136 related articles for article (PubMed ID: 15456480)
1. Real-time quantitative PCR analysis of factor XI mRNA variants in human platelets.
Podmore A; Smith M; Savidge G; Alhaq A
J Thromb Haemost; 2004 Oct; 2(10):1713-9. PubMed ID: 15456480
[TBL] [Abstract][Full Text] [Related]
2. Factor XI messenger RNA in human platelets.
Martincic D; Kravtsov V; Gailani D
Blood; 1999 Nov; 94(10):3397-404. PubMed ID: 10552949
[TBL] [Abstract][Full Text] [Related]
3. Nonsense mutation in exon V of the factor XI gene does not abolish platelet factor XI expression.
Shirk RA; Konkle BA; Walsh PN
Br J Haematol; 2000 Oct; 111(1):91-5. PubMed ID: 11091186
[TBL] [Abstract][Full Text] [Related]
4. [The inherited coagulation factor XI deficiency caused by intronic mutation IVS J-4delgttg].
Xie S; Wang HL; Wang XF; Wu WM; Zhou RF; Wang WB; Hu YQ; Wang ZY
Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):144-7. PubMed ID: 15946525
[TBL] [Abstract][Full Text] [Related]
5. Platelet factor XI: intracellular localization and mRNA splicing following platelet activation.
Zucker M; Hauschner H; Seligsohn U; Rosenberg N
Blood Cells Mol Dis; 2018 Mar; 69():30-37. PubMed ID: 28760385
[TBL] [Abstract][Full Text] [Related]
6. Factor XI promotes hemostasis in factor IX-deficient mice.
Mohammed BM; Cheng Q; Matafonov A; Monroe DM; Meijers JCM; Gailani D
J Thromb Haemost; 2018 Oct; 16(10):2044-2049. PubMed ID: 30007049
[TBL] [Abstract][Full Text] [Related]
7. Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China.
Shao Y; Cao Y; Lu Y; Dai J; Ding Q; Wang X; Xi X; Wang H
Blood Cells Mol Dis; 2016 May; 58():29-34. PubMed ID: 27067486
[TBL] [Abstract][Full Text] [Related]
8. Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defect.
Guella I; Soldà G; Spena S; Asselta R; Ghiotto R; Tenchini ML; Castaman G; Duga S
Thromb Haemost; 2008 Mar; 99(3):523-30. PubMed ID: 18327400
[TBL] [Abstract][Full Text] [Related]
9. Structure and function of factor XI.
Emsley J; McEwan PA; Gailani D
Blood; 2010 Apr; 115(13):2569-77. PubMed ID: 20110423
[TBL] [Abstract][Full Text] [Related]
10. Characterisation of blood coagulation factor XI T475I.
McVey JH; Lal K; Imanaka Y; Kemball-Cook G; Bolton-Maggs PH; Tuddenham EG
Thromb Haemost; 2005 Jun; 93(6):1082-8. PubMed ID: 15968392
[TBL] [Abstract][Full Text] [Related]
11. The spectrum of factor XI deficiency in Southeast China: four recurrent variants can explain most of the deficiencies.
Zhang K; Qin L; Xu F; Ye L; Wen M; Pan J; Yang L; Wang M; Xie H
Orphanet J Rare Dis; 2024 Jun; 19(1):224. PubMed ID: 38835089
[TBL] [Abstract][Full Text] [Related]
12. Factor XI-deficient mice exhibit increased bleeding after injury to the saphenous vein.
Ay C; Hisada Y; Cooley BC; Mackman N
J Thromb Haemost; 2017 Sep; 15(9):1829-1833. PubMed ID: 28677246
[TBL] [Abstract][Full Text] [Related]
13. The role of factor XI in the coagulant activity of platelets.
Connellan JM; Castaldi PA; Muntz RH
Haemostasis; 1977; 6(1):41-52. PubMed ID: 870397
[TBL] [Abstract][Full Text] [Related]
14. Tissue-specific expression of functional platelet factor XI is independent of plasma factor XI expression.
Hu CJ; Baglia FA; Mills DC; Konkle BA; Walsh PN
Blood; 1998 May; 91(10):3800-7. PubMed ID: 9573017
[TBL] [Abstract][Full Text] [Related]
15. Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families.
Colakoglu S; Bayhan T; Tavil B; Keskin EY; Cakir V; Gümrük F; Çetin M; Aytaç S; Berber E
Blood Transfus; 2018 Jan; 16(1):105-113. PubMed ID: 27723456
[TBL] [Abstract][Full Text] [Related]
16. Abnormal plasma clot structure and stability distinguish bleeding risk in patients with severe factor XI deficiency.
Zucker M; Seligsohn U; Salomon O; Wolberg AS
J Thromb Haemost; 2014 Jul; 12(7):1121-30. PubMed ID: 24815347
[TBL] [Abstract][Full Text] [Related]
17. Prospective analysis of factor XI deficiencies in the Marseilles area identified four novel mutations among 12 consecutive unrelated families.
Quélin F; Frère C; Pouymayou C; Morange P; de Mazancourt P; Juhan-Vague I
Blood Coagul Fibrinolysis; 2009 Jan; 20(1):84-8. PubMed ID: 20523169
[TBL] [Abstract][Full Text] [Related]
18. A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency.
Bozzao C; Rimoldi V; Asselta R; Landau M; Ghiotto R; Tenchini ML; De Cristofaro R; Castaman G; Duga S
FEBS J; 2007 Dec; 274(23):6128-38. PubMed ID: 17971173
[TBL] [Abstract][Full Text] [Related]
19. The spectrum of factor XI deficiency in Italy.
Castaman G; Giacomelli SH; Caccia S; Riccardi F; Rossetti G; Dragani A; Giuffrida AC; Biasoli C; Duga S
Haemophilia; 2014 Jan; 20(1):106-13. PubMed ID: 24112640
[TBL] [Abstract][Full Text] [Related]
20. Molecular genetic analysis of factor XI deficiency: identification of five novel gene alterations and the origin of type II mutation in Portuguese families.
Ventura C; Santos AI; Tavares A; Gago T; Lavinha J; McVey JH; David D
Thromb Haemost; 2000 Nov; 84(5):833-40. PubMed ID: 11127865
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]