Kieran Short
Kieran Short
Research Fellow, Monash University
Verified email at monash.edu
Title
Cited by
Cited by
Year
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
2932006
Global quantification of tissue dynamics in the developing mouse kidney
KM Short, AN Combes, J Lefevre, AL Ju, KM Georgas, T Lamberton, ...
Developmental cell 29 (2), 188-202, 2014
1812014
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), 1-14, 2002
1282002
Solution structure of the MID1 B-box2 CHC (D/C) C2H2 zinc-binding domain: insights into an evolutionarily conserved RING fold
MA Massiah, JAB Matts, KM Short, BN Simmons, S Singireddy, Z Yi, ...
Journal of molecular biology 369 (1), 1-10, 2007
1062007
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
1062006
Segmental territories along the cardinal veins generate lymph sacs via a ballooning mechanism during embryonic lymphangiogenesis in mice
M François, K Short, GA Secker, A Combes, Q Schwarz, TL Davidson, ...
Developmental biology 364 (2), 89-98, 2012
802012
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
LELM Vissers, TC Cox, AM Maga, KM Short, F Wiradjaja, IM Janssen, ...
PLoS Genet 7 (9), e1002278, 2011
732011
Spatial mapping and quantification of developmental branching morphogenesis
K Short, M Hodson, I Smyth
Development 140 (2), 471-478, 2013
722013
Structure of the MID1 Tandem B-Boxes Reveals an Interaction Reminiscent of Intermolecular Ring Heterodimers,
H Tao, BN Simmons, S Singireddy, M Jakkidi, KM Short, TC Cox, ...
Biochemistry 47 (8), 2450-2457, 2008
692008
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1
AM Slavotinek, SE Baranzini, D Schanze, C Labelle-Dumais, KM Short, ...
Journal of medical genetics 48 (6), 375-382, 2011
572011
Hox10 genes function in kidney development in the differentiation and integration of the cortical stroma
AR Yallowitz, SM Hrycaj, KM Short, IM Smyth, DM Wellik
PloS one 6 (8), e23410, 2011
552011
The contribution of branching morphogenesis to kidney development and disease
KM Short, IM Smyth
Nature Reviews Nephrology 12 (12), 754, 2016
542016
Tomographic quantification of branching morphogenesis and renal development
KM Short, MJ Hodson, IM Smyth
Kidney international 77 (12), 1132-1139, 2010
542010
Let's stick together: the role of the Fras1 and Frem proteins in epidermal adhesion
K Short, F Wiradjaja, I Smyth
IUBMB life 59 (7), 427-435, 2007
492007
Repression of Igf1 expression by Ezh2 prevents basal cell differentiation in the developing lung
LA Galvis, AZ Holik, KM Short, J Pasquet, ATL Lun, ME Blewitt, IM Smyth, ...
Development 142 (8), 1458-1469, 2015
472015
Altered ureteric branching morphogenesis and nephron endowment in offspring of diabetic and insulin-treated pregnancy
SN Hokke, JA Armitage, VG Puelles, KM Short, L Jones, IM Smyth, ...
PLoS One 8 (3), e58243, 2013
442013
FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules
J Perry, KM Short, JT Romer, S Swift, TC Cox, A Ashworth
Genomics 62 (3), 385-394, 1999
361999
Validation of a three-dimensional method for counting and sizing podocytes in whole glomeruli
VG Puelles, JW van der Wolde, KE Schulze, KM Short, MN Wong, ...
Journal of the American Society of Nephrology 27 (10), 3093-3104, 2016
332016
An integrated pipeline for the multidimensional analysis of branching morphogenesis
AN Combes, KM Short, J Lefevre, NA Hamilton, MH Little, IM Smyth
Nature protocols 9 (12), 2859, 2014
322014
A new X‐linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13
JM Graham Jr, P Wheeler, D Tackels‐Horne, AE Lin, BD Hall, M May, ...
American journal of medical genetics Part A 123 (1), 37-44, 2003
292003
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