Molecular mechanisms of complement component C6 deficiency; a hypervariable exon 6 region responsible for three of six reported defects (Q73348091)

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scientific article published on 01 February 2000

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English	Molecular mechanisms of complement component C6 deficiency; a hypervariable exon 6 region responsible for three of six reported defects	scientific article published on 01 February 2000

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scholarly article

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Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

editorial

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review article

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Europe PubMed Central

title

Molecular mechanisms of complement component C6 deficiency; a hypervariable exon 6 region responsible for three of six reported defects (English)

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stated in

Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

author name string

A Orren

series ordinal

1

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Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

publication date

1 February 2000

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stated in

Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

published in

Clinical and Experimental Immunology

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stated in

Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

volume

119

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stated in

Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

page(s)

255-258

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stated in

Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

cites work

High prevalence of complement component C6 deficiency among African-Americans in the south-eastern USA.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neisseria meningitidis and Neisseria gonorrhoeae Bacteremia Associated with C6, C7, or C8 Deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement deficiency states and infection: epidemiology, pathogenesis and consequences of neisserial and other infections in an immune deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of the sixth component of complement and susceptibility to Neisseria meningitidis infections: studies in 10 families and five isolated cases

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heberden oration 1986. Complement--friend or foe?

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement deficiencies in patients over ten years old with meningococcal disease due to uncommon serogroups

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited deficiencies of the late-acting complement components other than C9 found among healthy blood donors

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high incidence of C9 deficiency among healthy blood donors in Osaka, Japan

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infectious diseases associated with complement deficiencies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Properties of a low molecular weight complement component C6 found in human subjects with subtotal C6 deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited deficiencies of the terminal components of human complement

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meningococcal disease in patients with late complement component deficiency: studies in the U.S.S.R.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of strains of Neisseria meningitidis recovered from complement-sufficient and complement-deficient patients in the Western Cape Province, South Africa.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of subtotal complement C6 deficiency. A carboxy-terminally truncated but functionally active C6.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement component C6 and C7 haplotypes associated with deficiencies of C6.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular bases for inherited human complement component C6 deficiency in two unrelated individuals

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous C8beta complement deficiency does not predispose to meningococcal disease.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular defects leading to human complement component C6 deficiency in an African-American family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vaccination against meningococcus in complement-deficient individuals.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protection against meningococcal serogroup ACYW disease in complement-deficient individuals vaccinated with the tetravalent meningococcal capsular polysaccharide vaccine.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of C6 deficiency in the western Cape, South Africa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Blood group gene frequencies. An indication of the genetic constitution of population samples in Cape Town

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10632659

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1046/J.1365-2249.2000.01141.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

PMC publication ID

1905514

0 references

PubMed publication ID

10632659

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10632659

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10632659%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 November 2019

 

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