Sue CM - Search Results

1

Thioredoxin interacting protein (TXNIP) regulates tubular autophagy and mitophagy in diabetic nephropathy through the mTOR signaling pathway.

Huang C, Zhang Y, Kelly DJ, Tan CY, Gill A, Cheng D, Braet F, Park JS, Sue CM, Pollock CA, Chen XM. Huang C, et al. Among authors: sue cm. Sci Rep. 2016 Jul 6;6:29196. doi: 10.1038/srep29196. Sci Rep. 2016. PMID: 27381856 Free PMC article.

2

Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism.

Park JS, Mehta P, Cooper AA, Veivers D, Heimbach A, Stiller B, Kubisch C, Fung VS, Krainc D, Mackay-Sim A, Sue CM. Park JS, et al. Among authors: sue cm. Hum Mutat. 2011 Aug;32(8):956-64. doi: 10.1002/humu.21527. Epub 2011 Jul 12. Hum Mutat. 2011. PMID: 21542062

3

Phenotypic variability of parkin mutations in single kindred.

Koentjoro B, Park JS, Ha AD, Sue CM. Koentjoro B, et al. Among authors: sue cm. Mov Disord. 2012 Sep 1;27(10):1299-303. doi: 10.1002/mds.25041. Epub 2012 Jul 17. Mov Disord. 2012. PMID: 22807239

4

Parkinson's disease-associated human ATP13A2 (PARK9) deficiency causes zinc dyshomeostasis and mitochondrial dysfunction.

Park JS, Koentjoro B, Veivers D, Mackay-Sim A, Sue CM. Park JS, et al. Among authors: sue cm. Hum Mol Genet. 2014 Jun 1;23(11):2802-15. doi: 10.1093/hmg/ddt623. Epub 2014 Jan 7. Hum Mol Genet. 2014. PMID: 24399444 Free PMC article.

5

Parkin western blotting is useful for identification of patients with Parkin-related Parkinson's disease.

Koentjoro B, Park JS, Sue CM. Koentjoro B, et al. Among authors: sue cm. J Neurol Neurosurg Psychiatry. 2014 Dec;85(12):1436-7. doi: 10.1136/jnnp-2014-308142. Epub 2014 May 9. J Neurol Neurosurg Psychiatry. 2014. PMID: 24816420 No abstract available.

6

The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms.

Park JS, Blair NF, Sue CM. Park JS, et al. Among authors: sue cm. Mov Disord. 2015 May;30(6):770-9. doi: 10.1002/mds.26243. Epub 2015 Apr 21. Mov Disord. 2015. PMID: 25900096 Review.

7

Mutations in TUBB4A and spastic paraplegia.

Kumar KR, Vulinovic F, Lohmann K, Park JS, Schaake S, Sue CM, Klein C. Kumar KR, et al. Among authors: sue cm. Mov Disord. 2015 Nov;30(13):1857-8. doi: 10.1002/mds.26444. Epub 2015 Oct 19. Mov Disord. 2015. PMID: 26477786 No abstract available.

8

Hereditary Parkinsonism-Associated Genetic Variations in PARK9 Locus Lead to Functional Impairment of ATPase Type 13A2.

Park JS, Sue CM. Park JS, et al. Among authors: sue cm. Curr Protein Pept Sci. 2017;18(7):725-732. doi: 10.2174/1389203717666160311121534. Curr Protein Pept Sci. 2017. PMID: 26965689 Review.

9

Loss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell models.

Park JS, Koentjoro B, Davis RL, Sue CM. Park JS, et al. Among authors: sue cm. Parkinsonism Relat Disord. 2016 Jun;27:67-73. doi: 10.1016/j.parkreldis.2016.03.018. Epub 2016 Mar 22. Parkinsonism Relat Disord. 2016. PMID: 27039055

10

Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic Paraplegia.

Wali G, Sutharsan R, Fan Y, Stewart R, Tello Velasquez J, Sue CM, Crane DI, Mackay-Sim A. Wali G, et al. Among authors: sue cm. Sci Rep. 2016 May 27;6:27004. doi: 10.1038/srep27004. Sci Rep. 2016. PMID: 27229699 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

212 results

Search Page

Filters