(Q34537215)

English

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

scientific article

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scholarly article

1 reference

Europe PubMed Central

2 August 2017

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

1 reference

Europe PubMed Central

2 August 2017

author name string

P M Schneider

1

1 reference

Europe PubMed Central

2 August 2017

M C Carroll

2

1 reference

Europe PubMed Central

2 August 2017

C A Alper

3

1 reference

Europe PubMed Central

2 August 2017

C Rittner

4

1 reference

Europe PubMed Central

2 August 2017

A S Whitehead

5

1 reference

Europe PubMed Central

2 August 2017

E J Yunis

6

1 reference

Europe PubMed Central

2 August 2017

H R Colten

7

1 reference

Europe PubMed Central

2 August 2017

language of work or name

0 references

publication date

1 September 1986

1 reference

Europe PubMed Central

2 August 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

2 August 2017

78

1 reference

Europe PubMed Central

2 August 2017

650-657

1 reference

Europe PubMed Central

2 August 2017

3

1 reference

Europe PubMed Central

2 August 2017

On the significance of C2, C4, and factor B polymorphisms in disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

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=423642

7 July 2018

The molecular basis for the difference in immune hemolysis activity of the Chido and Rodgers isotypes 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=423642

7 July 2018

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=423642

7 July 2018

Cloning of a human complement component C4 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

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=423642

7 July 2018

The structural basis of the multiple forms 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=423642

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

A comparison of the properties of two classes, C4A and C4B, of 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=423642

7 July 2018

Correlation between a DNA restriction fragment length polymorphism and C4A6 protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

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=423642

7 July 2018

Thalassemia Revisited

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Evidence for linkage between HL-A histocompatibility genes and those involved in the synthesis of the second component of complement.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Isolation of high-molecular-weight DNA from mammalian cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Genetic polymorphism in human glycine-rich beta-glycoprotein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Clinical and endocrinological aspects of 21-hydroxylase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

The origin of the very variable haemolytic activities of the common human complement component C4 allotypes including C4-A6.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

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=423642

7 July 2018

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=423642

7 July 2018

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=423642

7 July 2018

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

The molecular basis for genetic deficiency of the second 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=423642

7 July 2018

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Inherited deficiency of the second component of complement. Rheumatic disease associations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423642

7 July 2018

Genetic polymorphism of human complement C4 and detection of heterozygotes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum complement 'supergenes' of the major histocompatibility complex in man (complotypes).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene order and gene distances in the HLA region studied by the haplotype method

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial C4 deficiency in subacute sclerosing panencephalitis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

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/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the human MHC-linked complement genes between HLA-B and HLA-DR by using HLA mutant cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unrelated individuals matched for MHC extended haplotypes and HLA-identical siblings show comparable responses in mixed lymphocyte culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C4B gene polymorphism detected in a human cosmid clone

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of HL-A and GBG

1 reference

https://pubmed.ncbi.nlm.nih.gov/3018042

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI112623

1 reference

Europe PubMed Central

2 August 2017

1 reference

Europe PubMed Central

2 August 2017

1 reference

Europe PubMed Central

2 August 2017

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