Byrne PC - Search Results

1

The hereditary spastic paraplegia protein spartin localises to mitochondria.

Lu J, Rashid F, Byrne PC. Lu J, et al. Among authors: byrne pc. J Neurochem. 2006 Sep;98(6):1908-19. doi: 10.1111/j.1471-4159.2006.04008.x. J Neurochem. 2006. PMID: 16945107 Free article.

2

Identification of novel spartin-interactors shows spartin is a multifunctional protein.

Milewska M, McRedmond J, Byrne PC. Milewska M, et al. Among authors: byrne pc. J Neurochem. 2009 Nov;111(4):1022-30. doi: 10.1111/j.1471-4159.2009.06382.x. Epub 2009 Sep 16. J Neurochem. 2009. PMID: 19765186 Free article.

3

Different expression levels of spartin cause broad spectrum of cellular consequences in human neuroblastoma cells.

Milewska M, Byrne PC. Milewska M, et al. Among authors: byrne pc. Cell Biol Int. 2015 Sep;39(9):1007-15. doi: 10.1002/cbin.10472. Epub 2015 May 8. Cell Biol Int. 2015. PMID: 25821002

4

Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p.

Webb S, Coleman D, Byrne P, Parfrey N, Burke T, Hutchinson J, Hutchinson M. Webb S, et al. Brain. 1998 Apr;121 ( Pt 4):601-9. doi: 10.1093/brain/121.4.601. Brain. 1998. PMID: 9577388

5

Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p.

Byrne PC, Mc Monagle P, Webb S, Fitzgerald B, Parfrey NA, Hutchinson M. Byrne PC, et al. Neurology. 2000 Apr 11;54(7):1510-7. doi: 10.1212/wnl.54.7.1510. Neurology. 2000. PMID: 10751268

6

Further evidence of dementia in SPG4-linked autosomal dominant hereditary spastic paraplegia.

McMonagle P, Byrne P, Hutchinson M. McMonagle P, et al. Neurology. 2004 Feb 10;62(3):407-10. doi: 10.1212/01.wnl.0000108629.04434.05. Neurology. 2004. PMID: 14872021

7

SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q.

Hughes CA, Byrne PC, Webb S, McMonagle P, Patterson V, Hutchinson M, Parfrey NA. Hughes CA, et al. Among authors: byrne pc. Neurology. 2001 May 8;56(9):1230-3. doi: 10.1212/wnl.56.9.1230. Neurology. 2001. PMID: 11342696

8

Dementia in SPG4 hereditary spastic paraplegia: clinical, genetic, and neuropathologic evidence.

Murphy S, Gorman G, Beetz C, Byrne P, Dytko M, McMonagle P, Kinsella K, Farrell M, Hutchinson M. Murphy S, et al. Neurology. 2009 Aug 4;73(5):378-84. doi: 10.1212/WNL.0b013e3181b04c6c. Neurology. 2009. PMID: 19652142

9

Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance.

Byrne PC, Webb S, McSweeney F, Burke T, Hutchinson M, Parfrey NA. Byrne PC, et al. Eur J Hum Genet. 1998 May-Jun;6(3):275-82. doi: 10.1038/sj.ejhg.5200185. Eur J Hum Genet. 1998. PMID: 9781032

10

Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein.

Mannan AU, Boehm J, Sauter SM, Rauber A, Byrne PC, Neesen J, Engel W. Mannan AU, et al. Among authors: byrne pc. Neurogenetics. 2006 May;7(2):93-103. doi: 10.1007/s10048-006-0034-4. Epub 2006 Apr 7. Neurogenetics. 2006. PMID: 16602018

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

27 results

Search Page

Filters