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Results: 1-18 |
Results: 18
THE MOLECULAR-BASES OF C6 DEFICIENCY IN THE WESTERN CAPE, SOUTH-AFRICA
Authors: HOBART MJ FERNIE BA FIJEN CAP ORREN A
Citation: Mj. Hobart et al., THE MOLECULAR-BASES OF C6 DEFICIENCY IN THE WESTERN CAPE, SOUTH-AFRICA, Molecular immunology, 35(6-7), 1998, pp. 42-42
PHENOTYPIC HETEROGENEITY OF TERMINAL COMPLEMENT C7 DEFICIENCIES
Authors: WURZNER R DIERICH MP ORREN A
Citation: R. Wurzner et al., PHENOTYPIC HETEROGENEITY OF TERMINAL COMPLEMENT C7 DEFICIENCIES, Molecular immunology, 35(11-12), 1998, pp. 765-765
HETEROGENEITY IN THE GENETIC-BASIS OF HUMAN-COMPLEMENT C9 DEFICIENCY
Authors: WITZELSCHLOMP K HOBART MJ FERNIE BA ORREN A WURZNER R RITTNER C KAUFMANN T SCHNEIDER PM
Citation: K. Witzelschlomp et al., HETEROGENEITY IN THE GENETIC-BASIS OF HUMAN-COMPLEMENT C9 DEFICIENCY, Immunogenetics (New York), 48(2), 1998, pp. 144-147
MOLECULAR-BASES OF C7-DEFICIENCY - 3 DIFFERENT DEFECTS
Authors: FERNIE BA ORREN A SHEEHAN G SCHLESINGER M HOBART MJ
Citation: Ba. Fernie et al., MOLECULAR-BASES OF C7-DEFICIENCY - 3 DIFFERENT DEFECTS, The Journal of immunology, 159(2), 1997, pp. 1019-1026
DNA HAPLOTYPES OF THE COMPLEMENT C6 AND C7 GENES ASSOCIATED WITH DEFICIENCIES OF THE 7TH COMPONENT - AND A NEW DNA POLYMORPHISM IN C7 EXON-13
Authors: FERNIE BA ORREN A SCHLESINGER M WURZNER R PLATONOV AE COOPER RC WILLIAMS YE HOBART MJ
Citation: Ba. Fernie et al., DNA HAPLOTYPES OF THE COMPLEMENT C6 AND C7 GENES ASSOCIATED WITH DEFICIENCIES OF THE 7TH COMPONENT - AND A NEW DNA POLYMORPHISM IN C7 EXON-13, Annals of Human Genetics, 61, 1997, pp. 287-298
COMPLEMENT C6 AND C7 DNA POLYMORPHISMS ANALYZED BY PCR IN 7 ETHNIC-GROUPS AND CHARACTERIZATION OF THE C6 MSPI RFLP
Authors: FERNIE BA FINLAY A PRICE D CHAN E ORREN A JOYSEY VC JOYSEY KA HOBART MJ
Citation: Ba. Fernie et al., COMPLEMENT C6 AND C7 DNA POLYMORPHISMS ANALYZED BY PCR IN 7 ETHNIC-GROUPS AND CHARACTERIZATION OF THE C6 MSPI RFLP, Experimental and clinical immunogenetics, 13(2), 1996, pp. 92-103
MOLECULAR-BASES OF COMBINED SUBTOTAL DEFICIENCIES OF C6 AND C7 - THEIR EFFECTS IN COMBINATION WITH OTHER C6 AND C7 DEFICIENCIES
Authors: FERNIE BA WURZNER R ORREN A MORGAN BP POTTER PC PLATONOV AE VERSHININA IV SHIPULIN GA LACHMANN PJ HOBART MJ
Citation: Ba. Fernie et al., MOLECULAR-BASES OF COMBINED SUBTOTAL DEFICIENCIES OF C6 AND C7 - THEIR EFFECTS IN COMBINATION WITH OTHER C6 AND C7 DEFICIENCIES, The Journal of immunology, 157(8), 1996, pp. 3648-3657
HOW PARTIAL C7 DEFICIENCY WITH CHRONIC AND RECURRENT BACTERIAL-INFECTIONS CAN MIMIC TOTAL C7 DEFICIENCY - TEMPORARY RESTORATION OF HOST C7 LEVELS FOLLOWING PLASMA TRANSFUSION
Authors: WURZNER R PLATONOV AE BELOBORODOV VB PEREVERZEV AI VERSHININA IV FERNIE BA HOBART MJ LACHMANN PJ ORREN A
Citation: R. Wurzner et al., HOW PARTIAL C7 DEFICIENCY WITH CHRONIC AND RECURRENT BACTERIAL-INFECTIONS CAN MIMIC TOTAL C7 DEFICIENCY - TEMPORARY RESTORATION OF HOST C7 LEVELS FOLLOWING PLASMA TRANSFUSION, Immunology, 88(3), 1996, pp. 407-411
A NEW INTRONIC POLYMORPHISM IN THE C7 GENE 36 BP FROM THE COMMON EXPRESSED C7 M N POLYMORPHISM/
Authors: FERNIE BA WURZNER R ORREN A HOBART M
Citation: Ba. Fernie et al., A NEW INTRONIC POLYMORPHISM IN THE C7 GENE 36 BP FROM THE COMMON EXPRESSED C7 M N POLYMORPHISM/, Annals of Human Genetics, 60, 1996, pp. 179-182
MOLECULAR-BASIS OF SUBTOTAL COMPLEMENT C6 DEFICIENCY - A CARBOXY-TERMINALLY TRUNCATED BUT FUNCTIONALLY ACTIVE C6
Authors: WURZNER R HOBART MJ FERNIE BA MEWAR D POTTER PC ORREN A LACHMANN PJ
Citation: R. Wurzner et al., MOLECULAR-BASIS OF SUBTOTAL COMPLEMENT C6 DEFICIENCY - A CARBOXY-TERMINALLY TRUNCATED BUT FUNCTIONALLY ACTIVE C6, The Journal of clinical investigation, 95(4), 1995, pp. 1877-1883
COMPLEMENT COMPONENT C6 AND C7 HAPLOTYPES ASSOCIATED WITH DEFICIENCIES OF C6
Authors: FERNIE BA ORREN A WURZNER R JONES AM POTTER PC LACHMANN PJ HOBART MJ
Citation: Ba. Fernie et al., COMPLEMENT COMPONENT C6 AND C7 HAPLOTYPES ASSOCIATED WITH DEFICIENCIES OF C6, Annals of Human Genetics, 59, 1995, pp. 183-195
A NOVEL HUMAN-COMPLEMENT COMPONENT C7 PHENOTYPE DETECTED IN SOUTH-AFRICA AND PROPOSED DESIGNATION OF THE ALLELE AS C7(ASTERISK)10
Authors: ORREN A WURZNER R LACHMANN PJ HOBART MJ
Citation: A. Orren et al., A NOVEL HUMAN-COMPLEMENT COMPONENT C7 PHENOTYPE DETECTED IN SOUTH-AFRICA AND PROPOSED DESIGNATION OF THE ALLELE AS C7(ASTERISK)10, European journal of immunogenetics, 21(3), 1994, pp. 181-187
HEREDITARY-DEFICIENCY OF THE 7TH COMPONENT OF COMPLEMENT AND RECURRENT MENINGOCOCCAL INFECTION - INVESTIGATIONS OF AN IRISH FAMILY USING A NOVEL HEMOLYTIC SCREENING ASSAY FOR COMPLEMENT ACTIVITY AND C7 M N ALLOTYPING/
Authors: EGAN LJ ORREN A DOHERTY J WURZNER R MCCARTHY CF
Citation: Lj. Egan et al., HEREDITARY-DEFICIENCY OF THE 7TH COMPONENT OF COMPLEMENT AND RECURRENT MENINGOCOCCAL INFECTION - INVESTIGATIONS OF AN IRISH FAMILY USING A NOVEL HEMOLYTIC SCREENING ASSAY FOR COMPLEMENT ACTIVITY AND C7 M N ALLOTYPING/, Epidemiology and infection, 113(2), 1994, pp. 275-281
CHARACTERIZATION OF STRAINS OF NEISSERIA-MENINGITIDIS RECOVERED FROM COMPLEMENT-SUFFICIENT AND COMPLEMENT-DEFICIENT PATIENTS IN THE WESTERNCAPE PROVINCE, SOUTH-AFRICA
Authors: ORREN A CAUGANT DA FIJEN CAP DANKERT J VANSCHALKWYK EJ POOLMAN JT COETZEE GJ
Citation: A. Orren et al., CHARACTERIZATION OF STRAINS OF NEISSERIA-MENINGITIDIS RECOVERED FROM COMPLEMENT-SUFFICIENT AND COMPLEMENT-DEFICIENT PATIENTS IN THE WESTERNCAPE PROVINCE, SOUTH-AFRICA, Journal of clinical microbiology, 32(9), 1994, pp. 2185-2191
PARADOXICAL RECONSTITUTION OF COMPLEMENT ACTIVITY FOLLOWING PLASMA TRANSFUSION OF AN INDIVIDUAL WITH DEFICIENCY OF THE 7TH-COMPONENT OF COMPLEMENT
Authors: PLATONOV AE WURZNER R BELOBORODOV VB JONES AM TROSHANSKY DV VERSHININA IV LACHMANN PJ ORREN A
Citation: Ae. Platonov et al., PARADOXICAL RECONSTITUTION OF COMPLEMENT ACTIVITY FOLLOWING PLASMA TRANSFUSION OF AN INDIVIDUAL WITH DEFICIENCY OF THE 7TH-COMPONENT OF COMPLEMENT, Immunology, 81(1), 1994, pp. 142-148
C6 HAPLOTYPES - ASSOCIATIONS OF A DDE-I SITE POLYMORPHISM TO COMPLEMENT DEFICIENCY GENES AND THE MSP-I RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM (RFLP) (VOL 95, PG 351, 1994)
Authors: FERNIE BA HOBART MJ DELBRIDGE G POTTER PC ORREN A LACHMANN PJ
Citation: Ba. Fernie et al., C6 HAPLOTYPES - ASSOCIATIONS OF A DDE-I SITE POLYMORPHISM TO COMPLEMENT DEFICIENCY GENES AND THE MSP-I RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM (RFLP) (VOL 95, PG 351, 1994), Clinical and experimental immunology, 98(1), 1994, pp. 174-174
C6 HAPLOTYPES - ASSOCIATIONS OF A DDE-I SITE POLYMORPHISM TO COMPLEMENT DEFICIENCY GENES AND THE MSP-I RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM (RFLP)
Authors: FERNIE BA HOBART MJ DELBRIDGE G POTTER PC ORREN A LACHMANN PJ
Citation: Ba. Fernie et al., C6 HAPLOTYPES - ASSOCIATIONS OF A DDE-I SITE POLYMORPHISM TO COMPLEMENT DEFICIENCY GENES AND THE MSP-I RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM (RFLP), Clinical and experimental immunology, 95(2), 1994, pp. 351-356
ASSOCIATION OF A 12.5-KILOBASE ALLELE OF THE MSPI RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM OF THE C6-GENE IN PATIENTS WITH TOTAL DEFICIENCYOF THE 6TH COMPONENT OF COMPLEMENT
Authors: POTTER PC WARBURTON C WURZNER R ORREN A DISCIPIO R
Citation: Pc. Potter et al., ASSOCIATION OF A 12.5-KILOBASE ALLELE OF THE MSPI RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM OF THE C6-GENE IN PATIENTS WITH TOTAL DEFICIENCYOF THE 6TH COMPONENT OF COMPLEMENT, Experimental and clinical immunogenetics, 10(1), 1993, pp. 38-44
Risultati: 1-18 |