| Mammalian AMP-activated protein kinase subfamily (∗) D Stapleton, KI Mitchelhill, G Gao, J Widmer, BJ Michell, T Teh, CM House, ... Journal of Biological Chemistry 271 (2), 611-614, 1996 | 823 | 1996 |
| Microtia: epidemiology and genetics DV Luquetti, CL Heike, AV Hing, ML Cunningham, TC Cox American Journal of Medical Genetics Part A 158 (1), 124-139, 2012 | 460 | 2012 |
| Human erythroid 5‐aminolevulinate synthase: promoter analysis and identification of an iron‐responsive element in the mRNA. TC Cox, MJ Bawden, A Martin, BK May The EMBO journal 10 (7), 1891-1902, 1991 | 451 | 1991 |
| THE α-1, 3-GALACTOSYLTRANSFERASE KNOCKOUT MOUSE: Implications for Xenotransplantation: 1 RG Tearle, MJ Tange, ZL Zannettino, M Katerelos, TA Shinkel, ... Transplantation 61 (1), 13-19, 1996 | 398 | 1996 |
| Subclassification of the RBCC/TRIM superfamily reveals a novel motif necessary for microtubule binding KM Short, TC Cox Journal of Biological Chemistry 281 (13), 8970-8980, 2006 | 372 | 2006 |
| Maternal ethanol consumption alters the epigenotype and the phenotype of offspring in a mouse model N Kaminen-Ahola, A Ahola, M Maga, KA Mallitt, P Fahey, TC Cox, ... PLoS genetics 6 (1), e1000811, 2010 | 364 | 2010 |
| Survey of spiking in the mouse visual system reveals functional hierarchy JH Siegle, X Jia, S Durand, S Gale, C Bennett, N Graddis, G Heller, ... Nature 592 (7852), 86-92, 2021 | 346 | 2021 |
| Compensatory growth of healthy cardiac cells in the presence of diseased cells restores tissue homeostasis during heart development JD Drenckhahn, QP Schwarz, S Gray, A Laskowski, H Kiriazis, Z Ming, ... Developmental cell 15 (4), 521-533, 2008 | 210 | 2008 |
| Efficacy of sonic and ultrasonic activation for removal of calcium hydroxide from mesial canals of mandibular molars: a microtomographic study A Wiseman, TC Cox, A Paranjpe, NM Flake, N Cohenca, JD Johnson Journal of endodontics 37 (2), 235-238, 2011 | 192 | 2011 |
| Taking it to the max: the genetic and developmental mechanisms coordinating midfacial morphogenesis and dysmorphology TC Cox Clinical genetics 65 (3), 163-176, 2004 | 183 | 2004 |
| Molecular regulation of heme biosynthesis in higher vertebrates BK May, SC Dogra, TJ Sadlon, CR Bhasker, TC Cox, SS Bottomley Progress in nucleic acid research and molecular biology 51, 1-51, 1995 | 177 | 1995 |
| Purifying natively folded proteins from inclusion bodies using sarkosyl, Triton X-100, and CHAPS H Tao, W Liu, BN Simmons, HK Harris, TC Cox, MA Massiah Biotechniques 48 (1), 61-64, 2010 | 173 | 2010 |
| Comparative computational modeling of airflows and vapor dosimetry in the respiratory tracts of rat, monkey, and human RA Corley, S Kabilan, AP Kuprat, JP Carson, KR Minard, RE Jacob, ... Toxicological Sciences 128 (2), 500-516, 2012 | 168 | 2012 |
| X-linked Pyridoxine-Responsive Sideroblastic Anemia Due to a Thr388-to-Ser Substitution in Erythroid 5-Aminolevulinate Synthase TC Cox, SS Bottomley, JS Wiley, MJ Bawden, CS Matthews, BK May New England Journal of Medicine 330 (10), 675-679, 1994 | 150 | 1994 |
| MID1 and MID2 homo-and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked … KM Short, B Hopwood, Z Yi, TC Cox BMC cell biology 3, 1-14, 2002 | 149 | 2002 |
| Retreatability of two endodontic sealers, EndoSequence BC Sealer and AH Plus: a micro-computed tomographic comparison E Oltra, TC Cox, MR LaCourse, JD Johnson, A Paranjpe Restorative dentistry & endodontics 42 (1), 19, 2017 | 142 | 2017 |
| A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development A Ashe, DK Morgan, NC Whitelaw, TJ Bruxner, NK Vickaryous, LL Cox, ... Genome biology 9, 1-16, 2008 | 140 | 2008 |
| Solution structure of the RBCC/TRIM B-box1 domain of human MID1: B-box with a RING MA Massiah, BN Simmons, KM Short, TC Cox Journal of molecular biology 358 (2), 532-545, 2006 | 138 | 2006 |
| Mutation discovery in mice by whole exome sequencing H Fairfield, GJ Gilbert, M Barter, RR Corrigan, M Curtain, Y Ding, ... Genome biology 12, 1-12, 2011 | 130 | 2011 |
| New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome TC Cox, LR Allen, LL Cox, B Hopwood, B Goodwin, E Haan, GK Suthers Human Molecular Genetics 9 (17), 2553-2562, 2000 | 129 | 2000 |
Kieran ShortResearch Fellow, Monash UniversityVerified email at monash.edu
