Thomas PQ - Search Results

1

Distribution of Parkinson's disease associated RAB39B in mouse brain tissue.

Gao Y, Wilson GR, Stephenson SEM, Oulad-Abdelghani M, Charlet-Berguerand N, Bozaoglu K, McLean CA, Thomas PQ, Finkelstein DI, Lockhart PJ. Gao Y, et al. Among authors: thomas pq. Mol Brain. 2020 Mar 30;13(1):52. doi: 10.1186/s13041-020-00584-7. Mol Brain. 2020. PMID: 32228644 Free PMC article.

2

Polyalanine expansion mutations in the X-linked hypopituitarism gene SOX3 result in aggresome formation and impaired transactivation.

Wong J, Farlie P, Holbert S, Lockhart P, Thomas PQ. Wong J, et al. Among authors: thomas pq. Front Biosci. 2007 Jan 1;12:2085-95. doi: 10.2741/2213. Front Biosci. 2007. PMID: 17127446

3

Deep sequencing analysis of the developing mouse brain reveals a novel microRNA.

Ling KH, Brautigan PJ, Hahn CN, Daish T, Rayner JR, Cheah PS, Raison JM, Piltz S, Mann JR, Mattiske DM, Thomas PQ, Adelson DL, Scott HS. Ling KH, et al. Among authors: thomas pq. BMC Genomics. 2011 Apr 5;12:176. doi: 10.1186/1471-2164-12-176. BMC Genomics. 2011. PMID: 21466694 Free PMC article.

4

Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency.

Cheah PS, Ramshaw HS, Thomas PQ, Toyo-Oka K, Xu X, Martin S, Coyle P, Guthridge MA, Stomski F, van den Buuse M, Wynshaw-Boris A, Lopez AF, Schwarz QP. Cheah PS, et al. Among authors: thomas pq. Mol Psychiatry. 2012 Apr;17(4):451-66. doi: 10.1038/mp.2011.158. Epub 2011 Nov 29. Mol Psychiatry. 2012. PMID: 22124272

5

Molecular pathology of polyalanine expansion disorders: new perspectives from mouse models.

Hughes JN, Thomas PQ. Hughes JN, et al. Among authors: thomas pq. Methods Mol Biol. 2013;1017:135-51. doi: 10.1007/978-1-62703-438-8_10. Methods Mol Biol. 2013. PMID: 23719913 Review.

6

Pcdh19 Loss-of-Function Increases Neuronal Migration In Vitro but is Dispensable for Brain Development in Mice.

Pederick DT, Homan CC, Jaehne EJ, Piltz SG, Haines BP, Baune BT, Jolly LA, Hughes JN, Gecz J, Thomas PQ. Pederick DT, et al. Among authors: thomas pq. Sci Rep. 2016 May 31;6:26765. doi: 10.1038/srep26765. Sci Rep. 2016. PMID: 27240640 Free PMC article.

7

Paroxysmal and cognitive phenotypes in Prrt2 mutant mice.

Robertson L, Featherby T, Howell S, Hughes J, Thomas P. Robertson L, et al. Genes Brain Behav. 2019 Jun;18(5):e12566. doi: 10.1111/gbb.12566. Epub 2019 Apr 1. Genes Brain Behav. 2019. PMID: 30884140 Free article.

8

Disrupted Excitatory Synaptic Contacts and Altered Neuronal Network Activity Underpins the Neurological Phenotype in PCDH19-Clustering Epilepsy (PCDH19-CE).

Mincheva-Tasheva S, Nieto Guil AF, Homan CC, Gecz J, Thomas PQ. Mincheva-Tasheva S, et al. Among authors: thomas pq. Mol Neurobiol. 2021 May;58(5):2005-2018. doi: 10.1007/s12035-020-02242-4. Epub 2021 Jan 7. Mol Neurobiol. 2021. PMID: 33411240

9

Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signalling.

Hughes J, Dawson R, Tea M, McAninch D, Piltz S, Jackson D, Stewart L, Ricos MG, Dibbens LM, Harvey NL, Thomas P. Hughes J, et al. Sci Rep. 2017 Oct 3;7(1):12618. doi: 10.1038/s41598-017-12574-2. Sci Rep. 2017. PMID: 28974734 Free PMC article.

10

Genome-wide DNA-binding profile of SRY-box transcription factor 3 (SOX3) in mouse testes.

McAninch D, Thomson EP, Thomas PQ. McAninch D, et al. Among authors: thomas pq. Reprod Fertil Dev. 2020 Nov;32(16):1260-1270. doi: 10.1071/RD20108. Reprod Fertil Dev. 2020. PMID: 33166488

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