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Kaplan, JM, H Kim, S, North, KN, Rennke, H, A Correia, L, Tong, H-Q, Mathis, BJ, Rodríguez-Pérez, J-C, Allen, PG, Beggs, AH, et al. Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis.
Nature Genetics
24(3)
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251 -256
2000
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Domazetovska, A, Ilkovski, B, Cooper, ST, Ghoddusi, M, Hardeman, EC, Minamide, LS, Gunning, PW, Bamburg, JR, North, KN. Mechanisms underlying intranuclear rod formation.
Brain
130(12)
:
3275 -3284
2007
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Punetha, J, Kesari, A, Uapinyoying, P, Giri, M, Clarke, NF, Waddell, LB, North, KN, Ghaoui, R, O'Grady, GL, Oates, EC, et al. Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases.
Journal of Neuromuscular Diseases
3(2)
:
209 -225
2016
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Clarke, NF, Ilkovski, B, Cooper, S, Valova, VA, Robinson, PJ, Nonaka, I, Feng, J, Marston, S, North, K. The pathogenesis of ACTA1‐related congenital fiber type disproportion.
Annals of Neurology
61(6)
:
552 -561
2007
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Liu, R, Ginn, SL, Lek, M, North, KN, Alexander, IE, Little, DG, Schindeler, A. Myoblast sensitivity and fibroblast insensitivity to osteogenic conversion by BMP-2 correlates with the expression of Bmpr-1a.
BMC Musculoskeletal Disorders
10(1)
:
51
2009
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