Sharpe PT - Search Results

1

Contribution of nuclear and extranuclear polyQ to neurological phenotypes in mouse models of Huntington's disease.

Benn CL, Landles C, Li H, Strand AD, Woodman B, Sathasivam K, Li SH, Ghazi-Noori S, Hockly E, Faruque SM, Cha JH, Sharpe PT, Olson JM, Li XJ, Bates GP. Benn CL, et al. Among authors: sharpe pt. Hum Mol Genet. 2005 Oct 15;14(20):3065-78. doi: 10.1093/hmg/ddi340. Epub 2005 Sep 23. Hum Mol Genet. 2005. PMID: 16183657

2

Disrupted mitochondrial function in the Opa3L122P mouse model for Costeff Syndrome impairs skeletal integrity.

Navein AE, Cooke EJ, Davies JR, Smith TG, Wells LH, Ohazama A, Healy C, Sharpe PT, Evans SL, Evans BA, Votruba M, Wells T. Navein AE, et al. Among authors: sharpe pt. Hum Mol Genet. 2016 Jun 15;25(12):2404-2416. doi: 10.1093/hmg/ddw107. Epub 2016 Apr 22. Hum Mol Genet. 2016. PMID: 27106103 Free PMC article.

3

Normal and abnormal dental development.

Miletich I, Sharpe PT. Miletich I, et al. Among authors: sharpe pt. Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R69-73. doi: 10.1093/hmg/ddg085. Hum Mol Genet. 2003. PMID: 12668599 Review.

4

Expression of Claudin-3 during chick development.

Haworth KE, El-Hanfy A, Prayag S, Healy C, Dietrich S, Sharpe P. Haworth KE, et al. Gene Expr Patterns. 2005 Dec;6(1):40-4. doi: 10.1016/j.modgep.2005.05.002. Epub 2005 Jul 18. Gene Expr Patterns. 2005. PMID: 16024293

5

The mouse as a developmental model.

Sharpe PT. Sharpe PT. Methods Mol Biol. 2008;461:3-5. doi: 10.1007/978-1-60327-483-8_1. Methods Mol Biol. 2008. PMID: 19030786 No abstract available.

6

Scube1 is expressed during facial development in the mouse.

Xavier GM, Sharpe PT, Cobourne MT. Xavier GM, et al. Among authors: sharpe pt. J Exp Zool B Mol Dev Evol. 2009 Jul 15;312B(5):518-24. doi: 10.1002/jez.b.21260. J Exp Zool B Mol Dev Evol. 2009. PMID: 19101956

7

Periodic stripe formation by a Turing mechanism operating at growth zones in the mammalian palate.

Economou AD, Ohazama A, Porntaveetus T, Sharpe PT, Kondo S, Basson MA, Gritli-Linde A, Cobourne MT, Green JB. Economou AD, et al. Among authors: sharpe pt. Nat Genet. 2012 Feb 19;44(3):348-51. doi: 10.1038/ng.1090. Nat Genet. 2012. PMID: 22344222 Free PMC article.

8

Multiple postnatal craniofacial anomalies are characterized by conditional loss of polycystic kidney disease 2 (Pkd2).

Khonsari RH, Ohazama A, Raouf R, Kawasaki M, Kawasaki K, Porntaveetus T, Ghafoor S, Hammond P, Suttie M, Odri GA, Sandford RN, Wood JN, Sharpe PT. Khonsari RH, et al. Among authors: sharpe pt. Hum Mol Genet. 2013 May 1;22(9):1873-85. doi: 10.1093/hmg/ddt041. Epub 2013 Feb 5. Hum Mol Genet. 2013. PMID: 23390131

9

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.

Hewitt JE, Lyle R, Clark LN, Valleley EM, Wright TJ, Wijmenga C, van Deutekom JC, Francis F, Sharpe PT, Hofker M, et al. Hewitt JE, et al. Among authors: sharpe pt. Hum Mol Genet. 1994 Aug;3(8):1287-95. doi: 10.1093/hmg/3.8.1287. Hum Mol Genet. 1994. PMID: 7987304

10

Granule cell development in the cerebellum is punctuated by changes in Sox gene expression.

Rex M, Church R, Tointon K, Ichihashi RM, Mokhtar S, Uwanogho D, Sharpe PT, Scotting PJ. Rex M, et al. Among authors: sharpe pt. Brain Res Mol Brain Res. 1998 Mar 30;55(1):28-34. doi: 10.1016/s0169-328x(97)00354-9. Brain Res Mol Brain Res. 1998. PMID: 9645957

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