Kefford RF - Search Results

1

Responses to ultraviolet-B in cell lines from hereditary melanoma kindreds.

Shannon JA, Kefford RF, Mann GJ. Shannon JA, et al. Among authors: kefford rf. Melanoma Res. 2001 Feb;11(1):1-9. doi: 10.1097/00008390-200102000-00001. Melanoma Res. 2001. PMID: 11254110

2

SCL gene in human tumors.

Rockman S, Begley CG, Kannourakis G, Mann GJ, Dobrovic AN, Kefford RF, McGrath K. Rockman S, et al. Among authors: kefford rf. Leukemia. 1992 Jul;6(7):623-5. Leukemia. 1992. PMID: 1625484

3

Clinical aspects of hereditary melanoma in Australia.

Salmon JA, Rivers JK, Donald JA, Shaw HM, McCarthy WH, Kefford RF. Salmon JA, et al. Among authors: kefford rf. Cytogenet Cell Genet. 1992;59(2-3):170-2. doi: 10.1159/000133235. Cytogenet Cell Genet. 1992. PMID: 1737490 No abstract available.

4

Isolation and preliminary characterisation of an X-ray-sensitive mammalian mutant cell line (WMXRS-1).

McKay MJ, Mann GJ, McDonald DA, Jones S, Kefford RF. McKay MJ, et al. Among authors: kefford rf. Mutat Res. 1994 May;314(3):261-71. doi: 10.1016/0921-8777(94)90070-1. Mutat Res. 1994. PMID: 7513058

5

Loss of heterozygosity in malignant melanoma at loci on chromosome 11 and 17 implicated in the pathogenesis of other cancers.

Tomlinson IP, Gammack AJ, Stickland JE, Mann GJ, MacKie RM, Kefford RF, McGee JO. Tomlinson IP, et al. Among authors: kefford rf. Genes Chromosomes Cancer. 1993 Jul;7(3):169-72. doi: 10.1002/gcc.2870070310. Genes Chromosomes Cancer. 1993. PMID: 7687871

6

The spectrum of in vitro radiosensitivity in four human melanoma cell lines is not accounted for by differential induction or rejoining of DNA double strand breaks.

McKay MJ, Kefford RF. McKay MJ, et al. Among authors: kefford rf. Int J Radiat Oncol Biol Phys. 1995 Jan 15;31(2):345-52. doi: 10.1016/0360-3016(94)e0147-c. Int J Radiat Oncol Biol Phys. 1995. PMID: 7836088

7

Testicular ultrasound in patients with testicular germ cell tumours.

Shannon JA, Kefford RF. Shannon JA, et al. Among authors: kefford rf. Aust N Z J Med. 1994 Aug;24(4):412-3. doi: 10.1111/j.1445-5994.1994.tb01478.x. Aust N Z J Med. 1994. PMID: 7980245 Review. No abstract available.

8

Loss of heterozygosity and homozygous deletions on 9p21-22 in melanoma.

Holland EA, Beaton SC, Edwards BG, Kefford RF, Mann GJ. Holland EA, et al. Among authors: kefford rf. Oncogene. 1994 May;9(5):1361-5. Oncogene. 1994. PMID: 8152796

9

Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds.

Holland EA, Beaton SC, Becker TM, Grulet OM, Peters BA, Rizos H, Kefford RF, Mann GJ. Holland EA, et al. Among authors: kefford rf. Oncogene. 1995 Dec 7;11(11):2289-94. Oncogene. 1995. PMID: 8570179

10

Differential expression of p16INK4a and p16beta transcripts in B-lymphoblastoid cells from members of hereditary melanoma families without CDKN2A exon mutations.

Rizos H, Becker TM, Holland EA, Kefford RF, Mann GJ. Rizos H, et al. Among authors: kefford rf. Oncogene. 1997 Jul 31;15(5):515-23. doi: 10.1038/sj.onc.1201217. Oncogene. 1997. PMID: 9247305

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