Professor Kate Quinlan

Biography

Kate is a Professor 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 ��Ʊ, 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 ��Ʊ Scientia Fellowship and became an independent group leader in 2018. She was promoted to Associate Professor in 2021 and to Professor in 2024. Kate mentors a number of PhD and Honours students.

E-mail

kate.quinlan@unsw.edu.au

Location

School of Biotechnology and Biomolecular Sciences Room 3102, Level 3, Biosciences South Building (E26) ��Ʊ Sydney NSW 2052 Australia

Book Chapters | 2018

Yik JJ; Crossley M; Quinlan KGR, 2018, 'Genome editing of erythroid cell culture model systems', in Lloyd JA (ed.), Erythropoiesis methods and protocols, Springer, pp. 245 - 257,
Journal articles | 2025

Hamey JJ; Shah M; Wade JD; Bartolec TK; Wettenhall REH; Quinlan KGR; Williamson NA; Wilkins MR, 2025, 'SMYD5 is a ribosomal methyltransferase that trimethylates RPL40 lysine 22 through recognition of a KXY motif', Cell Reports, 44,

Journal articles | 2024

Martyn GE; Doerfler PA; Yao Y; Quinlan KGR; Weiss MJ; Crossley M, 2024, 'Hydroxyurea reduces the levels of the fetal globin gene repressors ZBTB7A/LRF and BCL11A in erythroid cells in vitro', Journal of Sickle Cell Disease, 1,

Journal articles | 2024

Sikder S; Pierce D; Sarkar ER; McHugh C; Quinlan KGR; Giacomin P; Loukas A, 2024, 'Regulation of host metabolic health by parasitic helminths', Trends in Parasitology, 40, pp. 386 - 400,

Journal articles | 2023

Shah M; Knights AJ; Vohralik EJ; Psaila AM; Quinlan KGR, 2023, 'Blood and adipose-resident eosinophils are defined by distinct transcriptional profiles', Journal of Leukocyte Biology, 113, pp. 191 - 202,

Journal articles | 2022

Ly LC; Yang Y; Li F; Crossley M; Shi Y; Quinlan KGR, 2022, 'Protocols for protein-DNA binding analysis of a zinc finger transcription factor bound to its cognate promoter', STAR protocols, 3, pp. 101598,

Journal articles | 2022

Psaila AM; Vohralik EJ; Quinlan KGR, 2022, 'Shades of white: new insights into tissue-resident leukocyte heterogeneity', FEBS Journal, 289, pp. 308 - 318,

Journal articles | 2022

Topfer SK; Feng R; Huang P; Ly LC; Martyn GE; Blobel GA; Weiss MJ; Quinlan KGR; Crossley M, 2022, 'Disrupting the adult globin promoter alleviates promoter competition and reactivates fetal globin gene expression', Blood, 139, pp. 2107 - 2118,

Journal articles | 2021

Chen SY; Beretta M; Alexopoulos SJ; Shah DP; Olzomer EM; Hargett SR; Childress ES; Salamoun JM; Aleksovska I; Roseblade A; Cranfield C; Rawling T; Quinlan KGR; Morris MJ; Tucker SP; Santos WL; Hoehn KL, 2021, 'Mitochondrial uncoupler SHC517 reverses obesity in mice without affecting food intake', Metabolism: Clinical and Experimental, 117,

Journal articles | 2021

Seto JT; Roeszler KN; Meehan LR; Wood HD; Tiong C; Bek L; Lee SF; Shah M; Quinlan KGR; Gregorevic P; Houweling PJ; North KN, 2021, 'ACTN3 genotype influences skeletal muscle mass regulation and response to dexamethasone', Science Advances, 7,

Journal articles | 2021

Yang Y; Ren R; Ly LC; Horton JR; Li F; Quinlan KGR; Crossley M; Shi Y; Cheng X, 2021, 'Structural basis for human ZBTB7A action at the fetal globin promoter', Cell Reports, 36,

Journal articles | 2020

Byrne FL; Olzomer EM; Marriott GR; Quek LE; Katen A; Su J; Nelson ME; Hart-Smith G; Larance M; Sebesfi VF; Cuff J; Martyn GE; Childress E; Alexopoulos SJ; Poon IK; Faux MC; Burgess AW; Reid G; McCarroll JA; Santos WL; Quinlan KG; Turner N; Fazakerley DJ; Kumar N; Hoehn KL, 2020, 'Phenotypic screen for oxygen consumption rate identifies an anti-cancer naphthoquinone that induces mitochondrial oxidative stress', Redox Biology, 28, pp. 101374,

Journal articles | 2020

Knights AJ; Vohralik EJ; Houweling PJ; Stout ES; Norton LJ; Alexopoulos SJ; Yik JJ; Mat Jusoh H; Olzomer EM; Bell-Anderson KS; North KN; Hoehn KL; Crossley M; Quinlan KGR, 2020, 'Eosinophil function in adipose tissue is regulated by Krüppel-like factor 3 (KLF3)', Nature Communications, 11,

Journal articles | 2020

Knights AJ; Yang L; Shah M; Norton LJ; Green GS; Stout ES; Vohralik EJ; Crossley M; Quinlan KGR, 2020, 'Krüppel-like factor 3 (klf3) suppresses nf-b-driven inflammation in mice', Journal of Biological Chemistry, 295, pp. 608 - 6091,

Journal articles | 2020

Seto JT; Roeszler KN; Meehan LR; Wood HD; Tiong C; Bek L; Lee SF; Shah M; Quinlan KGR; Gregorevic P; Houweling PJ; North KN, 2020, 'ACTN3genotype influences skeletal muscle mass regulation and response to dexamethasone', ,

Journal articles | 2020

Vohralik EJ; Psaila AM; Knights AJ; Quinlan KGR, 2020, 'EoTHINophils: Eosinophils as key players in adipose tissue homeostasis', Clinical and Experimental Pharmacology and Physiology, 47, pp. 1495 - 1505,

Journal articles | 2020

Yang L; Chen Z; Stout ES; Delerue F; Ittner LM; Wilkins MR; Quinlan KGR; Crossley M, 2020, 'Methylation of a CGATA element inhibits binding and regulation by GATA-1', Nature Communications, 11,

Journal articles | 2019

Caruana BT; Byrne FL; Knights AJ; Quinlan KGR; Hoehn KL, 2019, 'Characterization of glucose transporter 6 in lipopolysaccharide-induced bone marrow-derived macrophage function', Journal of Immunology, 202, pp. 1826 - 1832,

Journal articles | 2019

Martyn GE; Wienert B; Kurita R; Nakamura Y; Quinlan KGR; Crossley M, 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,

Journal articles | 2019

Shah M; Funnell APW; Quinlan KGR; Crossley M, 2019, 'Hit and Run Transcriptional Repressors Are Difficult to Catch in the Act', BioEssays, 41, pp. e1900041,

Journal articles | 2018

Artuz CM; Knights AJ; Funnell APW; Gonda TJ; Ravid K; Pearson RCM; Quinlan KGR; Crossley M, 2018, 'Partial reprogramming of heterologous cells by defined factors to generate megakaryocyte lineage-restricted biomolecules', Biotechnology Reports, 20,

Journal articles | 2018

Knights AJ; Vohralik EJ; Hoehn KL; Crossley M; Quinlan KGR, 2018, 'Defining Eosinophil Function in Adiposity and Weight Loss', BioEssays, 40,

Journal articles | 2018

Martyn GE; Wienert B; Yang L; Shah M; Norton LJ; Burdach J; Kurita R; Nakamura Y; Pearson RCM; Funnell APW; Quinlan KGR; Crossley M, 2018, 'Natural regulatory mutations elevate the fetal globin gene via disruption of BCL11A or ZBTB7A binding', Nature Genetics, 50, pp. 498 - 503,

Journal articles | 2018

Summers MA; Rupasinghe T; Vasiljevski ER; Evesson FJ; Mikulec K; Peacock L; Quinlan KGR; 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,

Journal articles | 2018

Wienert B; Martyn GE; Funnell APW; Quinlan KGR; Crossley M, 2018, 'Wake-up Sleepy Gene: Reactivating Fetal Globin for β-Hemoglobinopathies', Trends in Genetics, 34, pp. 927 - 940,

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,

Journal articles | 2017

Baldwin JN; McKay MJ; Simic M; Hiller CE; Moloney N; Nightngale EJ; Burns J; 1000 Norms Project Consortium ; Huebscher M, 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, pp. 1282 - 1290,

Journal articles | 2017

Hamey JJ; Wienert B; Quinlan KGR; 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,

Journal articles | 2017

Houweling PJ; Berman YD; Turner N; Quinlan KGR; 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,

Journal articles | 2017

Martyn GE; Quinlan KGR; 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,

Journal articles | 2017

McKay MJ; Baldwin JN; Ferreira P; Simic M; Vanicek N; Burns J; Nightingale E; Pourkazemi F; Sman A; Hiller C; Mousavi S; Nicholson L; Rose K; Chard A; Mackey M; Moloney N; Raymond J; Yan AF; Hübscher M; Refshauge K; Wegener C; Lee F; North K; Quinlan K, 2017, 'Normative reference values for strength and flexibility of 1,000 children and adults', Neurology, 88, pp. 36 - 43,

Journal articles | 2017

McKay MJ; Baldwin JN; Ferreira P; Simic M; Vanicek N; Burns J; Nightingale E; Pourkazemi F; Sman A; Hiller C; Mousavi S; Nicholson L; Rose K; Chard A; Mackey M; Moloney N; Raymond J; Yan AF; Hübscher M; Refshauge K; Wegener C; Lee F; North K; Quinlan K, 2017, 'Reference values for developing responsive functional outcome measures across the lifespan', Neurology, 88, pp. 1512 - 1519,

Journal articles | 2017

Norton LJ; Funnell APW; Burdach J; Wienert B; Kurita R; Nakamura Y; Philipsen S; Pearson RCM; Quinlan KGR; Crossley M, 2017, 'KLF1 directly activates expression of the novel fetal globin repressor ZBTB7A/LRF in erythroid cells', Blood Advances, 1, pp. 685 - 692,

Journal articles | 2017

Norton LJ; Hallal S; Stout ES; Funnell APW; Pearson RCM; Crossley M; Quinlan KGR, 2017, 'Direct competition between DNA binding factors highlights the role of Krüppel-like Factor 1 in the erythroid/megakaryocyte switch', Scientific Reports, 7, pp. 3137,

Journal articles | 2017

Wienert B; Martyn GE; Kurita R; Nakamura Y; Quinlan KGR; Crossley M, 2017, 'KLF1 drives the expression of fetal hemoglobin in British HPFH', Blood, 130, pp. 803 - 807,

Journal articles | 2016

Hogarth MW; Garton FC; Houweling PJ; Tukiainen T; Lek M; Macarthur DG; Seto JT; Quinlan KGR; 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,

Journal articles | 2016

Knights AJ; Yik JJ; Jusoh HM; Norton LJ; Funnell APW; Pearson RCM; Bell-Anderson KS; Crossley M; Quinlan KGR, 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,

Journal articles | 2016

Lee FXZ; Houweling PJ; North KN; Quinlan KGR, 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,

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,

Journal articles | 2015

Dewi V; Kwok A; Lee S; Lee MM; Tan YM; Nicholas HR; Isono KI; Wienert B; Mak KS; Knights AJ; Quinlan KGR; Cordwell SJ; Funnell APW; Pearson RCM; 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,

Journal articles | 2015

Head SI; Chan S; Houweling PJ; Quinlan KGR; 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,

Journal articles | 2015

Houweling P; Seto J; Garton F; Quinlan K; Head S; North K, 2015, 'A gene for speed: The influence of ACTN3 on muscle performance in health and disease', NEUROMUSCULAR DISORDERS, 25, pp. S185 - S185,

Journal articles | 2015

Lim WF; Burdach J; Funnell APW; Pearson RCM; Quinlan KGR; 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,

Journal articles | 2015

Quinlan KG; Summers MA; Payne JM; Little DG; North KN; Schindeler A, 2015, 'Skeletal muscle and motor deficits in Neurofibromatosis Type 1', J Musculoskelet Neuronal Interact, 15, pp. 161 - 170

Journal articles | 2015

Wienert B; Funnell APW; Norton LJ; Pearson RCM; Wilkinson-White LE; Lester K; Vadolas J; Porteus MH; Matthews JM; Quinlan KGR; Crossley M, 2015, 'Editing the genome to introduce a beneficial naturally occurring mutation associated with increased fetal globin', Nature Communications, 6, pp. 7085,

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, pp. e106011,

Journal articles | 2014

Funnell APW; Vernimmen D; Lim WF; Mak KS; Wienert B; Martyn GE; Artuz CM; Burdach J; Quinlan KGR; Higgs DR; Whitelaw E; Pearson RCM; 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, pp. 8,

Journal articles | 2014

Garton FC; Seto JT; Quinlan KGR; 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,

Journal articles | 2014

Sullivan K; El-hoss J; Quinlan KGR; Deo N; Garton F; Seto JTC; 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,

Journal articles | 2014

Thomas KC; Zheng XF; Suarez FG; Raftery JM; Quinlan KGR; 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, pp. e88653,

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 CAC; 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,

Journal articles | 2013

Seto JT; Quinlan KGR; 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,

Journal articles | 2011

Nunez N; Clifton MM; Funnell AP; Artuz CM; Hallal S; Quinlan KG; Font J; Vandevenne M; Setiyaputra S; Pearson RC; Mackay JP; Crossley M, 2011, 'The multi-zinc finger protein ZNF217 contacts DNA through a two-finger domain', The Journal of Biological Chemistry, 286, pp. 38190 - 38201,

Journal articles | 2011

Seto JT; Chan SM; Turner N; MacArthur D; Raftery J; Berman Y; Quinlan KG; Cooney GJ; Head SI; Yang N; North K, 2011, 'The effect of alpha-actinin-3 deficiency on muscle aging', Experimental Gerontology, 46, pp. 292 - 302,

Journal articles | 2011

Seto JT; Lek M; Quinlan KG; Houweling PJ; Zheng XF; Garton F; MacArthur DG; Raftery JM; Garvey SM; Hauser MA; Yang N; Head SI; North K, 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,

Journal articles | 2011

Yang S; Schneider D; Mcdonald M; Setoh JWS; Houweling PJ; Lek M; Hograth P; Morse A; Raftery J; Balasuriya H; MacArthur D; Eisman JA; Berman Y; Quinlan K; Center JR; Nguyen TV; Prince R; Wilson S; Zhu S; Little S; North A, 2011, '&-Actinin-3 deficiency is associated with reducted bone mass in human and mouse', Bone, 49, pp. 790 - 798,

Journal articles | 2010

Lek M; Quinlan KGR; North KN, 2010, 'The evolution of skeletal muscle performance: Gene duplication and divergence of human sarcomeric α-actinins', BioEssays, 32, pp. 17 - 25,

Journal articles | 2010

Quinlan K; Seto JT; Turner N; Vandebrouck A; Floetenmeyer M; MacArthur D; Raftery J; Lek M; Yang N; Parton RG; Cooney GJ; North K, 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,

Journal articles | 2008

MacArthur DG; Seto JT; Chan S; Quinlan KG; Raftery JM; Turner N; Nicholson MD; Kee AJ; Hardeman EC; Gunning PW; Cooney GJ; Head SI; Yang N; North KN, 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,

Journal articles | 2007

MacArthur DG; Seto JT; Raftery JM; Quinlan KG; Huttley GA; Hook JW; Lemckert FA; Kee AJ; Edwards MR; Berman Y; Hardeman EC; Gunning PW; Easteal S; Yang N; North KN, 2007, 'Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans', Nature Genetics, 39, pp. 1261 - 1265

Journal articles | 2007

Quinlan KG; Verger A; Yaswen P; Crossley M, 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

Journal articles | 2006

Quinlan KG; Nardini M; Corda E; Yaswen P; Bolognesi M; Crossley M, 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,

Journal articles | 2006

Quinlan KG; Verger A; Kwok A; Lee SH; Perdomo JS; Nardini M; Bolognesi M; Crossley M, 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,

Journal articles | 2006

Stankovic-valentin N; Verger A; Deltour-valerdi S; Quinlan KG; Crossley M; Leprince D, 2006, 'A L225A substitution in the human tumour suppressor HIC1 abolishes its interaction with the corepressor CtBP', FEBS Journal, 273, pp. 2879 - 2890

Journal articles | 2006

Verger A; Quinlan KG; Crofts LA; Spano S; Corda E; Kable E; Braet F; Crossley M, 2006, 'Mechanisms directing the nuclear localization of the CtBP family', Molecular and Cellular Biology, 26, pp. 4882 - 4894,

Journal articles | 2006

van Vliet JL; Crofts LA; Quinlan KG; Czolij R; Perkins A; Crossley M, 2006, 'Human KLF17 is a new member of the Sp/KLF family of transcription factors', Genomics, 87, pp. 474 - 482

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,
Preprints | 2024

Hamey JJ; Shah M; Wade JD; Bartolec TK; Wettenhall REH; Quinlan KGR; Williamson NA; Wilkins MR, 2024, SMYD5 is a ribosomal methyltransferase which trimethylates RPL40 lysine 22 through recognition of a KXY motif,

Conference Abstracts | 2015

Wagner S; Chan S; Murphy R; Houweling PJ; Quinlan KGR; 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,

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 CAC; 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,

Conference Papers | 2012

Quinlan KGR; Seto JTC; 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,

Conference Papers | 2009

Quinlan KGR; 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,

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