Ian Smyth
Ian Smyth
Deputy Head (Research), Department of Anatomy and Developmental Biology; Co-Head Development and
Verified email at monash.edu
Cited by
Cited by
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome
H Hahn, C Wicking, PG Zaphiropoulos, MR Gailani, S Shanley, ...
Cell 85 (6), 841-851, 1996
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes
JK White, AK Gerdin, NA Karp, E Ryder, M Buljan, JN Bussell, J Salisbury, ...
Cell 154 (2), 452-464, 2013
Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident.
C Wicking, S Shanley, I Smyth, S Gillies, K Negus, S Graham, G Suthers, ...
American journal of human genetics 60 (1), 21, 1997
Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene in basal cell carcinoma and medulloblastoma on chromosome 1p32
I Smyth, MA Narang, T Evans, C Heimann, Y Nakamura, ...
Human molecular genetics 8 (2), 291-297, 1999
The hedgehog signalling pathway in tumorigenesis and development.
C Wicking, I Smyth, A Bale
Oncogene 18 (55), 7844, 1999
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
Human sebaceous tumors harbor inactivating mutations in LEF1
H Takeda, S Lyle, AJF Lazar, CC Zouboulis, I Smyth, FM Watt
Nature medicine 12 (4), 395-397, 2006
Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs
S Jadeja, I Smyth, JE Pitera, MS Taylor, M van Haelst, E Bentley, ...
Nature genetics 37 (5), 520-525, 2005
The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis
I Smyth, X Du, MS Taylor, MJ Justice, B Beutler, IJ Jackson
Proceedings of the National Academy of Sciences 101 (37), 13560-13565, 2004
Patched 1 conditional null allele in mice
T Ellis, I Smyth, E Riley, S Graham, K Elliot, M Narang, GF Kay, C Wicking, ...
Genesis 36 (3), 158-161, 2003
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
The genetics of Fraser syndrome and the blebs mouse mutants
I Smyth, P Scambler
Human Molecular Genetics 14 (suppl_2), R269-R274, 2005
Palmitoylation regulates epidermal homeostasis and hair follicle differentiation
P Mill, AWS Lee, Y Fukata, R Tsutsumi, M Fukata, M Keighren, RM Porter, ...
PLoS Genet 5 (11), e1000748, 2009
A mouse model of harlequin ichthyosis delineates a key role for Abca12 in lipid homeostasis
I Smyth, DF Hacking, AA Hilton, N Mukhamedova, PJ Meikle, S Ellis, ...
PLoS Genet 4 (9), e1000192, 2008
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
Spatial mapping and quantification of developmental branching morphogenesis
K Short, M Hodson, I Smyth
Development 140 (2), 471-478, 2013
INPP5E interacts with AURKA, linking phosphoinositide signaling to primary cilium stability
OV Plotnikova, S Seo, DL Cottle, S Conduit, S Hakim, JM Dyson, ...
Journal of cell science 128 (2), 364-372, 2015
INPP5E regulates phosphoinositide-dependent cilia transition zone function
JM Dyson, SE Conduit, SJ Feeney, S Hakim, T DiTommaso, AJ Fulcher, ...
Journal of Cell Biology 216 (1), 247-263, 2017
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
Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
T Ellis, I Smyth, E Riley, J Bowles, C Adolphe, JA Rothnagel, C Wicking, ...
Developmental biology 263 (2), 203-215, 2003
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