CD40-CD40L independent Ig gene hypermutation suggests a second B cell diversification pathway in humans

Proceedings of the National Academy of Sciences of the United States of America

Volumn 98, Issue 3, 2001, Pages 1166-1170

  Weller, Sandra ^a   Faili, Ahmad ^a   Garcia, Corinne ^a   Braun, Moritz C ^a   Le Deist, Françoise ^b   De Saint Basile, Geneviève ^b   Hermine, Olivier ^b   Fischer, Alain ^b   Reynaud, Claude Agnès ^a   Weill, Jean Claude ^a  

^a INSERM   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

CD27; Somatic hypermutation; X linked hyper IgM syndrome

Indexed keywords

CD27 ANTIGEN; CD40 ANTIGEN; GLYCOPROTEIN GP 39; IMMUNOGLOBULIN D; IMMUNOGLOBULIN M;

ANTIGEN EXPRESSION; ARTICLE; B LYMPHOCYTE; CONTROLLED STUDY; GENE MUTATION; HUMAN; HUMAN CELL; HYPERIMMUNOGLOBULINEMIA; IMMUNOGLOBULIN GENE; IMMUNOGLOBULIN STRUCTURE; PHENOTYPE; PRIORITY JOURNAL; SOMATIC MUTATION;

ADOLESCENT; ADULT; ALTERNATIVE SPLICING; ANTIGENS, CD40; B-LYMPHOCYTE SUBSETS; B-LYMPHOCYTES; CD40 LIGAND; CHILD; CHILD, PRESCHOOL; CODON, TERMINATOR; FETAL BLOOD; GENE REARRANGEMENT; GENES, IMMUNOGLOBULIN; HUMANS; IMMUNOGLOBULIN A; IMMUNOGLOBULIN D; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFANT, NEWBORN; MUTATION; REFERENCE VALUES; SEQUENCE DELETION;

EID: 0035970105     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.98.3.1166     Document Type: Article

References (37)