(Q37203068)

English

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

scientific article published on 11 September 2002

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scholarly article

1 reference

Europe PubMed Central

18 August 2017

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

Robert M Rennebohm

3

1 reference

Europe PubMed Central

18 August 2017

Marja-Liisa Lokki

4

1 reference

Europe PubMed Central

18 August 2017

Gloria C Higgins

5

1 reference

Europe PubMed Central

18 August 2017

Karla N Jones

6

1 reference

Europe PubMed Central

18 August 2017

Bi Zhou

7

1 reference

Europe PubMed Central

18 August 2017

Carol A Blanchong

8

1 reference

Europe PubMed Central

18 August 2017

C Yung Yu

9

1 reference

Europe PubMed Central

18 August 2017

language of work or name

0 references

publication date

11 September 2002

1 reference

Europe PubMed Central

18 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

18 August 2017

71

1 reference

Europe PubMed Central

18 August 2017

823-837

1 reference

Europe PubMed Central

18 August 2017

4

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

6 September 2017

Genetic organization of the human MHC class III region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

6 September 2017

Genetics of human complement component C4 and evolution the central MHC.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

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=378539

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=378539

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=378539

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=378539

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=378539

6 September 2017

Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

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=378539

6 September 2017

The 1982 revised criteria for the classification of systemic lupus erythematosus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

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=378539

6 September 2017

Human C4 haplotypes with duplicated C4A or C4B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

6 September 2017

A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

6 September 2017

A molecular basis for the two locus model of 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=378539

6 September 2017

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=378539

6 September 2017

Polymorphism of 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=378539

6 September 2017

Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

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=378539

6 September 2017

A structural model for the location of the Rodgers and the Chido antigenic determinants and their correlation with the human complement component C4A/C4B isotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

6 September 2017

Structural basis of the polymorphism of human complement components C4A and C4B: gene size, reactivity and antigenicity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

6 September 2017

Substitution of a single amino acid (aspartic acid for histidine) converts the functional activity of human complement C4B to C4A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

6 September 2017

Genetic polymorphism of C4 in man and localisation of a structural C4 locus to the HLA gene complex of chromosome 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

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=378539

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=378539

28 September 2017

Restriction fragment length polymorphisms of the complement component C4 loci on chromosome 6: studies with emphasis on the determination of gene number

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

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=378539

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=378539

26 June 2018

Quantitation of the human component C4: definition of C4 Q0 alleles and C4A duplications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

26 June 2018

An unequal crossover between the RCCX modules of the human MHC leading to the presence of a CYP21B gene and a tenascin TNXB/TNXA-RP2 recombinant between C4A and C4B genes in a patient with juvenile rheumatoid arthritis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378539

3 September 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=378539

3 September 2018

The C4 system: quantitative studies of different genotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12226794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of human C4 polymorphism: detection and segregation of rare and duplicated haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12226794

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/12226794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype study on C4 polymorphism in Japanese. Associations with MHC alleles, complotypes, and HLA-complement haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12226794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C4 phenotypic variation suggests an unusual class III gene organization

1 reference

https://pubmed.ncbi.nlm.nih.gov/12226794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a De Novo Conversion in Human Complement C4 Gene Producing a C4B5-Like Protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/12226794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of complete complement C4A and C4B deficiencies in a systemic lupus erythematosus patient with homozygous C4A and C4B mutant genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12226794

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/12226794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The study of a French family with two duplicated C4A haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12226794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel immunoassay for the quantitation of human C4 gene products

1 reference

https://pubmed.ncbi.nlm.nih.gov/12226794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genomic structure of two ancestral haplotypes carrying C4A duplications

1 reference

https://pubmed.ncbi.nlm.nih.gov/12226794

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

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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