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 *

132 related articles for article (PubMed ID: 10997988)

  • 1. Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene.
    Picard V; Bura A; Emmerich J; Alhenc-Gelas M; Biron C; Houbouyan-Reveillard LL; Molho P; Labatide-Alanore A; Sié P; Toulon P; Verdy E; Aiach M
    Br J Haematol; 2000 Sep; 110(3):731-4. PubMed ID: 10997988
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular analysis and genotype-phenotype correlation in patients with antithrombin deficiency from Southern Italy.
    Castaldo G; Cerbone AM; Guida A; Tandurella I; Ingino R; Tufano A; Ceglia C; Di Minno MN; Ruocco AL; Di Minno G
    Thromb Haemost; 2012 Apr; 107(4):673-80. PubMed ID: 22398878
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.
    Picard V; Nowak-Göttl U; Biron-Andreani C; Fouassier M; Frere C; Goualt-Heilman M; de Maistre E; Regina S; Rugeri L; Ternisien C; Trichet C; Vergnes C; Aiach M; Alhenc-Gelas M
    Hum Mutat; 2006 Jun; 27(6):600. PubMed ID: 16705712
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of two novel mutations (nt2762, exon 2, CAG to TAG, and nt2483 or 2484, exon 2, +A) in individuals with congenital type I antithrombin deficiencies.
    Nakahara Y; Tsuji H; Nakagawa K; Masuda H; Kitamura H; Nishimura H; Kasahara T; Sugano T; Sawada S; Sakata T; Miyata T; Inoue N; Nakagawa M
    Blood Coagul Fibrinolysis; 1999 Jul; 10(5):229-31. PubMed ID: 10456612
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Molecular basis of hereditary antithrombin defects in 10 Czech families].
    Hrachovinová I; Habart D; Salaj P; Matysková M; Vorlová Z
    Cas Lek Cesk; 2000 Sep; 139(19):596-8. PubMed ID: 11192751
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Antithrombin Katowice: exon 1 deletion in the SERPINC1 gene associated with type I antithrombin deficiency.
    Cieśla M; Wypasek E; Corral J; Alhenc-Gelas M; Undas A
    Blood Coagul Fibrinolysis; 2015 Jan; 26(1):95-7. PubMed ID: 25083771
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Antithrombin deficiency due to heterozygous antithrombin gene mutation and a pedigree study].
    Ye X; Feng Y; Jin PP; Zhou XH; Ding QL; Wang XF
    Zhonghua Xue Ye Xue Za Zhi; 2007 Sep; 28(9):587-9. PubMed ID: 18246812
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Report of a novel kindred with antithrombin heparin-binding site variant (47 Arg to His): demand for an automated progressive antithrombin assay to detect molecular variants with low thrombotic risk.
    Rossi E; Chiusolo P; Za T; Marietti S; Ciminello A; Leone G; De Stefano V
    Thromb Haemost; 2007 Sep; 98(3):695-7. PubMed ID: 17849067
    [No Abstract]   [Full Text] [Related]  

  • 9. SERPINC1 gene mutations in antithrombin deficiency.
    Mulder R; Croles FN; Mulder AB; Huntington JA; Meijer K; Lukens MV
    Br J Haematol; 2017 Jul; 178(2):279-285. PubMed ID: 28317092
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular basis of SERPINC1 mutations in Japanese patients with antithrombin deficiency.
    Tamura S; Hashimoto E; Suzuki N; Kakihara M; Odaira K; Hattori Y; Tokoro M; Suzuki S; Takagi A; Katsumi A; Hayakawa F; Suzuki A; Okamoto S; Kanematsu T; Matsushita T; Kojima T
    Thromb Res; 2019 Jun; 178():159-170. PubMed ID: 31030036
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two case reports of inherited antithrombin deficiency: a novel frameshift mutation and a large deletion including all seven exons detected using two methods.
    Sekiya A; Morishita E; Karato M; Maruyama K; Shimogawara I; Omote M; Wakugawa Y; Shinohara M; Hayashi T; Kadohira Y; Asakura H; Nakao S; Ohtake S
    Int J Hematol; 2011 Feb; 93(2):216-219. PubMed ID: 21240680
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Five antithrombin variants, four associated with thrombosis.
    Fitton HL; Walker ID; Jones L; Brown K; Carrell RW; Coughlin P
    Blood Coagul Fibrinolysis; 1997 Mar; 8(2):145-8. PubMed ID: 9518046
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic analysis of mutations in seven Japanese families with type I antithrombin deficiency.
    Ozawa T; Sakuragawa N
    Semin Thromb Hemost; 1998; 24(3):233-6. PubMed ID: 9701453
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. Retinal vein occlusion associated with antithrombin deficiency secondary to a novel G9840C missense mutation.
    Kuhli C; Jochmans K; Scharrer I; Lüchtenberg M; Hattenbach LO
    Arch Ophthalmol; 2006 Aug; 124(8):1165-9. PubMed ID: 16908819
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Amelioration of the severity of heparin-binding antithrombin mutations by posttranslational mosaicism.
    Martínez-Martínez I; Navarro-Fernández J; Østergaard A; Gutiérrez-Gallego R; Padilla J; Bohdan N; Miñano A; Pascual C; Martínez C; de la Morena-Barrio ME; Aguila S; Pedersen S; Kristensen SR; Vicente V; Corral J
    Blood; 2012 Jul; 120(4):900-4. PubMed ID: 22498748
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recurrent deletion in the human antithrombin III gene.
    Grundy CB; Thomas F; Millar DS; Krawczak M; Melissari E; Lindo V; Moffat E; Kakkar VV; Cooper DN
    Blood; 1991 Aug; 78(4):1027-32. PubMed ID: 1868237
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Antithrombin Krakow II (c.624+1 G > T): a novel mutation leading to type 1 antithrombin deficiency.
    Celinska-Löwenhoff M; Iwaniec T; Alhenc-Gelas M; Musial J; Undas A
    Blood Coagul Fibrinolysis; 2012 Jul; 23(5):454-5. PubMed ID: 22498983
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular basis for antithrombin III type I deficiency: three novel mutations located in exon IV.
    Vidaud D; Emmerich J; Sirieix ME; Sié P; Alhenc-Gelas M; Aiach M
    Blood; 1991 Nov; 78(9):2305-9. PubMed ID: 1932746
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A frameshift mutation leading to type 1 antithrombin deficiency and thrombosis.
    Olds RJ; Lane DA; Finazzi G; Barbui T; Thein SL
    Blood; 1990 Dec; 76(11):2182-6. PubMed ID: 1979501
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.