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Article

Genetic Sophistication of Human Complement Components C4A and C4B and RP-C4-CYP21-TNX (RCCX) Modules in the Major Histocompatibility Complex

1 Oct 2002

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 12226794
DOI: 10.1086/342777

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Genetic Sophistication of Human Complement Components C4A and C4B and RP-C4-CYP21-TNX (RCCX) Modules in the Major Histocompatibility ComplexPMID 12226794Read ↗

Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease.Semantic proximity Read ↗

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Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4.Semantic proximity Read ↗

Determining the one, two, three, or four long and short loci of human complement C4 in a major histocompatibility complex haplotype encoding C4A or C4B proteins.Semantic proximity Read ↗

Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations.Semantic proximity Read ↗

Modular Variations of the Human Major Histocompatibility Complex Class III Genes for Serine/Threonine Kinase RP, Complement Component C4, Steroid 21-Hydroxylase CYP21, and Tenascin TNX (the RCCX Module)Semantic proximity Read ↗

The intricate role of complement component C4 in human systemic lupus erythematosus.Semantic proximity Read ↗

Complete complement components C4A and C4B deficiencies in human kidney diseases and systemic lupus erythematosus.Semantic proximity Read ↗

Revised nomenclature for human complement component C4. WHO-IUIS Nomenclature Sub-Committee.Semantic proximity Read ↗

Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus.Semantic proximity Read ↗

Genetics of human complement component C4 and evolution the central MHC.Semantic proximity Read ↗

Sensitive and specific real-time polymerase chain reaction assays to accurately determine copy number variations (CNVs) of human complement C4A, C4B, C4-long, C4-short, and RCCX modules: elucidation of C4 CNVs in 50 consanguineous subjects with defined HLA genotypes.Semantic proximity Read ↗

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