Two novel mutations in the C7 gene in a Korean patient with complement C7 deficiency (Q33599495)

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English	Two novel mutations in the C7 gene in a Korean patient with complement C7 deficiency	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

15831990

retrieved

28 July 2017

title

Two novel mutations in the C7 gene in a Korean patient with complement C7 deficiency (English)

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Europe PubMed Central

PubMed publication ID

15831990

retrieved

28 July 2017

author name string

Chang-Seok Ki

series ordinal

1

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Europe PubMed Central

PubMed publication ID

15831990

retrieved

28 July 2017

Jong-Won Kim

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2

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Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

Hee-Jin Kim

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3

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Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

Sung-Min Choi

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4

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Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

Gyoung-Yim Ha

series ordinal

5

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Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

Hee Jung Kang

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6

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stated in

Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

Won-Duck Kim

series ordinal

7

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Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

publication date

1 April 2005

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stated in

Europe PubMed Central

PubMed publication ID

15831990

retrieved

28 July 2017

published in

Journal of Korean Medical Science

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stated in

Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

volume

20

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Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

issue

2

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stated in

Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

page(s)

220-224

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Europe PubMed Central

PubMed publication ID

15831990

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28 July 2017

copyright license

Creative Commons Attribution-NonCommercial 3.0 Unported

start time

1 January 2005

1 reference

stated in

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Investigation for complement deficiency following meningococcal disease

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

High prevalence of complement C7 deficiency among healthy blood donors of Moroccan Jewish ancestry

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PubMed Central

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21 June 2018

Reference typing report for complement components C6, C7 and C9 including mutations leading to deficiencies

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

Molecular bases of C7 deficiency: three different defects

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

retrieved

21 June 2018

Structure of the human C7 gene and comparison with the C6, C8A, C8B, and C9 genes

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

retrieved

21 June 2018

Hereditary complement deficiency in survivors of meningococcal disease: high prevalence of C7/C8 deficiency in Sephardic (Moroccan) Jews

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

The membrane attack complex of complement

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

Screening for complement deficiencies in unselected patients with meningitis.

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

The structure of human complement component C7 and the C5b-7 complex

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

Prevalence of hereditary properdin, C7 and C8 deficiencies in patients with meningococcal infections

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

Prophylaxis against Neisseria meningitidis infections and antibody responses in patients with deficiency of the sixth component of complement

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

Nonsense codons within the Rous sarcoma virus gag gene decrease the stability of unspliced viral RNA

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

Inherited deficiencies of the terminal components of human complement

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PubMed Central

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21 June 2018

Allelic polymorphisms of human Fc gamma receptor IIA and Fc gamma receptor IIIB. Independent mechanisms for differences in human phagocyte function

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PubMed Central

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21 June 2018

Interference of nonsense mutations with eukaryotic messenger RNA stability

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

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21 June 2018

Genetic bases of human complement C7 deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

retrieved

28 July 2018

Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficiencies

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

retrieved

28 July 2018

Screening for complement deficiencies in patients surviving from epidemic meningococcal disease

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808595

retrieved

30 October 2018

The assignment of the genes coding for human complement components C6 and C7 to chromosome 5

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15831990

retrieved

12 December 2020

based on heuristic

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Immune cell signaling defects in lupus: activation, anergy and death

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15831990

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of antibodies against tetravalent meningococcal polysaccharides in revaccinated complement-deficient patients

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15831990

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of Fcgamma receptor polymorphisms and C3 in the immune defence against Neisseria meningitidis in complement-deficient individuals

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15831990

retrieved

12 December 2020

based on heuristic

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Relevance of Fcgamma receptor and interleukin-10 polymorphisms for meningococcal disease

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15831990

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C7 complement deficiency in an Israeli Arab village

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15831990

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement component C7 deficiency in a Spanish family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15831990

retrieved

12 December 2020

based on heuristic

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Identifiers

DOI

10.3346/JKMS.2005.20.2.220

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15831990

retrieved

28 July 2017

Fatcat ID

release_l4u7gxywivazhmp7gfbu2dosni

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Fatcat

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https://api.fatcat.wiki/v0/release/l4u7gxywivazhmp7gfbu2dosni

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24 November 2022

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mapped directly with Wikidata item

PMC publication ID

2808595

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15831990

retrieved

28 July 2017

PubMed publication ID

15831990

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15831990

retrieved

28 July 2017

ResearchGate publication ID

7905142

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