(Q37203039)

English

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

scientific article published on 10 September 2002

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scholarly article

1 reference

Europe PubMed Central

18 August 2017

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 (English)

1 reference

Europe PubMed Central

18 August 2017

author name string

Erwin K Chung

1

1 reference

Europe PubMed Central

18 August 2017

Yan Yang

2

1 reference

Europe PubMed Central

18 August 2017

Kristi L Rupert

3

1 reference

Europe PubMed Central

18 August 2017

Karla N Jones

4

1 reference

Europe PubMed Central

18 August 2017

Robert M Rennebohm

5

1 reference

Europe PubMed Central

18 August 2017

Carol A Blanchong

6

1 reference

Europe PubMed Central

18 August 2017

C Yung Yu

7

1 reference

Europe PubMed Central

18 August 2017

language of work or name

0 references

publication date

10 September 2002

1 reference

Europe PubMed Central

18 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

18 August 2017

71

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Europe PubMed Central

18 August 2017

810-822

1 reference

Europe PubMed Central

18 August 2017

4

1 reference

Europe PubMed Central

18 August 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC378538/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Genetic sophistication of human complement components C4A and C4B and RP-C4-CYP21-TNX (RCCX) modules in the major histocompatibility complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Anaphylatoxins and infectious and non-infectious inflammatory diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Mannose-binding lectin: targeting the microbial world for complement attack and opsonophagocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Molecular aberrations in human systemic lupus erythematosus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

The human and mouse MHC class III region: a parade of 21 genes at the centromeric segment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Complete sequence and gene map of a human major histocompatibility complex. The MHC sequencing consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

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). A mechanism for gene deletions and disease as

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Studies of group B streptococcal infection in mice deficient in complement component C3 or C4 demonstrate an essential role for complement in both innate and acquired immunity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Structure and genetics of the partially duplicated gene RP located immediately upstream of the complement C4A and the C4B genes in the HLA class III region. Molecular cloning, exon-intron structure, composite retroposon, and breakpoint of gene dupli

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Kinetic PCR Analysis: Real-time Monitoring of DNA Amplification Reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

The dichotomous size variation of human complement C4 genes is mediated by a novel family of endogenous retroviruses, which also establishes species-specific genomic patterns among Old World primates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Inherited structural polymorphism of the fourth component of human complement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Reference ranges for serum C4 concentrations in subjects with and without C4 null alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Differences in gene copy number carried by different MHC ancestral haplotypes. Quantitation after physical separation of haplotypes by pulsed field gel electrophoresis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Mechanism and consequences of the duplication of the human C4/P450c21/gene X locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Consumption of classical complement components by heart subcellular membranes in vitro and in patients after acute myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

Two HLA-linked loci controlling the fourth component of human complement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

6 September 2017

The endogenous retroviral insertion in the human complement C4 gene modulates the expression of homologous genes by antisense inhibition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

28 September 2017

Complement deposition in early cardiac transplant biopsies is associated with ischemic injury and subsequent rejection episodes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

28 September 2017

Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

28 September 2017

Reference typing report for complement component C4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

26 June 2018

Neutralization of sensitized virus by the fourth component of complement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

26 June 2018

The effect of null C4 alleles on complement function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

26 June 2018

Phenotyping of human complement component C4, a class-III HLA antigen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

26 June 2018

Direct observation of the gene organization of the complement C4 and 21-hydroxylase loci by pulsed field gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

26 June 2018

C4B deficiency: a risk factor for bacteremia with encapsulated organisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

26 June 2018

The reaction mechanism of the internal thioester in the human complement component C4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378538

3 September 2018

C4a anaphylatoxin levels as an indicator of disease activity in systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/12224044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Capillary deposition of C4d complement fragment and early renal graft loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/12224044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma C3a and C4a levels in liver transplant recipients: a longitudinal study

1 reference

https://pubmed.ncbi.nlm.nih.gov/12224044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios

1 reference

https://pubmed.ncbi.nlm.nih.gov/12224044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphism of human complement C4 and detection of heterozygotes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12224044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The C4 system: quantitative studies of different genotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12224044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement polymorphism, the major histocompatibility complex and associated diseases: a speculation

1 reference

https://pubmed.ncbi.nlm.nih.gov/12224044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Major histocompatibility complex (MHC) class III genetics in two Amerindian tribes from southern Brazil: the Kaingang and the Guarani

1 reference

https://pubmed.ncbi.nlm.nih.gov/12224044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous deletion of the CYP21A-TNXA-RP2-C4B gene region conferring C4B deficiency associated with recurrent respiratory infections

1 reference

https://pubmed.ncbi.nlm.nih.gov/12224044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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Europe PubMed Central

18 August 2017

1 reference

Europe PubMed Central

18 August 2017

1 reference

Europe PubMed Central

18 August 2017

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