Complement genetics, deficiencies, and disease associations.
about
Systemic Lupus Erythematosus and Deficiencies of Early Components of the Complement Classical PathwayA reverse genetic approach identifies an ancestral frameshift mutation in RP1 causing recessive progressive retinal degeneration in European cattle breedsComplement regulator CD46: genetic variants and disease associationsCurrent evidence for the role of complement in the pathogenesis of Shiga toxin haemolytic uraemic syndrome.Transcriptome sequencing study implicates immune-related genes differentially expressed in schizophrenia: new data and a meta-analysis.Inhibition of c3 convertase activity by hepatitis C virus as an additional lesion in the regulation of complement componentsThe human serum protein C4b-binding protein inhibits pancreatic IAPP-induced inflammasome activation.Characterization of cellular and humoral immune responses after IBV infection in chicken lines differing in MBL serum concentration.Elucidation of molecular mechanisms of physiological variations between bovine subcutaneous and visceral fat depots under different nutritional regimes.CTRP6 is an endogenous complement regulator that can effectively treat induced arthritis.Adeno-associated virus mediated delivery of an engineered protein that combines the complement inhibitory properties of CD46, CD55 and CD59Keeping It All Going-Complement Meets MetabolismA novel immunodeficiency syndrome associated with partial trisomy 19p13.Genetic dissection of NK cell responses.Inflammatory cytokine network in schizophrenia.Identifying key genes in rheumatoid arthritis by weighted gene co-expression network analysis.Inherited variation in immune response genes in follicular lymphoma and diffuse large B-cell lymphoma.A Plasma α-Tocopherome Can Be Identified from Proteins Associated with Vitamin E Status in School-Aged Children of Nepal.Cervicovaginal microbiome dysbiosis is associated with proteome changes related to alterations of the cervicovaginal mucosal barrier.Dysregulation of adaptive immune responses in complement C3-deficient patients.The impact of micronutrient status on health: correlation network analysis to understand the role of micronutrients in metabolic-inflammatory processes regulating homeostasis and phenotypic flexibility.Clinical, cellular, microscopic, and ultrastructural studies of a case of fibrogenesis imperfecta ossium.Positive selection on human gamete-recognition genes.The plasma proteome identifies expected and novel proteins correlated with micronutrient status in undernourished Nepalese children.Persistent changes in circulating white blood cell populations after splenectomy.Targeting complement-mediated immunoregulation for cancer immunotherapy.Cutaneous Vasculitis and Recurrent Infection Caused by Deficiency in Complement Factor I.Autoimmune phenotypes in schizophrenia reveal novel treatment targets.Plasma proteins associated with circulating carotenoids in Nepalese school-aged children.
P2860
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P2860
Complement genetics, deficiencies, and disease associations.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Complement genetics, deficiencies, and disease associations.
@en
type
label
Complement genetics, deficiencies, and disease associations.
@en
prefLabel
Complement genetics, deficiencies, and disease associations.
@en
P2860
P1433
P1476
Complement genetics, deficiencies, and disease associations.
@en
P2093
Karine R Mayilyan
P2860
P2888
P304
P356
10.1007/S13238-012-2924-6
P577
2012-07-10T00:00:00Z