Ashton GH - Search Results

1

A novel Src kinase inhibitor reduces tumour formation in a skin carcinogenesis model.

Serrels B, Serrels A, Mason SM, Baldeschi C, Ashton GH, Canel M, Mackintosh LJ, Doyle B, Green TP, Frame MC, Sansom OJ, Brunton VG. Serrels B, et al. Among authors: ashton gh. Carcinogenesis. 2009 Feb;30(2):249-57. doi: 10.1093/carcin/bgn278. Epub 2008 Dec 5. Carcinogenesis. 2009. PMID: 19060248

2

Identification of potential biomarkers for measuring inhibition of Src kinase activity in colon cancer cells following treatment with dasatinib.

Serrels A, Macpherson IR, Evans TR, Lee FY, Clark EA, Sansom OJ, Ashton GH, Frame MC, Brunton VG. Serrels A, et al. Among authors: ashton gh. Mol Cancer Ther. 2006 Dec;5(12):3014-22. doi: 10.1158/1535-7163.MCT-06-0382. Epub 2006 Dec 5. Mol Cancer Ther. 2006. PMID: 17148760

3

Focal adhesion kinase is required for intestinal regeneration and tumorigenesis downstream of Wnt/c-Myc signaling.

Ashton GH, Morton JP, Myant K, Phesse TJ, Ridgway RA, Marsh V, Wilkins JA, Athineos D, Muncan V, Kemp R, Neufeld K, Clevers H, Brunton V, Winton DJ, Wang X, Sears RC, Clarke AR, Frame MC, Sansom OJ. Ashton GH, et al. Dev Cell. 2010 Aug 17;19(2):259-69. doi: 10.1016/j.devcel.2010.07.015. Dev Cell. 2010. PMID: 20708588 Free PMC article.

4

Loss of Apc allows phenotypic manifestation of the transforming properties of an endogenous K-ras oncogene in vivo.

Sansom OJ, Meniel V, Wilkins JA, Cole AM, Oien KA, Marsh V, Jamieson TJ, Guerra C, Ashton GH, Barbacid M, Clarke AR. Sansom OJ, et al. Among authors: ashton gh. Proc Natl Acad Sci U S A. 2006 Sep 19;103(38):14122-7. doi: 10.1073/pnas.0604130103. Epub 2006 Sep 7. Proc Natl Acad Sci U S A. 2006. PMID: 16959882 Free PMC article.

5

Prenatal diagnosis for inherited skin diseases.

Ashton GH, Eady RA, McGrath JA. Ashton GH, et al. Clin Dermatol. 2000 Nov-Dec;18(6):643-8. doi: 10.1016/s0738-081x(00)00153-x. Clin Dermatol. 2000. PMID: 11173198 Review. No abstract available.

6

Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1.

Hamada T, South AP, Mitsuhashi Y, Kinebuchi T, Bleck O, Ashton GH, Hozumi Y, Suzuki T, Hashimoto T, Eady RA, McGrath JA. Hamada T, et al. Among authors: ashton gh. Exp Dermatol. 2002 Apr;11(2):107-14. doi: 10.1034/j.1600-0625.2002.110202.x. Exp Dermatol. 2002. PMID: 11994137

7

Properties of the Binary Black Hole Merger GW150914.

Abbott BP, Abbott R, Abbott TD, Abernathy MR, Acernese F, Ackley K, Adams C, Adams T, Addesso P, Adhikari RX, Adya VB, Affeldt C, Agathos M, Agatsuma K, Aggarwal N, Aguiar OD, Aiello L, Ain A, Ajith P, Allen B, Allocca A, Altin PA, Anderson SB, Anderson WG, Arai K, Araya MC, Arceneaux CC, Areeda JS, Arnaud N, Arun KG, Ascenzi S, Ashton G, Ast M, Aston SM, Astone P, Aufmuth P, Aulbert C, Babak S, Bacon P, Bader MK, Baker PT, Baldaccini F, Ballardin G, Ballmer SW, Barayoga JC, Barclay SE, Barish BC, Barker D, Barone F, Barr B, Barsotti L, Barsuglia M, Barta D, Bartlett J, Bartos I, Bassiri R, Basti A, Batch JC, Baune C, Bavigadda V, Bazzan M, Behnke B, Bejger M, Bell AS, Bell CJ, Berger BK, Bergman J, Bergmann G, Berry CP, Bersanetti D, Bertolini A, Betzwieser J, Bhagwat S, Bhandare R, Bilenko IA, Billingsley G, Birch J, Birney R, Birnholtz O, Biscans S, Bisht A, Bitossi M, Biwer C, Bizouard MA, Blackburn JK, Blair CD, Blair DG, Blair RM, Bloemen S, Bock O, Bodiya TP, Boer M, Bogaert G, Bogan C, Bohe A, Bojtos P, Bond C, Bondu F, Bonnand R, Boom BA, Bork R, Boschi V, Bose S, Bouffanais Y, Bozzi A, Bradaschia C, Brady PR, Braginsky VB, Branchesi M, Brau JE, Briant T, Brillet A… See abstract for full author list ➔ Abbott BP, et al. Among authors: ashton g. Phys Rev Lett. 2016 Jun 17;116(24):241102. doi: 10.1103/PhysRevLett.116.241102. Epub 2016 Jun 14. Phys Rev Lett. 2016. PMID: 27367378 Free article.

8

EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis.

South AP, Ashton GH, Willoughby C, Ellis IH, Bleck O, Hamada T, Mannion G, Wessagowit V, Hashimoto T, Eady RA, McGrath JA. South AP, et al. Among authors: ashton gh. Br J Dermatol. 2002 Feb;146(2):216-20. doi: 10.1046/j.1365-2133.2002.04638.x. Br J Dermatol. 2002. PMID: 11903230

9

Prenatal diagnosis of Herlitz junctional epidermolysis bullosa in nonidentical twins.

Fassihi H, Ashton GH, Denyer J, Mellerio JE, Mason G, McGrath JA. Fassihi H, et al. Among authors: ashton gh. Clin Exp Dermatol. 2005 Mar;30(2):180-2. doi: 10.1111/j.1365-2230.2004.01704.x. Clin Exp Dermatol. 2005. PMID: 15725250

10

Prenatal diagnosis for severe inherited skin disorders: 25 years' experience.

Fassihi H, Eady RA, Mellerio JE, Ashton GH, Dopping-Hepenstal PJ, Denyer JE, Nicolaides KH, Rodeck CH, McGrath JA. Fassihi H, et al. Among authors: ashton gh. Br J Dermatol. 2006 Jan;154(1):106-13. doi: 10.1111/j.1365-2133.2005.07012.x. Br J Dermatol. 2006. PMID: 16403102

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