(Q33844920)

English

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

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scholarly article

1 reference

Europe PubMed Central

29 July 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 (English)

1 reference

Europe PubMed Central

29 July 2017

author name string

Z Yang

1

1 reference

Europe PubMed Central

29 July 2017

A R Mendoza

2

1 reference

Europe PubMed Central

29 July 2017

T R Welch

3

1 reference

Europe PubMed Central

29 July 2017

W B Zipf

4

1 reference

Europe PubMed Central

29 July 2017

C Y Yu

5

1 reference

Europe PubMed Central

29 July 2017

language of work or name

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publication date

1 April 1999

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Europe PubMed Central

29 July 2017

Journal of Biological Chemistry

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Europe PubMed Central

29 July 2017

274

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Europe PubMed Central

29 July 2017

12147-12156

1 reference

Europe PubMed Central

29 July 2017

17

1 reference

Europe PubMed Central

29 July 2017

Molecular genetics of the human MHC complement gene cluster

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

The molecular genetics of 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

C4 polymorphism in multiplex families with insulin dependent diabetes in the Tunisian population: standard C4 typing methods and RFLP analysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Ancestral haplotypes reveal the role of the central MHC in the immunogenetics of IDDM

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Major histocompatibility complex haplotypes and class II genes in non-Jewish patients with pemphigus vulgaris

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Possible association of the extended MHC haplotype B44-SC30-DR4 with autism.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Human histocompatibility leukocyte antigen (HLA) haplotype frequencies estimated from the data on HLA class I, II, and III antigens in 111 Japanese narcoleptics

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

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://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Identification of a novel family of human endogenous retroviruses and characterization of one family member, HERV-K(C4), located in the complement C4 gene cluster.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

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://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Four ubiquitously expressed genes, RD (D6S45)-SKI2W (SKIV2L)-DOM3Z-RP1 (D6S60E), are present between complement component genes factor B and C4 in the class III region of the HLA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

A Previously Undetected MHC Gene with an Unusual Periodic Structure

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

The human DEVH-box protein Ski2w from the HLA is localized in nucleoli and ribosomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Characterisation of the novel gene G11 lying adjacent to the complement C4A gene in the human major histocompatibility complex

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

The G11 gene located in the major histocompatibility complex encodes a novel nuclear serine/threonine protein kinase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Structure of human steroid 21-hydroxylase genes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Cluster of fibronectin type III repeats found in the human major histocompatibility complex class III region shows the highest homology with the repeats in an extracellular matrix protein, tenascin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

A cDNA clone for cytotactin contains sequences similar to epidermal growth factor-like repeats and segments of fibronectin and fibrinogen

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Inherited structural polymorphism of the fourth component of human complement

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

The structural basis of the multiple forms of human complement component C4.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Sequences promoting the transcription of the human XA gene overlapping P450c21A correctly predict the presence of a novel, adrenal-specific, truncated form of tenascin-X

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

When is a deletion not a deletion? When it is converted

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Genes for SMA: multum in parvo

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

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://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

The HLA-A3, Cw6,B47,DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with at least two crossover sites in the class III region.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasia.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Tenascin-X deficiency is associated with Ehlers-Danlos syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.12147

21 January 2018

Identifiers

10.1074/JBC.274.17.12147

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

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