(Q74220418)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9475353%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

The phenotype of SLE associated with complete deficiency of complement isotype C4A (English)

1 reference

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9 November 2019

1 reference

T R Welch

1

1 reference

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9 November 2019

C Brickman

2

1 reference

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9 November 2019

N Bishof

3

1 reference

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9 November 2019

S Maringhini

4

1 reference

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9 November 2019

M Rutkowski

5

1 reference

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9 November 2019

M Frenzke

6

1 reference

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9 November 2019

N Kantor

7

1 reference

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9 November 2019

publication date

1 January 1998

1 reference

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Journal of Clinical Immunology

9 November 2019

published in

1 reference

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9 November 2019

volume

18

1 reference

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9 November 2019

issue

1

1 reference

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9 November 2019

page(s)

48-51

1 reference

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https://scigraph.springernature.com/pub.10.1023/a:1023287820786

9 November 2019

exact match

0 references

cites work

Genetic deficiency of C4, C2 or C1q and lupus syndromes. Association with anti-Ro (SS-A) antibodies

1 reference

12 December 2020

C4 isotype deficiency in IgA nephropathy

1 reference

12 December 2020

Clinical aspects of systemic lupus erythematosus in childhood

1 reference

12 December 2020

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

12 December 2020

Null alleles of human complement C4. Evidence for pseudogenes at the C4A locus and for gene conversion at the C4B locus

1 reference

12 December 2020

C4B deficiency: a risk factor for bacteremia with encapsulated organisms

1 reference

12 December 2020

Major histocompatibility complex extended haplotypes in systemic lupus erythematosus

1 reference

12 December 2020

Inherited deficiency of the fourth component of human complement

1 reference

12 December 2020

Glomerulonephritis associated with complete deficiency of the fourth component of complement. Response to intravenous immunoglobulin

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Disease States in Genetic Complement Deficiencies

1 reference

12 December 2020

Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and black Americans.

1 reference

12 December 2020

Comparative analysis of the disease-associated complement C4 gene from the HLA-A1, B8, DR3 haplotype

1 reference

12 December 2020

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

1 reference

12 December 2020

Major-histocompatibility-complex extended haplotypes in membranoproliferative glomerulonephritis

1 reference

12 December 2020

The effect of null C4 alleles on complement function.

1 reference

12 December 2020

Molecular genetics of C4B deficiency in IgA nephropathy

1 reference

12 December 2020