Case MC - Search Results

1

A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups.

Sulong S, Moorman AV, Irving JA, Strefford JC, Konn ZJ, Case MC, Minto L, Barber KE, Parker H, Wright SL, Stewart AR, Bailey S, Bown NP, Hall AG, Harrison CJ. Sulong S, et al. Among authors: case mc. Blood. 2009 Jan 1;113(1):100-7. doi: 10.1182/blood-2008-07-166801. Epub 2008 Oct 6. Blood. 2009. PMID: 18838613 Free article.

2

Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis.

Irving JA, Bloodworth L, Bown NP, Case MC, Hogarth LA, Hall AG. Irving JA, et al. Among authors: case mc. Cancer Res. 2005 Apr 15;65(8):3053-8. doi: 10.1158/0008-5472.CAN-04-2604. Cancer Res. 2005. PMID: 15833833

3

The V617F mutation in Jak2 is not found in childhood acute lymphoblastic leukaemia.

Sulong S, Case M, Minto L, Wilkins B, Hall A, Irving J. Sulong S, et al. Br J Haematol. 2005 Sep;130(6):964-5. doi: 10.1111/j.1365-2141.2005.05697.x. Br J Haematol. 2005. PMID: 16156866 Free article. No abstract available.

4

Expression levels of asparagine synthetase in blasts from children and adults with acute lymphoblastic leukaemia.

Leslie M, Case MC, Hall AG, Coulthard SA. Leslie M, et al. Among authors: case mc. Br J Haematol. 2006 Mar;132(6):740-2. doi: 10.1111/j.1365-2141.2005.05945.x. Br J Haematol. 2006. PMID: 16487174 Free article.

5

DHFR and MSH3 co-amplification in childhood acute lymphoblastic leukaemia, in vitro and in vivo.

Matheson EC, Hogarth LA, Case MC, Irving JA, Hall AG. Matheson EC, et al. Among authors: case mc. Carcinogenesis. 2007 Jun;28(6):1341-6. doi: 10.1093/carcin/bgl235. Epub 2006 Dec 5. Carcinogenesis. 2007. PMID: 17148505

6

High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.

Carr J, Bown NP, Case MC, Hall AG, Lunec J, Tweddle DA. Carr J, et al. Among authors: case mc. Cancer Genet Cytogenet. 2007 Jan 15;172(2):127-38. doi: 10.1016/j.cancergencyto.2006.08.012. Cancer Genet Cytogenet. 2007. PMID: 17213021

7

Mutation of genes affecting the RAS pathway is common in childhood acute lymphoblastic leukemia.

Case M, Matheson E, Minto L, Hassan R, Harrison CJ, Bown N, Bailey S, Vormoor J, Hall AG, Irving JA. Case M, et al. Cancer Res. 2008 Aug 15;68(16):6803-9. doi: 10.1158/0008-5472.CAN-08-0101. Cancer Res. 2008. PMID: 18701506

8

The effect of thiopurine drugs on DNA methylation in relation to TPMT expression.

Hogarth LA, Redfern CP, Teodoridis JM, Hall AG, Anderson H, Case MC, Coulthard SA. Hogarth LA, et al. Among authors: case mc. Biochem Pharmacol. 2008 Oct 15;76(8):1024-35. doi: 10.1016/j.bcp.2008.07.026. Epub 2008 Jul 30. Biochem Pharmacol. 2008. PMID: 18708030

9

The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1.

Parker H, An Q, Barber K, Case M, Davies T, Konn Z, Stewart A, Wright S, Griffiths M, Ross FM, Moorman AV, Hall AG, Irving JA, Harrison CJ, Strefford JC. Parker H, et al. Genes Chromosomes Cancer. 2008 Dec;47(12):1118-25. doi: 10.1002/gcc.20613. Genes Chromosomes Cancer. 2008. PMID: 18767146

10

Establishment and validation of a standard protocol for the detection of minimal residual disease in B lineage childhood acute lymphoblastic leukemia by flow cytometry in a multi-center setting.

Irving J, Jesson J, Virgo P, Case M, Minto L, Eyre L, Noel N, Johansson U, Macey M, Knotts L, Helliwell M, Davies P, Whitby L, Barnett D, Hancock J, Goulden N, Lawson S; UKALL Flow MRD Group; UK MRD steering Group. Irving J, et al. Haematologica. 2009 Jun;94(6):870-4. doi: 10.3324/haematol.2008.000414. Epub 2009 Apr 18. Haematologica. 2009. PMID: 19377076 Free PMC article.

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