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Author Correction: RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells.
Qutob N, Masuho I, Alon M, Emmanuel R, Cohen I, Di Pizio A, Madore J, Elkahloun A, Ziv T, Levy R, Gartner JJ, Hill VK, Lin JC, Hevroni Y, Greenberg P, Brodezki A, Rosenberg SA, Kosloff M, Hayward NK, Admon A, Niv MY, Scolyer RA, Martemyanov KA, Samuels Y. Qutob N, et al. Among authors: samuels y. Sci Rep. 2019 Mar 9;9(1):4523. doi: 10.1038/s41598-018-37932-6. Sci Rep. 2019. PMID: 30850615 Free PMC article.
Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanoma.
Palavalli LH, Prickett TD, Wunderlich JR, Wei X, Burrell AS, Porter-Gill P, Davis S, Wang C, Cronin JC, Agrawal NS, Lin JC, Westbroek W, Hoogstraten-Miller S, Molinolo AA, Fetsch P, Filie AC, O'Connell MP, Banister CE, Howard JD, Buckhaults P, Weeraratna AT, Brody LC, Rosenberg SA, Samuels Y. Palavalli LH, et al. Among authors: samuels y. Nat Genet. 2009 May;41(5):518-20. doi: 10.1038/ng.340. Epub 2009 Mar 29. Nat Genet. 2009. PMID: 19330028 Free PMC article.
Frequent mutations in the MITF pathway in melanoma.
Cronin JC, Wunderlich J, Loftus SK, Prickett TD, Wei X, Ridd K, Vemula S, Burrell AS, Agrawal NS, Lin JC, Banister CE, Buckhaults P, Rosenberg SA, Bastian BC, Pavan WJ, Samuels Y. Cronin JC, et al. Among authors: samuels y. Pigment Cell Melanoma Res. 2009 Aug;22(4):435-44. doi: 10.1111/j.1755-148X.2009.00578.x. Epub 2009 Apr 29. Pigment Cell Melanoma Res. 2009. PMID: 19422606 Free PMC article.
Novel somatic mutations in heterotrimeric G proteins in melanoma.
Cárdenas-Navia LI, Cruz P, Lin JC; NISC Comparative Sequencing Program; Rosenberg SA, Samuels Y. Cárdenas-Navia LI, et al. Among authors: samuels y. Cancer Biol Ther. 2010 Jul 1;10(1):33-7. doi: 10.4161/cbt.10.1.11949. Cancer Biol Ther. 2010. PMID: 20424519 Free PMC article.
Mutational and functional analysis reveals ADAMTS18 metalloproteinase as a novel driver in melanoma.
Wei X, Prickett TD, Viloria CG, Molinolo A, Lin JC, Cardenas-Navia I, Cruz P; NISC Comparative Sequencing Program; Rosenberg SA, Davies MA, Gershenwald JE, López-Otín C, Samuels Y. Wei X, et al. Among authors: samuels y. Mol Cancer Res. 2010 Nov;8(11):1513-25. doi: 10.1158/1541-7786.MCR-10-0262. Epub 2010 Oct 13. Mol Cancer Res. 2010. PMID: 21047771 Free PMC article.
Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
Wei X, Walia V, Lin JC, Teer JK, Prickett TD, Gartner J, Davis S; NISC Comparative Sequencing Program; Stemke-Hale K, Davies MA, Gershenwald JE, Robinson W, Robinson S, Rosenberg SA, Samuels Y. Wei X, et al. Among authors: samuels y. Nat Genet. 2011 May;43(5):442-6. doi: 10.1038/ng.810. Epub 2011 Apr 15. Nat Genet. 2011. PMID: 21499247 Free PMC article.
Mutational inactivation of STAG2 causes aneuploidy in human cancer.
Solomon DA, Kim T, Diaz-Martinez LA, Fair J, Elkahloun AG, Harris BT, Toretsky JA, Rosenberg SA, Shukla N, Ladanyi M, Samuels Y, James CD, Yu H, Kim JS, Waldman T. Solomon DA, et al. Among authors: samuels y. Science. 2011 Aug 19;333(6045):1039-43. doi: 10.1126/science.1203619. Science. 2011. PMID: 21852505 Free PMC article.
109 results