(Q77650371)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9844043%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

title

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

1 reference

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7 December 2019

author name string

A M O'Hara

1

1 reference

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7 December 2019

B A Fernie

2

1 reference

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7 December 2019

A P Moran

3

1 reference

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7 December 2019

Y E Williams

4

1 reference

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7 December 2019

J J Connaughton

5

1 reference

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7 December 2019

A Orren

6

1 reference

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7 December 2019

M J Hobart

7

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7 December 2019

publication date

1 December 1998

1 reference

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Clinical and Experimental Immunology

7 December 2019

published in

1 reference

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7 December 2019

volume

114

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7 December 2019

issue

3

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7 December 2019

page(s)

355-361

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TaqI polymorphism in the complement component C7 gene

7 December 2019

cites work

1 reference

12 December 2020

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

1 reference

12 December 2020

DNA polymorphisms and linkage relationship of the human complement component C6, C7, and C9 genes

1 reference

12 December 2020

Inherited deficiencies of the terminal components of human complement

1 reference

12 December 2020

A novel protein polymorphism of human complement C7 detected by a monoclonal antibody

1 reference

12 December 2020

Correlation of a Glu/Ala substitution at position 98 with the complement C6 A/B phenotypes

1 reference

12 December 2020

Polymorphism of Human Complement Component C6: An Amino Acid Substitution (GLU/ALA) within the Second Thrombospondin Repeat Differentiates between the Two Common Allotypes C6A and C6B

1 reference

12 December 2020

A physical map of the human complement component C6, C7, and C9 genes

1 reference

12 December 2020

A physical map of the C6 and C7 complement component gene region on chromosome 5p13.

1 reference

12 December 2020

Hereditary deficiency of the seventh component of complement and recurrent meningococcal infection: investigations of an Irish family using a novel haemolytic screening assay for complement activity and C7 M/N allotyping

1 reference

12 December 2020

A common Ser/Thr polymorphism in the perforin-homologous region of human complement component C7

1 reference

12 December 2020

Molecular basis of the complement C7 M/N polymorphism. A neutral amino acid substitution outside the epitope of the allospecific monoclonal antibody WU 4-15.

1 reference

12 December 2020

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

1 reference

12 December 2020

DNA polymorphisms of the complement C6 and C7 genes

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A new intronic polymorphism in the C7 gene 36 bp from the common expressed C7 M/N polymorphism

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic bases of human complement C7 deficiency

1 reference

12 December 2020

Complement C6 and C7 DNA polymorphisms analysed by PCR in seven ethnic groups and characterisation of the C6 MspI RFLP.

1 reference

12 December 2020

Heterozygous C8beta complement deficiency does not predispose to meningococcal disease.

1 reference

12 December 2020

Molecular bases of C7 deficiency: three different defects.

1 reference

12 December 2020

DNA haplotypes of the complement C6 and C7 genes associated with deficiencies of the seventh component; and a new DNA polymorphism in C7 exon 13

1 reference

12 December 2020

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

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Enhanced autoradiographic detection of 32P and 125I using intensifying screens and hypersensitized film

1 reference

12 December 2020

DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man

1 reference

12 December 2020

Ultrasensitive stain for proteins in polyacrylamide gels shows regional variation in cerebrospinal fluid proteins

1 reference

12 December 2020

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

1 reference

12 December 2020

The membrane attack complex of complement

1 reference

12 December 2020

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

12 December 2020

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

1 reference

12 December 2020

Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1046/J.1365-2249.1998.00737.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9844043%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

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