Smyth I - Search Results

1

Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32.

Smyth I, Narang MA, Evans T, Heimann C, Nakamura Y, Chenevix-Trench G, Pietsch T, Wicking C, Wainwright BJ. Smyth I, et al. Hum Mol Genet. 1999 Feb;8(2):291-7. doi: 10.1093/hmg/8.2.291. Hum Mol Genet. 1999. PMID: 9931336

2

The molecular and cellular anatomy of a fetal programming defect - the impact of low protein diet on the developing kidney.

Short KM, Tortelote GG, Jones LK, Diniz F, Edgington-Giordano F, Cullen-McEwen LA, Schröder J, Spencer A, Keniry A, Polo JM, Bertram JF, Blewitt ME, Smyth IM, El-Dahr SS. Short KM, et al. Among authors: smyth im. bioRxiv [Preprint]. 2023 Dec 5:2023.12.04.569988. doi: 10.1101/2023.12.04.569988. bioRxiv. 2023. PMID: 38106143 Free PMC article. Preprint.

3

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome.

Hahn H, Wicking C, Zaphiropoulous PG, Gailani MR, Shanley S, Chidambaram A, Vorechovsky I, Holmberg E, Unden AB, Gillies S, Negus K, Smyth I, Pressman C, Leffell DJ, Gerrard B, Goldstein AM, Dean M, Toftgard R, Chenevix-Trench G, Wainwright B, Bale AE. Hahn H, et al. Among authors: smyth i. Cell. 1996 Jun 14;85(6):841-51. doi: 10.1016/s0092-8674(00)81268-4. Cell. 1996. PMID: 8681379 Free article.

4

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, Chenevix-Trench G. Wicking C, et al. Among authors: smyth i. Am J Hum Genet. 1997 Jan;60(1):21-6. Am J Hum Genet. 1997. PMID: 8981943 Free PMC article.

5

De novo mutations of the Patched gene in nevoid basal cell carcinoma syndrome help to define the clinical phenotype.

Wicking C, Gillies S, Smyth I, Shanley S, Fowles L, Ratcliffe J, Wainwright B, Chenevix-Trench G. Wicking C, et al. Among authors: smyth i. Am J Med Genet. 1997 Dec 19;73(3):304-7. Am J Med Genet. 1997. PMID: 9415689

6

The effects of splice site mutations in patients with naevoid basal cell carcinoma syndrome.

Smyth I, Wicking C, Wainwright B, Chenevix-Trench G. Smyth I, et al. Hum Genet. 1998 May;102(5):598-601. doi: 10.1007/s004390050747. Hum Genet. 1998. PMID: 9654212

7

The hedgehog signalling pathway in tumorigenesis and development.

Wicking C, Smyth I, Bale A. Wicking C, et al. Among authors: smyth i. Oncogene. 1999 Dec 20;18(55):7844-51. doi: 10.1038/sj.onc.1203282. Oncogene. 1999. PMID: 10630637 Review.

8

The spectrum of patched mutations in a collection of Australian basal cell carcinomas.

Evans T, Boonchai W, Shanley S, Smyth I, Gillies S, Georgas K, Wainwright B, Chenevix-Trench G, Wicking C. Evans T, et al. Among authors: smyth i. Hum Mutat. 2000;16(1):43-8. doi: 10.1002/1098-1004(200007)16:1<43::AID-HUMU8>3.0.CO;2-7. Hum Mutat. 2000. PMID: 10874304

9

Patched 1 conditional null allele in mice.

Ellis T, Smyth I, Riley E, Graham S, Elliot K, Narang M, Kay GF, Wicking C, Wainwright B. Ellis T, et al. Among authors: smyth i. Genesis. 2003 Jul;36(3):158-61. doi: 10.1002/gene.10208. Genesis. 2003. PMID: 12872247

10

Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis.

Ellis T, Smyth I, Riley E, Bowles J, Adolphe C, Rothnagel JA, Wicking C, Wainwright BJ. Ellis T, et al. Among authors: smyth i. Dev Biol. 2003 Nov 15;263(2):203-15. doi: 10.1016/s0012-1606(03)00394-4. Dev Biol. 2003. PMID: 14597196 Free article.

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