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 *

80 related articles for article (PubMed ID: 9579556)

  • 1. A novel donor splice site mutation in the C1 inhibitor gene of a patient with type I hereditary angioneurotic edema.
    Kawachi Y; Hibi T; Yamazaki S; Otsuka F
    J Invest Dermatol; 1998 May; 110(5):837-9. PubMed ID: 9579556
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An RNA splice site mutation in the C1-inhibitor gene causes type I hereditary angio-oedema.
    Siddique Z; McPhaden AR; Lappin DF; Whaley K
    Hum Genet; 1991 Dec; 88(2):231-2. PubMed ID: 1684567
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel RNA splice site mutation in the C1 inhibitor gene of a patient with type I hereditary angioedema.
    Sekijima Y; Hashimoto T; Kawachi Y; Koshihara H; Otsuka F; Ikeda S
    Intern Med; 2004 Mar; 43(3):253-5. PubMed ID: 15098611
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Identification and characterization of a novel splice site mutation in the SERPING1 gene in a family with hereditary angioedema.
    Colobran R; Lois S; de la Cruz X; Pujol-Borrell R; Hernández-González M; Guilarte M
    Clin Immunol; 2014 Feb; 150(2):143-8. PubMed ID: 24412907
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Molecular genetics of C1 inhibitor.
    Tosi M
    Immunobiology; 1998 Aug; 199(2):358-65. PubMed ID: 9777419
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. A de novo deletion in the C1 inhibitor gene in a case of sporadic hereditary angioneurotic edema.
    Ariga T; Hoshioka A; Kohno Y; Sakamaki T; Matsumoto S
    Clin Immunol Immunopathol; 1993 Oct; 69(1):103-5. PubMed ID: 8403537
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. [Identification of a novel mutation of C1 inhibitor gene in a Chinese family with hereditary angioedema].
    Zhi YX; Zhang HY; Huang SZ
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Dec; 25(6):664-6. PubMed ID: 14714307
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.