Berber E - Search Results

1

Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease.

O'Brien LA, James PD, Othman M, Berber E, Cameron C, Notley CR, Hegadorn CA, Sutherland JJ, Hough C, Rivard GE, O'Shaunessey D, Lillicrap D; Association of Hemophilia Clinic Directors of Canada. O'Brien LA, et al. Among authors: berber e. Blood. 2003 Jul 15;102(2):549-57. doi: 10.1182/blood-2002-12-3693. Epub 2003 Mar 20. Blood. 2003. PMID: 12649144 Free article.

2

Cell type-specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressor.

Hough C, Cuthbert CD, Notley C, Brown C, Hegadorn C, Berber E, Lillicrap D. Hough C, et al. Among authors: berber e. Blood. 2005 Feb 15;105(4):1531-9. doi: 10.1182/blood-2002-10-3093. Epub 2004 Oct 21. Blood. 2005. PMID: 15498853 Free article.

3

Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p.M771I, p.L881R and p.P1413L.

Berber E, Ozbil M, Brown C, Baslar Z, Caglayan SH, Lillicrap D. Berber E, et al. Blood Transfus. 2017 Oct;15(6):548-556. doi: 10.2450/2016.0034-16. Epub 2016 Jul 25. Blood Transfus. 2017. PMID: 27483487 Free PMC article.

4

An assessment of the pathogenic significance of the R924Q von Willebrand factor substitution.

Berber E, James PD, Hough C, Lillicrap D. Berber E, et al. J Thromb Haemost. 2009 Oct;7(10):1672-9. doi: 10.1111/j.1538-7836.2009.03551.x. Epub 2009 Jul 17. J Thromb Haemost. 2009. PMID: 19624459 Free article.

5

Influence of a GT repeat element on shear stress responsiveness of the VWF gene promoter.

Hough C, Cameron CL, Notley CR, Brown C, O'Brien L, Keightley AM, Berber E, Lillicrap D. Hough C, et al. Among authors: berber e. J Thromb Haemost. 2008 Jul;6(7):1183-90. doi: 10.1111/j.1538-7836.2008.03011.x. Epub 2008 Jul 1. J Thromb Haemost. 2008. PMID: 18485092 Free article.

6

DNA microarray analysis for the detection of mutations in hemophilia A.

Berber E, Leggo J, Brown C, Berber E, Gallo N, Feilotter H, Lillicrap D. Berber E, et al. J Thromb Haemost. 2006 Aug;4(8):1756-62. doi: 10.1111/j.1538-7836.2006.02055.x. J Thromb Haemost. 2006. PMID: 16879218 Free article.

7

Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N.

Berber E, Fidanci ID, Un C, El-Maarri O, Aktuglu G, Gurgey A, Celkan T, Meral A, Oldenburg J, Graw J, Akar N, Caglayan H. Berber E, et al. Haemophilia. 2006 Jul;12(4):398-400. doi: 10.1111/j.1365-2516.2006.01302.x. Haemophilia. 2006. PMID: 16834740

8

A common VWF exon 28 haplotype in the Turkish population.

Berber E, Pehlevan F, Akin M, Capan OY, Kavakli K, Çaglayan SH. Berber E, et al. Clin Appl Thromb Hemost. 2013 Sep;19(5):550-6. doi: 10.1177/1076029612441054. Epub 2012 Apr 2. Clin Appl Thromb Hemost. 2013. PMID: 22473027 Free article.

9

Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation.

Kılıç SÇ, İçağasıoğlu FD, Güven AS, Berber E. Kılıç SÇ, et al. Among authors: berber e. Blood Transfus. 2014 Jul;12(3):446-8. doi: 10.2450/2014.0022-14. Blood Transfus. 2014. PMID: 25074526 Free PMC article. No abstract available.

10

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. Colakoglu S, et al. Among authors: berber e. Blood Transfus. 2018 Jan;16(1):105-113. doi: 10.2450/2016.0098-16. Epub 2016 Oct 4. Blood Transfus. 2018. PMID: 27723456 Free PMC article. Clinical Trial.

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