(Q46987642)

27 December 2017

title

Rapid quantification of human complement component C4A and C4B genes by capillary gel electrophoresis (English)

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27 December 2017

author

Zsolt Ronai

3

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27 December 2017

author name string

Agnes Szilagyi

1

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27 December 2017

Bernadett Blasko

2

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27 December 2017

Gyorgy Fust

4

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27 December 2017

Maria Sasvari-Szekely

5

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27 December 2017

András Guttman

6

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27 December 2017

language of work or name

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1 April 2006

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27 December 2017

published in

Electrophoresis

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27 December 2017

volume

27

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27 December 2017

issue

8

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27 December 2017

page(s)

1437-1443

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27 December 2017

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

cites work

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Complement allotyping in SLE: association with C4A null

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https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

The phenotype of SLE associated with complete deficiency of complement isotype C4A

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https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Association of homozygous C4B deficiency with bacterial meningitis

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https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Association between circulating immune complexes, complement C4 null alleles, and myocardial infarction before age 45 years

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

C4 null alleles and myocardial infarction

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

C4A gene deletion: association with Graves' disease.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Complement polymorphism in herpes gestationis: association with C4 null allele

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Association of C4B deficiency (C4B*Q0) with erythema nodosum in leprosy

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https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Molecular genetics of C4B deficiency in IgA nephropathy

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https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

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

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Polymerase chain reaction based C4AQ0 and C4BQ0 genotyping: association with systemic lupus erythematosus in southwest Han Chinese.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Long PCR detection of the C4A null allele in B8-C4AQ0-C4B1-DR3

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Analysis of dopamine D4 receptor gene polymorphism using microchip electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

A comparison between SNaPshot, pyrosequencing, and biplex invader SNP genotyping methods: accuracy, cost, and throughput

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Genotyping and haplotyping of the dopamine D4 receptor gene by capillary electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Quantitative analysis of gene expression by reverse transcription polymerase chain reaction and capillary electrophoresis with laser-induced fluorescence detection

1 reference

https://api.crossref.org/works/10.1002%2FELPS.200500779

7 January 2021

Identifiers

DOI

10.1002/ELPS.200500779

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27 December 2017

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27 December 2017