(Q37277776)

English

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

scientific article published on 09 January 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

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 (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Kapil Saxena

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Kathryn J Kitzmiller

2

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Yee Ling Wu

3

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Bi Zhou

4

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Nazreen Esack

5

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Leena Hiremath

6

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Erwin K Chung

7

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Yan Yang

8

1 reference

Europe PubMed Central

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19 August 2017

C Yung Yu

9

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

publication date

9 January 2009

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19 August 2017

Molecular Immunology

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Europe PubMed Central

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19 August 2017

46

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Europe PubMed Central

PMC publication ID

19 August 2017

7

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

1289-1303

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2716727/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Extending genome-wide association studies to copy-number variation

1 reference

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Antibodies, isotypes and complement in allograft rejection.

1 reference

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6 September 2017

Induction of truncated form of tenascin-X (XB-S) through dissociation of HDAC1 from SP-1/HDAC1 complex in response to hypoxic conditions

1 reference

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6 September 2017

Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project

1 reference

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Diet and the evolution of human amylase gene copy number variation

1 reference

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6 September 2017

1 reference

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Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

1 reference

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6 September 2017

Congenital adrenal hyperplasia: focus on the molecular basis of 21-hydroxylase deficiency.

1 reference

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Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

1 reference

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6 September 2017

Global variation in copy number in the human genome

1 reference

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6 September 2017

Extensive clinical experience: nonclassical 21-hydroxylase deficiency

1 reference

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6 September 2017

Diagnostic value of C4d in renal biopsies

1 reference

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A protective role for innate immunity in systemic lupus erythematosus

1 reference

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6 September 2017

Large-scale copy number polymorphism in the human genome

1 reference

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6 September 2017

Dancing with Complement C4 and the RP-C4-CYP21-TNX (RCCX) Modules of the Major Histocompatibility Complex

1 reference

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6 September 2017

Diversity in intrinsic strengths of the human complement system: serum C4 protein concentrations correlate with C4 gene size and polygenic variations, hemolytic activities, and body mass index

1 reference

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6 September 2017

Complement C4d in graft capillaries -- the missing link in the recognition of humoral alloreactivity

1 reference

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6 September 2017

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

1 reference

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6 September 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

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6 September 2017

Complement. First of two parts

1 reference

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6 September 2017

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

1 reference

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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=2716727

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=2716727

6 September 2017

Genomics of the major histocompatibility complex: haplotypes, duplication, retroviruses and disease

1 reference

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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

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6 September 2017

Genetic variation in India.

1 reference

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6 September 2017

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

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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

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6 September 2017

Length polymorphism of the human complement component C4 gene is due to an ancient retroviral integration

1 reference

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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

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6 September 2017

Inherited structural polymorphism of the fourth component of human complement

1 reference

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Primate erythrocyte-immune complex-clearing mechanism

1 reference

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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

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6 September 2017

Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.

1 reference

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HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation

1 reference

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A molecular basis for the two locus model of human complement component C4

1 reference

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6 September 2017

Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

1 reference

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6 September 2017

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

1 reference

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6 September 2017

Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia

1 reference

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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

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6 September 2017

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

1 reference

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6 September 2017

The complete exon-intron structure of a human complement component C4A gene. DNA sequences, polymorphism, and linkage to the 21-hydroxylase gene

1 reference

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6 September 2017

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

1 reference

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

1 reference

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6 September 2017

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

1 reference

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Complete MHC haplotype sequencing for common disease gene mapping

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14 September 2017

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

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28 September 2017

Tenascin-X deficiency is associated with Ehlers-Danlos syndrome

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26 June 2018

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

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26 June 2018

An epitope on C4 beta light (L) chains detected by human anti-Rg; its relationship with beta chain polymorphism and MHC associations

1 reference

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26 June 2018

Definitive RFLPs to distinguish between the human complement C4A/C4B isotypes and the major Rodgers/Chido determinants: application to the study of C4 null alleles

1 reference

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The role of C4d immunostaining in the evaluation of the causes of renal allograft dysfunction.

1 reference

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Newborn screening in India

1 reference

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3 September 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

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3 September 2018

Statement on the nomenclature of human C4 allotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2716727

3 September 2018

Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/19135723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antigenic determinants expressed by human C4 allotypes; a study of 325 families provides evidence for the structural antigenic model

1 reference

https://pubmed.ncbi.nlm.nih.gov/19135723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in gene copy number and polymorphism of the human salivary amylase isoenzyme system in Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/19135723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of systemic lupus erythematosus in India

1 reference

https://pubmed.ncbi.nlm.nih.gov/19135723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IFN-gamma mediates stimulation of complement C4 biosynthesis in human proximal tubular epithelial cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19135723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement and the kidney: what the nephrologist needs to know in 2006?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19135723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural variation in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19135723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chido‐Substance in Plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/19135723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A New Antibody Specificity, Anti-Rga, Reacting with a Red Cell and Serum Antigen

1 reference

https://pubmed.ncbi.nlm.nih.gov/19135723

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/19135723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.MOLIMM.2008.11.018

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

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