Smith R - Search Results

1

Eye movement disorders are an early manifestation of CACNA1A mutations in children.

Tantsis EM, Gill D, Griffiths L, Gupta S, Lawson J, Maksemous N, Ouvrier R, Riant F, Smith R, Troedson C, Webster R, Menezes MP. Tantsis EM, et al. Among authors: smith r. Dev Med Child Neurol. 2016 Jun;58(6):639-44. doi: 10.1111/dmcn.13033. Epub 2016 Jan 27. Dev Med Child Neurol. 2016. PMID: 26814174 Free article.

2

Expression of glucocorticoid and progesterone nuclear receptor genes in archival breast cancer tissue.

Smith RA, Lea RA, Curran JE, Weinstein SR, Griffiths LR. Smith RA, et al. Breast Cancer Res. 2003;5(1):R9-12. doi: 10.1186/bcr556. Epub 2002 Nov 7. Breast Cancer Res. 2003. PMID: 12559052 Free PMC article.

3

Detection of mRNA levels for the estrogen alpha, estrogen beta and androgen nuclear receptor genes in archival breast cancer tissue.

Smith RA, Lea RA, Weinstein SR, Griffiths LR. Smith RA, et al. Cancer Lett. 2006 Jun 18;237(2):248-55. doi: 10.1016/j.canlet.2005.06.013. Epub 2005 Jul 20. Cancer Lett. 2006. PMID: 16046054

4

Progesterone, glucocorticoid, but not estrogen receptor mRNA is altered in breast cancer stroma.

Smith RA, Lea RA, Weinstein SR, Griffiths LR. Smith RA, et al. Cancer Lett. 2007 Sep 18;255(1):77-84. doi: 10.1016/j.canlet.2007.03.019. Epub 2007 May 23. Cancer Lett. 2007. PMID: 17512111

5

Investigation of the NOTCH3 and TNFSF7 genes on C19p13 as candidates for migraine.

Smith RA, Curtain R, Ovcaric M, Tajouri L, Macmillan J, Griffiths L. Smith RA, et al. Open Neurol J. 2008;2:1-7. doi: 10.2174/1874205X00802010001. Epub 2008 Apr 23. Open Neurol J. 2008. PMID: 19018300 Free PMC article.

6

Two novel mutations and a previously unreported intronic polymorphism in the NOTCH3 gene.

Roy B, Maksemous N, Smith RA, Menon S, Davies G, Griffiths LR. Roy B, et al. Among authors: smith ra. Mutat Res. 2012 Apr 1;732(1-2):3-8. doi: 10.1016/j.mrfmmm.2012.02.004. Epub 2012 Feb 21. Mutat Res. 2012. PMID: 22373597

7

Investigation of two Wnt signalling pathway single nucleotide polymorphisms in a breast cancer-affected Australian population.

Gabrovska PN, Smith RA, Haupt LM, Griffiths LR. Gabrovska PN, et al. Among authors: smith ra. Twin Res Hum Genet. 2011 Dec;14(6):562-7. doi: 10.1375/twin.14.6.562. Twin Res Hum Genet. 2011. PMID: 22506312

8

A genetic variant located in miR-423 is associated with reduced breast cancer risk.

Smith RA, Jedlinski DJ, Gabrovska PN, Weinstein SR, Haupt L, Griffiths LR. Smith RA, et al. Cancer Genomics Proteomics. 2012 May-Jun;9(3):115-8. Cancer Genomics Proteomics. 2012. PMID: 22593246

9

Detection of a novel mutation in the CACNA1A gene.

Stuart S, Roy B, Davies G, Maksemous N, Smith R, Griffiths LR. Stuart S, et al. Among authors: smith r. Twin Res Hum Genet. 2012 Feb;15(1):120-5. doi: 10.1375/twin.15.1.120. Twin Res Hum Genet. 2012. PMID: 22784462 Free article.

10

Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine.

Rodriguez-Acevedo AJ, Smith RA, Roy B, Sutherland H, Lea RA, Frith A, MacGregor EA, Griffiths LR. Rodriguez-Acevedo AJ, et al. Among authors: smith ra. J Headache Pain. 2014 Oct 14;15(1):62. doi: 10.1186/1129-2377-15-62. J Headache Pain. 2014. PMID: 25315199 Free PMC article.

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