Dai L - Search Results

1

Stabilization of fibrin clots by activated prothrombin complex concentrate and tranexamic acid in FVIII inhibitor plasma.

Dai L, Bevan D, Rangarajan S, Sørensen B, Mitchell M. Dai L, et al. Haemophilia. 2011 Sep;17(5):e944-8. doi: 10.1111/j.1365-2516.2011.02491.x. Epub 2011 Mar 3. Haemophilia. 2011. PMID: 21371192

2

The profibrinolytic effect of plasma thrombomodulin in factor XI deficiency and its implications in hemostasis.

Dai L, Mitchell M, Savidge G, Alhaq A. Dai L, et al. J Thromb Haemost. 2004 Dec;2(12):2200-4. doi: 10.1111/j.1538-7836.2004.01034.x. J Thromb Haemost. 2004. PMID: 15613027 Free article.

3

Three dominant-negative mutations in factor XI-deficient patients.

Dai L, Rangarajan S, Mitchell M. Dai L, et al. Haemophilia. 2011 Sep;17(5):e919-22. doi: 10.1111/j.1365-2516.2011.02519.x. Epub 2011 Apr 3. Haemophilia. 2011. PMID: 21457405

4

Characterisation of five factor XI mutations.

Mitchell MJ, Dai L, Clarke JB, Bolton-Maggs PH, Savidge GF, Alhaq A. Mitchell MJ, et al. Among authors: dai l. Thromb Haemost. 2007 Jun;97(6):884-9. doi: 10.1160/th06-12-0704. Thromb Haemost. 2007. PMID: 17549289

5

An Alu-mediated 31.5-kb deletion as the cause of factor XI deficiency in 2 unrelated patients.

Mitchell M, Dai L, Savidge G, Alhaq A. Mitchell M, et al. Among authors: dai l. Blood. 2004 Oct 15;104(8):2394-6. doi: 10.1182/blood-2004-04-1318. Epub 2004 Jun 29. Blood. 2004. PMID: 15226185 Free article.

6

Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families.

Keskin EY, Gürsel T, Kaya Z, Dai L, Koçak Ü, Yenicesu İ, Belen FB, Mitchell M. Keskin EY, et al. Among authors: dai l. Blood Coagul Fibrinolysis. 2015 Jan;26(1):63-8. doi: 10.1097/MBC.0000000000000185. Blood Coagul Fibrinolysis. 2015. PMID: 25158988

7

Effects of regional citrate anticoagulation on thrombin generation, fibrinolysis and platelet function in critically ill patients receiving continuous renal replacement therapy for acute kidney injury: a prospective study.

Fisher R, Moore GW, Mitchell MJ, Dai L, Crichton S, Lumlertgul N, Ostermann M. Fisher R, et al. Among authors: dai l. Ann Intensive Care. 2022 Mar 31;12(1):29. doi: 10.1186/s13613-022-01004-w. Ann Intensive Care. 2022. PMID: 35355147 Free PMC article.

8

Spectrum of factor XI (F11) mutations in the UK population--116 index cases and 140 mutations.

Mitchell M, Mountford R, Butler R, Alhaq A, Dai L, Savidge G, Bolton-Maggs PH. Mitchell M, et al. Among authors: dai l. Hum Mutat. 2006 Aug;27(8):829. doi: 10.1002/humu.9439. Hum Mutat. 2006. PMID: 16835901

9

Homocysteine metabolism and the associations of global DNA methylation with selected gene polymorphisms and nutritional factors in patients with dementia.

Bednarska-Makaruk M, Graban A, Sobczyńska-Malefora A, Harrington DJ, Mitchell M, Voong K, Dai L, Łojkowska W, Bochyńska A, Ryglewicz D, Wiśniewska A, Wehr H. Bednarska-Makaruk M, et al. Among authors: dai l. Exp Gerontol. 2016 Aug;81:83-91. doi: 10.1016/j.exger.2016.05.002. Epub 2016 May 7. Exp Gerontol. 2016. PMID: 27167582

10

Characterization of a causative mutation of hemophilia A identified in the promoter region of the factor VIII gene (F8).

Dai L, Cutler JA, Savidge GF, Mitchell MJ. Dai L, et al. J Thromb Haemost. 2008 Jan;6(1):193-5. doi: 10.1111/j.1538-7836.2007.02806.x. Epub 2007 Oct 16. J Thromb Haemost. 2008. PMID: 17944985 Free article. No abstract available.

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