Seiamak Bahram

A cluster of ten novel MHC class I related genes on human chromosome 6q24.2-q25.3.

A basolateral sorting motif in the MICA cytoplasmic tail.

Iron overload in mice expressing HFE exclusively in the intestinal villi provides evidence that HFE regulates a functional cross-talk between crypt and villi enterocytes.

Duodenal nonheme iron content correlates with iron stores in mice, but the relationship is altered by Hfe gene knock-out.

Identification of I kappa BL as the second major histocompatibility complex-linked susceptibility locus for rheumatoid arthritis.

Selection of evolutionarily conserved mucosal-associated invariant T cells by MR1.

In vivo immunogenetics: from MIC to RAET1 loci.

Comparative sequencing of human and chimpanzee MHC class I regions unveils insertions/deletions as the major path to genomic divergence.

Hypoxic response of iron absorption is not affected by the Hfe gene knock-out in mice.

Effect of hepcidin on intestinal iron absorption in mice.

Multigenic control of hepatic iron loading in a murine model of hemochromatosis.

Genetics of the central MHC.

A direct role for NKG2D/MICA interaction in villous atrophy during celiac disease.

Association of the R92Q TNFRSF1A mutation and extracranial deep vein thrombosis in patients with Behçet's disease.

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

MIC and other NKG2D ligands: from none to too many.

Differential expression of genes related to HFE and iron status in mouse duodenal epithelium.

Rapid evolution of major histocompatibility complex class I genes in primates generates new disease alleles in humans via hitchhiking diversity.

[Toll-dependent and toll-independent innate antiviral immunity].

Two critical genes (HLA-DRB1 and ABCF1)in the HLA region are associated with the susceptibility to autoimmune pancreatitis.

Lipolysis is altered in MHC class I zinc-alpha(2)-glycoprotein deficient mice.

In vivo expression pattern of MICA and MICB and its relevance to auto-immunity and cancer.

A gene in the human major histocompatibility complex class II region controlling the class I antigen presentation pathway. 1990.

A novel immunoglobulin-immunoglobulin interaction in autoimmunity.

Genetics of Behçet disease inside and outside the MHC.

The heterogeneous allelic repertoire of human toll-like receptor (TLR) genes.

Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.

Virus-host interactions in hepatitis C virus infection: implications for molecular pathogenesis and antiviral strategies.

Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci.

The non-conventional MHC class I MR1 molecule controls infection by Klebsiella pneumoniae in mice.

A unique proteomic profile on surface IgM ligation in unmutated chronic lymphocytic leukemia.

Deregulation of type I IFN-dependent genes correlates with increased susceptibility to cytomegalovirus acute infection of dicer mutant mice.

MiR-20a regulates ASK1 expression and TLR4-dependent cytokine release in rheumatoid fibroblast-like synoviocytes.

Reverse-engineering the genetic circuitry of a cancer cell with predicted intervention in chronic lymphocytic leukemia.

The miR-17 ∼ 92 Cluster: A Key Player in the Control of Inflammation during Rheumatoid Arthritis.