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Items: 29

1.

MACROD2 Haploinsufficiency Impairs Catalytic Activity of PARP1 and Promotes Chromosome Instability and Growth of Intestinal Tumors.

Sakthianandeswaren A, Parsons M, Mouradov D, MacKinnon RN, Catimel B, Liu S, Palmieri M, Love CG, Jorissen RN, Li S, Whitehead L, Putoczki TL, Preaudet A, Tsui C, Nowell CJ, Ward RL, Hawkins NJ, Desai J, Gibbs P, Ernst M, Street I, Buchert M, Sieber OM.

Cancer Discov. 2018 Jun 7. pii: CD-17-0909. doi: 10.1158/2159-8290.CD-17-0909. [Epub ahead of print]

PMID:
29880585
2.

Analysis of Chromothripsis by Combined FISH and Microarray Analysis.

MacKinnon RN.

Methods Mol Biol. 2018;1769:53-77. doi: 10.1007/978-1-4939-7780-2_5.

PMID:
29564818
3.

The Dicentric Chromosome dic(20;22) Is a Recurrent Abnormality in Myelodysplastic Syndromes and Is a Product of Telomere Fusion.

MacKinnon RN, Duivenvoorden HM, Campbell LJ, Wall M.

Cytogenet Genome Res. 2016;150(3-4):262-272. doi: 10.1159/000456677. Epub 2017 Mar 4.

PMID:
28259884
4.

Active centromere and chromosome identification in fixed cell lines.

Beh TT, MacKinnon RN, Kalitsis P.

Mol Cytogenet. 2016 Mar 22;9:28. doi: 10.1186/s13039-016-0236-x. eCollection 2016.

5.

Src family kinases and their role in hematological malignancies.

Ku M, Wall M, MacKinnon RN, Walkley CR, Purton LE, Tam C, Izon D, Campbell L, Cheng HC, Nandurkar H.

Leuk Lymphoma. 2015 Mar;56(3):577-86. doi: 10.3109/10428194.2014.907897. Epub 2015 Jan 21. Review.

PMID:
24898666
6.

Genome organization and the role of centromeres in evolution of the erythroleukaemia cell line HEL.

Mackinnon RN, Wall M, Zordan A, Nutalapati S, Mercer B, Peverall J, Campbell LJ.

Evol Med Public Health. 2013 Jan;2013(1):225-40. doi: 10.1093/emph/eot020. Epub 2013 Oct 1.

7.

Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangement.

Mackinnon RN, Campbell LJ.

Cancer Genet. 2013 Jun;206(6):238-51. doi: 10.1016/j.cancergen.2013.05.021. Epub 2013 Aug 2.

PMID:
23911237
8.

ETV6 deletion is a common additional abnormality in patients with myelodysplastic syndromes or acute myeloid leukemia and monosomy 7.

Wall M, Rayeroux KC, MacKinnon RN, Zordan A, Campbell LJ.

Haematologica. 2012 Dec;97(12):1933-6. doi: 10.3324/haematol.2012.069716. Epub 2012 Aug 8. No abstract available.

9.

11q23 rearrangement and duplication of MLLT1-MLL gene fusion in therapy-related acute myeloid leukemia.

Chin LK, Cheah CY, Michael PM, MacKinnon RN, Campbell LJ.

Leuk Lymphoma. 2012 Oct;53(10):2066-8. doi: 10.3109/10428194.2012.666663. Epub 2012 Mar 16. No abstract available.

PMID:
22335556
10.

CGH and SNP array using DNA extracted from fixed cytogenetic preparations and long-term refrigerated bone marrow specimens.

Mackinnon RN, Selan C, Zordan A, Wall M, Nandurkar H, Campbell LJ.

Mol Cytogenet. 2012 Feb 2;5:10. doi: 10.1186/1755-8166-5-10.

11.

A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromes.

MacKinnon RN, Kannourakis G, Wall M, Campbell LJ.

Cancer Genet. 2011 Apr;204(4):187-94. doi: 10.1016/j.cancergen.2011.02.001.

PMID:
21536236
12.

Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20q.

MacKinnon RN, Duivenvoorden HM, Campbell LJ.

Cancer Genet. 2011 Mar;204(3):153-61. doi: 10.1016/j.cancergen.2010.12.001.

PMID:
21504715
13.

The use of M-FISH and M-BAND to define chromosome abnormalities.

Mackinnon RN, Chudoba I.

Methods Mol Biol. 2011;730:203-18. doi: 10.1007/978-1-61779-074-4_15.

PMID:
21431644
14.

The role of dicentric chromosome formation and secondary centromere deletion in the evolution of myeloid malignancy.

Mackinnon RN, Campbell LJ.

Genet Res Int. 2011;2011:643628. doi: 10.4061/2011/643628. Epub 2011 Sep 27.

15.

The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion.

Mackinnon RN, Selan C, Wall M, Baker E, Nandurkar H, Campbell LJ.

Genes Chromosomes Cancer. 2010 Nov;49(11):998-1013. doi: 10.1002/gcc.20806.

PMID:
20645416
16.

Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20.

Mackinnon RN, Campbell LJ.

Cytogenet Genome Res. 2007;119(3-4):211-20. doi: 10.1159/000112063. Epub 2008 Feb 1.

PMID:
18253031
19.
20.

Linkage analysis of spinal muscular atrophy.

Daniels RJ, Thomas NH, MacKinnon RN, Lehner T, Ott J, Flint TJ, Dubowitz V, Ignatius J, Donner M, Zerres K, et al.

Genomics. 1992 Feb;12(2):335-9.

PMID:
1346777
21.
22.

A YAC contig across the fragile X site defines the region of fragility.

Hirst MC, Rack K, Nakahori Y, Roche A, Bell MV, Flynn G, Christadoulou Z, MacKinnon RN, Francis M, Littler AJ, et al.

Nucleic Acids Res. 1991 Jun 25;19(12):3283-8.

23.

Linear order of new and established DNA markers around the fragile site at Xq27.3.

Hirst MC, Roche A, Flint TJ, MacKinnon RN, Bassett JH, Nakahori Y, Watson JE, Bell MV, Patterson MN, Boyd Y, et al.

Genomics. 1991 May;10(1):243-9.

PMID:
2045104
24.

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.

Bell MV, Hirst MC, Nakahori Y, MacKinnon RN, Roche A, Flint TJ, Jacobs PA, Tommerup N, Tranebjaerg L, Froster-Iskenius U, et al.

Cell. 1991 Feb 22;64(4):861-6.

PMID:
1997211
25.

Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site.

Hirst MC, Bell MV, MacKinnon RN, Watson JE, Callen D, Sutherland G, Dahl N, Patterson MN, Schwartz C, Ledbetter D, et al.

Am J Med Genet. 1991 Feb-Mar;38(2-3):354-6.

PMID:
1673311
26.

An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15.

MacKinnon PJ, Powell BC, Rogers GE, Baker EG, MacKinnon RN, Hyland VJ, Callen DF, Sutherland GR.

Mamm Genome. 1991;1(1):53-6.

PMID:
1724400
27.

Microdissection of the fragile X region.

MacKinnon RN, Hirst MC, Bell MV, Watson JE, Claussen U, Ludecke HJ, Senger G, Horsthemke B, Davies KE.

Am J Hum Genet. 1990 Aug;47(2):181-6.

28.

Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1.

Hyland VJ, Suthers GK, Friend K, MacKinnon RN, Callen DF, Breuning MH, Keith T, Brown VA, Phipps P, Sutherland GR.

Hum Genet. 1990 Feb;84(3):286-8.

PMID:
1968038
29.

Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.

Hyland VJ, Fernandez KE, Callen DF, MacKinnon RN, Baker E, Friend K, Sutherland GR.

Hum Genet. 1989 Aug;83(1):61-6.

PMID:
2570019

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