Cairns PM - Search Results

1

Characterisation of Wnt gene expression during the differentiation of murine embryonic stem cells in vitro: role of Wnt3 in enhancing haematopoietic differentiation.

Lako M, Lindsay S, Lincoln J, Cairns PM, Armstrong L, Hole N. Lako M, et al. Among authors: cairns pm. Mech Dev. 2001 May;103(1-2):49-59. doi: 10.1016/s0925-4773(01)00331-8. Mech Dev. 2001. PMID: 11335111 Free article.

2

mTert expression correlates with telomerase activity during the differentiation of murine embryonic stem cells.

Armstrong L, Lako M, Lincoln J, Cairns PM, Hole N. Armstrong L, et al. Among authors: cairns pm. Mech Dev. 2000 Oct;97(1-2):109-16. doi: 10.1016/s0925-4773(00)00423-8. Mech Dev. 2000. PMID: 11025212 Free article.

3

Hair follicle dermal cells repopulate the mouse haematopoietic system.

Lako M, Armstrong L, Cairns PM, Harris S, Hole N, Jahoda CA. Lako M, et al. Among authors: cairns pm. J Cell Sci. 2002 Oct 15;115(Pt 20):3967-74. doi: 10.1242/jcs.00060. J Cell Sci. 2002. PMID: 12244134

4

Haploinsufficiency of the germ cell-specific nuclear RNA binding protein hnRNP G-T prevents functional spermatogenesis in the mouse.

Ehrmann I, Dalgliesh C, Tsaousi A, Paronetto MP, Heinrich B, Kist R, Cairns P, Li W, Mueller C, Jackson M, Peters H, Nayernia K, Saunders P, Mitchell M, Stamm S, Sette C, Elliott DJ. Ehrmann I, et al. Hum Mol Genet. 2008 Sep 15;17(18):2803-18. doi: 10.1093/hmg/ddn179. Epub 2008 Jun 18. Hum Mol Genet. 2008. PMID: 18562473

5

Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia.

Kist R, Watson M, Wang X, Cairns P, Miles C, Reid DJ, Peters H. Kist R, et al. Hum Mol Genet. 2005 Dec 1;14(23):3605-17. doi: 10.1093/hmg/ddi388. Epub 2005 Oct 19. Hum Mol Genet. 2005. PMID: 16236760

6

Somatic mutations of the von Hippel-Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma.

Foster K, Prowse A, van den Berg A, Fleming S, Hulsbeek MM, Crossey PA, Richards FM, Cairns P, Affara NA, Ferguson-Smith MA, et al. Foster K, et al. Hum Mol Genet. 1994 Dec;3(12):2169-73. doi: 10.1093/hmg/3.12.2169. Hum Mol Genet. 1994. PMID: 7881415

7

Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22.

Foster K, Crossey PA, Cairns P, Hetherington JW, Richards FM, Jones MH, Bentley E, Affara NA, Ferguson-Smith MA, Maher ER. Foster K, et al. Br J Cancer. 1994 Feb;69(2):230-4. doi: 10.1038/bjc.1994.44. Br J Cancer. 1994. PMID: 8297719 Free PMC article.

8

Identification of a splice acceptor site mutation in p16INK4A/p14ARF within a breast cancer, melanoma, neurofibroma prone kindred.

Prowse AH, Schultz DC, Guo S, Vanderveer L, Dangel J, Bove B, Cairns P, Daly M, Godwin AK. Prowse AH, et al. J Med Genet. 2003 Aug;40(8):e102. doi: 10.1136/jmg.40.8.e102. J Med Genet. 2003. PMID: 12920094 Free PMC article. No abstract available.

9

Initiation of bladder cancer may involve deletion of a tumour-suppressor gene on chromosome 9.

Cairns P, Shaw ME, Knowles MA. Cairns P, et al. Oncogene. 1993 Apr;8(4):1083-5. Oncogene. 1993. PMID: 8096074

10

Somatic mutations of PTEN in glioblastoma multiforme.

Wang SI, Puc J, Li J, Bruce JN, Cairns P, Sidransky D, Parsons R. Wang SI, et al. Cancer Res. 1997 Oct 1;57(19):4183-6. Cancer Res. 1997. PMID: 9331071

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