Dr Kate Quinlan
TitleCited byYear
Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans
DG MacArthur, JT Seto, JM Raftery, KG Quinlan, GA Huttley, JW Hook, ...
Nature genetics 39 (10), 1261, 2007
2732007
An Actn3 knockout mouse provides mechanistic insights into the association between α-actinin-3 deficiency and human athletic performance
DG MacArthur, JT Seto, S Chan, KGR Quinlan, JM Raftery, N Turner, ...
Human molecular genetics 17 (8), 1076-1086, 2008
2622008
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy
M Yuen, SA Sandaradura, JJ Dowling, AS Kostyukova, N Moroz, ...
The Journal of clinical investigation 124 (11), 4693-4708, 2014
1212014
Human KLF17 is a new member of the Sp/KLF family of transcription factors
J van Vliet, LA Crofts, KGR Quinlan, R Czolij, AC Perkins, M Crossley
Genomics 87 (4), 474-482, 2006
1082006
ACTN3 genotype influences muscle performance through the regulation of calcineurin signaling
JT Seto, KGR Quinlan, M Lek, XF Zheng, F Garton, DG MacArthur, ...
The Journal of clinical investigation 123 (10), 4255-4263, 2013
922013
Specific recognition of ZNF217 and other zinc finger proteins at a surface groove of C-terminal binding proteins
KGR Quinlan, M Nardini, A Verger, P Francescato, P Yaswen, D Corda, ...
Molecular and cellular biology 26 (21), 8159-8172, 2006
832006
α-Actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle
KGR Quinlan, JT Seto, N Turner, A Vandebrouck, M Floetenmeyer, ...
Human molecular genetics 19 (7), 1335-1346, 2010
792010
Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling
JT Seto, M Lek, KGR Quinlan, PJ Houweling, XF Zheng, F Garton, ...
Human molecular genetics 20 (15), 2914-2927, 2011
752011
Mechanisms directing the nuclear localization of the CtBP family proteins
A Verger, KGR Quinlan, LA Crofts, S SpanÚ, D Corda, EPW Kable, F Braet, ...
Molecular and cellular biology 26 (13), 4882-4894, 2006
702006
Editing the genome to introduce a beneficial naturally occurring mutation associated with increased fetal globin
B Wienert, APW Funnell, LJ Norton, RCM Pearson, LE Wilkinson-White, ...
Nature communications 6, 7085, 2015
612015
Copper binding is the governing determinant of prion protein turnover
CL Haigh, K Edwards, DR Brown
Molecular and Cellular Neuroscience 30 (2), 186-196, 2005
612005
Amplification of zinc finger gene 217 (ZNF217) and cancer: when good fingers go bad
KGR Quinlan, A Verger, P Yaswen, M Crossley
Biochimica et Biophysica Acta (BBA)-Reviews on Cancer 1775 (2), 333-340, 2007
582007
Role of the C-terminal binding protein PXDLS motif binding cleft in protein interactions and transcriptional repression
KGR Quinlan, A Verger, A Kwok, SHY Lee, J Perdomo, M Nardini, ...
Molecular and cellular biology 26 (21), 8202-8213, 2006
502006
The effect of α-actinin-3 deficiency on muscle aging
JT Seto, S Chan, N Turner, DG MacArthur, JM Raftery, YD Berman, ...
Experimental gerontology 46 (4), 292-302, 2011
472011
The evolution of skeletal muscle performance: gene duplication and divergence of human sarcomeric α‐actinins
M Lek, KGR Quinlan, KN North
Bioessays 32 (1), 17-25, 2010
412010
Normative reference values for strength and flexibility of 1,000 children and adults
MJ McKay, JN Baldwin, P Ferreira, M Simic, N Vanicek, J Burns, ...
Neurology 88 (1), 36-43, 2017
402017
Natural regulatory mutations elevate the fetal globin gene via disruption of BCL11A or ZBTB7A binding
GE Martyn, B Wienert, L Yang, M Shah, LJ Norton, J Burdach, R Kurita, ...
Nature genetics 50 (4), 498, 2018
372018
α-Actinin-3 deficiency is associated with reduced bone mass in human and mouse
N Yang, A Schindeler, MM McDonald, JT Seto, PJ Houweling, M Lek, ...
Bone 49 (4), 790-798, 2011
342011
Evidence based selection of commonly used RT-qPCR reference genes for the analysis of mouse skeletal muscle
KC Thomas, XF Zheng, FG Suarez, JM Raftery, KGR Quinlan, N Yang, ...
PloS one 9 (2), e88653, 2014
302014
How does α-actinin-3 deficiency alter muscle function? Mechanistic insights into ACTN3, the ‘gene for speed’
FXZ Lee, PJ Houweling, KN North, KGR Quinlan
Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1863 (4), 686-693, 2016
282016
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Articles 1–20