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Results: 1-9 |
Results: 9
GENETIC AND MOLECULAR DEFINITION OF COMPLEMENTATION GROUP-D IN MHC CLASS-II DEFICIENCY
Authors: FONDANECHE MC VILLARD J WISZNIEWSKI W JOUANGUY E ETZIONI A LEDEIST F PEIJNENBURG A CASANOVA JL REITH W MACH B FISCHER A LISOWSKAGROSPIERRE B
Citation: Mc. Fondaneche et al., GENETIC AND MOLECULAR DEFINITION OF COMPLEMENTATION GROUP-D IN MHC CLASS-II DEFICIENCY, Human molecular genetics, 7(5), 1998, pp. 879-885
A CAUSATIVE RELATIONSHIP BETWEEN MUTANT IFNGR1 ALLELES AND IMPAIRED CELLULAR-RESPONSE TO IFN-GAMMA IN A COMPOUND HETEROZYGOUS CHILD
Authors: ALTARE F JOUANGUY E LAMHAMEDICHERRADI S FONDANECHE MC FIZAME C RIBIERRE F MERLIN G DEMBIC Z SCHREIBER R LISOWSKAGROSPIERRE B FISCHER A SEBOUN E CASANOVA JL
Citation: F. Altare et al., A CAUSATIVE RELATIONSHIP BETWEEN MUTANT IFNGR1 ALLELES AND IMPAIRED CELLULAR-RESPONSE TO IFN-GAMMA IN A COMPOUND HETEROZYGOUS CHILD, American journal of human genetics, 62(3), 1998, pp. 723-726
CLASS-II DEFICIENCY (BARE LYMPHOCYTE SYNDROME) - CHARACTERIZING A NEWCOMPLEMENTATION GROUP
Authors: ETZIONI A FONDANECHE M POLLACK S FISCHER A LISOWSKAGROSPIERRE B
Citation: A. Etzioni et al., CLASS-II DEFICIENCY (BARE LYMPHOCYTE SYNDROME) - CHARACTERIZING A NEWCOMPLEMENTATION GROUP, Journal of allergy and clinical immunology, 99(1), 1997, pp. 310-310
MUTATION OF RFXAP, A REGULATOR OF MHC CLASS-II GENES, IN PRIMARY MHC CLASS-II DEFICIENCY
Authors: VILLARD J LISOWSKAGROSPIERRE B VANDENELSEN P FISCHER A REITH W MACH B
Citation: J. Villard et al., MUTATION OF RFXAP, A REGULATOR OF MHC CLASS-II GENES, IN PRIMARY MHC CLASS-II DEFICIENCY, The New England journal of medicine, 337(11), 1997, pp. 748-753
UNDETECTABLE CD40 LIGAND EXPRESSION ON T-CELLS AND LOW B-CELL RESPONSES TO CD40 BINDING AGONISTS IN HUMAN NEWBORNS
Authors: DURANDY A DESAINTBASILE G LISOWSKAGROSPIERRE B GAUCHAT JF FORVEILLE M KROCZEK RA BONNEFOY JY FISCHER A
Citation: A. Durandy et al., UNDETECTABLE CD40 LIGAND EXPRESSION ON T-CELLS AND LOW B-CELL RESPONSES TO CD40 BINDING AGONISTS IN HUMAN NEWBORNS, The Journal of immunology, 154(4), 1995, pp. 1560-1568
BONE-MARROW TRANSPLANTATION IN MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II DEFICIENCY - A SINGLE-CENTER STUDY OF 19 PATIENTS
Authors: KLEIN C CAVAZZANACALVO M LEDEIST F JABADO N BENKERROU M BLANCHE S LISOWSKAGROSPIERRE B GRISCELLI C FISCHER A
Citation: C. Klein et al., BONE-MARROW TRANSPLANTATION IN MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II DEFICIENCY - A SINGLE-CENTER STUDY OF 19 PATIENTS, Blood, 85(2), 1995, pp. 580-587
2 COMPLEMENTATION GROUPS ACCOUNT FOR MOST CASES OF INHERITED MHC CLASS-II DEFICIENCY
Authors: LISOWSKAGROSPIERRE B FONDANECHE MC ROLS MP GRISCELLI C FISCHER A
Citation: B. Lisowskagrospierre et al., 2 COMPLEMENTATION GROUPS ACCOUNT FOR MOST CASES OF INHERITED MHC CLASS-II DEFICIENCY, Human molecular genetics, 3(6), 1994, pp. 953-958
REGULATION OF MHC CLASS-II EXPRESSION BY INTERFERON-GAMMA MEDIATED BYTHE TRANSACTIVATOR GENE CIITA
Authors: STEIMLE V SIEGRIST CA MOTTET A LISOWSKAGROSPIERRE B MACH B
Citation: V. Steimle et al., REGULATION OF MHC CLASS-II EXPRESSION BY INTERFERON-GAMMA MEDIATED BYTHE TRANSACTIVATOR GENE CIITA, Science, 265(5168), 1994, pp. 106-109
MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II DEFICIENCY - CLINICAL MANIFESTATIONS, IMMUNOLOGICAL FEATURES, AND OUTCOME
Authors: KLEIN C LISOWSKAGROSPIERRE B LEDEIST F FISCHER A GRISCELLI C
Citation: C. Klein et al., MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II DEFICIENCY - CLINICAL MANIFESTATIONS, IMMUNOLOGICAL FEATURES, AND OUTCOME, The Journal of pediatrics, 123(6), 1993, pp. 921-928
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