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Journal Abstract Search

296 related items for PubMed ID: 12690309

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  • 2. Loss of heterozygosity and homozygous deletions on 9p21-22 in melanoma.
    Holland EA, Beaton SC, Edwards BG, Kefford RF, Mann GJ.
    Oncogene; 1994 May; 9(5):1361-5. PubMed ID: 8152796
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  • 3. Molecular alterations at chromosome 9p21 in melanocytic naevi and melanoma.
    Sini MC, Manca A, Cossu A, Budroni M, Botti G, Ascierto PA, Cremona F, Muggiano A, D'Atri S, Casula M, Baldinu P, Palomba G, Lissia A, Tanda F, Palmieri G.
    Br J Dermatol; 2008 Feb; 158(2):243-50. PubMed ID: 18028495
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  • 4. [Detailed mapping and clinical significance of loss of heterozygosity on 9p13-23 in laryngeal squamous cell carcinoma by microsatellite analysis].
    Xu XF, Tang PZ, Cheng SJ.
    Ai Zheng; 2003 May; 22(5):452-7. PubMed ID: 12753701
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  • 6. Morphologic diversity in malignant melanoma: the potential use of microdissection and the polymerase chain reaction for diagnosis.
    Quezado MM, Abati AD, Albuquerque AV, Wilson J, Merino MJ, Filie AC.
    Mod Pathol; 1998 Oct; 11(10):1010-5. PubMed ID: 9796732
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  • 7. p16INK4a inactivation is not frequent in uncultured sporadic primary cutaneous melanoma.
    Fujimoto A, Morita R, Hatta N, Takehara K, Takata M.
    Oncogene; 1999 Apr 15; 18(15):2527-32. PubMed ID: 10229204
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  • 8. CDKN2A mutation and deletion status in thin and thick primary melanoma.
    Cachia AR, Indsto JO, McLaren KM, Mann GJ, Arends MJ.
    Clin Cancer Res; 2000 Sep 15; 6(9):3511-5. PubMed ID: 10999737
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  • 12. Loss of heterozygosity in the MXI1 gene is a frequent occurrence in melanoma.
    Ariyanayagam-Baksh SM, Baksh FK, Swalsky PA, Finkelstein SD.
    Mod Pathol; 2003 Oct 15; 16(10):992-5. PubMed ID: 14559981
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  • 16. Detailed deletion mapping of loss of heterozygosity on 9p13-23 in laryngeal squamous cell carcinoma by microsatellite analysis.
    Xu XF, Gao YN, Cheng SJ.
    Chin Med J (Engl); 2004 Aug 15; 117(8):1204-9. PubMed ID: 15361296
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  • 17. Deletion mapping of chromosome region 9p21-p22 surrounding the CDKN2 locus in melanoma.
    Ohta M, Berd D, Shimizu M, Nagai H, Cotticelli M-G, Mastrangelo M, Shields JA, Shields CL, Croce CM, Huebner K.
    Int J Cancer; 1996 Mar 15; 65(6):762-7. PubMed ID: 8631588
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  • 18. Spitz nevi display allelic deletions.
    Bogdan I, Burg G, Böni R.
    Arch Dermatol; 2001 Nov 15; 137(11):1417-20. PubMed ID: 11708943
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  • 19. Loss of heterozygosity on chromosome 1 and 9 and hormone receptor analysis of metastatic malignant melanoma presenting in breast.
    Beaty MW, Quezado M, Sobel ME, Duray P, Merino MJ.
    Int J Surg Pathol; 2005 Jan 15; 13(1):9-18. PubMed ID: 15735850
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  • 20. Loss of heterozygosity at chromosome 9p21 (INK4-p14ARF locus): homozygous deletions and mutations in the p16 and p14ARF genes in sporadic primary melanomas.
    Kumar R, Smeds J, Lundh Rozell B, Hemminki K.
    Melanoma Res; 1999 Apr 15; 9(2):138-47. PubMed ID: 10380936
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