Molecular mechanisms in genetically defined autoinflammatory diseases: disorders of amplified danger signaling.
de Jesus, Adriana Almeida; Canna, Scott W; Liu, Yin; Goldbach-Mansky, Raphaela.
Annu Rev Immunol
; 33: 823-74, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25706096
SLAM family receptors and SAP adaptors in immunity.
Function of a Foxp3 cis-element in protecting regulatory T cell identity.
X-linked inhibitor of apoptosis protein deficiency: more than an X-linked lymphoproliferative syndrome.
Analytická interference muze vést k diagnostice lymfoproliferativního onemocnení.
Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation.
The nuclear matrix protein CIZ1 facilitates localization of Xist RNA to the inactive X-chromosome territory.
Nucleotide-binding oligomerization domain (NOD) signaling defects and cell death susceptibility cannot be uncoupled in X-linked inhibitor of apoptosis (XIAP)-driven inflammatory disease.
Risk factors and clinical outcomes of Epstein-Barr virus DNAemia and post-transplant lymphoproliferative disorders after haploidentical and matched-sibling PBSCT in patients with hematologic malignancies.
Progressive reduction of circulating B lymphocytes in patients with X-linked lymphoproliferative disease (XLP).
Consistency of the Moreau CLL score.