Burley MW - Search Results

1

The -1021C->T DBH gene variant is not associated with epilepsy or antiepileptic drug response.

Depondt C, Cock HR, Healy DG, Burley MW, Weinshenker D, Wood NW, Goldstein DB, Sisodiya SM. Depondt C, et al. Among authors: burley mw. Neurology. 2004 Oct 26;63(8):1497-9. doi: 10.1212/01.wnl.0000142092.16719.ad. Neurology. 2004. PMID: 15505174

2

Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?

Cavalleri GL, Lynch JM, Depondt C, Burley MW, Wood NW, Sisodiya SM, Goldstein DB. Cavalleri GL, et al. Among authors: burley mw. Brain. 2005 Aug;128(Pt 8):1832-40. doi: 10.1093/brain/awh524. Epub 2005 May 11. Brain. 2005. PMID: 15888540

3

Lack of support for a role for RLIP76 (RALBP1) in response to treatment or predisposition to epilepsy.

Soranzo N, Kelly L, Martinian L, Burley MW, Thom M, Sali A, Kroetz DL, Goldstein DB, Sisodiya SM. Soranzo N, et al. Among authors: burley mw. Epilepsia. 2007 Apr;48(4):674-83. doi: 10.1111/j.1528-1167.2007.00926.x. Epilepsia. 2007. PMID: 17437410 Free article.

4

A 19 bp deletion polymorphism adjacent to a dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase locus.

Nahmias J, Burley MW, Povey S, Porter C, Craig I, Wolfe J. Nahmias J, et al. Among authors: burley mw. Hum Mol Genet. 1992 Jul;1(4):286. doi: 10.1093/hmg/1.4.286. Hum Mol Genet. 1992. PMID: 1339474 No abstract available.

5

A BamHI polymorphism at the DBH locus.

Porter CJ, Craig SP, Burley M, Levy ER, Hinds H, Williams A, Craig IW. Porter CJ, et al. Nucleic Acids Res. 1990 Sep 25;18(18):5581. doi: 10.1093/nar/18.18.5581-a. Nucleic Acids Res. 1990. PMID: 1977125 Free PMC article.

6

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

Povey S, Burley MW, Attwood J, Benham F, Hunt D, Jeremiah SJ, Franklin D, Gillett G, Malas S, Robson EB. Povey S, et al. Among authors: burley mw. Ann Hum Genet. 1994 May;58(2):107-27. doi: 10.1111/j.1469-1809.1994.tb01881.x. Ann Hum Genet. 1994. PMID: 7979156

7

Mapping ESTs to the TSC1 candidate interval by use of the 'Science 96' transcript map.

Wolfe J, Jeremiah S, Young J, Burley MW, Stewart H, McCulley M, Grant C, Naz K, Povey S. Wolfe J, et al. Among authors: burley mw. Ann Hum Genet. 1997 Sep;61(Pt 5):401-9. doi: 10.1046/j.1469-1809.1997.6150401.x. Ann Hum Genet. 1997. PMID: 9459002

8

A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients.

Young JM, Burley MW, Jeremiah SJ, Jeganathan D, Ekong R, Osborne JP, Povey S. Young JM, et al. Among authors: burley mw. Ann Hum Genet. 1998 May;62(Pt 3):203-13. doi: 10.1046/j.1469-1809.1998.6230203.x. Ann Hum Genet. 1998. PMID: 9803264

9

An attempt to map two genes for tuberous sclerosis using novel two-point methods.

Povey S, Attwood J, Janssen LA, Burley M, Smith M, Flodman P, Morton NE, Edwards JH, Sampson JR, Yates JR, et al. Povey S, et al. Ann N Y Acad Sci. 1991;615:298-305. doi: 10.1111/j.1749-6632.1991.tb37771.x. Ann N Y Acad Sci. 1991. PMID: 1674846 No abstract available.

10

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.

van Slegtenhorst M, de Hoogt R, Hermans C, Nellist M, Janssen B, Verhoef S, Lindhout D, van den Ouweland A, Halley D, Young J, Burley M, Jeremiah S, Woodward K, Nahmias J, Fox M, Ekong R, Osborne J, Wolfe J, Povey S, Snell RG, Cheadle JP, Jones AC, Tachataki M, Ravine D, Sampson JR, Reeve MP, Richardson P, Wilmer F, Munro C, Hawkins TL, Sepp T, Ali JB, Ward S, Green AJ, Yates JR, Kwiatkowska J, Henske EP, Short MP, Haines JH, Jozwiak S, Kwiatkowski DJ. van Slegtenhorst M, et al. Science. 1997 Aug 8;277(5327):805-8. doi: 10.1126/science.277.5327.805. Science. 1997. PMID: 9242607

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