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Four and a half LIM protein 1 gene mutations cause four distinct human myopathies: a comprehensive review of the clinical, histological and pathological features.
Neuromuscul Disord. 2011 Apr;21(4):237-51. doi: 10.1016/j.nmd.2011.01.001.
Neuromuscul Disord. 2011.
PMID: 21310615
Review.
A transgenic zebrafish model of hepatocyte function in human Z α1-antitrypsin deficiency.
Yip E, Giousoh A, Fung C, Wilding B, Prakash MD, Williams C, Verkade H, Bryson-Richardson RJ, Bird PI.
Yip E, et al. Among authors: wilding b.
Biol Chem. 2019 Nov 26;400(12):1603-1616. doi: 10.1515/hsz-2018-0391.
Biol Chem. 2019.
PMID: 31091192
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Expression of the Z Variant of α1-Antitrypsin Suppresses Hepatic Cholesterol Biosynthesis in Transgenic Zebrafish.
Fung C, Wilding B, Schittenhelm RB, Bryson-Richardson RJ, Bird PI.
Fung C, et al. Among authors: wilding b.
Int J Mol Sci. 2023 Jan 27;24(3):2475. doi: 10.3390/ijms24032475.
Int J Mol Sci. 2023.
PMID: 36768797
Free PMC article.
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Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy.
Friedrich FW, Wilding BR, Reischmann S, Crocini C, Lang P, Charron P, Müller OJ, McGrath MJ, Vollert I, Hansen A, Linke WA, Hengstenberg C, Bonne G, Morner S, Wichter T, Madeira H, Arbustini E, Eschenhagen T, Mitchell CA, Isnard R, Carrier L.
Friedrich FW, et al. Among authors: wilding br.
Hum Mol Genet. 2012 Jul 15;21(14):3237-54. doi: 10.1093/hmg/dds157. Epub 2012 Apr 20.
Hum Mol Genet. 2012.
PMID: 22523091
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FHL1 mutants that cause clinically distinct human myopathies form protein aggregates and impair myoblast differentiation.
Wilding BR, McGrath MJ, Bonne G, Mitchell CA.
Wilding BR, et al.
J Cell Sci. 2014 May 15;127(Pt 10):2269-81. doi: 10.1242/jcs.140905. Epub 2014 Mar 14.
J Cell Sci. 2014.
PMID: 24634512
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SLIMMER (FHL1B/KyoT3) interacts with the proapoptotic protein Siva-1 (CD27BP) and delays skeletal myoblast apoptosis.
Cottle DL, McGrath MJ, Wilding BR, Cowling BS, Kane JM, D'Arcy CE, Holdsworth M, Hatzinisiriou I, Prescott M, Brown S, Mitchell CA.
Cottle DL, et al. Among authors: wilding br.
J Biol Chem. 2009 Sep 25;284(39):26964-77. doi: 10.1074/jbc.M109.036293. Epub 2009 Jul 29.
J Biol Chem. 2009.
PMID: 19643733
Free PMC article.
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X-linked Recessive Distal Myopathy With Hypertrophic Cardiomyopathy Caused by a Novel Mutation in the FHL1 Gene.
D'Arcy C, Kanellakis V, Forbes R, Wilding B, McGrath M, Howell K, Ryan M, McLean C.
D'Arcy C, et al. Among authors: wilding b.
J Child Neurol. 2015 Aug;30(9):1211-7. doi: 10.1177/0883073814549807. Epub 2014 Sep 22.
J Child Neurol. 2015.
PMID: 25246303
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