22 results for author:"Smyth I." in Literature citations
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| Spatial mapping and quantification of developmental branching morphogenesis. Short K., Hodson M., Smyth I. Development 140:471-478(2013) · Mapped (5) |
| Segmental territories along the cardinal veins generate lymph sacs via a ballooning mechanism during embryonic lymphangiogenesis in mice. Francois M., Short K., Secker G.A., Combes A., Schwarz Q., Davidson T.L., Smyth I., Hong Y.K., Harvey N.L., Koopman P. Dev. Biol. 364:89-98(2012) · Mapped (37) |
| Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice. Vissers L.E.L.M., Cox T.C., Maga A.M., Short K.M., Wiradjaja F., Janssen I.M., Jehee F., Bertola D., Liu J., Yagnik G. et al. PLoS Genet. 7:E1002278-E1002278(2011) · UniProtKB (1) · Mapped (21) |
| Hox10 genes function in kidney development in the differentiation and integration of the cortical stroma. Yallowitz A.R., Hrycaj S.M., Short K.M., Smyth I.M., Wellik D.M. PLoS ONE 6:e23410-e23410(2011) · Mapped (52) |
| Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1. Slavotinek A.M., Baranzini S.E., Schanze D., Labelle-Dumais C., Short K.M., Chao R., Yahyavi M., Bijlsma E.K., Chu C., Musone S. et al. J. Med. Genet. 48:375-382(2011) · UniProtKB (1) · Mapped (1) |
| A breathtaking phenotype: unexpected roles of the DNA base damage response protein ASCIZ as a key regulator of early lung development. Heierhorst J., Smyth I., Jurado S. Cell Cycle 10:1222-1224(2011) · Mapped (1) |
| Dual functions of ASCIZ in the DNA base damage response and pulmonary organogenesis. Jurado S., Smyth I., van Denderen B., Tenis N., Hammet A., Hewitt K., Ng J.L., McNees C.J., Kozlov S.V., Oka H. et al. PLoS Genet. 6:e1001170-e1001170(2010) · Mapped (45) |
| Tomographic quantification of branching morphogenesis and renal development. Short K.M., Hodson M.J., Smyth I.M. Kidney Int. 77:1132-1139(2010) · Mapped (5) |
| Palmitoylation regulates epidermal homeostasis and hair follicle differentiation. Mill P., Lee A.W., Fukata Y., Tsutsumi R., Fukata M., Keighren M., Porter R.M., McKie L., Smyth I., Jackson I.J. PLoS Genet. 5:e1000748-e1000748(2009) · Mapped (98) |
| Expression of the fras1/frem gene family during zebrafish development and fin morphogenesis. Gautier P., Naranjo-Golborne C., Taylor M.S., Jackson I.J., Smyth I. |
| A mouse model of harlequin ichthyosis delineates a key role for Abca12 in lipid homeostasis. Smyth I., Hacking D.F., Hilton A.A., Mukhamedova N., Meikle P.J., Ellis S., Satterley K., Slattery K., Collinge J.E., de Graaf C.A. et al. PLoS Genet. 4:e1000192-e1000192(2008) · Mapped (22) |
| Human sebaceous tumors harbor inactivating mutations in LEF1. Takeda H., Lyle S., Lazar A.J., Zouboulis C.C., Smyth I., Watt F.M. Nat. Med. 12:395-397(2006) · Mapped (5) |
| Genomic anatomy of the Tyrp1 (brown) deletion complex. Smyth I.M., Wilming L., Lee A.W., Taylor M.S., Gautier P., Barlow K., Wallis J., Martin S., Glithero R., Phillimore B. et al. Proc. Natl. Acad. Sci. U.S.A. 103:3704-3709(2006) · Mapped (5) |
| The genetics of Fraser syndrome and the blebs mouse mutants. Smyth I., Scambler P. Hum. Mol. Genet. 14 Spec No. 2:R269-74(2005) · Mapped (2) |
| Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs. Jadeja S., Smyth I., Pitera J.E., Taylor M.S., van Haelst M., Bentley E., McGregor L., Hopkins J., Chalepakis G., Philip N. et al. |
| The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis. Smyth I., Du X., Taylor M.S., Justice M.J., Beutler B., Jackson I.J. Proc. Natl. Acad. Sci. U.S.A. 101:13560-13565(2004) · UniProtKB (3) · Mapped (30) |
| Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis. Ellis T., Smyth I., Riley E., Bowles J., Adolphe C., Rothnagel J.A., Wicking C., Wainwright B.J. Dev. Biol. 263:203-215(2003) · Mapped (38) |
| Patched 1 conditional null allele in mice. Ellis T., Smyth I., Riley E., Graham S., Elliot K., Narang M., Kay G.F., Wicking C., Wainwright B. Genesis 36:158-161(2003) · Mapped (9) |
| The hedgehog signalling pathway in tumorigenesis and development. Wicking C., Smyth I., Bale A. Oncogene 18:7844-7851(1999) · Mapped (24) |
| Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene in basal cell carcinoma and medulloblastoma on chromosome 1p32. Smyth I., Narang M.A., Evans T., Heimann C., Nakamura Y., Chenevix-Trench G., Pietsch T., Wicking C., Wainwright B.J. Hum. Mol. Genet. 8:291-297(1999) · UniProtKB (1) |
| 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. Wicking C., Shanley S., Smyth I., Gillies S., Negus K., Graham S., Suthers G., Haites N., Edwards M., Wainwright B.J. et al. Am. J. Hum. Genet. 60:21-26(1997) · UniProtKB (1) |
| Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Hahn H., Wicking C., Zaphiropoulous P.G., Gailani M.R., Shanley S., Chidambaram A., Vorechovsky I., Holmberg E., Unden A.B., Gillies S. et al. Cell 85:841-851(1996) · Mapped (9) |