Premarathne S - Search Results

1

Evidence of a Recessively Inherited CCN3 Mutation as a Rare Cause of Early-Onset Parkinsonism.

Bentley SR, Khan S, Öchsner M, Premarathne S, Aslam Z, Fowdar JY, Iqbal J, Naeem M, Love CA, Wood SA, Mellick GD, Sykes AM. Bentley SR, et al. Among authors: premarathne s. Front Neurol. 2020 May 15;11:331. doi: 10.3389/fneur.2020.00331. eCollection 2020. Front Neurol. 2020. PMID: 32499748 Free PMC article.

2

Proteomic profiling of idiopathic Parkinson's disease primary patient cells by SWATH-MS.

Wood SA, Hains PG, Muller A, Hill M, Premarathne S, Murtaza M, Robinson PJ, Mellick GD, Sykes AM. Wood SA, et al. Among authors: premarathne s. Proteomics Clin Appl. 2022 Sep;16(5):e2200015. doi: 10.1002/prca.202200015. Epub 2022 Jun 7. Proteomics Clin Appl. 2022. PMID: 35579911 Free PMC article.

3

USP9X deletion elevates the density of oligodendrocytes within the postnatal dentate gyrus.

Oishi S, Zalucki O, Premarathne S, Wood SA, Piper M. Oishi S, et al. Among authors: premarathne s. Neurogenesis (Austin). 2016 Sep 30;3(1):e1235524. doi: 10.1080/23262133.2016.1235524. eCollection 2016. Neurogenesis (Austin). 2016. PMID: 27830160 Free PMC article.

4

Loss of Usp9x disrupts cell adhesion, and components of the Wnt and Notch signaling pathways in neural progenitors.

Premarathne S, Murtaza M, Matigian N, Jolly LA, Wood SA. Premarathne S, et al. Sci Rep. 2017 Aug 14;7(1):8109. doi: 10.1038/s41598-017-05451-5. Sci Rep. 2017. PMID: 28808228 Free PMC article.

5

The Ubiquitin System: a Regulatory Hub for Intellectual Disability and Autism Spectrum Disorder.

Kasherman MA, Premarathne S, Burne THJ, Wood SA, Piper M. Kasherman MA, et al. Among authors: premarathne s. Mol Neurobiol. 2020 May;57(5):2179-2193. doi: 10.1007/s12035-020-01881-x. Epub 2020 Jan 23. Mol Neurobiol. 2020. PMID: 31974941 Review.

6

Usp9x-deficiency disrupts the morphological development of the postnatal hippocampal dentate gyrus.

Oishi S, Premarathne S, Harvey TJ, Iyer S, Dixon C, Alexander S, Burne TH, Wood SA, Piper M. Oishi S, et al. Among authors: premarathne s. Sci Rep. 2016 May 16;6:25783. doi: 10.1038/srep25783. Sci Rep. 2016. PMID: 27181636 Free PMC article.

7

Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis.

Stegeman S, Jolly LA, Premarathne S, Gecz J, Richards LJ, Mackay-Sim A, Wood SA. Stegeman S, et al. Among authors: premarathne s. PLoS One. 2013 Jul 5;8(7):e68287. doi: 10.1371/journal.pone.0068287. Print 2013. PLoS One. 2013. PMID: 23861879 Free PMC article.

8

Usp9X Controls Ankyrin-Repeat Domain Protein Homeostasis during Dendritic Spine Development.

Yoon S, Parnell E, Kasherman M, Forrest MP, Myczek K, Premarathne S, Sanchez Vega MC, Piper M, Burne THJ, Jolly LA, Wood SA, Penzes P. Yoon S, et al. Among authors: premarathne s. Neuron. 2020 Feb 5;105(3):506-521.e7. doi: 10.1016/j.neuron.2019.11.003. Epub 2019 Dec 5. Neuron. 2020. PMID: 31813652 Free PMC article.

9

USP9X deubiquitylating enzyme maintains RAPTOR protein levels, mTORC1 signalling and proliferation in neural progenitors.

Bridges CR, Tan MC, Premarathne S, Nanayakkara D, Bellette B, Zencak D, Domingo D, Gecz J, Murtaza M, Jolly LA, Wood SA. Bridges CR, et al. Among authors: premarathne s. Sci Rep. 2017 Mar 24;7(1):391. doi: 10.1038/s41598-017-00149-0. Sci Rep. 2017. PMID: 28341829 Free PMC article.

10

Taxonomic status of Pseudophilautus conniffae (Anura: Rhacophoridae) an endemic shrub frog restricted to South-Western wet zone of Sri Lanka.

Abeysekara S, Samarasinghe H, Manamendra-Arachchi K, Adhikari H, Premarathne S, Bandara C, Perera U, Wijayathilaka N. Abeysekara S, et al. Among authors: premarathne s. Zootaxa. 2023 Mar 27;5258(1):130-140. doi: 10.11646/zootaxa.5258.1.6. Zootaxa. 2023. PMID: 37044606

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