Detalhe da pesquisa
1.
An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complex.
J Allergy Clin Immunol
; 135(4): 998-1007.e6, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25312759
2.
Human MSH6 deficiency is associated with impaired antibody maturation.
J Immunol
; 188(4): 2023-9, 2012 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22250089
3.
Restoration of human B-cell differentiation into NOD-SCID mice engrafted with gene-corrected CD34+ cells isolated from Artemis or RAG1-deficient patients.
Mol Ther
; 16(2): 396-403, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18223550
4.
Hyper-IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination.
J Clin Invest
; 112(1): 136-42, 2003 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12840068
5.
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey.
Medicine (Baltimore)
; 91(4): e1-e19, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22751495
6.
Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.
Nat Immunol
; 4(10): 1023-8, 2003 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12958596