-
1
-
-
33846457870
-
Cancer statistics, 2007
-
Jemal A, Siegel R, Ward E, et al. Cancer statistics, 2007. CA Cancer J Clin. 2007;57:43-66.
-
(2007)
CA Cancer J Clin
, vol.57
, pp. 43-66
-
-
Jemal, A.1
Siegel, R.2
Ward, E.3
-
2
-
-
0021743724
-
A study of tumor progression: The precursor lesions of superficial spreading and nodular melanoma
-
Clark WH Jr, Elder DE, Guerry DT, et al. A study of tumor progression: the precursor lesions of superficial spreading and nodular melanoma. Hum Pathol. 1984;15:1147-1165.
-
(1984)
Hum Pathol
, vol.15
, pp. 1147-1165
-
-
Clark Jr, W.H.1
Elder, D.E.2
Guerry, D.T.3
-
3
-
-
0023212156
-
Dysplastic nevus in histologic contiguity with acquired nonfamilial melanoma. Clinicopathologic experience in a 100-bed hospital
-
Duray PH, Ernstoff MS. Dysplastic nevus in histologic contiguity with acquired nonfamilial melanoma. Clinicopathologic experience in a 100-bed hospital. Arch Dermatol. 1987;123:80-84.
-
(1987)
Arch Dermatol
, vol.123
, pp. 80-84
-
-
Duray, P.H.1
Ernstoff, M.S.2
-
4
-
-
0020610772
-
Dysplastic melanocytic nevi in histologic association with 234 primary cutaneous melanomas
-
Rhodes AR, Harrist TJ, Day CL, et al. Dysplastic melanocytic nevi in histologic association with 234 primary cutaneous melanomas. J Am Acad Dermatol. 1983;9:563-574.
-
(1983)
J Am Acad Dermatol
, vol.9
, pp. 563-574
-
-
Rhodes, A.R.1
Harrist, T.J.2
Day, C.L.3
-
5
-
-
0028593972
-
Precursors to skin cancer
-
Sober AJ, Burstein JM. Precursors to skin cancer. Cancer. 1995;75: 645-650.
-
(1995)
Cancer
, vol.75
, pp. 645-650
-
-
Sober, A.J.1
Burstein, J.M.2
-
6
-
-
0037079003
-
Rules for making human tumor cells
-
Hahn WC, Weinberg RA. Rules for making human tumor cells. N Engl J Med. 2002;347:1593-1603.
-
(2002)
N Engl J Med
, vol.347
, pp. 1593-1603
-
-
Hahn, W.C.1
Weinberg, R.A.2
-
7
-
-
0034486175
-
The genetics of cutaneous melanoma
-
Pollock PM, Trent JM. The genetics of cutaneous melanoma. Clin Lab Med. 2000;20:667-690.
-
(2000)
Clin Lab Med
, vol.20
, pp. 667-690
-
-
Pollock, P.M.1
Trent, J.M.2
-
8
-
-
0036850146
-
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, et al. Screening of N-ras codon 61 mutations in paired primary and metastatic cutaneous melanomas: mutations occur early and persist throughout tumor progression. Clin Cancer Res. 2002;8:3468-3474.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 3468-3474
-
-
Omholt, K.1
Karsberg, S.2
Platz, A.3
-
9
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies H, Bignell GR, Cox C, et al. Mutations of the BRAF gene in human cancer. Nature. 2002;417:949-954.
-
(2002)
Nature
, vol.417
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
-
10
-
-
0029919109
-
Hereditary cancer: Two hits revisited
-
Knudson AG. Hereditary cancer: two hits revisited. J Cancer Res Clin Oncol. 1996;122:135-140.
-
(1996)
J Cancer Res Clin Oncol
, vol.122
, pp. 135-140
-
-
Knudson, A.G.1
-
11
-
-
0030062357
-
Allelotypes of primary cutaneous melanoma and benign melanocytic nevi
-
Healy E, Belgaid CE, Takata M, et al. Allelotypes of primary cutaneous melanoma and benign melanocytic nevi. Cancer Res. 1996;56: 589-593.
-
(1996)
Cancer Res
, vol.56
, pp. 589-593
-
-
Healy, E.1
Belgaid, C.E.2
Takata, M.3
-
12
-
-
0028879183
-
Microsatellite instability and loss of heterozygosity in melanoma
-
Peris K, Keller G, Chimenti S, et al. Microsatellite instability and loss of heterozygosity in melanoma. J Invest Dermatol. 1995;105:625-628.
-
(1995)
J Invest Dermatol
, vol.105
, pp. 625-628
-
-
Peris, K.1
Keller, G.2
Chimenti, S.3
-
13
-
-
0034295281
-
Microsatellite analysis of melanoma lesions using (CA)13 oligonucleotides as an internal probe
-
Fujiwara Y, Hoon DS. Microsatellite analysis of melanoma lesions using (CA)13 oligonucleotides as an internal probe. Int J Oncol. 2000;17: 783-787.
-
(2000)
Int J Oncol
, vol.17
, pp. 783-787
-
-
Fujiwara, Y.1
Hoon, D.S.2
-
14
-
-
0033587013
-
Functional localization of a melanoma tumor suppressor gene to a small (< or = 2 Mb) region on 11q23
-
Robertson GP, Goldberg EK, Lugo TG, et al. Functional localization of a melanoma tumor suppressor gene to a small (< or = 2 Mb) region on 11q23. Oncogene. 1999;18:3173-3180.
-
(1999)
Oncogene
, vol.18
, pp. 3173-3180
-
-
Robertson, G.P.1
Goldberg, E.K.2
Lugo, T.G.3
-
15
-
-
0030249881
-
Allele loss on chromosome 11q and microsatellite instability in malignant melanoma
-
Tomlinson IP, Beck NE, Bodmer WF. Allele loss on chromosome 11q and microsatellite instability in malignant melanoma. Eur J Cancer. 1996; 32A:1797-1802.
-
(1996)
Eur J Cancer
, vol.32 A
, pp. 1797-1802
-
-
Tomlinson, I.P.1
Beck, N.E.2
Bodmer, W.F.3
-
16
-
-
34047258036
-
Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays
-
Stark M, Hayward N. Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays. Cancer Res. 2007;67:2632-2642.
-
(2007)
Cancer Res
, vol.67
, pp. 2632-2642
-
-
Stark, M.1
Hayward, N.2
-
17
-
-
0031589485
-
Genetic alterations of p16INK4a and p53 genes in sporadic dysplastic nevus
-
Lee JY, Dong SM, Shin MS, et al. Genetic alterations of p16INK4a and p53 genes in sporadic dysplastic nevus. Biochem Biophys Res Commun. 1997;237:667-672.
-
(1997)
Biochem Biophys Res Commun
, vol.237
, pp. 667-672
-
-
Lee, J.Y.1
Dong, S.M.2
Shin, M.S.3
-
18
-
-
0031909301
-
Allelic deletion at chromosome 9p21(p16) and 17p13(p53) in microdissected sporadic dysplastic nevus
-
Park WS, Vortmeyer AO, Pack S, et al. Allelic deletion at chromosome 9p21(p16) and 17p13(p53) in microdissected sporadic dysplastic nevus. Hum Pathol. 1998;29:127-130.
-
(1998)
Hum Pathol
, vol.29
, pp. 127-130
-
-
Park, W.S.1
Vortmeyer, A.O.2
Pack, S.3
-
19
-
-
0036219402
-
Loss of heterozygosity analysis of cutaneous melanoma and benign melanocytic nevi: Laser capture microdissection demonstrates clonal genetic changes in acquired nevocellular nevi
-
Maitra A, Gazdar AF, Moore TO, et al. Loss of heterozygosity analysis of cutaneous melanoma and benign melanocytic nevi: laser capture microdissection demonstrates clonal genetic changes in acquired nevocellular nevi. Hum Pathol. 2002;33:191-197.
-
(2002)
Hum Pathol
, vol.33
, pp. 191-197
-
-
Maitra, A.1
Gazdar, A.F.2
Moore, T.O.3
-
20
-
-
0036713522
-
Alteration of chromosome 9p21 and/or p16 in benign and dysplastic nevi suggests a role in early melanoma progression (United States)
-
Tran TP, Titus-Ernstoff L, Perry AE, et al. Alteration of chromosome 9p21 and/or p16 in benign and dysplastic nevi suggests a role in early melanoma progression (United States). Cancer Causes Control. 2002;13: 675-682.
-
(2002)
Cancer Causes Control
, vol.13
, pp. 675-682
-
-
Tran, T.P.1
Titus-Ernstoff, L.2
Perry, A.E.3
-
21
-
-
0036241674
-
Loss of heterozygosity, microsatellite instability, and mismatch repair protein alterations in the radial growth phase of cutaneous malignant melanomas
-
Hussein MR, Sun M, Roggero E, et al. Loss of heterozygosity, microsatellite instability, and mismatch repair protein alterations in the radial growth phase of cutaneous malignant melanomas. Mol Carcinog. 2002;34:35-44.
-
(2002)
Mol Carcinog
, vol.34
, pp. 35-44
-
-
Hussein, M.R.1
Sun, M.2
Roggero, E.3
-
22
-
-
0034033843
-
Detection of microsatellite alterations in the spectrum of melanocytic nevi in patients with or without individual or family history of melanoma
-
Birindelli S, Tragni G, Bartoli C, et al. Detection of microsatellite alterations in the spectrum of melanocytic nevi in patients with or without individual or family history of melanoma. Int J Cancer. 2000;86: 255-261.
-
(2000)
Int J Cancer
, vol.86
, pp. 255-261
-
-
Birindelli, S.1
Tragni, G.2
Bartoli, C.3
-
23
-
-
0034918766
-
Comprehensive analysis of 112 melanocytic skin lesions demonstrates microsatellite instability in melanomas and dysplastic nevi, but not in benign nevi
-
Hussein MR, Sun M, Tuthill RJ, et al. Comprehensive analysis of 112 melanocytic skin lesions demonstrates microsatellite instability in melanomas and dysplastic nevi, but not in benign nevi. J Cutan Pathol. 2001;28:343-350.
-
(2001)
J Cutan Pathol
, vol.28
, pp. 343-350
-
-
Hussein, M.R.1
Sun, M.2
Tuthill, R.J.3
-
24
-
-
0035674998
-
X inactivation, DNA deletion, and microsatellite instability in common acquired melanocytic nevi
-
Indsto JO, Cachia AR, Kefford RF, et al. X inactivation, DNA deletion, and microsatellite instability in common acquired melanocytic nevi. Clin Cancer Res. 2001;7:4054-4059.
-
(2001)
Clin Cancer Res
, vol.7
, pp. 4054-4059
-
-
Indsto, J.O.1
Cachia, A.R.2
Kefford, R.F.3
-
25
-
-
0038242006
-
Assessment of genetic instability in melanocytic skin lesions through microsatellite analysis of benign naevi, dysplastic naevi, and primary melanomas and their metastases
-
Palmieri G, Ascierto PA, Cossu A, et al. Assessment of genetic instability in melanocytic skin lesions through microsatellite analysis of benign naevi, dysplastic naevi, and primary melanomas and their metastases. Melanoma Res. 2003;13:167-170.
-
(2003)
Melanoma Res
, vol.13
, pp. 167-170
-
-
Palmieri, G.1
Ascierto, P.A.2
Cossu, A.3
-
26
-
-
0034949093
-
Instability at sequence repeats in melanocytic tumours
-
Richetta A, Ottini L, Falchetti M, et al. Instability at sequence repeats in melanocytic tumours. Melanoma Res. 2001;11:283-289.
-
(2001)
Melanoma Res
, vol.11
, pp. 283-289
-
-
Richetta, A.1
Ottini, L.2
Falchetti, M.3
-
27
-
-
0036050753
-
Loss of heterozygosity and microsatellite instability in acquired melanocytic nevi: Towards a molecular definition of the dysplastic nevus
-
Rubben A, Bogdan I, Grussendorf-Conen EI, et al. Loss of heterozygosity and microsatellite instability in acquired melanocytic nevi: towards a molecular definition of the dysplastic nevus. Recent Results Cancer Res. 2002;160:100-110.
-
(2002)
Recent Results Cancer Res
, vol.160
, pp. 100-110
-
-
Rubben, A.1
Bogdan, I.2
Grussendorf-Conen, E.I.3
-
28
-
-
0034762203
-
The Raf/MEK/ERK pathway: New concepts of activation
-
Peyssonnaux C, Eychene A. The Raf/MEK/ERK pathway: new concepts of activation. Biol Cell. 2001;93:53-62.
-
(2001)
Biol Cell
, vol.93
, pp. 53-62
-
-
Peyssonnaux, C.1
Eychene, A.2
-
29
-
-
0141565499
-
BRAF mutation: A frequent event in benign, atypical, and malignant melanocytic lesions of the skin
-
Uribe P, Wistuba II, Gonzalez S. BRAF mutation: a frequent event in benign, atypical, and malignant melanocytic lesions of the skin. Am J Dermatopathol. 2003;25:365-370.
-
(2003)
Am J Dermatopathol
, vol.25
, pp. 365-370
-
-
Uribe, P.1
Wistuba, I.I.2
Gonzalez, S.3
-
31
-
-
0037194728
-
Tumorigenesis: RAF/RAS oncogenes and mismatch-repair status
-
Rajagopalan H, Bardelli A, Lengauer C, et al. Tumorigenesis: RAF/RAS oncogenes and mismatch-repair status. Nature. 2002;418:934.
-
(2002)
Nature
, vol.418
, pp. 934
-
-
Rajagopalan, H.1
Bardelli, A.2
Lengauer, C.3
-
32
-
-
17444443790
-
Comparison of molecular changes in lung cancers in HIV-positive and HIV-indeterminate subjects
-
Wistuba II, Behrens C, Milchgrub S, et al. Comparison of molecular changes in lung cancers in HIV-positive and HIV-indeterminate subjects. JAMA. 1998;279:1554-1559.
-
(1998)
JAMA
, vol.279
, pp. 1554-1559
-
-
Wistuba, I.I.1
Behrens, C.2
Milchgrub, S.3
-
33
-
-
0033927099
-
Molecular changes in the bronchial epithelium of patients with small cell lung cancer
-
Wistuba II, Berry J, Behrens C, et al. Molecular changes in the bronchial epithelium of patients with small cell lung cancer. Clin Cancer Res. 2000; 6:2604-2610.
-
(2000)
Clin Cancer Res
, vol.6
, pp. 2604-2610
-
-
Wistuba, I.I.1
Berry, J.2
Behrens, C.3
-
34
-
-
0028896973
-
Loss of heterozygosity in sporadic primary cutaneous melanoma
-
Healy E, Rehman I, Angus B, et al. Loss of heterozygosity in sporadic primary cutaneous melanoma. Genes Chromosomes Cancer. 1995;12: 152-156.
-
(1995)
Genes Chromosomes Cancer
, vol.12
, pp. 152-156
-
-
Healy, E.1
Rehman, I.2
Angus, B.3
-
35
-
-
0032580365
-
Prognostic significance of allelic losses in primary melanoma
-
Healy E, Belgaid C, Takata M, et al. Prognostic significance of allelic losses in primary melanoma. Oncogene. 1998;16:2213-2218.
-
(1998)
Oncogene
, vol.16
, pp. 2213-2218
-
-
Healy, E.1
Belgaid, C.2
Takata, M.3
-
36
-
-
0025021774
-
Identifying tumor suppressor genes in human colorectal cancer
-
Stanbridge EJ. Identifying tumor suppressor genes in human colorectal cancer. Science. 1990;247:12-13.
-
(1990)
Science
, vol.247
, pp. 12-13
-
-
Stanbridge, E.J.1
-
37
-
-
0032490119
-
Analysis of loss of heterozygosity in 399 premalignant breast lesions at 15 genetic loci
-
O'Connell P, Pekkel V, Fuqua SA, et al. Analysis of loss of heterozygosity in 399 premalignant breast lesions at 15 genetic loci. J Natl Cancer Inst. 1998;90:697-703.
-
(1998)
J Natl Cancer Inst
, vol.90
, pp. 697-703
-
-
O'Connell, P.1
Pekkel, V.2
Fuqua, S.A.3
-
38
-
-
0032957132
-
Recognition and evaluation of cytological dysplasia in acquired melanocytic nevi
-
Murphy GF, Mihm MC Jr. Recognition and evaluation of cytological dysplasia in acquired melanocytic nevi. Hum Pathol. 1999;30:506-512.
-
(1999)
Hum Pathol
, vol.30
, pp. 506-512
-
-
Murphy, G.F.1
Mihm Jr., M.C.2
-
39
-
-
27844567142
-
Distinct sets of genetic alterations in melanoma
-
Curtin JA, Fridlyand J, Kageshita T, et al. Distinct sets of genetic alterations in melanoma. N Engl J Med. 2005;353:2135-2147.
-
(2005)
N Engl J Med
, vol.353
, pp. 2135-2147
-
-
Curtin, J.A.1
Fridlyand, J.2
Kageshita, T.3
-
40
-
-
33644775655
-
Lack of association between BRAF mutation and MAPK ERK activation in melanocytic nevi
-
Uribe P, Andrade L, Gonzalez S. Lack of association between BRAF mutation and MAPK ERK activation in melanocytic nevi. J Invest Dermatol. 2006;126:161-166.
-
(2006)
J Invest Dermatol
, vol.126
, pp. 161-166
-
-
Uribe, P.1
Andrade, L.2
Gonzalez, S.3
-
41
-
-
0032900869
-
Comparison of features of human lung cancer cell lines and their corresponding tumors
-
Wistuba II, Bryant D, Behrens C, et al. Comparison of features of human lung cancer cell lines and their corresponding tumors. Clin Cancer Res. 1999;5:991-1000.
-
(1999)
Clin Cancer Res
, vol.5
, pp. 991-1000
-
-
Wistuba, I.I.1
Bryant, D.2
Behrens, C.3
-
42
-
-
0023748414
-
Genetic alterations during colorectal-tumor development
-
Vogelstein B, Fearon ER, Hamilton SR, et al. Genetic alterations during colorectal-tumor development. N Engl J Med. 1988;319:525-532.
-
(1988)
N Engl J Med
, vol.319
, pp. 525-532
-
-
Vogelstein, B.1
Fearon, E.R.2
Hamilton, S.R.3
-
43
-
-
19244370711
-
High resolution chromosome 3p allelotyping of human lung cancer and preneoplastic/preinvasive bronchial epithelium reveals multiple, discontinuous sites of 3p allele loss and three regions of frequent breakpoints
-
Wistuba II, Behrens C, Virmani AK, et al. High resolution chromosome 3p allelotyping of human lung cancer and preneoplastic/preinvasive bronchial epithelium reveals multiple, discontinuous sites of 3p allele loss and three regions of frequent breakpoints. Cancer Res. 2000;60: 1949-1960.
-
(2000)
Cancer Res
, vol.60
, pp. 1949-1960
-
-
Wistuba, I.I.1
Behrens, C.2
Virmani, A.K.3
-
44
-
-
16944366174
-
Deletions of chromosome 3p are frequent and early events in the pathogenesis of uterine cervical carcinoma
-
Wistuba II, Montellano FD, Milchgrub S, et al. Deletions of chromosome 3p are frequent and early events in the pathogenesis of uterine cervical carcinoma. Cancer Res. 1997;57:3154-3158.
-
(1997)
Cancer Res
, vol.57
, pp. 3154-3158
-
-
Wistuba, I.I.1
Montellano, F.D.2
Milchgrub, S.3
-
45
-
-
0034327412
-
The 630-kb lung cancer homozygous deletion region on human chromosome 3p21.3: Identification and evaluation of the resident candidate tumor suppressor genes. The International Lung Cancer Chromosome 3p21.3 Tumor Suppressor Gene Consortium
-
Lerman MI, Minna JD. The 630-kb lung cancer homozygous deletion region on human chromosome 3p21.3: identification and evaluation of the resident candidate tumor suppressor genes. The International Lung Cancer Chromosome 3p21.3 Tumor Suppressor Gene Consortium. Cancer Res. 2000;60:6116-6133.
-
(2000)
Cancer Res
, vol.60
, pp. 6116-6133
-
-
Lerman, M.I.1
Minna, J.D.2
-
46
-
-
0029921612
-
Deletion mapping of chromosome region 9p21-p22 surrounding the CDKN2 locus in melanoma
-
Ohta M, Berd D, Shimizu M, et al. Deletion mapping of chromosome region 9p21-p22 surrounding the CDKN2 locus in melanoma. Int J Cancer. 1996;65:762-767.
-
(1996)
Int J Cancer
, vol.65
, pp. 762-767
-
-
Ohta, M.1
Berd, D.2
Shimizu, M.3
-
47
-
-
0035119327
-
Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development
-
Pollock PM, Welch J, Hayward NK. Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development. Cancer Res. 2001;61:1154-1161.
-
(2001)
Cancer Res
, vol.61
, pp. 1154-1161
-
-
Pollock, P.M.1
Welch, J.2
Hayward, N.K.3
-
48
-
-
0033812198
-
Allelic losses in carcinoma in situ and testicular germ cell tumours of adolescents and adults: Evidence suggestive of the linear progression model
-
Faulkner SW, Leigh DA, Oosterhuis JW, et al. Allelic losses in carcinoma in situ and testicular germ cell tumours of adolescents and adults: evidence suggestive of the linear progression model. Br J Cancer. 2000;83: 729-736.
-
(2000)
Br J Cancer
, vol.83
, pp. 729-736
-
-
Faulkner, S.W.1
Leigh, D.A.2
Oosterhuis, J.W.3
-
49
-
-
21744443423
-
High-resolution detection and mapping of genomic DNA alterations in neuroblastoma
-
Mosse YP, Greshock J, Margolin A, et al. High-resolution detection and mapping of genomic DNA alterations in neuroblastoma. Genes Chromosomes Cancer. 2005;43:390-403.
-
(2005)
Genes Chromosomes Cancer
, vol.43
, pp. 390-403
-
-
Mosse, Y.P.1
Greshock, J.2
Margolin, A.3
-
50
-
-
0012905718
-
Frequent loss of heterozygosity on chromosome 5 in non-small cell lung carcinoma
-
Mendes-da-Silva P, Moreira A, Duro-da-Costa J, et al. Frequent loss of heterozygosity on chromosome 5 in non-small cell lung carcinoma. Mol Pathol. 2000;53:184-187.
-
(2000)
Mol Pathol
, vol.53
, pp. 184-187
-
-
Mendes-da-Silva, P.1
Moreira, A.2
Duro-da-Costa, J.3
-
51
-
-
0033119008
-
Plasma DNA microsatellites as tumor-specific markers and indicators of tumor progression in melanoma patients
-
Fujiwara Y, Chi DD, Wang H, et al. Plasma DNA microsatellites as tumor-specific markers and indicators of tumor progression in melanoma patients. Cancer Res. 1999;59:1567-1571.
-
(1999)
Cancer Res
, vol.59
, pp. 1567-1571
-
-
Fujiwara, Y.1
Chi, D.D.2
Wang, H.3
-
52
-
-
0026049238
-
Loss of heterozygosity for loci on the long arm of chromosome 6 in human malignant melanoma
-
Millikin D, Meese E, Vogelstein B, et al. Loss of heterozygosity for loci on the long arm of chromosome 6 in human malignant melanoma. Cancer Res. 1991;51:5449-5453.
-
(1991)
Cancer Res
, vol.51
, pp. 5449-5453
-
-
Millikin, D.1
Meese, E.2
Vogelstein, B.3
-
53
-
-
0034103092
-
A human melanoma metastasis-suppressor locus maps to 6q16.3-q23
-
Miele ME, Jewett MD, Goldberg SF, et al. A human melanoma metastasis-suppressor locus maps to 6q16.3-q23. Int J Cancer. 2000;86:524-528.
-
(2000)
Int J Cancer
, vol.86
, pp. 524-528
-
-
Miele, M.E.1
Jewett, M.D.2
Goldberg, S.F.3
-
54
-
-
0034970550
-
Putative tumor suppressor loci at 6q22 and 6q23-q24 are involved in the malignant progression of sporadic endocrine pancreatic tumors
-
Barghorn A, Speel EJ, Farspour B, et al. Putative tumor suppressor loci at 6q22 and 6q23-q24 are involved in the malignant progression of sporadic endocrine pancreatic tumors. Am J Pathol. 2001;158:1903-1911.
-
(2001)
Am J Pathol
, vol.158
, pp. 1903-1911
-
-
Barghorn, A.1
Speel, E.J.2
Farspour, B.3
-
55
-
-
32244435895
-
Epigenetic regulation of the tumor suppressor gene TCF21 on 6q23-q24 in lung and head and neck cancer
-
Smith LT, Lin M, Brena RM, et al. Epigenetic regulation of the tumor suppressor gene TCF21 on 6q23-q24 in lung and head and neck cancer. Proc Natl Acad Sci USA. 2006;103:982-987.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 982-987
-
-
Smith, L.T.1
Lin, M.2
Brena, R.M.3
-
56
-
-
85047698772
-
Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancer
-
Liu Y, Emilion G, Mungall AJ, et al. Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancer. Oncogene. 2002; 21:387-399.
-
(2002)
Oncogene
, vol.21
, pp. 387-399
-
-
Liu, Y.1
Emilion, G.2
Mungall, A.J.3
-
57
-
-
0033166650
-
A novel region of deletion on chromosome 6q23.3 spanning less than 500 Kb in high grade invasive epithelial ovarian cancer
-
Shridhar V, Staub J, Huntley B, et al. A novel region of deletion on chromosome 6q23.3 spanning less than 500 Kb in high grade invasive epithelial ovarian cancer. Oncogene. 1999;18:3913-3918.
-
(1999)
Oncogene
, vol.18
, pp. 3913-3918
-
-
Shridhar, V.1
Staub, J.2
Huntley, B.3
-
58
-
-
0344141317
-
Identification of three commonly deleted regions on chromosome arm 6q in human pancreatic cancer
-
Abe T, Makino N, Furukawa T, et al. Identification of three commonly deleted regions on chromosome arm 6q in human pancreatic cancer. Genes Chromosomes Cancer. 1999;25:60-64.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 60-64
-
-
Abe, T.1
Makino, N.2
Furukawa, T.3
-
59
-
-
0033865957
-
Roles of BRCA1 and its interacting proteins
-
Deng CX, Brodie SG. Roles of BRCA1 and its interacting proteins. Bioessays. 2000;22:728-737.
-
(2000)
Bioessays
, vol.22
, pp. 728-737
-
-
Deng, C.X.1
Brodie, S.G.2
-
60
-
-
0034688123
-
Genomic alterations (LOH, MI) on chromosome 17q21-23 and prognosis of sporadic colorectal cancer
-
Berney CR, Fisher RJ, Yang J, et al. Genomic alterations (LOH, MI) on chromosome 17q21-23 and prognosis of sporadic colorectal cancer. Int J Cancer. 2000;89:1-7.
-
(2000)
Int J Cancer
, vol.89
, pp. 1-7
-
-
Berney, C.R.1
Fisher, R.J.2
Yang, J.3
-
61
-
-
0035251772
-
A common deletion at chromosomal region 17q21 in sporadic prostate tumors distal to BRCA1
-
Dai Q, Deubler DA, Maxwell TM, et al. A common deletion at chromosomal region 17q21 in sporadic prostate tumors distal to BRCA1. Genomics. 2001;71:324-329.
-
(2001)
Genomics
, vol.71
, pp. 324-329
-
-
Dai, Q.1
Deubler, D.A.2
Maxwell, T.M.3
-
62
-
-
3042823534
-
Candidate target genes for loss of heterozygosity on human chromosome 17q21
-
De Marchis L, Cropp C, Sheng ZM, et al. Candidate target genes for loss of heterozygosity on human chromosome 17q21. Br J Cancer. 2004;90: 2384-2389.
-
(2004)
Br J Cancer
, vol.90
, pp. 2384-2389
-
-
De Marchis, L.1
Cropp, C.2
Sheng, Z.M.3
-
63
-
-
0035138814
-
Estrogens reduce and withdrawal of estrogens increase risk of microsatellite instability-positive colon cancer
-
Slattery ML, Potter JD, Curtin K, et al. Estrogens reduce and withdrawal of estrogens increase risk of microsatellite instability-positive colon cancer. Cancer Res. 2001;61:126-130.
-
(2001)
Cancer Res
, vol.61
, pp. 126-130
-
-
Slattery, M.L.1
Potter, J.D.2
Curtin, K.3
-
64
-
-
0347382321
-
Mutations of BRAF are associated with extensive hMLH1 promoter methylation in sporadic colorectal carcinomas
-
Koinuma K, Shitoh K, Miyakura Y, et al. Mutations of BRAF are associated with extensive hMLH1 promoter methylation in sporadic colorectal carcinomas. Int J Cancer. 2004;108:237-242.
-
(2004)
Int J Cancer
, vol.108
, pp. 237-242
-
-
Koinuma, K.1
Shitoh, K.2
Miyakura, Y.3
-
65
-
-
0141593677
-
BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair
-
Wang L, Cunningham JM, Winters JL, et al. BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair. Cancer Res. 2003;63:5209-5212.
-
(2003)
Cancer Res
, vol.63
, pp. 5209-5212
-
-
Wang, L.1
Cunningham, J.M.2
Winters, J.L.3
-
66
-
-
33749021085
-
Somatic activation of KIT in distinct subtypes of melanoma
-
Curtin JA, Busam K, Pinkel D, et al. Somatic activation of KIT in distinct subtypes of melanoma. J Clin Oncol. 2006;24:4340-4346.
-
(2006)
J Clin Oncol
, vol.24
, pp. 4340-4346
-
-
Curtin, J.A.1
Busam, K.2
Pinkel, D.3
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