about
A genetic association study of serum acute-phase C-reactive protein levels in rheumatoid arthritis: implications for clinical interpretationResequencing the susceptibility gene, ITGAM, identifies two functionally deleterious rare variants in systemic lupus erythematosus cases.The genetics of SLE: an update in the light of genome-wide association studies.Evaluation of imputation-based association in and around the integrin-alpha-M (ITGAM) gene and replication of robust association between a non-synonymous functional variant within ITGAM and systemic lupus erythematosus (SLE).Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at MSH5, HLA-DPB1 and HLA-GOsteoclast Differentiation Is Impaired in a Subgroup of SLE Patients and Correlates Inversely with Mycophenolate Mofetil TreatmentThe rs1143679 (R77H) lupus associated variant of ITGAM (CD11b) impairs complement receptor 3 mediated functions in human monocytesGenetic determinants of basal C-reactive protein expression in Filipino systemic lupus erythematosus families.General aspects of the genetics of SLE.Fine-mapping the genetic basis of CRP regulation in African Americans: a Bayesian approachThe complement receptor 3 (CD11b/CD18) agonist Leukadherin-1 suppresses human innate inflammatory signalling.C-reactive protein in rheumatology: biology and genetics.Systemic lupus erythematosus: An update for ophthalmologists.Familial clustering of non-nuclear autoantibodies and C3 and C4 complement components in systemic lupus erythematosus.The potential overlapping populations for treatment with belimumab and rituximab using current NHS England and National Institute for Health and Care Excellence Guidelines in England and Wales.The potential overlapping populations for treatment with belimumab and rituximab using current NHS England and National Institute for Health and Care Excellence Guidelines in England and Wales.Quantification of the genetic component of basal C-reactive protein expression in SLE nuclear families.Association of LY9 in UK and Canadian SLE families.The heritability and genetics of complement C3 expression in UK SLE families.Using genetics to deliver personalized SLE therapy-a realistic prospect?Genetics core learning outcomes.Paget's disease of bone: osteitis deformans or osteodystrophia deformans?Variation in IGHMBP2 is not associated with IgA nephropathy in independent studies of UK Caucasian and Chinese Han patientsChanging patterns of sedation use for routine out-patient diagnostic gastroscopy between 1989 and 1998Kikuchi's diseaseErdheim-Chester disease
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description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Benjamin Rhodes
@ast
Benjamin Rhodes
@en
Benjamin Rhodes
@es
Benjamin Rhodes
@nl
Benjamin Rhodes
@sl
type
label
Benjamin Rhodes
@ast
Benjamin Rhodes
@en
Benjamin Rhodes
@es
Benjamin Rhodes
@nl
Benjamin Rhodes
@sl
prefLabel
Benjamin Rhodes
@ast
Benjamin Rhodes
@en
Benjamin Rhodes
@es
Benjamin Rhodes
@nl
Benjamin Rhodes
@sl
P106
P21
P31
P496
0000-0001-7554-5409