATION
    18. Fischer, A; Hacein-Bey, S; Le Deist, F; de Saint Basile, G; de Villartay, JP; Cavazzana-Calvo, M
      Gene therapy of immunodeficiency disorders

      BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
    19. Conley, ME
      Genetic effects on immunity - New genes - how do they fit? Editorial overview

      CURRENT OPINION IN IMMUNOLOGY
    20. Cohen, SY; Roifman, CM
      Signal transduction - Lessons learned from rare pediatric immunodeficiencies

      IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA
    21. Peijnenburg, A; Van Eggermond, MCJA; Van den Berg, R; Sanal, O; Vossen, JMJJ; Van den Elsen, PJ
      Molecular analysis of an MHC class II deficiency patient reveals a novel mutation in the RFX5 gene

      IMMUNOGENETICS
    22. CANDOTTI F; BLAESE RM
      GENE-THERAPY OF PRIMARY IMMUNODEFICIENCIES

      Perspectives in mathematical logic
    23. BOULOC A; CAVANI A; KATZ SI
      CONTACT HYPERSENSITIVITY IN MHC CLASS II-DEFICIENT MICE DEPENDS ON CD8 T-LYMPHOCYTES PRIMED BY IMMUNOSTIMULATING LANGERHANS CELLS

      Journal of investigative dermatology
    24. CANIONI D; PATEY N; CUENOD B; BENKERROU M; BROUSSE N
      MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II DEFICIENCY NEEDS AN EARLY DIAGNOSIS - REPORT OF A CASE

      PEDIATRIC PATHOLOGY & LABORATORY MEDICINE
    25. VILLARD J; REITH W; BARRAS E; GOS A; MORRIS MA; ANTONARAKIS SE; VANDENELSEN PJ; MACH B
      ANALYSIS OF MUTATIONS AND CHROMOSOMAL LOCALIZATION OF THE GENE ENCODING RFX5, A NOVEL TRANSCRIPTION FACTOR AFFECTED IN MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II DEFICIENCY

      Human mutation
    26. DOOIJES D; CLEVERS H
      CONTROL OF GEM EXPRESSION DURING LYMPHOID DEVELOPMENT - TARGETED GENEDISRUPTION PROVIDES NEW CLUES

      APMIS. Acta pathologica, microbiologica et immunologica Scandinavica
    27. DURAND B; SPERISEN P; EMERY P; BARRAS E; ZUFFEREY M; MACH B; REITH W
      RFXAP, A NOVEL SUBUNIT OF THE RFX DNA-BINDING COMPLEX IS MUTATED IN MHC CLASS-II DEFICIENCY

      EMBO journal
    28. PUCK JM
      PRIMARY IMMUNODEFICIENCY DISEASES

      JAMA, the journal of the American Medical Association
    29. SCHWARTZ RS
      THE CASE OF THE BARE LYMPHOCYTE SYNDROME - TRACKING DOWN FAULTY TRANSCRIPTION FACTORS

      The New England journal of medicine
    30. FISCHER A
      GENETIC-DISORDERS OF THE HUMAN SYSTEM IN HUMANS

      Bulletin de l'Academie nationale de medecine
    31. PUEL A; MOUTON D
      GENES RESPONSIBLE FOR QUANTITATIVE REGULATION OF ANTIBODY-PRODUCTION

      Critical reviews in immunology
    32. CANDOTTI F; BLAESE RM
      THE USE OF GENE-THERAPY FOR IMMUNODEFICIENCY DISEASE

      Immunology and allergy clinics of North America
    33. MACH B; STEIMLE V; MARTINEZSORIA E; REITH W
      REGULATION OF MHC CLASS-II GENES - LESSONS FROM A DISEASE

      Annual review of immunology
    34. SCHWARZ K; GAUSS GH; LUDWIG L; PANNICKE U; LI Z; LINDNER D; FRIEDRICH W; SEGER RA; HANSENHAGGE TE; DESIDERIO S; LIEBER MR; BARTRAM CR
      RAG MUTATIONS IN HUMAN B-CELL-NEGATIVE SCID

      Science
    35. STEIMLE V; DURAND B; BARRAS E; ZUFFEREY M; HADAM MR; MACH B; REITH W
      A NOVEL DNA-BINDING REGULATORY FACTOR IS MUTATED IN PRIMARY MHC CLASS-II DEFICIENCY (BARE LYMPHOCYTE SYNDROME)

      Genes & development
    36. MANNHALTER JW; WOLF HM; HAUBER I; MIRICKA M; GADNER H; EIBL MM
      T-CELL DIFFERENTIATION AND GENERATION OF THE ANTIGEN-SPECIFIC T-CELL REPERTOIRE IN MAN - OBSERVATIONS IN MHC CLASS-II DEFICIENCY

      Clinical and experimental immunology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 10/08/20 alle ore 02:12:02