Theo dõi
Ian Smyth
Ian Smyth
Associate Dean, Research and Research Infrastructure, Faculty of Medicine, Nursing and Health
Email được xác minh tại monash.edu
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
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
24751996
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
5492013
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
3361997
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
2862014
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
2811999
The hedgehog signalling pathway in tumorigenesis and development.
C Wicking, I Smyth, A Bale
Oncogene 18 (55), 7844, 1999
2581999
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
1862005
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
1742006
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
1372004
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
1152003
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
1142017
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
1092012
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 genetics 7 (9), e1002278, 2011
1072011
Attenuated palmitoylation of serotonin receptor 5-HT1A affects receptor function and contributes to depression-like behaviors
N Gorinski, M Bijata, S Prasad, A Wirth, D Abdel Galil, A Zeug, ...
Nature Communications 10 (1), 3924, 2019
1052019
Palmitoylation regulates epidermal homeostasis and hair follicle differentiation
P Mill, AWS Lee, Y Fukata, R Tsutsumi, M Fukata, M Keighren, RM Porter, ...
PLoS genetics 5 (11), e1000748, 2009
1002009
Spatial mapping and quantification of developmental branching morphogenesis
K Short, M Hodson, I Smyth
Development 140 (2), 471-478, 2013
962013
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
952015
The contribution of branching morphogenesis to kidney development and disease
KM Short, IM Smyth
Nature Reviews Nephrology 12 (12), 754-767, 2016
942016
The genetics of Fraser syndrome and the blebs mouse mutants
I Smyth, P Scambler
Human Molecular Genetics 14 (suppl_2), R269-R274, 2005
932005
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 genetics 4 (9), e1000192, 2008
852008
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