CHARACTERIZATION OF THE MOLECULAR BASES OF PRIMARY IMMUNODEFICIENCIES DUE TO DEFECTS IN TERMINAL B-CELL DIFFERENTIATION
- 3 Anni 1998/2001
 - 108.456€ Totale Fondi
 
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Pubblicazioni Scientifiche
- 2001-01-01 ADVANCES IN GENETICS, VOL 43 
Primary immunodeficiency mutation databases
 - 2000-03-05 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 
Structural basis for SH2D1A mutations in X-linked lymphoproliferative disease
 - 1999-11-15 BLOOD 
Intrathymic restriction and peripheral expansion of the T-cell repertoire in Omenn syndrome
 - 2001-01-01 BLOOD 
V(D)J recombination defects in lymphocytes due to RAG mutations:: severe immunodeficiency with a spectrum of clinical presentations
 - 2000-09-01 CELL 
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper-IgM syndrome (HIGM2)
 - 1998-05-29 CELL 
Partial V(D)J recombination activity leads to Omenn syndrome
 - 2000-06-01 CLINICAL AND EXPERIMENTAL IMMUNOLOGY 
X-linked immunodeficiency with hyper-IgM (XHIM)
 - 2001-01-01 CURRENT OPINION IN HEMATOLOGY 
Recombinase activating gene enzymes of lymphocytes
 - 1999-08-01 CURRENT OPINION IN IMMUNOLOGY 
RAG and RAG defects
 - 2000-01-01 HUMAN GENETICS 
Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism
 - 2000-12-01 IMMUNOLOGICAL REVIEWS 
Of genes and phenotypes:: the immunological and molecular spectrum of combined immune deficiency.: Defects of the γc-JAK3 signaling pathway as a model
 - 1999-03-01 JOURNAL OF CLINICAL IMMUNOLOGY 
Omenn syndrome: A disorder of Rag1 and Rag2 genes
 - 2000-08-07 JOURNAL OF EXPERIMENTAL MEDICINE 
X-linked lymphoproliferative disease: 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cells
 - 2000-02-01 MOLECULAR AND CELLULAR BIOLOGY 
Complex effects of naturally occurring mutations in the JAK3 pseudokinase domain: Evidence for interactions between the kinase and pseudokinase domains
 - 1999-07-01 PRENATAL DIAGNOSIS 
Prenatal diagnosis of JAK3 deficient SCID
 - 2000-01-01 PRENATAL DIAGNOSIS 
Prenatal diagnosis of RAG-deficient Omenn syndrome