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South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
March 31, 1979
Serum complement concentrations, nutritional status and the outcome of measles and measles pneumonia
A Orren, A Kipps, E B Dowdle, et al.
Clinical and Experimental Immunology
|
April 4, 2017
Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub-Saharan Africa: implications for the susceptibility to meningococcal disease
C Franco-Jarava, D Comas, A Orren, et al.
Epidemiology and Infection
|
October 1, 1994
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
L J Egan, A Orren, J Doherty, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1993
Association of a 12.5-kilobase allele of the MspI restriction fragment length polymorphism of the C6 gene in patients with total deficiency of the sixth component of complement
P C Potter, C Warburton, R Würzner, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 15, 1997
Molecular bases of C7 deficiency: three different defects
B A Fernie, A Orren, G Sheehan, et al.
Immunogenetics
|
January 1, 1988
Allotypes of mouse complement component C6 in inbred strains and some wild populations
A Orren, J Hayakawa, J E Johnson, et al.
Molecular Immunology
|
December 31, 2011
Characterization of a large genomic deletion in four Irish families with C7 deficiency
A D Thomas, A Orren, J Connaughton, et al.
Clinical and Experimental Immunology
|
September 1, 1992
C7 M/N protein polymorphism typing applied to inherited deficiencies of human complement proteins C6 and C7
R Würzner, N Rance, P C Potter, et al.
Experimental and Clinical Immunogenetics
|
March 11, 1999
Reference typing report for complement components C6, C7 and C9 including mutations leading to deficiencies
R Würzner, K Witzel-Schlömp, K Tokunaga, et al.
Clinical and Experimental Immunology
|
February 1, 1994
C6 haplotypes: associations of a Dde I site polymorphism to complement deficiency genes and the Msp I restriction fragment length polymorphism (RFLP)
B A Fernie, M J Hobart, G Delbridge, et al.
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of 5
Search research articles
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Showing results (21-30 of 49) with videos related to
Sort By:
Page
of 5
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
March 31, 1979
Serum complement concentrations, nutritional status and the outcome of measles and measles pneumonia
A Orren, A Kipps, E B Dowdle, et al.
Clinical and Experimental Immunology
|
April 4, 2017
Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub-Saharan Africa: implications for the susceptibility to meningococcal disease
C Franco-Jarava, D Comas, A Orren, et al.
Epidemiology and Infection
|
October 1, 1994
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
L J Egan, A Orren, J Doherty, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1993
Association of a 12.5-kilobase allele of the MspI restriction fragment length polymorphism of the C6 gene in patients with total deficiency of the sixth component of complement
P C Potter, C Warburton, R Würzner, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 15, 1997
Molecular bases of C7 deficiency: three different defects
B A Fernie, A Orren, G Sheehan, et al.
Immunogenetics
|
January 1, 1988
Allotypes of mouse complement component C6 in inbred strains and some wild populations
A Orren, J Hayakawa, J E Johnson, et al.
Molecular Immunology
|
December 31, 2011
Characterization of a large genomic deletion in four Irish families with C7 deficiency
A D Thomas, A Orren, J Connaughton, et al.
Clinical and Experimental Immunology
|
September 1, 1992
C7 M/N protein polymorphism typing applied to inherited deficiencies of human complement proteins C6 and C7
R Würzner, N Rance, P C Potter, et al.
Experimental and Clinical Immunogenetics
|
March 11, 1999
Reference typing report for complement components C6, C7 and C9 including mutations leading to deficiencies
R Würzner, K Witzel-Schlömp, K Tokunaga, et al.
Clinical and Experimental Immunology
|
February 1, 1994
C6 haplotypes: associations of a Dde I site polymorphism to complement deficiency genes and the Msp I restriction fragment length polymorphism (RFLP)
B A Fernie, M J Hobart, G Delbridge, et al.
Page
of 5