George PM - Search Results

1

The characterization of ovine genes for atrial, brain, and C-type natriuretic peptides.

Aitken GD, Raizis AM, Yandle TG, George PM, Espiner EA, Cameron VA. Aitken GD, et al. Among authors: george pm. Domest Anim Endocrinol. 1999 Feb;16(2):115-21. doi: 10.1016/s0739-7240(99)00005-3. Domest Anim Endocrinol. 1999. PMID: 10219521

2

Effect of nonsense mutations on PTEN mRNA stability.

Raizis AM, Ferguson MM, George PM. Raizis AM, et al. Among authors: george pm. Hum Genet. 2000 Jul;107(1):24-7. doi: 10.1007/s004390000317. Hum Genet. 2000. PMID: 10982030

3

Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndrome.

Raizis AM, Ferguson MM, Robinson BA, Atkinson CH, George PM. Raizis AM, et al. Among authors: george pm. Mol Pathol. 1998 Dec;51(6):339-41. doi: 10.1136/mp.51.6.339. Mol Pathol. 1998. PMID: 10193515 Free PMC article.

4

Spectrum of MECP2 mutations in New Zealand Rett syndrome patients.

Raizis AM, Saleem M, MacKay R, George PM. Raizis AM, et al. Among authors: george pm. N Z Med J. 2009 Jun 5;122(1296):21-8. N Z Med J. 2009. PMID: 19652677

5

Improved clinical management of retinoblastoma through gene testing.

Raizis A, Clemett R, Corbett R, McGaughran J, Evans J, George P. Raizis A, et al. N Z Med J. 2002 May 24;115(1154):231-4. N Z Med J. 2002. PMID: 12117173

6

Four cases of autosomal dominant hypocalcaemia with hypercalciuria including two with novel mutations in the calcium-sensing receptor gene.

Schouten BJ, Raizis AM, Soule SG, Cole DR, Frengley PA, George PM, Florkowski CM. Schouten BJ, et al. Among authors: george pm. Ann Clin Biochem. 2011 May;48(Pt 3):286-90. doi: 10.1258/acb.2010.010139. Epub 2011 Mar 25. Ann Clin Biochem. 2011. PMID: 21441391

7

Trilateral retinoblastoma in a patient with Peutz-Jeghers syndrome.

Raizis AM, Van Mater D, Aaltonen LA, Lohmann D, Cheale MS, Bickley VM, George PM, Zhou Y, Rosoff PM. Raizis AM, et al. Among authors: george pm. Am J Med Genet A. 2013 May;161A(5):1096-100. doi: 10.1002/ajmg.a.35748. Epub 2013 Mar 5. Am J Med Genet A. 2013. PMID: 23463749

8

Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients.

Palmer BR, Slow S, Ellis KL, Pilbrow AP, Skelton L, Frampton CM, Palmer SC, Troughton RW, Yandle TG, Doughty RN, Whalley GA, Lever M, George PM, Chambers ST, Ellis C, Richards AM, Cameron VA. Palmer BR, et al. Among authors: george pm. PLoS One. 2014 Mar 11;9(3):e89029. doi: 10.1371/journal.pone.0089029. eCollection 2014. PLoS One. 2014. PMID: 24618918 Free PMC article.

9

DNA hypermethylation/boundary control loss identified in retinoblastomas associated with genetic and epigenetic inactivation of the RB1 gene promoter.

Raizis AM, Racher HM, Foucal A, Dimaras H, Gallie BL, George PM. Raizis AM, et al. Among authors: george pm. Epigenetics. 2021 Sep;16(9):940-954. doi: 10.1080/15592294.2020.1834911. Epub 2020 Dec 1. Epigenetics. 2021. PMID: 33258708 Free PMC article.

10

Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy.

Lacey CJ, Doudney K, Bridgman PG, George PM, Mulder RT, Zarifeh JJ, Kimber B, Cadzow MJ, Black MA, Merriman TR, Lehnert K, Bickley VM, Pearson JF, Cameron VA, Kennedy MA. Lacey CJ, et al. Among authors: george pm. Sci Rep. 2018 May 15;8(1):7548. doi: 10.1038/s41598-018-25827-5. Sci Rep. 2018. PMID: 29765130 Free PMC article.

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