Bates GP - Search Results

1

Expression of mutant exon 1 huntingtin fragments in human neural stem cells and neurons causes inclusion formation and mitochondrial dysfunction.

Ghosh R, Wood-Kaczmar A, Dobson L, Smith EJ, Sirinathsinghji EC, Kriston-Vizi J, Hargreaves IP, Heaton R, Herrmann F, Abramov AY, Lam AJ, Heales SJ, Ketteler R, Bates GP, Andre R, Tabrizi SJ. Ghosh R, et al. Among authors: bates gp. FASEB J. 2020 Jun;34(6):8139-8154. doi: 10.1096/fj.201902277RR. Epub 2020 Apr 23. FASEB J. 2020. PMID: 32329133 Free PMC article.

2

Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?

Davies SW, Beardsall K, Turmaine M, DiFiglia M, Aronin N, Bates GP. Davies SW, et al. Among authors: bates gp. Lancet. 1998 Jan 10;351(9096):131-3. doi: 10.1016/S0140-6736(97)08360-8. Lancet. 1998. PMID: 9439509

3

Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouse.

Tabrizi SJ, Workman J, Hart PE, Mangiarini L, Mahal A, Bates G, Cooper JM, Schapira AH. Tabrizi SJ, et al. Ann Neurol. 2000 Jan;47(1):80-6. doi: 10.1002/1531-8249(200001)47:1<80::aid-ana13>3.3.co;2-b. Ann Neurol. 2000. PMID: 10632104

4

Inclusion formation in Huntington's disease R6/2 mouse muscle cultures.

Orth M, Cooper JM, Bates GP, Schapira AH. Orth M, et al. Among authors: bates gp. J Neurochem. 2003 Oct;87(1):1-6. doi: 10.1046/j.1471-4159.2003.02009.x. J Neurochem. 2003. PMID: 12969246 Free article.

5

Biomarkers for neurodegenerative diseases.

Henley SM, Bates GP, Tabrizi SJ. Henley SM, et al. Among authors: bates gp. Curr Opin Neurol. 2005 Dec;18(6):698-705. doi: 10.1097/01.wco.0000186842.51129.cb. Curr Opin Neurol. 2005. PMID: 16280682 Review.

6

Metabolic characterization of the R6/2 transgenic mouse model of Huntington's disease by high-resolution MAS 1H NMR spectroscopy.

Tsang TM, Woodman B, McLoughlin GA, Griffin JL, Tabrizi SJ, Bates GP, Holmes E. Tsang TM, et al. Among authors: bates gp. J Proteome Res. 2006 Mar;5(3):483-92. doi: 10.1021/pr050244o. J Proteome Res. 2006. PMID: 16512662

7

Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease.

Björkqvist M, Petersén A, Bacos K, Isaacs J, Norlén P, Gil J, Popovic N, Sundler F, Bates GP, Tabrizi SJ, Brundin P, Mulder H. Björkqvist M, et al. Among authors: bates gp. Hum Mol Genet. 2006 May 15;15(10):1713-21. doi: 10.1093/hmg/ddl094. Epub 2006 Apr 13. Hum Mol Genet. 2006. PMID: 16613897

8

The Hdh(Q150/Q150) knock-in mouse model of HD and the R6/2 exon 1 model develop comparable and widespread molecular phenotypes.

Woodman B, Butler R, Landles C, Lupton MK, Tse J, Hockly E, Moffitt H, Sathasivam K, Bates GP. Woodman B, et al. Among authors: bates gp. Brain Res Bull. 2007 Apr 30;72(2-3):83-97. doi: 10.1016/j.brainresbull.2006.11.004. Epub 2006 Dec 5. Brain Res Bull. 2007. PMID: 17352931

9

Hsp27 overexpression in the R6/2 mouse model of Huntington's disease: chronic neurodegeneration does not induce Hsp27 activation.

Zourlidou A, Gidalevitz T, Kristiansen M, Landles C, Woodman B, Wells DJ, Latchman DS, de Belleroche J, Tabrizi SJ, Morimoto RI, Bates GP. Zourlidou A, et al. Among authors: bates gp. Hum Mol Genet. 2007 May 1;16(9):1078-90. doi: 10.1093/hmg/ddm057. Epub 2007 Mar 14. Hum Mol Genet. 2007. PMID: 17360721

10

A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease.

Björkqvist M, Wild EJ, Thiele J, Silvestroni A, Andre R, Lahiri N, Raibon E, Lee RV, Benn CL, Soulet D, Magnusson A, Woodman B, Landles C, Pouladi MA, Hayden MR, Khalili-Shirazi A, Lowdell MW, Brundin P, Bates GP, Leavitt BR, Möller T, Tabrizi SJ. Björkqvist M, et al. Among authors: bates gp. J Exp Med. 2008 Aug 4;205(8):1869-77. doi: 10.1084/jem.20080178. Epub 2008 Jul 14. J Exp Med. 2008. PMID: 18625748 Free PMC article.

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