Lo HP - Search Results

1

Limb-girdle muscular dystrophy: diagnostic evaluation, frequency and clues to pathogenesis.

Lo HP, Cooper ST, Evesson FJ, Seto JT, Chiotis M, Tay V, Compton AG, Cairns AG, Corbett A, MacArthur DG, Yang N, Reardon K, North KN. Lo HP, et al. Neuromuscul Disord. 2008 Jan;18(1):34-44. doi: 10.1016/j.nmd.2007.08.009. Epub 2007 Sep 25. Neuromuscul Disord. 2008. PMID: 17897828

2

Single section Western blot: improving the molecular diagnosis of the muscular dystrophies.

Cooper ST, Lo HP, North KN. Cooper ST, et al. Among authors: lo hp. Neurology. 2003 Jul 8;61(1):93-7. doi: 10.1212/01.wnl.0000069460.53438.38. Neurology. 2003. PMID: 12847163

3

Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesis.

Cooper ST, Kizana E, Yates JD, Lo HP, Yang N, Wu ZH, Alexander IE, North KN. Cooper ST, et al. Among authors: lo hp. Neuromuscul Disord. 2007 Apr;17(4):276-84. doi: 10.1016/j.nmd.2006.12.010. Epub 2007 Feb 15. Neuromuscul Disord. 2007. PMID: 17303423

4

Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodies.

Lo HP, Bertini E, Mirabella M, Domazetovska A, Dale RC, Petrini S, D'Amico A, Valente EM, Barresi R, Roberts M, Tozzi G, Tasca G, Cooper ST, Straub V, North KN. Lo HP, et al. Neuromuscul Disord. 2011 Mar;21(3):194-203. doi: 10.1016/j.nmd.2010.11.015. Epub 2011 Feb 4. Neuromuscul Disord. 2011. PMID: 21295981

5

Expression of aquaporin 1 in human cardiac and skeletal muscle.

Au CG, Cooper ST, Lo HP, Compton AG, Yang N, Wintour EM, North KN, Winlaw DS. Au CG, et al. Among authors: lo hp. J Mol Cell Cardiol. 2004 May;36(5):655-62. doi: 10.1016/j.yjmcc.2004.01.009. J Mol Cell Cardiol. 2004. PMID: 15135660

6

Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3.

Hernández-Deviez DJ, Martin S, Laval SH, Lo HP, Cooper ST, North KN, Bushby K, Parton RG. Hernández-Deviez DJ, et al. Among authors: lo hp. Hum Mol Genet. 2006 Jan 1;15(1):129-42. doi: 10.1093/hmg/ddi434. Epub 2005 Nov 30. Hum Mol Genet. 2006. PMID: 16319126

7

Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients.

Au CG, Butler TL, Egan JR, Cooper ST, Lo HP, Compton AG, North KN, Winlaw DS. Au CG, et al. Among authors: lo hp. Acta Neuropathol. 2008 Sep;116(3):235-46. doi: 10.1007/s00401-008-0369-z. Epub 2008 Apr 8. Acta Neuropathol. 2008. PMID: 18392839

8

Muscular dystrophy associated with alpha-dystroglycan deficiency in Sphynx and Devon Rex cats.

Martin PT, Shelton GD, Dickinson PJ, Sturges BK, Xu R, LeCouteur RA, Guo LT, Grahn RA, Lo HP, North KN, Malik R, Engvall E, Lyons LA. Martin PT, et al. Among authors: lo hp. Neuromuscul Disord. 2008 Dec;18(12):942-52. doi: 10.1016/j.nmd.2008.08.002. Epub 2008 Nov 5. Neuromuscul Disord. 2008. PMID: 18990577 Free PMC article.

9

Reduced plasma membrane expression of dysferlin mutants is attributed to accelerated endocytosis via a syntaxin-4-associated pathway.

Evesson FJ, Peat RA, Lek A, Brilot F, Lo HP, Dale RC, Parton RG, North KN, Cooper ST. Evesson FJ, et al. Among authors: lo hp. J Biol Chem. 2010 Sep 10;285(37):28529-39. doi: 10.1074/jbc.M110.111120. Epub 2010 Jul 1. J Biol Chem. 2010. PMID: 20595382 Free PMC article.

10

Rippling muscle disease.

Roberts HL, Day B, Lo H, McLean C, North K. Roberts HL, et al. J Clin Neurosci. 2006 Jun;13(5):576-8. doi: 10.1016/j.jocn.2005.06.015. Epub 2006 May 24. J Clin Neurosci. 2006. PMID: 16723230

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