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 *

135 related articles for article (PubMed ID: 15140147)

  • 1. Factor XI gene analysis in thrombophilia and factor XI deficiency.
    Gerdes VE; Kraaijenhagen RA; Vogels EW; ten Cate H; Reitsma PH
    J Thromb Haemost; 2004 Jun; 2(6):1015-7. PubMed ID: 15140147
    [No Abstract]   [Full Text] [Related]  

  • 2. Severe factor XI deficiency in the Abruzzo region of Italy is associated to different FXI gene mutations.
    Castaman G; Giacomelli SH; Dragani A; Iuliani O; Duga S; Rodeghiero F
    Haematologica; 2008 Jun; 93(6):957-8. PubMed ID: 18515884
    [No Abstract]   [Full Text] [Related]  

  • 3. Successful treatment of a lung cancer patient with factor XI deficiency.
    Yamagishi T; Ochi N; Yamane H; Fukazawa T; Wada H; Takigawa N
    Haemophilia; 2013 Nov; 19(6):e367-9. PubMed ID: 23992470
    [No Abstract]   [Full Text] [Related]  

  • 4. Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency.
    Mulder R; Wiewel-Verschueren S; Meijer K; Mulder AB
    Thromb Haemost; 2013 Jun; 109(6):1183-5. PubMed ID: 23494098
    [No Abstract]   [Full Text] [Related]  

  • 5. Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency.
    Spena S; Asselta R; Caccia S; Rimoldi V; Giacomelli SH; Tagliaferri A; Peyvandi F; Castaman G; Duga S
    Thromb Haemost; 2009 Sep; 102(3):603-6. PubMed ID: 19718484
    [No Abstract]   [Full Text] [Related]  

  • 6. Identification of a novel F11 missense mutation (Ile463Ser) in a family with congenital factor XI deficiency.
    Tirefort Y; Uhr MR; Neerman-Arbez M; de Moerloose P
    Blood Coagul Fibrinolysis; 2012 Apr; 23(3):251-2. PubMed ID: 22322133
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular investigation of 41 patients affected by coagulation factor XI deficiency.
    Rimoldi V; Paraboschi EM; Menegatti M; Peyvandi F; Salomon O; Duga S; Asselta R
    Haemophilia; 2018 Mar; 24(2):e50-e55. PubMed ID: 29178608
    [No Abstract]   [Full Text] [Related]  

  • 8. Partial and severe factor XI deficiency in South Australia and the usefulness of factor XI mutation analysis for diagnosis.
    Duncan EM; Casey GJ; Fenech MP; Lerda NV; Casey CR; Rodgers SE; Lee SH; Chunilal S; Robinson K; Lloyd JV
    Pathology; 2008 Jun; 40(4):401-6. PubMed ID: 18446632
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency.
    Quélin F; Mathonnet F; Potentini-Esnault C; Trigui N; Peynet J; Bastenaire B; Guillon L; Bigel ML; Sauger A; Mazurier C; de Mazancourt P
    Blood Coagul Fibrinolysis; 2006 Jan; 17(1):69-73. PubMed ID: 16607084
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular analysis of severe factor XI deficiency in three Italian patients.
    Bicocchi MP; Marotta F; Banov L; Acquila M
    Haemophilia; 2011 Sep; 17(5):e835-6. PubMed ID: 21649796
    [No Abstract]   [Full Text] [Related]  

  • 11. [Identification of two novel factor XI non-sense mutation Trp228stop and Trp383stop in a Chinese pedigree of congenital factor XI deficiency].
    Wu WM; Wang HL; Wang XF; Chu HY; Fu QH; Ding QL; Hu YQ; Shen ZX; Wang ZY
    Zhonghua Xue Ye Xue Za Zhi; 2003 Mar; 24(3):126-8. PubMed ID: 12697122
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recurrent mutations of factor XI gene in Japanese.
    Okumura K; Kyotani M; Kawai R; Takagi A; Murate T; Yamamoto K; Takamatsu J; Matsushita T; Saito H; Kojima T
    Int J Hematol; 2006 Jun; 83(5):462-3. PubMed ID: 16787881
    [No Abstract]   [Full Text] [Related]  

  • 13. Four novel FXI gene mutations in three factor XI- deficient patients.
    de Raucourt E; de Mazancourt P; Quélin F
    Blood Coagul Fibrinolysis; 2008 Apr; 19(3):240-2. PubMed ID: 18388506
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and molecular epidemiology of factor XI deficiency in India.
    Kawankar N; Rathi J; Ghosh K; Shetty S
    Thromb Res; 2016 Nov; 147():85-87. PubMed ID: 27710856
    [No Abstract]   [Full Text] [Related]  

  • 15. A novel c.290G>A mutation in the Factor 11 gene in a Dutch Caucasian family with a Factor XI deficiency.
    Mulder R; Croles FN; Lukens MV; Meijer K; Mulder AB
    Thromb Res; 2015 Apr; 135(4):767-9. PubMed ID: 25618263
    [No Abstract]   [Full Text] [Related]  

  • 16. Archeogenetics of
    de la Morena-Barrio ME; Salloum-Asfar S; Esteban J; de la Morena-Barrio B; Altisent C; Martin-Fernández L; Gueguen P; Padilla J; Miñano A; Parra R; Vicente V; Vidal F; Bauduer F; Carbonell P; Corral J
    Blood; 2019 Jun; 133(24):2618-2622. PubMed ID: 31043424
    [No Abstract]   [Full Text] [Related]  

  • 17. A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency.
    Soldà G; Asselta R; Ghiotto R; Tenchini ML; Castaman G; Duga S
    Haematologica; 2005 Dec; 90(12):1716-8. PubMed ID: 16330457
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of mutations and polymorphisms in the factor XI genes of an African American family by dideoxyfingerprinting.
    Martincic D; Zimmerman SA; Ware RE; Sun MF; Whitlock JA; Gailani D
    Blood; 1998 Nov; 92(9):3309-17. PubMed ID: 9787168
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.
    Choi SJ; Kim J; Lee KA; Choi JR; Yoo J
    Ann Lab Med; 2014 Jul; 34(4):332-5. PubMed ID: 24982842
    [No Abstract]   [Full Text] [Related]  

  • 20. A novel factor XI gene mutation associated with mild factor XI deficiency in a symptomatic patient.
    Ramadan KM; McNulty O; Anderson JA; Jones FG; Winter PC
    Blood Coagul Fibrinolysis; 2006 Sep; 17(6):499-502. PubMed ID: 16905957
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.