The genetics of systemic lupus erythematosus: putting the pieces together. - Wikidata - wikimedia - TriplyDB

The genetics of systemic lupus erythematosus: putting the pieces together.

The genetics of systemic lupus erythematosus: putting the pieces together.

http://www.wikidata.org/entity/Q34148175

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Systemic lupus erythematosus and the type I interferon system Will investments in large-scale prospective cohorts and biobanks limit our ability to discover weaker, less common genetic and environmental contributors to complex diseases?A practice approach for identifying previously unsuspected environmental contributors to systemic lupus erythematosus and other complex diseases Replication of recently identified systemic lupus erythematosus genetic associations: a case-control study.A naturally occurring variant in human TLR9, P99L, is associated with loss of CpG oligonucleotide responsiveness.Functional promoter haplotypes of the human FAS gene are associated with the phenotype of SLE characterized by thrombocytopenia.A genomewide screen for generalized vitiligo: confirmation of AIS1 on chromosome 1p31 and evidence for additional susceptibility loci Linkage at 12q24 with systemic lupus erythematosus (SLE) is established and confirmed in Hispanic and European American families.Spontaneous lupus-like syndrome in HLA-DQ2 transgenic mice with a mixed genetic background.Role of Fc gamma receptor IIb polymorphism in the genetic background of systemic lupus erythematosus: insights from Asia.An extensive screen of the HLA region reveals an independent association of HLA class I and class II with susceptibility for systemic lupus erythematosus.Loss of LFA-1, but not Mac-1, protects MRL/MpJ-Fas(lpr) mice from autoimmune disease Environmental exposure, estrogen and two X chromosomes are required for disease development in an epigenetic model of lupus T-cell tolerance and autoimmunity to systemic and tissue-restricted self-antigens.Current status of lupus genetics SH2D1A regulates T-dependent humoral autoimmunity.Active inhibition of plasma cell development in resting B cells by microphthalmia-associated transcription factor Cutaneous lupus erythematosus: understanding of clinical features, genetic basis, and pathobiology of disease guides therapeutic strategies.Familial lupus and antiphospholipid syndrome.Altered expression of Fcgamma and complement receptors on B cells in systemic lupus erythematosus.Fc receptor genes and the systemic lupus erythematosus diathesis.Diet influences expression of autoimmune-associated genes and disease severity by epigenetic mechanisms in a transgenic mouse model of lupus.TLR9 polymorphisms and systemic lupus erythematosus risk: an update meta-analysis study.FcgammaRIIB Ile232Thr transmembrane polymorphism associated with human systemic lupus erythematosus decreases affinity to lipid rafts and attenuates inhibitory effects on B cell receptor signaling.Clinicopathological characteristics of familial SLE patients with lupus nephritis.Linkage analysis of SLE susceptibility: confirmation of SLER1 at 5p15.3.A novel single-nucleotide polymorphism of the Fcgamma receptor IIIa gene is associated with genetic susceptibility to systemic lupus erythematosus in Chinese populations: a family-based association study.CD72 polymorphisms associated with alternative splicing modify susceptibility to human systemic lupus erythematosus through epistatic interaction with FCGR2B.Relation between HLA typing and clinical presentations in Systemic Lupus Erythematosus patients in Al-Qassim region, Saudi Arabia.Association of Fcgamma receptor IIb polymorphism with susceptibility to systemic lupus erythematosus in Chinese: a common susceptibility gene in the Asian populations.Systemic lupus erythematosus with and without a family history: a meta-analysis.Natural killer cell activity in families of patients with systemic lupus erythematosus: demonstration of a killing defect in patients.C-reactive protein +1444CT (rs1130864) genetic polymorphism is associated with the susceptibility to systemic lupus erythematosus and C-reactive protein levels.Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus Genetic linkage of systemic lupus erythematosus with chromosome 11q14 (SLEH1) in African-American families stratified by a nucleolar antinuclear antibody pattern Genome scan stratified by the presence of anti-double-stranded DNA (dsDNA) autoantibody in pedigrees multiplex for systemic lupus erythematosus (SLE) establishes linkages at 19p13.2 (SLED1) and 18q21.1 (SLED2)Effects of Major Epigenetic Factors on Systemic Lupus Erythematosus

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The genetics of systemic lupus erythematosus: putting the pieces together.

http://www.wikidata.org/entity/Q34148175

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The genetics of systemic lupus erythematosus: putting the pieces together.

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The genetics of systemic lupus erythematosus: putting the pieces together.

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The genetics of systemic lupus erythematosus: putting the pieces together.

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The genetics of systemic lupus erythematosus: putting the pieces together.

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The genetics of systemic lupus erythematosus: putting the pieces together.

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The genetics of systemic lupus erythematosus: putting the pieces together.

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A second serine protease associated with mannan-binding lectin that activates complement

cDNA cloning and primary structure analysis of C1qR(P), the human C1q/MBL/SPA receptor that mediates enhanced phagocytosis in vitro

Interleukin 10 is a potent growth and differentiation factor for activated human B lymphocytes

Evidence for a susceptibility gene, SLEV1, on chromosome 17p13 in families with vitiligo-related systemic lupus erythematosus

Fc gamma RIIA alleles are heritable risk factors for lupus nephritis in African Americans

Sequences of complementary DNAs that encode the NA1 and NA2 forms of Fc receptor III on human neutrophils

Alternative membrane forms of Fc gamma RIII(CD16) on human natural killer cells and neutrophils. Cell type-specific expression of two genes that differ in single nucleotide substitutions

Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosus

Fas ligand mutation in a patient with systemic lupus erythematosus and lymphoproliferative disease

High frequencies in African and non-African populations of independent mutations in the mannose binding protein gene

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