These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 9670930)

  • 1. A novel type II complement C2 deficiency allele in an African-American family.
    Zhu ZB; Atkinson TP; Volanakis JE
    J Immunol; 1998 Jul; 161(2):578-84. PubMed ID: 9670930
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing.
    Johnson CA; Densen P; Hurford RK; Colten HR; Wetsel RA
    J Biol Chem; 1992 May; 267(13):9347-53. PubMed ID: 1577763
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular heterogeneity in deficiency of complement protein C2 type I.
    Wang X; Circolo A; Lokki ML; Shackelford PG; Wetsel RA; Colten HR
    Immunology; 1998 Feb; 93(2):184-91. PubMed ID: 9616367
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretion.
    Wetsel RA; Kulics J; Lokki ML; Kiepiela P; Akama H; Johnson CA; Densen P; Colten HR
    J Biol Chem; 1996 Mar; 271(10):5824-31. PubMed ID: 8621452
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevalence of a mutation causing C2 deficiency in systemic lupus erythematosus.
    Sullivan KE; Petri MA; Schmeckpeper BJ; McLean RH; Winkelstein JA
    J Rheumatol; 1994 Jun; 21(6):1128-33. PubMed ID: 7932427
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Serologic studies in a family with heterozygous C2 deficiency.
    McCarty DJ; Tan EM; Zvaifler NJ; Koethe S; Duquesnoy RJ
    Am J Med; 1981 Dec; 71(6):945-8. PubMed ID: 6797295
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular defects leading to human complement component C6 deficiency in an African-American family.
    Zhu ZB; Totemchokchyakarn K; Atkinson TP; Volanakis JE
    Clin Exp Immunol; 1998 Jan; 111(1):91-6. PubMed ID: 9472666
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Combined heterozygous deficiency of the classical complement pathway proteins C2 and C4.
    Hartmann D; Fremeaux-Bacchi V; Weiss L; Meyer A; Blouin J; Hauptmann G; Kazatchkine M; Uring-Lambert B
    J Clin Immunol; 1997 Mar; 17(2):176-84. PubMed ID: 9083894
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Simultaneous occurrence of hereditary C6 and C2 deficiency in a French-Canadian family.
    Delâge JM; Lehner-Netsch G; Lafleur R; Simard J; Brun G; Prochazka E
    Immunology; 1979 Jun; 37(2):419-28. PubMed ID: 468307
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evidence for a silent or null gene in hereditary C2 deficiency.
    Pariser KM; Raum D; Berkman EM; Alper CA; Agnello V
    J Immunol; 1978 Dec; 121(6):2580-1. PubMed ID: 722085
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Selective deficiencies in complement component : a family with hereditary C2 deficiency.
    Dantant M; Rivat C; Gilbert D; Fontaine M; Cavelier B; Godin M; Fillastre JP
    Biomedicine; 1978; 28(3):185-90. PubMed ID: 698338
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Subacute cutaneous lupus erythematosus in multiple members of a family with C2 deficiency.
    Callen JP; Hodge SJ; Kulick KB; Stelzer G; Buchino JJ
    Arch Dermatol; 1987 Jan; 123(1):66-70. PubMed ID: 3467658
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Frequency in Spanish population of familial complement factor 2 type I deficits and associated HLA haplotypes.
    Antolín SC; Del Rey Cerros MJ; Sierra EM; Miñarro DO; Clemente J; Martínez LA; Peña PV; Panete MJ; Pérez PM; Paz-Artal E
    Hum Immunol; 2005 Oct; 66(10):1093-8. PubMed ID: 16386652
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system.
    Venneker GT; van Meegen M; de Kok-Nazaruk M; Hulsmans RF; de Waall LP; Bos JD; Asghar SS
    Exp Clin Immunogenet; 1996; 13(2):104-11. PubMed ID: 9063702
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inherited deficiency of second component of complement and HLA haplotype A10,B18 associated with inflammatory bowel disease.
    Slade JD; Luskin AT; Gewurz H; Kraft SC; Kirsner JB; Zeitz HJ
    Ann Intern Med; 1978 Jun; 88(6):796-8. PubMed ID: 666136
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular bases for inherited human complement component C6 deficiency in two unrelated individuals.
    Nishizaka H; Horiuchi T; Zhu ZB; Fukumori Y; Nagasawa K; Hayashi K; Krumdieck R; Cobbs CG; Higuchi M; Yasunaga S; Niho Y; Volanakis JE
    J Immunol; 1996 Mar; 156(6):2309-15. PubMed ID: 8690922
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Studies on the C2-deficiency gene in man.
    Mortensen JP; Buskjaer L; Lamm LU
    Immunology; 1980 Apr; 39(4):541-9. PubMed ID: 7380478
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Renal transplantation in a patient with hereditary deficiency of the second component of complement.
    Zeitz HJ; Gewurz A; Jonasson O; Geis WP; Gewurz H
    Clin Exp Immunol; 1981 Nov; 46(2):420-4. PubMed ID: 7039890
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deficiency of C2, the second complement component, in the family of a patient with SLE-like syndrome: the first case of hereditary C2 deficiency in Czechoslovakia.
    Starsia Z; Zitnan D; Loos M; Stefanovic J; Bosák V; Niks M; Tomanová H; Lukác J; Lulovicová M
    Haematologia (Budap); 1987; 20(4):215-20. PubMed ID: 3428724
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of mutations and polymorphisms in the factor XI genes of an African American family by dideoxyfingerprinting.
    Martincic D; Zimmerman SA; Ware RE; Sun MF; Whitlock JA; Gailani D
    Blood; 1998 Nov; 92(9):3309-17. PubMed ID: 9787168
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.