Keeney S - Search Results

1

Expression of diverse AML1/MTG8 transcripts is a consistent feature in acute myeloid leukemia with t(8;21) irrespective of disease phase.

Saunders MJ, Tobal K, Keeney S, Liu Yin JA. Saunders MJ, et al. Among authors: keeney s. Leukemia. 1996 Jul;10(7):1139-42. Leukemia. 1996. PMID: 8683993

2

The molecular biology of von Willebrand disease.

Keeney S, Cumming AM. Keeney S, et al. Clin Lab Haematol. 2001 Aug;23(4):209-30. doi: 10.1046/j.1365-2257.2001.00400.x. Clin Lab Haematol. 2001. PMID: 11683782 Review.

3

HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. UKHCDO Inhibitor Working Party.

Hay CR, Ollier W, Pepper L, Cumming A, Keeney S, Goodeve AC, Colvin BT, Hill FG, Preston FE, Peake IR. Hay CR, et al. Among authors: keeney s. Thromb Haemost. 1997 Feb;77(2):234-7. Thromb Haemost. 1997. PMID: 9157572

4

Development of resistance to activated protein C during pregnancy.

Cumming AM, Tait RC, Fildes S, Yoong A, Keeney S, Hay CR. Cumming AM, et al. Among authors: keeney s. Br J Haematol. 1995 Jul;90(3):725-7. doi: 10.1111/j.1365-2141.1995.tb05610.x. Br J Haematol. 1995. PMID: 7647019

5

Clinical utility gene card for: von Willebrand disease.

Cumming AM, Keeney S, Jenkins PV, Nash MJ, O'Donnell JS. Cumming AM, et al. Among authors: keeney s. Eur J Hum Genet. 2011 May;19(5). doi: 10.1038/ejhg.2010.222. Epub 2011 Jan 5. Eur J Hum Genet. 2011. PMID: 21206511 Free PMC article. No abstract available.

6

A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiency.

Bolton-Maggs PH, Peretz H, Butler R, Mountford R, Keeney S, Zacharski L, Zivelin A, Seligsohn U. Bolton-Maggs PH, et al. Among authors: keeney s. J Thromb Haemost. 2004 Jun;2(6):918-24. doi: 10.1111/j.1538-7836.2004.00723.x. J Thromb Haemost. 2004. PMID: 15140127 Free article.

7

The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population.

Cumming AM, Keeney S, Salden A, Bhavnani M, Shwe KH, Hay CR. Cumming AM, et al. Among authors: keeney s. Br J Haematol. 1997 Aug;98(2):353-5. doi: 10.1046/j.1365-2141.1997.2353052.x. Br J Haematol. 1997. PMID: 9266933 Free article.

8

C1584 in von Willebrand factor is necessary for enhanced proteolysis by ADAMTS13 in vitro.

Keeney S, Grundy P, Collins PW, Bowen DJ. Keeney S, et al. Haemophilia. 2007 Jul;13(4):405-8. doi: 10.1111/j.1365-2516.2007.01470.x. Haemophilia. 2007. PMID: 17610557

9

The methylenetetrahydrofolate reductase gene C677T polymorphism in patients with homozygous sickle cell disease and stroke.

Cumming AM, Olujohungbe A, Keeney S, Singh H, Hay CR, Serjeant GR. Cumming AM, et al. Among authors: keeney s. Br J Haematol. 1999 Dec;107(3):569-71. doi: 10.1046/j.1365-2141.1999.01728.x. Br J Haematol. 1999. PMID: 10583261 Free article.

10

The molecular analysis of haemophilia B: a guideline from the UK haemophilia centre doctors' organization haemophilia genetics laboratory network.

Mitchell M, Keeney S, Goodeve A; UK Haemophilia Centre Doctors' Organization Haemophilia Genetics Laboratory Network. Mitchell M, et al. Among authors: keeney s. Haemophilia. 2005 Jul;11(4):398-404. doi: 10.1111/j.1365-2516.2005.01112.x. Haemophilia. 2005. PMID: 16011594

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