-
1
-
-
0019163016
-
Malignant melanoma: a unifying concept
-
Ackerman, A.B. (1980). Malignant melanoma: a unifying concept. Hum. Pathol. 11, 591-595.
-
(1980)
Hum. Pathol.
, vol.11
, pp. 591-595
-
-
Ackerman, A.B.1
-
2
-
-
84862314014
-
Genetic alterations of PTEN in human melanoma
-
Aguissa-Toure, A.H., and Li, G. (2012). Genetic alterations of PTEN in human melanoma. Cell. Mol. Life Sci. 69, 1475-1491.
-
(2012)
Cell. Mol. Life Sci.
, vol.69
, pp. 1475-1491
-
-
Aguissa-Toure, A.H.1
Li, G.2
-
3
-
-
77951765345
-
Subtle variations in Pten dose determine cancer susceptibility
-
Alimonti, A., Carracedo, A., Clohessy, J.G. et al. (2010). Subtle variations in Pten dose determine cancer susceptibility. Nat. Genet. 42, 454-458.
-
(2010)
Nat. Genet.
, vol.42
, pp. 454-458
-
-
Alimonti, A.1
Carracedo, A.2
Clohessy, J.G.3
-
4
-
-
33846004477
-
PTEN enters the nuclear age
-
Baker, S.J. (2007). PTEN enters the nuclear age. Cell 128, 25-28.
-
(2007)
Cell
, vol.128
, pp. 25-28
-
-
Baker, S.J.1
-
5
-
-
78650027929
-
Haplo-insufficiency: a driving force in cancer
-
Berger, A.H., and Pandolfi, P.P. (2011). Haplo-insufficiency: a driving force in cancer. J. Pathol. 223, 137-146.
-
(2011)
J. Pathol.
, vol.223
, pp. 137-146
-
-
Berger, A.H.1
Pandolfi, P.P.2
-
6
-
-
84861427327
-
Melanoma genome sequencing reveals frequent PREX2 mutations
-
Berger, M.F., Hodis, E., Heffernan, T.P. et al. (2012). Melanoma genome sequencing reveals frequent PREX2 mutations. Nature 485, 502-506.
-
(2012)
Nature
, vol.485
, pp. 502-506
-
-
Berger, M.F.1
Hodis, E.2
Heffernan, T.P.3
-
7
-
-
0033852872
-
Mutations of the human PTEN gene
-
Bonneau, D., and Longy, M. (2000). Mutations of the human PTEN gene. Hum. Mutat. 16, 109-122.
-
(2000)
Hum. Mutat.
, vol.16
, pp. 109-122
-
-
Bonneau, D.1
Longy, M.2
-
8
-
-
79951785364
-
Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair
-
Bradford, P.T., Goldstein, A.M., Tamura, D. et al. (2011). Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair. J. Med. Genet. 48, 168-176.
-
(2011)
J. Med. Genet.
, vol.48
, pp. 168-176
-
-
Bradford, P.T.1
Goldstein, A.M.2
Tamura, D.3
-
9
-
-
79958066836
-
KIT as a therapeutic target in metastatic melanoma
-
Carvajal, R.D., Antonescu, C.R., Wolchok, J.D. et al. (2011). KIT as a therapeutic target in metastatic melanoma. JAMA 305, 2327-2334.
-
(2011)
JAMA
, vol.305
, pp. 2327-2334
-
-
Carvajal, R.D.1
Antonescu, C.R.2
Wolchok, J.D.3
-
10
-
-
0021743724
-
A study of tumor progression: the precursor lesions of superficial spreading and nodular melanoma
-
Clark, W.H. Jr, Elder, D.E., Guerry, D., Epstein, M.N., Greene, M.H., and Van, H.M. (1984). A study of tumor progression: the precursor lesions of superficial spreading and nodular melanoma. Hum. Pathol. 15, 1147-1165.
-
(1984)
Hum. Pathol.
, vol.15
, pp. 1147-1165
-
-
Clark Jr, W.H.1
Elder, D.E.2
Guerry, D.3
Epstein, M.N.4
Greene, M.H.5
Van, H.M.6
-
11
-
-
27844567142
-
Distinct sets of genetic alterations in melanoma. N.Engl
-
Curtin, J.A., Fridlyand, J., Kageshita, T. et al. (2005). Distinct sets of genetic alterations in melanoma. N.Engl. J. Med. 353, 2135-2147.
-
(2005)
J. Med.
, vol.353
, pp. 2135-2147
-
-
Curtin, J.A.1
Fridlyand, J.2
Kageshita, T.3
-
12
-
-
33749021085
-
Somatic activation of KIT in distinct subtypes of melanoma
-
Curtin, J.A., Busam, K., Pinkel, D., and Bastian, B.C. (2006). Somatic activation of KIT in distinct subtypes of melanoma. J. Clin. Oncol. 24, 4340-4346.
-
(2006)
J. Clin. Oncol.
, vol.24
, pp. 4340-4346
-
-
Curtin, J.A.1
Busam, K.2
Pinkel, D.3
Bastian, B.C.4
-
13
-
-
65649147543
-
Braf (V600E) cooperates with Pten loss to induce metastatic melanoma
-
Dankort, D., Curley, D.P., Cartlidge, R.A., Nelson, B., Karnezis, A.N., Damsky, W.E. Jr, You, M.J., DePinho, R.A., McMahon, M., and Bosenberg, M. (2009). Braf (V600E) cooperates with Pten loss to induce metastatic melanoma. Nat. Genet. 41, 544-552.
-
(2009)
Nat. Genet.
, vol.41
, pp. 544-552
-
-
Dankort, D.1
Curley, D.P.2
Cartlidge, R.A.3
Nelson, B.4
Karnezis, A.N.5
Damsky Jr, W.E.6
You, M.J.7
DePinho, R.A.8
McMahon, M.9
Bosenberg, M.10
-
14
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies, H., Bignell, G.R., Cox, C. et al. (2002). Mutations of the BRAF gene in human cancer. Nature 417, 949-954.
-
(2002)
Nature
, vol.417
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
-
15
-
-
14644430466
-
The role of UV induced lesions in skin carcinogenesis: an overview of oncogene and tumor suppressor gene modifications in xeroderma pigmentosum skin tumors
-
Daya-Grosjean, L., and Sarasin, A. (2005). The role of UV induced lesions in skin carcinogenesis: an overview of oncogene and tumor suppressor gene modifications in xeroderma pigmentosum skin tumors. Mutat. Res. 571, 43-56.
-
(2005)
Mutat. Res.
, vol.571
, pp. 43-56
-
-
Daya-Grosjean, L.1
Sarasin, A.2
-
16
-
-
0034688339
-
UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients
-
D'Errico, M., Calcagnile, A., Canzona, F. et al. (2000). UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients. Oncogene 19, 463-467.
-
(2000)
Oncogene
, vol.19
, pp. 463-467
-
-
D'Errico, M.1
Calcagnile, A.2
Canzona, F.3
-
17
-
-
84857041145
-
Shining a light on xeroderma pigmentosum
-
DiGiovanna, J.J., and Kraemer, K.H. (2012). Shining a light on xeroderma pigmentosum. J. Invest. Dermatol. 132, 785-796.
-
(2012)
J. Invest. Dermatol.
, vol.132
, pp. 785-796
-
-
DiGiovanna, J.J.1
Kraemer, K.H.2
-
18
-
-
33845287261
-
Participation of mouse DNA polymerase iota in strand-biased mutagenic bypass of UV photoproducts and suppression of skin cancer
-
Dumstorf, C.A., Clark, A.B., Lin, Q., Kissling, G.E., Yuan, T., Kucherlapati, R., McGregor, W.G., and Kunkel, T.A. (2006). Participation of mouse DNA polymerase iota in strand-biased mutagenic bypass of UV photoproducts and suppression of skin cancer. Proc. Natl Acad. Sci. USA 103, 18083-18088.
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, pp. 18083-18088
-
-
Dumstorf, C.A.1
Clark, A.B.2
Lin, Q.3
Kissling, G.E.4
Yuan, T.5
Kucherlapati, R.6
McGregor, W.G.7
Kunkel, T.A.8
-
19
-
-
84882330643
-
Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma
-
Gartner, J.J., Parker, S.C., Prickett, T.D. et al. (2013). Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma. Proc. Natl Acad. Sci. USA 110, 13481-13486.
-
(2013)
Proc. Natl Acad. Sci. USA
, vol.110
, pp. 13481-13486
-
-
Gartner, J.J.1
Parker, S.C.2
Prickett, T.D.3
-
20
-
-
79958043675
-
-
eds). (Bethesda, MD: National Cancer Institute), (based on November 2012 SEER data submission, posted to the SEER web site, April 2013).
-
Howlader, N., Noone, AM., Krapcho, M., Garshell, J., Neyman, N., Altekruse, SF., Kosary, CL., Yu, M., Ruhl, J., Tatalovich, Z., Cho, H., Mariotto, A., Lewis, DR., Chen, HS., Feuer, EJ., Cronin, KA. (eds). (2013). SEER Cancer Statistics Review, 1975-2010. (Bethesda, MD: National Cancer Institute), http://seer.cancer.gov/csr/1975_2010/ (based on November 2012 SEER data submission, posted to the SEER web site, April 2013).
-
(2013)
SEER Cancer Statistics Review, 1975-2010
-
-
Howlader, N.1
Noone, A.M.2
Krapcho, M.3
Garshell, J.4
Neyman, N.5
Altekruse, S.F.6
Kosary, C.L.7
Yu, M.8
Ruhl, J.9
Tatalovich, Z.10
Cho, H.11
Mariotto, A.12
Lewis, D.R.13
Chen, H.S.14
Feuer, E.J.15
Cronin, K.A.16
-
21
-
-
0032102944
-
The (6-4) photoproduct of thymine-thymine induces targeted substitution mutations in mammalian cells
-
Kamiya, H., Iwai, S., and Kasai, H. (1998). The (6-4) photoproduct of thymine-thymine induces targeted substitution mutations in mammalian cells. Nucleic Acids Res. 26, 2611-2617.
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 2611-2617
-
-
Kamiya, H.1
Iwai, S.2
Kasai, H.3
-
22
-
-
40649126759
-
mTOR is activated in the majority of malignant melanomas
-
Karbowniczek, M., Spittle, C.S., Morrison, T., Wu, H., and Henske, E.P. (2008). mTOR is activated in the majority of malignant melanomas. J. Invest. Dermatol. 128, 980-987.
-
(2008)
J. Invest. Dermatol.
, vol.128
, pp. 980-987
-
-
Karbowniczek, M.1
Spittle, C.S.2
Morrison, T.3
Wu, H.4
Henske, E.P.5
-
23
-
-
0028110878
-
The role of sunlight and DNA repair in melanoma and nonmelanoma skin cancer. The xeroderma pigmentosum paradigm
-
Kraemer, K.H., Lee, M.M., Andrews, A.D., and Lambert, W.C. (1994). The role of sunlight and DNA repair in melanoma and nonmelanoma skin cancer. The xeroderma pigmentosum paradigm. Arch. Dermatol. 130, 1018-1021.
-
(1994)
Arch. Dermatol.
, vol.130
, pp. 1018-1021
-
-
Kraemer, K.H.1
Lee, M.M.2
Andrews, A.D.3
Lambert, W.C.4
-
24
-
-
0025950131
-
The thymine-thymine pyrimidine-pyrimidone (6-4) ultraviolet light photoproduct is highly mutagenic and specifically induces 3' thymine-to-cytosine transitions in Escherichia coli
-
LeClerc, J.E., Borden, A., and Lawrence, C.W. (1991). The thymine-thymine pyrimidine-pyrimidone (6-4) ultraviolet light photoproduct is highly mutagenic and specifically induces 3' thymine-to-cytosine transitions in Escherichia coli. Proc. Natl Acad. Sci. USA 88, 9685-9689.
-
(1991)
Proc. Natl Acad. Sci. USA
, vol.88
, pp. 9685-9689
-
-
LeClerc, J.E.1
Borden, A.2
Lawrence, C.W.3
-
25
-
-
42149191944
-
Mesenchymal-epithelial interactions involving epiregulin in tuberous sclerosis complex hamartomas
-
Li, S., Takeuchi, F., Wang, J.A., Fan, Q., Komurasaki, T., Billings, E.M., Pacheco-Rodriguez, G., Moss, J., and Darling, T.N. (2008). Mesenchymal-epithelial interactions involving epiregulin in tuberous sclerosis complex hamartomas. Proc. Natl Acad. Sci. USA 105, 3539-3544.
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 3539-3544
-
-
Li, S.1
Takeuchi, F.2
Wang, J.A.3
Fan, Q.4
Komurasaki, T.5
Billings, E.M.6
Pacheco-Rodriguez, G.7
Moss, J.8
Darling, T.N.9
-
26
-
-
33947230256
-
Distinct clinical and pathological features are associated with the BRAF (T1799A (V600E)) mutation in primary melanoma
-
Liu, W., Kelly, J.W., Trivett, M. et al. (2007). Distinct clinical and pathological features are associated with the BRAF (T1799A (V600E)) mutation in primary melanoma. J. Invest Dermatol. 127, 900-905.
-
(2007)
J. Invest Dermatol.
, vol.127
, pp. 900-905
-
-
Liu, W.1
Kelly, J.W.2
Trivett, M.3
-
27
-
-
84890062777
-
Differential AKT dependency displayed by mouse models of BRAFV600E-initiated melanoma
-
Marsh, D.V., Deuker, M.M., Bosenberg, M.W., Phillips, W., and McMahon, M. (2013). Differential AKT dependency displayed by mouse models of BRAFV600E-initiated melanoma. J. Clin. Invest. 123, 5104-5118.
-
(2013)
J. Clin. Invest.
, vol.123
, pp. 5104-5118
-
-
Marsh, D.V.1
Deuker, M.M.2
Bosenberg, M.W.3
Phillips, W.4
McMahon, M.5
-
28
-
-
33745684404
-
Melanoma. N.Engl
-
Miller, A.J., and Mihm, M.C. Jr (2006). Melanoma. N.Engl. J. Med. 355, 51-65.
-
(2006)
J. Med.
, vol.355
, pp. 51-65
-
-
Miller, A.J.1
Mihm Jr, M.C.2
-
29
-
-
84857053657
-
Melanoma: new insights and new therapies
-
Nikolaou, V.A., Stratigos, A.J., Flaherty, K.T., and Tsao, H. (2012). Melanoma: new insights and new therapies. J. Invest Dermatol. 132, 854-863.
-
(2012)
J. Invest Dermatol.
, vol.132
, pp. 854-863
-
-
Nikolaou, V.A.1
Stratigos, A.J.2
Flaherty, K.T.3
Tsao, H.4
-
30
-
-
78651444805
-
mTOR pathway activation in cutaneous melanoma is associated with poorer prognosis characteristics
-
Populo, H., Soares, P., Faustino, A., Rocha, A.S., Silva, P., Azevedo, F., and Lopes, J.M. (2011). mTOR pathway activation in cutaneous melanoma is associated with poorer prognosis characteristics. Pigment Cell Melanoma Res. 24, 254-257.
-
(2011)
Pigment Cell Melanoma Res.
, vol.24
, pp. 254-257
-
-
Populo, H.1
Soares, P.2
Faustino, A.3
Rocha, A.S.4
Silva, P.5
Azevedo, F.6
Lopes, J.M.7
-
31
-
-
84862516323
-
Insights into melanoma: targeting the mTOR pathway for therapeutics
-
Populo, H., Soares, P., and Lopes, J.M. (2012). Insights into melanoma: targeting the mTOR pathway for therapeutics. Expert Opin. Ther. Targets 16, 689-705.
-
(2012)
Expert Opin. Ther. Targets
, vol.16
, pp. 689-705
-
-
Populo, H.1
Soares, P.2
Lopes, J.M.3
-
32
-
-
33746263912
-
BRAF and NRAS mutations in melanoma and melanocytic nevi
-
Poynter, J.N., Elder, J.T., Fullen, D.R., Nair, R.P., Soengas, M.S., Johnson, T.M., Redman, B., Thomas, N.E., and Gruber, S.B. (2006). BRAF and NRAS mutations in melanoma and melanocytic nevi. Melanoma Res. 16, 267-273.
-
(2006)
Melanoma Res.
, vol.16
, pp. 267-273
-
-
Poynter, J.N.1
Elder, J.T.2
Fullen, D.R.3
Nair, R.P.4
Soengas, M.S.5
Johnson, T.M.6
Redman, B.7
Thomas, N.E.8
Gruber, S.B.9
-
33
-
-
0036713510
-
Human non-synonymous SNPs: server and survey
-
Ramensky, V., Bork, P., and Sunyaev, S. (2002). Human non-synonymous SNPs: server and survey. Nucleic Acids Res. 30, 3894-3900.
-
(2002)
Nucleic Acids Res.
, vol.30
, pp. 3894-3900
-
-
Ramensky, V.1
Bork, P.2
Sunyaev, S.3
-
34
-
-
80053984176
-
A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes
-
Rodriguez-Escudero, I., Oliver, M.D., Andres-Pons, A., Molina, M., Cid, V.J., and Pulido, R. (2011). A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes. Hum. Mol. Genet. 20, 4132-4142.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 4132-4142
-
-
Rodriguez-Escudero, I.1
Oliver, M.D.2
Andres-Pons, A.3
Molina, M.4
Cid, V.J.5
Pulido, R.6
-
35
-
-
84898927037
-
-
Sanger Institute Catalogue of Somatic Mutations in Cancer.
-
Sanger Institute (2012). Catalogue of Somatic Mutations in Cancer. http://cancer.sanger.ac.uk/cancergenome/projects/cosmic/
-
(2012)
-
-
-
36
-
-
0027450194
-
Malignant melanoma in xeroderma pigmentosum: search for a precursor lesion
-
Stern, J.B., Peck, G.L., Haupt, H.M., Hollingsworth, H.C., and Beckerman, T. (1993). Malignant melanoma in xeroderma pigmentosum: search for a precursor lesion. J. Am. Acad. Dermatol. 28, 591-594.
-
(1993)
J. Am. Acad. Dermatol.
, vol.28
, pp. 591-594
-
-
Stern, J.B.1
Peck, G.L.2
Haupt, H.M.3
Hollingsworth, H.C.4
Beckerman, T.5
-
37
-
-
0034085811
-
Relative reciprocity of NRAS and PTEN/MMAC1 alterations in cutaneous melanoma cell lines
-
Tsao, H., Zhang, X., Fowlkes, K., and Haluska, F.G. (2000). Relative reciprocity of NRAS and PTEN/MMAC1 alterations in cutaneous melanoma cell lines. Cancer Res. 60, 1800-1804.
-
(2000)
Cancer Res.
, vol.60
, pp. 1800-1804
-
-
Tsao, H.1
Zhang, X.2
Fowlkes, K.3
Haluska, F.G.4
-
38
-
-
0142244844
-
PTEN expression in normal skin, acquired melanocytic nevi, and cutaneous melanoma
-
Tsao, H., Mihm, M.C. Jr, and Sheehan, C. (2003). PTEN expression in normal skin, acquired melanocytic nevi, and cutaneous melanoma. J. Am. Acad. Dermatol. 49, 865-872.
-
(2003)
J. Am. Acad. Dermatol.
, vol.49
, pp. 865-872
-
-
Tsao, H.1
Mihm Jr, M.C.2
Sheehan, C.3
-
39
-
-
1442274619
-
Genetic interaction between NRAS and BRAF mutations and PTEN/MMAC1 inactivation in melanoma
-
Tsao, H., Goel, V., Wu, H., Yang, G., and Haluska, F.G. (2004). Genetic interaction between NRAS and BRAF mutations and PTEN/MMAC1 inactivation in melanoma. J. Invest Dermatol. 122, 337-341.
-
(2004)
J. Invest Dermatol.
, vol.122
, pp. 337-341
-
-
Tsao, H.1
Goel, V.2
Wu, H.3
Yang, G.4
Haluska, F.G.5
-
40
-
-
84857043139
-
Evaluation of three DNA extraction protocols for forensic STR typing after laser capture microdissection
-
Vandewoestyne, M., Van, N.F., Van, H.D., and Deforce, D. (2012). Evaluation of three DNA extraction protocols for forensic STR typing after laser capture microdissection. Forensic Sci. Int. Genet. 6, 258-262.
-
(2012)
Forensic Sci. Int. Genet.
, vol.6
, pp. 258-262
-
-
Vandewoestyne, M.1
Van, N.F.2
Van, H.D.3
Deforce, D.4
-
41
-
-
34248195087
-
Evidence that in xeroderma pigmentosum variant cells, which lack DNA polymerase eta, DNA polymerase iota causes the very high frequency and unique spectrum of UV-induced mutations
-
Wang, Y., Woodgate, R., McManus, T.P., Mead, S., McCormick, J.J., and Maher, V.M. (2007). Evidence that in xeroderma pigmentosum variant cells, which lack DNA polymerase eta, DNA polymerase iota causes the very high frequency and unique spectrum of UV-induced mutations. Cancer Res. 67, 3018-3026.
-
(2007)
Cancer Res.
, vol.67
, pp. 3018-3026
-
-
Wang, Y.1
Woodgate, R.2
McManus, T.P.3
Mead, S.4
McCormick, J.J.5
Maher, V.M.6
-
42
-
-
65549163889
-
Evidence of ultraviolet type mutations in xeroderma pigmentosum melanomas
-
Wang, Y., DiGiovanna, J.J., Stern, J.B., Hornyak, T.J., Raffeld, M., Khan, S.G., Oh, K.S., Hollander, M.C., Dennis, P.A., and Kraemer, K.H. (2009). Evidence of ultraviolet type mutations in xeroderma pigmentosum melanomas. Proc. Natl Acad. Sci. USA 106, 6279-6284.
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 6279-6284
-
-
Wang, Y.1
DiGiovanna, J.J.2
Stern, J.B.3
Hornyak, T.J.4
Raffeld, M.5
Khan, S.G.6
Oh, K.S.7
Hollander, M.C.8
Dennis, P.A.9
Kraemer, K.H.10
-
43
-
-
0037453898
-
Repair of UV light-induced DNA damage and risk of cutaneous malignant melanoma
-
Wei, Q., Lee, J.E., Gershenwald, J.E. et al. (2003). Repair of UV light-induced DNA damage and risk of cutaneous malignant melanoma. J. Natl Cancer Inst. 95, 308-315.
-
(2003)
J. Natl Cancer Inst.
, vol.95
, pp. 308-315
-
-
Wei, Q.1
Lee, J.E.2
Gershenwald, J.E.3
-
44
-
-
85027946522
-
Exome sequencing identifies GRIN2A as frequently mutated in melanoma
-
Wei, X., Walia, V., Lin, J.C. et al. (2011). Exome sequencing identifies GRIN2A as frequently mutated in melanoma. Nat. Genet. 43, 442-446.
-
(2011)
Nat. Genet.
, vol.43
, pp. 442-446
-
-
Wei, X.1
Walia, V.2
Lin, J.C.3
-
45
-
-
80053928911
-
The melanomas: a synthesis of epidemiological, clinical, histopathological, genetic, and biological aspects, supporting distinct subtypes, causal pathways, and cells of origin
-
Whiteman, D.C., Pavan, W.J., and Bastian, B.C. (2011). The melanomas: a synthesis of epidemiological, clinical, histopathological, genetic, and biological aspects, supporting distinct subtypes, causal pathways, and cells of origin. Pigment Cell Melanoma Res. 24, 879-897.
-
(2011)
Pigment Cell Melanoma Res.
, vol.24
, pp. 879-897
-
-
Whiteman, D.C.1
Pavan, W.J.2
Bastian, B.C.3
-
46
-
-
0032755991
-
A high frequency of sequence alterations is due to formalin fixation of archival specimens
-
Williams, C., Ponten, F., Moberg, C., Soderkvist, P., Uhlen, M., Ponten, J., Sitbon, G., and Lundeberg, J. (1999). A high frequency of sequence alterations is due to formalin fixation of archival specimens. Am. J. Pathol. 155, 1467-1471.
-
(1999)
Am. J. Pathol.
, vol.155
, pp. 1467-1471
-
-
Williams, C.1
Ponten, F.2
Moberg, C.3
Soderkvist, P.4
Uhlen, M.5
Ponten, J.6
Sitbon, G.7
Lundeberg, J.8
-
47
-
-
84887163012
-
KIT, NRAS, BRAF and PTEN mutations in a sample of Swedish patients with acral lentiginous melanoma
-
Zebary, A., Omholt, K., Vassilaki, I., Hoiom, V., Linden, D., Viberg, L., Kanter-Lewensohn, L., Johansson, C.H., and Hansson, J. (2013). KIT, NRAS, BRAF and PTEN mutations in a sample of Swedish patients with acral lentiginous melanoma. J. Dermatol. Sci. 72, 284-289.
-
(2013)
J. Dermatol. Sci.
, vol.72
, pp. 284-289
-
-
Zebary, A.1
Omholt, K.2
Vassilaki, I.3
Hoiom, V.4
Linden, D.5
Viberg, L.6
Kanter-Lewensohn, L.7
Johansson, C.H.8
Hansson, J.9
-
48
-
-
0027166864
-
Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers
-
Ziegler, A., Leffell, D.J., Kunala, S. et al. (1993). Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers. Proc. Natl Acad. Sci. USA 90, 4216-4220.
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 4216-4220
-
-
Ziegler, A.1
Leffell, D.J.2
Kunala, S.3
|