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 *

164 related articles for article (PubMed ID: 1656734)

  • 1. Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients.
    Stoppa-Lyonnet D; Duponchel C; Meo T; Laurent J; Carter PE; Arala-Chaves M; Cohen JH; Dewald G; Goetz J; Hauptmann G
    Am J Hum Genet; 1991 Nov; 49(5):1055-62. PubMed ID: 1656734
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements.
    Stoppa-Lyonnet D; Carter PE; Meo T; Tosi M
    Proc Natl Acad Sci U S A; 1990 Feb; 87(4):1551-5. PubMed ID: 2154751
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recombinations between Alu repeat sequences that result in partial deletions within the C1 inhibitor gene.
    Ariga T; Carter PE; Davis AE
    Genomics; 1990 Dec; 8(4):607-13. PubMed ID: 2276734
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular defects of the C1-inhibitor gene in hereditary angioedema.
    Tosi M; Stoppa-Lyonnet D; Carter P; Meo T
    Behring Inst Mitt; 1989 Jul; (84):173-9. PubMed ID: 2572212
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rapid detection by fluorescent multiplex PCR of exon deletions and duplications in the C1 inhibitor gene of hereditary angioedema patients.
    Duponchel C; Di Rocco C; Cicardi M; Tosi M
    Hum Mutat; 2001; 17(1):61-70. PubMed ID: 11139243
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alpha-galactosidase A gene rearrangements causing Fabry disease. Identification of short direct repeats at breakpoints in an Alu-rich gene.
    Kornreich R; Bishop DF; Desnick RJ
    J Biol Chem; 1990 Jun; 265(16):9319-26. PubMed ID: 2160973
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Complete nucleotide sequence of the gene for human C1 inhibitor with an unusually high density of Alu elements.
    Carter PE; Duponchel C; Tosi M; Fothergill JE
    Eur J Biochem; 1991 Apr; 197(2):301-8. PubMed ID: 2026152
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

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

  • 10. A cluster of mutations within a short triplet repeat in the C1 inhibitor gene.
    Bissler JJ; Cicardi M; Donaldson VH; Gatenby PA; Rosen FS; Sheffer AL; Davis AE
    Proc Natl Acad Sci U S A; 1994 Sep; 91(20):9622-5. PubMed ID: 7937817
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Hereditary angioedema caused by a point mutation of exon 7 in the C1 inhibitor gene.
    Ishii N; Ono H; Kawaguchi H; Nakajima H
    Br J Dermatol; 1996 Apr; 134(4):731-3. PubMed ID: 8733381
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Type II hereditary angio-oedema associated with two mutations in one allele of the C1-inhibitor gene around the reactive-site coding region.
    Siddique Z; McPhaden AR; Whaley K
    Hum Hered; 1992; 42(5):298-301. PubMed ID: 1459574
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Altered C1 inhibitor genes in type I hereditary angioedema.
    Stoppa-Lyonnet D; Tosi M; Laurent J; Sobel A; Lagrue G; Meo T
    N Engl J Med; 1987 Jul; 317(1):1-6. PubMed ID: 3587308
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gene mapping strategy for Alu elements rearrangements: Detection of new large deletions in the SERPING1 gene causing hereditary angioedema in Brazilian families.
    Nicolicht P; Faria DOS; Martins-Silva L; Maia LSM; Moreno AS; Arruda LK; Motta AA; Grumach AS; Pesquero JB
    Gene; 2019 Feb; 685():179-185. PubMed ID: 30389558
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The 5' region of the MSH2 gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences.
    Charbonnier F; Baert-Desurmont S; Liang P; Di Fiore F; Martin C; Frerot S; Olschwang S; Wang Q; Buisine MP; Gilbert B; Nilbert M; Lindblom A; Frebourg T
    Hum Mutat; 2005 Sep; 26(3):255-61. PubMed ID: 16086322
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in the C1 inhibitor gene that result in hereditary angioneurotic edema.
    Davis AE; Bissler JJ; Cicardi M
    Behring Inst Mitt; 1993 Dec; (93):313-20. PubMed ID: 8172583
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detection of C1 inhibitor mutations in patients with hereditary angioedema.
    Zuraw BL; Herschbach J
    J Allergy Clin Immunol; 2000 Mar; 105(3):541-6. PubMed ID: 10719305
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A single base deletion from the C1-inhibitor gene causes type I hereditary angio-oedema.
    Siddique Z; McPhaden AR; McCluskey D; Whaley K
    Hum Hered; 1992; 42(4):231-4. PubMed ID: 1339401
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.