A/Prof Kate Quinlan
Sitert av
Sitert av
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), 1261-1265, 2007
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
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), 498-503, 2018
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
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
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
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
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
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 (1), 7085, 2015
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
Wake-up sleepy gene: reactivating fetal globin for β-hemoglobinopathies
B Wienert, GE Martyn, APW Funnell, KGR Quinlan, M Crossley
Trends in Genetics 34 (12), 927-940, 2018
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
Mechanisms directing the nuclear localization of the CtBP family proteins
A Verger, KGR Quinlan, LA Crofts, S Spanò, D Corda, EPW Kable, F Braet, ...
Molecular and cellular biology 26 (13), 4882-4894, 2006
KLF1 drives the expression of fetal hemoglobin in British HPFH
B Wienert, GE Martyn, R Kurita, Y Nakamura, KGR Quinlan, M Crossley
Blood, The Journal of the American Society of Hematology 130 (6), 803-807, 2017
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
Evidence based selection of commonly used RT-qPCR reference genes for the analysis of mouse skeletal muscle
KC Thomas, XF Zheng, F Garces Suarez, JM Raftery, KGR Quinlan, ...
PloS one 9 (2), e88653, 2014
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
Reference values for developing responsive functional outcome measures across the lifespan
MJ McKay, JN Baldwin, P Ferreira, M Simic, N Vanicek, J Burns, ...
Neurology 88 (16), 1512-1519, 2017
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
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
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