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 *

136 related articles for article (PubMed ID: 8476848)

  • 1. Complete nucleotide sequence of the antithrombin gene: evidence for homologous recombination causing thrombophilia.
    Olds RJ; Lane DA; Chowdhury V; De Stefano V; Leone G; Thein SL
    Biochemistry; 1993 Apr; 32(16):4216-24. PubMed ID: 8476848
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Major structural defects in the antithrombin gene in four families with type I antithrombin deficiency--partial/complete deletions and rearrangement of the antithrombin gene.
    Beauchamp NJ; Makris M; Preston FE; Peake IR; Daly ME
    Thromb Haemost; 2000 May; 83(5):715-21. PubMed ID: 10823268
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Type I antithrombin deficiency due to 13389G deletion in antithrombin gene].
    Fu Q; Xu X; Ding Q; Hu Y; Wang X; Wang H
    Zhonghua Xue Ye Xue Za Zhi; 2002 Nov; 23(11):588-90. PubMed ID: 12482344
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular basis of inherited antithrombin deficiency in Portuguese families: identification of genetic alterations and screening for additional thrombotic risk factors.
    David D; Ribeiro S; Ferrão L; Gago T; Crespo F
    Am J Hematol; 2004 Jun; 76(2):163-71. PubMed ID: 15164384
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 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. Low-density lipoprotein receptor mutation that deletes exons 2 and 3 by Alu-Alu recombination.
    Kigawa K; Kihara K; Miyake Y; Tajima S; Funahashi T; Yamamura T; Yamamoto A
    J Biochem; 1993 Mar; 113(3):372-6. PubMed ID: 8486609
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A deletion/insertion leading to the generation of a direct repeat as a result of slipped mispairing and intragenic recombination in the factor VIII gene.
    Tavassoli K; Eigel A; Horst J
    Hum Genet; 1999 May; 104(5):435-7. PubMed ID: 10394938
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Antithrombin and its inherited deficiencies.
    Perry DJ
    Blood Rev; 1994 Mar; 8(1):37-55. PubMed ID: 8205009
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Antithrombin and its deficiency states.
    Lane DA; Olds RR; Thein SL
    Blood Coagul Fibrinolysis; 1992 Jun; 3(3):315-41. PubMed ID: 1643210
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nucleotide sequence of the gene for the b subunit of human factor XIII.
    Bottenus RE; Ichinose A; Davie EW
    Biochemistry; 1990 Dec; 29(51):11195-209. PubMed ID: 2271707
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency.
    Picard V; Chen JM; Tardy B; Aillaud MF; Boiteux-Vergnes C; Dreyfus M; Emmerich J; Lavenu-Bombled C; Nowak-Göttl U; Trillot N; Aiach M; Alhenc-Gelas M
    Hum Genet; 2010 Jan; 127(1):45-53. PubMed ID: 19760264
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Adenosine deaminase (ADA) deficiency due to deletion of the ADA gene promoter and first exon by homologous recombination between two Alu elements.
    Markert ML; Hutton JJ; Wiginton DA; States JC; Kaufman RE
    J Clin Invest; 1988 May; 81(5):1323-7. PubMed ID: 3366897
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular analysis of human glycophorin MiIX gene shows a silent segment transfer and untemplated mutation resulting from gene conversion via sequence repeats.
    Huang CH; Skov F; Daniels G; Tippett P; Blumenfeld OO
    Blood; 1992 Nov; 80(9):2379-87. PubMed ID: 1421409
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of a splicing mutation in group A xeroderma pigmentosum.
    Satokata I; Tanaka K; Miura N; Miyamoto I; Satoh Y; Kondo S; Okada Y
    Proc Natl Acad Sci U S A; 1990 Dec; 87(24):9908-12. PubMed ID: 1702221
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel and de novo spontaneous point mutation (Glu271STOP) of the antithrombin gene results in a type I deficiency and thrombophilia.
    Tarantino MD; Curtis SM; Johnson GS; Waye JS; Blajchman MA
    Am J Hematol; 1999 Feb; 60(2):126-9. PubMed ID: 9929104
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A novel mutation in antithrombin gene results in hereditary antithrombin deficiency].
    Zhang FH; Ding QL; Wu JS; Zhou RF; Wang XF; Xu XC
    Zhonghua Xue Ye Xue Za Zhi; 2006 Sep; 27(9):598-601. PubMed ID: 17278425
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structural organization of glycophorin A and B genes: glycophorin B gene evolved by homologous recombination at Alu repeat sequences.
    Kudo S; Fukuda M
    Proc Natl Acad Sci U S A; 1989 Jun; 86(12):4619-23. PubMed ID: 2734312
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The 5' region of the human thyroglobulin gene contains members of the Alu family.
    Targovnik H; Paz C; Corach D; Christophe D
    Thyroid; 1992; 2(4):321-4. PubMed ID: 1493374
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular basis of antithrombin type I deficiency: the first large in-frame deletion and two novel mutations in exon 6.
    Emmerich J; Chadeuf G; Alhenc-Gelas M; Gouault-Heilman M; Toulon P; Fiessinger JN; Aiach M
    Thromb Haemost; 1994 Oct; 72(4):534-9. PubMed ID: 7878627
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.