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 *

197 related articles for article (PubMed ID: 1885769)

  • 1. Nonsense mutations affect C1 inhibitor messenger RNA levels in patients with type I hereditary angioneurotic edema.
    Frangi D; Cicardi M; Sica A; Colotta F; Agostoni A; Davis AE
    J Clin Invest; 1991 Sep; 88(3):755-9. PubMed ID: 1885769
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Normal C1 inhibitor mRNA expression level in type I hereditary angioedema patients: newly found C1 inhibitor gene mutations.
    Kang HR; Yim EY; Oh SY; Chang YS; Kim YK; Cho SH; Min KU; Kim YY
    Allergy; 2006 Feb; 61(2):260-4. PubMed ID: 16409206
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation screening of the C1 inhibitor gene among Hungarian patients with hereditary angioedema.
    Kalmár L; Bors A; Farkas H; Vas S; Fandl B; Varga L; Füst G; Tordai A
    Hum Mutat; 2003 Dec; 22(6):498. PubMed ID: 14635117
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.
    Cicardi M; Igarashi T; Rosen FS; Davis AE
    J Clin Invest; 1987 Mar; 79(3):698-702. PubMed ID: 3818946
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Type II hereditary angioneurotic edema that may result from a single nucleotide change in the codon for alanine-436 in the C1 inhibitor gene.
    Levy NJ; Ramesh N; Cicardi M; Harrison RA; Davis AE
    Proc Natl Acad Sci U S A; 1990 Jan; 87(1):265-8. PubMed ID: 2296585
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Transinhibition of C1 inhibitor synthesis in type I hereditary angioneurotic edema.
    Kramer J; Rosen FS; Colten HR; Rajczy K; Strunk RC
    J Clin Invest; 1993 Mar; 91(3):1258-62. PubMed ID: 8450054
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Restriction fragment length polymorphism of the C1 inhibitor gene in hereditary angioneurotic edema.
    Cicardi M; Igarashi T; Kim MS; Frangi D; Agostoni A; Davis AE
    J Clin Invest; 1987 Dec; 80(6):1640-3. PubMed ID: 2890659
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Type I C1 inhibitor deficiency with a small messenger RNA resulting from deletion of one exon.
    Ariga T; Igarashi T; Ramesh N; Parad R; Cicardi M; Davis AE
    J Clin Invest; 1989 Jun; 83(6):1888-93. PubMed ID: 2723063
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A mutation unique in serine protease inhibitors (serpins) identified in a family with type II hereditary angioneurotic edema.
    Ocejo-Vinyals JG; Leyva-Cobián F; Fernández-Luna JL
    Mol Med; 1995 Sep; 1(6):700-5. PubMed ID: 8529136
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dysfunctional C1 inhibitor Ta: deletion of Lys-251 results in acquisition of an N-glycosylation site.
    Parad RB; Kramer J; Strunk RC; Rosen FS; Davis AE
    Proc Natl Acad Sci U S A; 1990 Sep; 87(17):6786-90. PubMed ID: 2118657
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I hereditary angioedema.
    Freiberger T; Kolárová L; Mejstrík P; Vyskocilová M; Kuklínek P; Litzman J
    Hum Mutat; 2002 Apr; 19(4):461. PubMed ID: 11933207
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation in exon 8 of C1 inhibitor (C1INH) gene leads to abolish its physiological stop codon in a large Chinese family with hereditary angioedema type I.
    Qu L; Wei B; Liu M; Zhang L; Xiao T; Chen HD; Zhou L; Mi QS; He C
    Exp Dermatol; 2012 Oct; 21(10):788-91. PubMed ID: 22882460
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A point mutation in exon 7 of the C1-inhibitor gene causing type I hereditary angioedema.
    Ono H; Kawaguchi H; Ishii N; Nakajima H
    Hum Genet; 1996 Oct; 98(4):452-3. PubMed ID: 8792821
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema.
    Quastel M; Harrison R; Cicardi M; Alper CA; Rosen FS
    J Clin Invest; 1983 Apr; 71(4):1041-6. PubMed ID: 6833491
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular defects in hereditary angioneurotic edema.
    Bissler JJ; Aulak KS; Donaldson VH; Rosen FS; Cicardi M; Harrison RA; Davis AE
    Proc Assoc Am Physicians; 1997 Mar; 109(2):164-73. PubMed ID: 9069585
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family.
    Ferraro MF; Moreno AS; Castelli EC; Donadi EA; Palma MS; Arcuri HA; Lange AP; Bork K; Sarti W; Arruda LK
    Allergy; 2011 Oct; 66(10):1384-90. PubMed ID: 21623829
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Contiguous deletion and duplication mutations resulting in type 1 hereditary angioneurotic edema.
    Bissler JJ; Donaldson VH; Davis AE
    Hum Genet; 1994 Mar; 93(3):265-9. PubMed ID: 8125476
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A review of the reported defects in the human C1 esterase inhibitor gene producing hereditary angioedema including four new mutations.
    Bowen B; Hawk JJ; Sibunka S; Hovick S; Weiler JM
    Clin Immunol; 2001 Feb; 98(2):157-63. PubMed ID: 11161971
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Impaired production of both normal and mutant C1 inhibitor proteins in type I hereditary angioedema with a duplication in exon 8.
    Ernst SC; Circolo A; Davis AE; Gheesling-Mullis K; Fliesler M; Strunk RC
    J Immunol; 1996 Jul; 157(1):405-10. PubMed ID: 8683145
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedema.
    Gösswein T; Kocot A; Emmert G; Kreuz W; Martinez-Saguer I; Aygören-Pürsün E; Rusicke E; Bork K; Oldenburg J; Müller CR
    Cytogenet Genome Res; 2008; 121(3-4):181-8. PubMed ID: 18758157
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.