Platz A - Search Results

1

Expression and localization of mutant p16 proteins in melanocytic lesions from familial melanoma patients.

Ghiorzo P, Villaggio B, Sementa AR, Hansson J, Platz A, Nicoló G, Spina B, Canepa M, Palmer JM, Hayward NK, Bianchi-Scarrà G. Ghiorzo P, et al. Among authors: platz a. Hum Pathol. 2004 Jan;35(1):25-33. doi: 10.1016/j.humpath.2003.08.017. Hum Pathol. 2004. PMID: 14745721

2

A melanoma-predisposing germline CDKN2A mutation with functional significance for both p16 and p14ARF.

Hashemi J, Lindström MS, Asker C, Platz A, Hansson J, Wiman KG. Hashemi J, et al. Among authors: platz a. Cancer Lett. 2002 Jun 28;180(2):211-21. doi: 10.1016/s0304-3835(02)00027-7. Cancer Lett. 2002. PMID: 12175554

3

Screening of germline mutations in the CDK4, CDKN2C and TP53 genes in familial melanoma: a clinic-based population study.

Platz A, Hansson J, Ringborg U. Platz A, et al. Int J Cancer. 1998 Sep 25;78(1):13-5. doi: 10.1002/(sici)1097-0215(19980925)78:1<13::aid-ijc3>3.0.co;2-#. Int J Cancer. 1998. PMID: 9724087

4

Melanoma development in relation to non-functional p16/INK4A protein and dysplastic naevus syndrome in Swedish melanoma kindreds.

Hashemi J, Linder S, Platz A, Hansson J. Hashemi J, et al. Among authors: platz a. Melanoma Res. 1999 Feb;9(1):21-30. doi: 10.1097/00008390-199902000-00004. Melanoma Res. 1999. PMID: 10338331

5

Hereditary cutaneous melanoma.

Platz A, Ringborg U, Hansson J. Platz A, et al. Semin Cancer Biol. 2000 Aug;10(4):319-26. doi: 10.1006/scbi.2000.0149. Semin Cancer Biol. 2000. PMID: 10966854 Review.

6

Biallelic deletions in INK4 in cutaneous melanoma are common and associated with decreased survival.

Grafström E, Egyházi S, Ringborg U, Hansson J, Platz A. Grafström E, et al. Among authors: platz a. Clin Cancer Res. 2005 Apr 15;11(8):2991-7. doi: 10.1158/1078-0432.CCR-04-1731. Clin Cancer Res. 2005. PMID: 15837753

7

Geographical variation in the penetrance of CDKN2A mutations for melanoma.

Bishop DT, Demenais F, Goldstein AM, Bergman W, Bishop JN, Bressac-de Paillerets B, Chompret A, Ghiorzo P, Gruis N, Hansson J, Harland M, Hayward N, Holland EA, Mann GJ, Mantelli M, Nancarrow D, Platz A, Tucker MA; Melanoma Genetics Consortium. Bishop DT, et al. Among authors: platz a. J Natl Cancer Inst. 2002 Jun 19;94(12):894-903. doi: 10.1093/jnci/94.12.894. J Natl Cancer Inst. 2002. PMID: 12072543

8

Frequency of UV-inducible NRAS mutations in melanomas of patients with germline CDKN2A mutations.

Eskandarpour M, Hashemi J, Kanter L, Ringborg U, Platz A, Hansson J. Eskandarpour M, et al. Among authors: platz a. J Natl Cancer Inst. 2003 Jun 4;95(11):790-8. doi: 10.1093/jnci/95.11.790. J Natl Cancer Inst. 2003. PMID: 12783933

9

Screening of N-ras codon 61 mutations in paired primary and metastatic cutaneous melanomas: mutations occur early and persist throughout tumor progression.

Omholt K, Karsberg S, Platz A, Kanter L, Ringborg U, Hansson J. Omholt K, et al. Among authors: platz a. Clin Cancer Res. 2002 Nov;8(11):3468-74. Clin Cancer Res. 2002. PMID: 12429636

10

NRAS and BRAF mutations arise early during melanoma pathogenesis and are preserved throughout tumor progression.

Omholt K, Platz A, Kanter L, Ringborg U, Hansson J. Omholt K, et al. Among authors: platz a. Clin Cancer Res. 2003 Dec 15;9(17):6483-8. Clin Cancer Res. 2003. PMID: 14695152

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