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Results: 1-25 | 26-27
Results: 1-25/27
C7 DEFICIENCY - 7 FURTHER MOLECULAR DEFECTS AND THEIR ASSOCIATED MARKER HAPLOTYPES, INCLUDING 5 NEW POLYMORPHISMS
Authors: FERNIE BA HOBART MJ
Citation: Ba. Fernie et Mj. Hobart, C7 DEFICIENCY - 7 FURTHER MOLECULAR DEFECTS AND THEIR ASSOCIATED MARKER HAPLOTYPES, INCLUDING 5 NEW POLYMORPHISMS, Molecular immunology, 35(6-7), 1998, pp. 41-41
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
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
AN UNUSUAL COMBINED INSERTION DELETION POLYMORPHISM IN INTRON-10 OF THE HUMAN-COMPLEMENT C6 GENE/
Authors: FERNIE BA HOBART MJ
Citation: Ba. Fernie et Mj. Hobart, AN UNUSUAL COMBINED INSERTION DELETION POLYMORPHISM IN INTRON-10 OF THE HUMAN-COMPLEMENT C6 GENE/, Human genetics, 100(1), 1997, pp. 104-108
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
THE HUMAN-COMPLEMENT C9 GENE - IDENTIFICATION OF 2 MUTATIONS CAUSING DEFICIENCY AND REVISION OF THE GENE STRUCTURE
Authors: WITZELSCHLOMP K SPATH PJ HOBART MJ FERNIE BA RITTNER C KAUFMANN T SCHNEIDER PM
Citation: K. Witzelschlomp et al., THE HUMAN-COMPLEMENT C9 GENE - IDENTIFICATION OF 2 MUTATIONS CAUSING DEFICIENCY AND REVISION OF THE GENE STRUCTURE, The Journal of immunology, 158(10), 1997, pp. 5043-5049
DIFFICULTIES IN THE ASCERTAINMENT OF C9 DEFICIENCY - LESSONS TO BE DRAWN FROM A COMPOUND HETEROZYGOTE C9-DEFICIENT SUBJECT
Authors: HOBART MJ FERNIE BA WURZNER R OLDROYD RG HARRISON RA JOYSEY V LACHMANN PJ
Citation: Mj. Hobart et al., DIFFICULTIES IN THE ASCERTAINMENT OF C9 DEFICIENCY - LESSONS TO BE DRAWN FROM A COMPOUND HETEROZYGOTE C9-DEFICIENT SUBJECT, Clinical and experimental immunology, 108(3), 1997, pp. 500-506
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
PHYSICAL LINKAGE AND ORIENTATION OF THE HUMAN-COMPLEMENT C8-ALPHA ANDC8-BETA GENES ON CHROMOSOME 1P32
Authors: PLATTEBORZE PL HOBART MJ SODETZ JM
Citation: Pl. Platteborze et al., PHYSICAL LINKAGE AND ORIENTATION OF THE HUMAN-COMPLEMENT C8-ALPHA ANDC8-BETA GENES ON CHROMOSOME 1P32, Human genetics, 98(4), 1996, pp. 443-446
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
STUDY OF THE IN-VITRO ACTIVATION OF THE COMPLEMENT ALTERNATIVE PATHWAY BY ECHINOCOCCUS-GRANULOSUS HYDATID CYST FLUID
Authors: FERREIRA AM WURZNER R HOBART MJ LACHMANN PJ
Citation: Am. Ferreira et al., STUDY OF THE IN-VITRO ACTIVATION OF THE COMPLEMENT ALTERNATIVE PATHWAY BY ECHINOCOCCUS-GRANULOSUS HYDATID CYST FLUID, Parasite immunology, 17(5), 1995, pp. 245-251
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/
Authors: WURZNER R FERNIE BA JONES AM LACHMANN PJ HOBART MJ
Citation: R. Wurzner et al., 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/, The Journal of immunology, 154(9), 1995, pp. 4813-4819
STRUCTURE OF THE HUMAN C7 GENE AND COMPARISON WITH THE C6, C8A, C8B, AND C9 GENES
Authors: HOBART MJ FERNIE BA DISCIPIO RG
Citation: Mj. Hobart et al., STRUCTURE OF THE HUMAN C7 GENE AND COMPARISON WITH THE C6, C8A, C8B, AND C9 GENES, The Journal of immunology, 154(10), 1995, pp. 5188-5194
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
IMPORTANCE OF THE 3RD THROMBOSPONDIN REPEAT OF C6 FOR TERMINAL COMPLEMENT COMPLEX ASSEMBLY
Authors: WURZNER R MEWAR D FERNIE BA HOBART MJ LACHMANN PJ
Citation: R. Wurzner et al., IMPORTANCE OF THE 3RD THROMBOSPONDIN REPEAT OF C6 FOR TERMINAL COMPLEMENT COMPLEX ASSEMBLY, Immunology, 85(2), 1995, pp. 214-219
DNA POLYMORPHISMS OF THE COMPLEMENT C6 AND C7 GENES (VOL 59, PG 163, 1995)
Authors: FERNIE BA WURZNER R UNSWORTH DJ TUXWORTH RI HOBART MJ
Citation: Ba. Fernie et al., DNA POLYMORPHISMS OF THE COMPLEMENT C6 AND C7 GENES (VOL 59, PG 163, 1995), Annals of Human Genetics, 59, 1995, pp. 337-337
DNA POLYMORPHISMS OF THE COMPLEMENT C6 AND C7 GENES
Authors: FERNIE BA WURZNER R UNSWORTH DJ TUXWORTH RI HOBART MJ
Citation: Ba. Fernie et al., DNA POLYMORPHISMS OF THE COMPLEMENT C6 AND C7 GENES, Annals of Human Genetics, 59, 1995, pp. 163-181
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
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
A PHYSICAL MAP OF THE C6 AND C7 COMPLEMENT COMPONENT GENE REGION ON CHROMOSOME-5P13
Authors: HOBART MJ FERNIE BA DISCIPIO RG LACHMANN PJ
Citation: Mj. Hobart et al., A PHYSICAL MAP OF THE C6 AND C7 COMPLEMENT COMPONENT GENE REGION ON CHROMOSOME-5P13, Human molecular genetics, 2(7), 1993, pp. 1035-1036
CORRELATION OF A GLU ALA SUBSTITUTION AT POSITION 98 WITH THE COMPLEMENT C6 A B PHENOTYPES/
Authors: FERNIE BA DELBRIDGE G HOBART MJ
Citation: Ba. Fernie et al., CORRELATION OF A GLU ALA SUBSTITUTION AT POSITION 98 WITH THE COMPLEMENT C6 A B PHENOTYPES/, Human molecular genetics, 2(5), 1993, pp. 591-592
Risultati: 1-25 | 26-27