Walker KR - Search Results

1

Production of human skeletal alpha-actin proteins by the baculovirus expression system.

Anthony Akkari P, Nowak KJ, Beckman K, Walker KR, Schachat F, Laing NG. Anthony Akkari P, et al. Among authors: walker kr. Biochem Biophys Res Commun. 2003 Jul 18;307(1):74-9. doi: 10.1016/s0006-291x(03)01133-1. Biochem Biophys Res Commun. 2003. PMID: 12849983

2

Nemaline myopathy caused by absence of alpha-skeletal muscle actin.

Nowak KJ, Sewry CA, Navarro C, Squier W, Reina C, Ricoy JR, Jayawant SS, Childs AM, Dobbie JA, Appleton RE, Mountford RC, Walker KR, Clement S, Barois A, Muntoni F, Romero NB, Laing NG. Nowak KJ, et al. Among authors: walker kr. Ann Neurol. 2007 Feb;61(2):175-84. doi: 10.1002/ana.21035. Ann Neurol. 2007. PMID: 17187373

3

Expression of cardiac alpha-actin spares extraocular muscles in skeletal muscle alpha-actin diseases--quantification of striated alpha-actins by MRM-mass spectrometry.

Ravenscroft G, Colley SM, Walker KR, Clement S, Bringans S, Lipscombe R, Fabian VA, Laing NG, Nowak KJ. Ravenscroft G, et al. Among authors: walker kr. Neuromuscul Disord. 2008 Dec;18(12):953-8. doi: 10.1016/j.nmd.2008.09.010. Epub 2008 Oct 25. Neuromuscul Disord. 2008. PMID: 18952430

4

Disease severity and thin filament regulation in M9R TPM3 nemaline myopathy.

Ilkovski B, Mokbel N, Lewis RA, Walker K, Nowak KJ, Domazetovska A, Laing NG, Fowler VM, North KN, Cooper ST. Ilkovski B, et al. J Neuropathol Exp Neurol. 2008 Sep;67(9):867-77. doi: 10.1097/NEN.0b013e318183a44f. J Neuropathol Exp Neurol. 2008. PMID: 18716557 Free PMC article.

5

Actin mutations are one cause of congenital fibre type disproportion.

Laing NG, Clarke NF, Dye DE, Liyanage K, Walker KR, Kobayashi Y, Shimakawa S, Hagiwara T, Ouvrier R, Sparrow JC, Nishino I, North KN, Nonaka I. Laing NG, et al. Among authors: walker kr. Ann Neurol. 2004 Nov;56(5):689-94. doi: 10.1002/ana.20260. Ann Neurol. 2004. PMID: 15468086

6

Adenovirus and adeno-associated virus-mediated delivery of human myophosphorylase cDNA and LacZ cDNA to muscle in the ovine model of McArdle's disease: expression and re-expression of glycogen phosphorylase.

Howell JM, Walker KR, Davies L, Dunton E, Everaardt A, Laing N, Karpati G. Howell JM, et al. Among authors: walker kr. Neuromuscul Disord. 2008 Mar;18(3):248-58. doi: 10.1016/j.nmd.2007.10.006. Epub 2008 Mar 14. Neuromuscul Disord. 2008. PMID: 18343113

7

Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease.

Howell JM, Walker KR, Creed KE, Dunton E, Davies L, Quinlivan R, Karpati G. Howell JM, et al. Among authors: walker kr. Neuromuscul Disord. 2014 Feb;24(2):167-77. doi: 10.1016/j.nmd.2013.10.003. Epub 2013 Oct 26. Neuromuscul Disord. 2014. PMID: 24309536

8

Intraprofessional Education Experiences in Dentistry: Dental hygienists' perceptions of collaboration with dentists.

Walker KRJ, Giblin-Scanlon LJ, Vineyard J, McCarthy J. Walker KRJ, et al. J Dent Hyg. 2024 Oct;98(5):22-33. J Dent Hyg. 2024. PMID: 39406488

9

UCI EyeMobile Exam Findings from School Children Following on-Site Screening.

Hong JD, Choi EH, Suh S, Bui JH, Storch AM, Walker KR, Shahraki K, Yanez C, Torres D, Espinoza J, Molina I, Suh DW. Hong JD, et al. Among authors: walker kr. Clin Ophthalmol. 2024 Jun 6;18:1667-1678. doi: 10.2147/OPTH.S460879. eCollection 2024. Clin Ophthalmol. 2024. PMID: 38860118 Free PMC article.

10

Exploring Pediatric Vision Care: Insights from Five Years of Referral Cases in the UCI Eye Mobile and Implications of COVID-19.

Choi EH, Hong JD, Suh S, Menezes CR, Walker KR, Bui J, Storch A, Torres D, Espinoza J, Shahraki K, Molina I, Suh DW. Choi EH, et al. Among authors: walker kr. J Pediatr Ophthalmol Strabismus. 2024 Sep-Oct;61(5):309-316. doi: 10.3928/01913913-20240314-01. Epub 2024 Apr 25. J Pediatr Ophthalmol Strabismus. 2024. PMID: 38661310

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