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 *

98 related articles for article (PubMed ID: 7947262)

  • 1. The molecular genetics of antithrombin deficiency.
    Olds RJ; Lane DA; Thein SL
    Br J Haematol; 1994 Jun; 87(2):221-6. PubMed ID: 7947262
    [No Abstract]   [Full Text] [Related]  

  • 2. Two new antithrombin variants support a role for K114 and R13 in heparin binding.
    Picard V; Susen S; Bellucci S; Aiach M; Alhenc-Gelas M
    J Thromb Haemost; 2003 Feb; 1(2):386-7. PubMed ID: 12871518
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis.
    Chowdhury V; Lane DA; Mille B; Auberger K; Gandenberger-Bachem S; Pabinger I; Olds RJ; Thein SL
    Thromb Haemost; 1994 Aug; 72(2):198-202. PubMed ID: 7831651
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular genetics of human antithrombin deficiency.
    Perry DJ; Carrell RW
    Hum Mutat; 1996; 7(1):7-22. PubMed ID: 8664906
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Protein C and antithrombin deficiency are important risk factors for deep vein thrombosis in Japanese.
    Sakata T; Okamoto A; Mannami T; Matsuo H; Miyata T
    J Thromb Haemost; 2004 Mar; 2(3):528-30. PubMed ID: 15009480
    [No Abstract]   [Full Text] [Related]  

  • 8. Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate.
    Baud O; Picard V; Durand P; Duchemin J; Proulle V; Alhenc-Gelas M; Devictor D; Dreyfus M
    J Pediatr; 2001 Nov; 139(5):741-3. PubMed ID: 11713457
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Antithrombin-TRI (Ala382 to Thr) causing severe thromboembolic tendency undergoes the S-to-R transition and is associated with a plasma-inactive high-molecular-weight complex of aggregated antithrombin.
    Lindo VS; Kakkar VV; Learmonth M; Melissari E; Zappacosta F; Panico M; Morris HR
    Br J Haematol; 1995 Mar; 89(3):589-601. PubMed ID: 7734359
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of the novel signal peptide mutation, antithrombin-Siriraj causes type-I antithrombin deficiency in thai patients.
    Chinthammitr Y; Chinchang W; Ruchutrakool T; Viprakasit V
    Thromb Haemost; 2005 Sep; 94(3):678-9. PubMed ID: 16268490
    [No Abstract]   [Full Text] [Related]  

  • 12. Thrombophilia: a genetic predisposition to thrombosis.
    Sacher RA
    Trans Am Clin Climatol Assoc; 1999; 110():51-60; discussion 60-1. PubMed ID: 10344006
    [No Abstract]   [Full Text] [Related]  

  • 13. [Type I hereditary antithrombin deficiency due to C2757T heterozygotic mutation in antithrombin gene].
    Zhou RF; Dai Q; Fu QH; Wang WB; Xue S; Ding QL; Hu YQ; Wang XF; Wang HL
    Zhonghua Yi Xue Za Zhi; 2005 Jun; 85(23):1640-2. PubMed ID: 16185535
    [No Abstract]   [Full Text] [Related]  

  • 14. Identification of six novel mutations in type I antithrombin deficient Italian families.
    Di Perna P; Vecchione G; D'Andrea G; Scenna G; Brancaccio V; Margaglione M
    Haematologica; 2004 Jan; 89(1):117-8. PubMed ID: 14754620
    [No Abstract]   [Full Text] [Related]  

  • 15. [Familial antithrombin deficiency].
    Eide D; Odegaard OR
    Tidsskr Nor Laegeforen; 1989 Mar; 109(7-8):836-7. PubMed ID: 2705167
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Antithrombins Southport (Leu 99 to Val) and Vienna (Gln 118 to Pro): two novel antithrombin variants with abnormal heparin binding.
    Chowdhury V; Mille B; Olds RJ; Lane DA; Watton J; Barrowcliffe TW; Pabinger I; Woodcock BE; Thein SL
    Br J Haematol; 1995 Mar; 89(3):602-9. PubMed ID: 7734360
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Introduction: hypercoagulable states.
    Bertina RM
    Semin Hematol; 1997 Jul; 34(3):167-70. PubMed ID: 9241703
    [No Abstract]   [Full Text] [Related]  

  • 18. Familial antithrombin III deficiency.
    Br Med J; 1978 Feb; 1(6111):508. PubMed ID: 626859
    [No Abstract]   [Full Text] [Related]  

  • 19. Antithrombin niigata: a novel missense mutation (Thr194-Ile) of the antithrombin gene results in type I deficiency.
    Fuse I; Ozawa T; Higuchi W; Aizawa Y
    Thromb Haemost; 2000 Dec; 84(6):1126. PubMed ID: 11154130
    [No Abstract]   [Full Text] [Related]  

  • 20. Antithrombin: structure and function.
    Pratt CW; Church FC
    Semin Hematol; 1991 Jan; 28(1):3-9. PubMed ID: 2017689
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.