Associate Professor Kate Quinlan
Associate Professor

Associate Professor Kate Quinlan

Science
School of Biotech & Biomolecular Science

Biography

Kate is is Scientia Fellow (Level C) in the School of Biotechnology and Biomolecular Sciences (BABS).  She runs a research group interested in gene regulation, with a particular focus on understanding the communication between immune cells and fat cells within adipose tissue to uncover new therapeutic targets for obesity.  Kate completed her Bsc (Hons) (Advanced) at the University of Sydney in 2000.  She went to overseas to work as a Research Assistant at the University of Cambridge for a year before returning to the University of Sydney to complete her PhD under the supervision of Professor Merlin Crossley (2002-2006) in transcription factor biology.  Kate moved to the Children's Hospital at Westmead as a post doc under the mentorship of Professor Kathryn North in 2006, where she studied the effects of the human ACTN3 gene polymorphism on skeletal muscle performance and metabolism.  She continued her post doctoral training at the University of Cambridge (2008-2010) under the mentorship of Professor Roger Pedersen with the aid of an NHMRC CJ Martin Fellowship, researching pluripotency of embryonic stem cells and targeted differentiation of these cells towards skeletal muscle satellite cells.  She then returned to the University of Sydney to collaborate with Professor Kathryn North and to lead a program of research into the human ACTN3 gene polymorphism, with the aims of uncovering mechanisms behind changes to muscle function and metabolism in individuals homozygous for this polymorphism, and translating findings from model organisms to humans.  In 2014 Kate joined UNSW, working with Professor Merlin Crossley to study the transcriptional regulation of haematopoiesis and transcription factor mechanisms in addition to continuing an independent research program focussed on skeletal muscle metabolism.  She was awarded a UNSW Scientia Fellowship and became an independent group leader in 2018.  Kate mentors a number of PhD and Honours students.

Location
School of Biotechnology and Biomolecular Sciences Room 3102, Level 3, Biosciences South Building (E26) UNSW Sydney NSW 2052 Australia
  • Book Chapters | 2018
    2018, 'Genome editing of erythroid cell culture model systems', in Erythropoiesis methods and protocols, Springer, pp. 245 - 257, http://dx.doi.org/10.1007/978-1-4939-7428-3_15
  • Journal articles | 2023
    2023, 'Blood and adipose-resident eosinophils are defined by distinct transcriptional profiles', Journal of leukocyte biology, 113, pp. 191 - 202, http://dx.doi.org/10.1093/jleuko/qiac009
    Journal articles | 2022
    2022, 'Disrupting the adult globin promoter alleviates promoter competition and reactivates fetal globin gene expression', Blood, 139, pp. 2107 - 2118, http://dx.doi.org/10.1182/blood.2021014205
    Journal articles | 2022
    2022, 'Protocols for protein-DNA binding analysis of a zinc finger transcription factor bound to its cognate promoter', STAR protocols, 3, pp. 101598, http://dx.doi.org/10.1016/j.xpro.2022.101598
    Journal articles | 2022
    2022, 'Shades of white: new insights into tissue-resident leukocyte heterogeneity', FEBS Journal, 289, pp. 308 - 318, http://dx.doi.org/10.1111/febs.15737
    Journal articles | 2021
    2021, 'ACTN3 genotype influences skeletal muscle mass regulation and response to dexamethasone', Science Advances, 7, http://dx.doi.org/10.1126/sciadv.abg0088
    Journal articles | 2021
    2021, 'Mitochondrial uncoupler SHC517 reverses obesity in mice without affecting food intake', Metabolism: Clinical and Experimental, 117, pp. 154724, http://dx.doi.org/10.1016/j.metabol.2021.154724
    Journal articles | 2021
    2021, 'Structural basis for human ZBTB7A action at the fetal globin promoter', Cell Reports, 36, pp. 109759, http://dx.doi.org/10.1016/j.celrep.2021.109759
    Journal articles | 2020
    2020, 'ACTN3 genotype influences skeletal muscle mass regulation and response to dexamethasone', , http://dx.doi.org/10.1101/2020.11.20.392282
    Journal articles | 2020
    2020, 'EoTHINophils: Eosinophils as key players in adipose tissue homeostasis', Clinical and Experimental Pharmacology and Physiology, 47, pp. 1495 - 1505, http://dx.doi.org/10.1111/1440-1681.13304
    Journal articles | 2020
    2020, 'Eosinophil function in adipose tissue is regulated by Krüppel-like factor 3 (KLF3)', Nature Communications, 11, pp. 2922, http://dx.doi.org/10.1038/s41467-020-16758-9
    Journal articles | 2020
    2020, 'Krüppel-like factor 3 (klf3) suppresses nf-b-driven inflammation in mice', Journal of Biological Chemistry, 295, pp. 608 - 6091, http://dx.doi.org/10.1074/jbc.RA120.013114
    Journal articles | 2020
    2020, 'Methylation of a CGATA element inhibits binding and regulation by GATA-1', Nature Communications, 11, pp. 2560, http://dx.doi.org/10.1038/s41467-020-16388-1
    Journal articles | 2020
    2020, 'Phenotypic screen for oxygen consumption rate identifies an anti-cancer naphthoquinone that induces mitochondrial oxidative stress', Redox Biology, 28, pp. 101374 - 101374, http://dx.doi.org/10.1016/j.redox.2019.101374
    Journal articles | 2019
    2019, 'A natural regulatory mutation in the proximal promoter elevates fetal globin expression by creating a de novo GATA1 site', Blood, 133, pp. 852 - 856, http://dx.doi.org/10.1182/blood-2018-07-863951
    Journal articles | 2019
    2019, 'Characterization of glucose transporter 6 in lipopolysaccharide-induced bone marrow-derived macrophage function', Journal of Immunology, 202, pp. 1826 - 1832, http://dx.doi.org/10.4049/jimmunol.1801063
    Journal articles | 2019
    2019, 'Hit and Run Transcriptional Repressors Are Difficult to Catch in the Act', BioEssays, 41, pp. e1900041, http://dx.doi.org/10.1002/bies.201900041
    Journal articles | 2018
    Artuz CM; Knights AJ; Funnell AP W; Gonda TJ; Ravid K; Pearson RC M; Quinlan KG R; Crossley M, 2018, 'Partial reprogramming of heterologous cells by defined factors to generate megakaryocyte lineage-restricted biomolecules', Biotechnology Reports, 20, http://dx.doi.org/10.1016/j.btre.2018.e00285
    Journal articles | 2018
    Knights AJ; Vohralik EJ; Hoehn KL; Crossley M; Quinlan KG R, 2018, 'Defining Eosinophil Function in Adiposity and Weight Loss', BioEssays, 40, http://dx.doi.org/10.1002/bies.201800098
    Journal articles | 2018
    Martyn GE; Wienert B; Yang L; Shah M; Norton LJ; Burdach J; Kurita R; Nakamura Y; Pearson RC M; Funnell AP W; Quinlan KG R; Crossley M, 2018, 'Natural regulatory mutations elevate the fetal globin gene via disruption of BCL11A or ZBTB7A binding', Nature Genetics, 50, pp. 498 - 503, http://dx.doi.org/10.1038/s41588-018-0085-0
    Journal articles | 2018
    Summers MA; Rupasinghe T; Vasiljevski ER; Evesson FJ; Mikulec K; Peacock L; Quinlan KG R; Cooper ST; Roessner U; Stevenson DA; Little DG; Schindeler A, 2018, 'Dietary intervention rescues myopathy associated with neurofibromatosis type 1', Human Molecular Genetics, 27, pp. 577 - 588, http://dx.doi.org/10.1093/hmg/ddx423
    Journal articles | 2018
    Wienert B; Martyn GE; Funnell AP W; Quinlan KG R; Crossley M, 2018, 'Wake-up Sleepy Gene: Reactivating Fetal Globin for β-Hemoglobinopathies', Trends in Genetics, 34, pp. 927 - 940, http://dx.doi.org/10.1016/j.tig.2018.09.004
    Journal articles | 2017
    Baldwin JN; McKay MJ; Hiller CE; Nightingale EJ; Moloney N; Burns J; Chard A; Ferreira P; Yan AF; Hawke F; Lee (née Zheng) F; Mackey M; Mousavi S; Nicholson L; Pourkazemi F; Raymond J; Rose K; Simic M; Sman A; Wegener C; Refshauge KM; Hübscher M; Vanicek N; Quinlan K; North K, 2017, 'Correlates of Perceived Ankle Instability in Healthy Individuals Aged 8 to 101 Years', Archives of Physical Medicine and Rehabilitation, 98, pp. 72 - 79, http://dx.doi.org/10.1016/j.apmr.2016.08.474
    Journal articles | 2017
    Hamey JJ; Wienert B; Quinlan KG R; Wilkins MR, 2017, 'METTL21B Is a Novel Human lysine methyltransferase of translation elongation factor 1A: Discovery by CRISPR/Cas9 Knockout', Molecular and Cellular Proteomics, 16, pp. 2229 - 2242, http://dx.doi.org/10.1074/mcp.M116.066308
    Journal articles | 2017
    Houweling PJ; Berman YD; Turner N; Quinlan KG R; Seto JT; Yang N; Lek M; MacArthur DG; Cooney G; North KN, 2017, 'Exploring the relationship between α-actinin-3 deficiency and obesity in mice and humans', International Journal of Obesity, 41, pp. 1154 - 1157, http://dx.doi.org/10.1038/ijo.2017.72
    Journal articles | 2017
    Martyn GE; Quinlan KG R; Crossley M, 2017, 'The regulation of human globin promoters by CCAAT box elements and the recruitment of NF-Y', Biochimica et Biophysica Acta - Gene Regulatory Mechanisms, 1860, pp. 525 - 536, http://dx.doi.org/10.1016/j.bbagrm.2016.10.002
    Journal articles | 2017
    Norton LJ; Hallal S; Stout ES; Funnell AP W; Pearson RC M; Crossley M; Quinlan KG R, 2017, 'Direct competition between DNA binding factors highlights the role of Krüppel-like Factor 1 in the erythroid/megakaryocyte switch', Scientific Reports, 7, http://dx.doi.org/10.1038/s41598-017-03289-5
    Journal articles | 2017
    Wienert B; Martyn GE; Kurita R; Nakamura Y; Quinlan KG R; Crossley M, 2017, 'KLF1 drives the expression of fetal hemoglobin in British HPFH', Blood, 130, pp. 803 - 807, http://dx.doi.org/10.1182/blood-2017-02-767400
    Journal articles | 2017
    2017, 'KLF1 directly activates expression of the novel fetal globin repressor ZBTB7A/LRF in erythroid cells', Blood Advances, 1, pp. 685 - 692, http://dx.doi.org/10.1182/bloodadvances.2016002303
    Journal articles | 2017
    2017, 'Normative reference values for strength and flexibility of 1,000 children and adults', Neurology, 88, pp. 36 - 43, http://dx.doi.org/10.1212/WNL.0000000000003466
    Journal articles | 2017
    2017, 'Reference values for developing responsive functional outcome measures across the lifespan', Neurology, 88, pp. 1512 - 1519, http://dx.doi.org/10.1212/WNL.0000000000003847
    Journal articles | 2017
    2017, 'Self-reported knee pain and disability among healthy individuals: reference data and factors associated with the Knee injury and Osteoarthritis Outcome Score (KOOS) and KOOS-Child', Osteoarthritis and Cartilage, 25, pp. 1282 - 1290, http://dx.doi.org/10.1016/j.joca.2017.03.007
    Journal articles | 2016
    Hogarth MW; Garton FC; Houweling PJ; Tukiainen T; Lek M; Macarthur DG; Seto JT; Quinlan KG R; Yang N; Head SI; North KN, 2016, 'Analysis of the ACTN3 heterozygous genotype suggests that α-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion', Human Molecular Genetics, 25, pp. 866 - 877, http://dx.doi.org/10.1093/hmg/ddv613
    Journal articles | 2016
    Knights AJ; Yik JJ; Jusoh HM; Norton LJ; Funnell AP W; Pearson RC M; Bell-Anderson KS; Crossley M; Quinlan KG R, 2016, 'Krüppel-like factor 3 (KLF3/BKLF) is required for widespread repression of the inflammatory modulator galectin-3 (Lgals3)', Journal of Biological Chemistry, 291, pp. 16048 - 16058, http://dx.doi.org/10.1074/jbc.M116.715748
    Journal articles | 2016
    Lee FX Z; Houweling PJ; North KN; Quinlan KG R, 2016, 'How does α-actinin-3 deficiency alter muscle function? Mechanistic insights into ACTN3, the 'gene for speed'', Biochimica et Biophysica Acta - Molecular Cell Research, 1863, pp. 686 - 693, http://dx.doi.org/10.1016/j.bbamcr.2016.01.013
    Journal articles | 2016
    McKay MJ; Baldwin JN; Ferreira P; Simic M; Vanicek N; Hiller CE; Nightingale EJ; Moloney NA; Quinlan KG; Pourkazemi F; Sman AD; Nicholson LL; Mousavi SJ; Rose K; Raymond J; Mackey MG; Chard A; Hübscher M; Wegener C; Fong Yan A; Refshauge KM; Burns J, 2016, '1000 Norms Project: Protocol of a cross-sectional study cataloging human variation', Physiotherapy (United Kingdom), 102, pp. 50 - 56, http://dx.doi.org/10.1016/j.physio.2014.12.002
    Journal articles | 2015
    Dewi V; Kwok A; Lee S; Lee MM; Tan YM; Nicholas HR; Isono KI; Wienert B; Mak KS; Knights AJ; Quinlan KG R; Cordwell SJ; Funnell AP W; Pearson RC M; Crossley M, 2015, 'Phosphorylation of krüppel-like factor 3 (KLF3/BKLF) and C-terminal binding protein 2 (CtBP2) by homeodomaininteracting protein kinase 2 (HIPK2) modulates KLF3 DNA binding and activity', Journal of Biological Chemistry, 290, pp. 8591 - 8605, http://dx.doi.org/10.1074/jbc.M115.638338
    Journal articles | 2015
    Head SI; Chan S; Houweling PJ; Quinlan KG R; Murphy R; Wagner S; Friedrich O; North KN, 2015, 'Altered Ca2+ kinetics associated with α-actinin-3 deficiency may explain positive selection for ACTN3 null allele in human evolution', PLoS genetics, 11, pp. e1004862, http://dx.doi.org/10.1371/journal.pgen.1004862
    Journal articles | 2015
    Lim WF; Burdach J; Funnell AP W; Pearson RC M; Quinlan KG R; Crossley M, 2015, 'Directing an artificial zinc finger protein to new targets by fusion to a non-DNA-binding domain', Nucleic Acids Research, 44, pp. 3118 - 3130, http://dx.doi.org/10.1093/nar/gkv1380
    Journal articles | 2015
    Wienert B; Funnell AP W; Norton LJ; Pearson RC M; Wilkinson-White LE; Lester K; Vadolas J; Porteus MH; Matthews JM; Quinlan KG R; Crossley M, 2015, 'Editing the genome to introduce a beneficial naturally occurring mutation associated with increased fetal globin', Nature Communications, 6, pp. 7085, http://dx.doi.org/10.1038/ncomms8085
    Journal articles | 2015
    2015, 'A gene for speed: The influence of ACTN3 on muscle performance in health and disease', NEUROMUSCULAR DISORDERS, 25, pp. S185 - S185, http://dx.doi.org/10.1016/j.nmd.2015.06.011
    Journal articles | 2015
    2015, 'Skeletal muscle and motor deficits in Neurofibromatosis Type 1', J Musculoskelet Neuronal Interact, 15, pp. 161 - 170
    Journal articles | 2014
    Clifton MK; Westman BJ; Thong SY; O'Connell MR; Webster MW; Shepherd NE; Quinlan KG; Crossley M; Blobel GA; Mackay JP, 2014, 'The identification and structure of an N-terminal PR domain show that FOG1 is a member of the PRDM family of proteins', PLoS ONE, 9, http://dx.doi.org/10.1371/journal.pone.0106011
    Journal articles | 2014
    Funnell AP W; Vernimmen D; Lim WF; Mak KS; Wienert B; Martyn GE; Artuz CM; Burdach J; Quinlan KG R; Higgs DR; Whitelaw E; Pearson RC M; Crossley M, 2014, 'Differential regulation of the α-globin locus by Krüppel-like factor 3 in erythroid and non-erythroid cells', BMC Molecular Biology, 15, http://dx.doi.org/10.1186/1471-2199-15-8
    Journal articles | 2014
    Garton FC; Seto JT; Quinlan KG R; Yang N; Houweling PJ; North KN, 2014, 'α-Actinin-3 deficiency alters muscle adaptation in response to denervation and immobilization', Human molecular genetics, 23, pp. 1879 - 1893, http://dx.doi.org/10.1093/hmg/ddt580
    Journal articles | 2014
    Sullivan K; El-hoss J; Quinlan KG R; Deo N; Garton F; Seto JT C; Gdalevitch M; Turner N; Cooney GJ; Kolanczyk M; North KN; Little DG; Schindeler A, 2014, 'NF1 is a critical regulator of muscle development and metabolism', Human Molecular Genetics, 23, pp. 1250 - 1259, http://dx.doi.org/10.1093/hmg/ddt515
    Journal articles | 2014
    Thomas KC; Zheng XF; Suarez FG; Raftery JM; Quinlan KG R; Yang N; North KN; Houweling PJ, 2014, 'Evidence based selection of commonly used RT-qPCR reference genes for the analysis of mouse skeletal muscle', PLoS ONE, 9, http://dx.doi.org/10.1371/journal.pone.0088653
    Journal articles | 2014
    Yuen M; Sandaradura SA; Dowling JJ; Kostyukova AS; Moroz N; Quinlan KG; Lehtokari VL; Ravenscroft G; Todd EJ; Ceyhan-Birsoy O; Gokhin DS; Maluenda J; Lek M; Nolent F; Pappas CT; Novak SM; D'Amico A; Malfatti E; Thomas BP; Gabriel SB; Gupta N; Daly MJ; Ilkovski B; Houweling PJ; Davidson AE; Swanson LC; Brownstein CA; Gupta VA; Medne L; Shannon P; Martin N; Bick DP; Flisberg A; Holmberg E; Van Den Bergh P; Lapunzina P; Waddell LB; Sloboda DD; Bertini E; Chitayat D; Telfer WR; Laquerrière A; Gregorio CC; Ottenheijm CA C; Bönnemann CG; Pelin K; Beggs AH; Hayashi YK; Romero NB; Laing NG; Nishino I; Wallgren-Pettersson C; Melki J; Fowler VM; MacArthur DG; North KN; Clarke NF, 2014, 'Leiomodin-dysfunction results in thin filament disorganization and nemaline myopathy', Journal of Clinical Investigation, 124, pp. 4693 - 4708, http://dx.doi.org/10.1172/JCI75199
    Journal articles | 2013
    Seto JT; Quinlan KG R; Lek M; Zheng XF; Garton F; Macarthur DG; Hogarth MW; Houweling PJ; Gregorevic P; Turner N; Cooney GJ; Yang N; North KN, 2013, 'ACTN3 genotype infuences muscle performance through the regulation of calcineurin signaling', Journal of Clinical Investigation, 123, pp. 4255 - 4263, http://dx.doi.org/10.1172/JCI67691
    Journal articles | 2011
    2011, '&-Actinin-3 deficiency is associated with reducted bone mass in human and mouse', Bone, 49, pp. 790 - 798, http://dx.doi.org/10.1016/j.bone.2011.07.009
    Journal articles | 2011
    2011, 'Deficiency of alpha-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling', Human Molecular Genetics, 20, pp. 2914 - 2927, http://dx.doi.org/10.1093/hmg/ddr196
    Journal articles | 2011
    2011, 'The effect of alpha-actinin-3 deficiency on muscle aging', Experimental Gerontology, 46, pp. 292 - 302, http://dx.doi.org/10.1016/j.exger.2010.11.006
    Journal articles | 2011
    2011, 'The multi-zinc finger protein ZNF217 contacts DNA through a two-finger domain', The Journal of Biological Chemistry, 286, pp. 38190 - 38201, http://dx.doi.org/10.1074/jbc.M111.301234
    Journal articles | 2010
    Lek M; Quinlan KG R; North KN, 2010, 'The evolution of skeletal muscle performance: Gene duplication and divergence of human sarcomeric α-actinins', BioEssays, 32, pp. 17 - 25, http://dx.doi.org/10.1002/bies.200900110
    Journal articles | 2010
    2010, 'Alpha-actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle', Human Molecular Genetics, 19, pp. 1335 - 1346, http://dx.doi.org/10.1093/hmg/ddq010
    Journal articles | 2008
    2008, 'An Actn3 knockout mouse provides mechanistic insights into the association between alpha-actinin-3 deficiency and human athletic performance', Human Molecular Genetics, 17, pp. 1076 - 1086, http://dx.doi.org/10.1093/hmg/ddm380
    Journal articles | 2007
    2007, 'Amplification of zinc finger gene 217 (ZNF217) and cancer: When good fingers go bad', Biochimica et Biophysica ACTA - Reviews on Cancer, 1775, pp. 333 - 340, http://dx.doi.org/10.1016/j.bbcan.2007.05.001
    Journal articles | 2007
    2007, 'Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans', Nature Genetics, 39, pp. 1261 - 1265, http://dx.doi.org/10.1038/ng2122
    Journal articles | 2006
    2006, 'A L225A substitution in the human tumour suppressor HIC1 abolishes its interaction with the corepressor CtBP', FEBS Journal, 273, pp. 2879 - 2890, http://dx.doi.org/10.1111/j.1742-4658.2006.05301.x
    Journal articles | 2006
    2006, 'Human KLF17 is a new member of the Sp/KLF family of transcription factors', Genomics, 87, pp. 474 - 482, http://dx.doi.org/10.1016/j.ygeno.2005.12.011
    Journal articles | 2006
    2006, 'Mechanisms directing the nuclear localization of the CtBP family', Molecular and Cellular Biology, 26, pp. 4882 - 4894, http://dx.doi.org/10.1128/MCB.02402-05
    Journal articles | 2006
    2006, 'Role of the C-terminal binding protein PXDLS motif binding cleft in protein interactions and transcriptional repression', Molecular and Cellular Biology, 26, pp. 8202 - 8213, http://dx.doi.org/10.1128/MCB.00445-06
    Journal articles | 2006
    2006, 'Specific recognition of ZNF217 and other zinc-finger proteins at a surface groove of C-terminal binding proteins', Molecular and Cellular Biology, 26, pp. 8159 - 8172, http://dx.doi.org/10.1128/MCB.00680-06
    Journal articles | 2005
    Haigh CL; Edwards K; Brown DR, 2005, 'Copper binding is the governing determinant of prion protein turnover', Molecular and Cellular Neuroscience, 30, pp. 186 - 196, http://dx.doi.org/10.1016/j.mcn.2005.07.001
  • Conference Abstracts | 2015
    Wagner S; Chan S; Murphy R; Houweling PJ; Quinlan KG R; North KN; Head SI; Friedrich O, 2015, 'Speed of shortening is not altered in the alpha-actinin-3 (ACTN3) 'gene of speed' knock-out mutation in fast-twitch skeletal muscle', in ACTA PHYSIOLOGICA, WILEY-BLACKWELL, Vol. 213, pp. 66 - 66, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000362554200139&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Papers | 2014
    Kreissl M; Sandaradura SA; Dowling JJ; Kostyukova AS; Moroz N; Quinlan KG; Lehtokari V; Ravenscroft G; Todd EJ; Ceyhan-Birsoy O; Gokhin DS; Maluenda J; Lek M; Nolent F; Pappas CT; Novak SM; D'Amico A; Malfatti E; Thomas BP; Gabriel SB; Gupta N; Daly MJ; Ilkovski B; Houweling PJ; Swanson LC; Brownstein CA; Gupta VA; Medne L; Shannon P; Flisberg A; Holmberg E; Van den Bergh P; Lapunzina P; Waddell LB; Sloboda DD; Bertini E; Chitayat D; Telfer WR; Laquerriere A; Gregorio CC; Ottenheijm CA C; Boennemann CG; Pelin K; Beggs AH; Hayashi YK; Romero NB; Laing NG; Nishino I; Wallgren-Pettersson C; Melki J; Fowler VM; MacArthur DG; North KN; Clarke NF, 2014, 'Mutations in LMOD3 cause severe nemaline myopathy by disrupting thin filament organisation in skeletal muscle', in NEUROMUSCULAR DISORDERS, PERGAMON-ELSEVIER SCIENCE LTD, GERMANY, Berlin, pp. 792 - 793, presented at 19th International Congress of the World-Muscle-Society, GERMANY, Berlin, 07 October 2014 - 11 October 2014, http://dx.doi.org/10.1016/j.nmd.2014.06.010
    Conference Papers | 2012
    Quinlan KG R; Seto JT C; Lek M; Zheng FX; Garton F; Houweling PJ; North KN, 2012, 'ACTN3 genotype influences skeletal muscle performance through alterations in calcineurin signaling', in NEUROMUSCULAR DISORDERS, PERGAMON-ELSEVIER SCIENCE LTD, AUSTRALIA, Perth, pp. 904 - 904, presented at 17th International Congress of the World-Muscle-Society (WMS), AUSTRALIA, Perth, 09 October 2012 - 13 October 2012, http://dx.doi.org/10.1016/j.nmd.2012.06.331
    Conference Papers | 2009
    Quinlan KG R; Seto JT; Turner N; Floetenmeyer M; Macarthur DG; Raftery JM; Yang N; Parton RG; Cooney GJ; North KN, 2009, 'alpha-Actinin-3 regulates muscle glycogen phosphorylase: A potential mechanism for the metabolic consequences of the common human null allele of ACTN3', in NEUROMUSCULAR DISORDERS, PERGAMON-ELSEVIER SCIENCE LTD, SWITZERLAND, Geneva, pp. 545 - 546, presented at 14th International Congress of the World-Muscle-Society, SWITZERLAND, Geneva, 09 September 2009 - 12 September 2009, http://dx.doi.org/10.1016/j.nmd.2009.06.011