Human genes differ by their UV sensitivity estimated through analysis of UV‐induced silent mutations in melanoma
暂无分享,去创建一个
C. Begg | J. Parker | C. Amos | I. Gorlov | R. Shen | S. Tsavachidis | O. Gorlova | M. Ernstoff | I. Orlow | M. Berwick | E. Hernando | N. Thomas | Chao Cheng | L. Luo | J. Parker | R. Shen
[1] E. Larsson,et al. Intragenomic variability and extended sequence patterns in the mutational signature of ultraviolet light , 2019, Proceedings of the National Academy of Sciences.
[2] Z. Pursell,et al. POLE proofreading defects: Contributions to mutagenesis and cancer. , 2019, DNA repair.
[3] A. Gonzalez-Perez,et al. Local Determinants of the Mutational Landscape of the Human Genome , 2019, Cell.
[4] M. Stratton,et al. Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis , 2019, Cell.
[5] B. Jean-Claude,et al. Temozolomide Induced Hypermutation in Glioma: Evolutionary Mechanisms and Therapeutic Opportunities , 2019, Front. Oncol..
[6] M. Ohno. Spontaneous de novo germline mutations in humans and mice: rates, spectra, causes and consequences. , 2019, Genes & genetic systems.
[7] The UniProt Consortium,et al. UniProt: a worldwide hub of protein knowledge , 2018, Nucleic Acids Res..
[8] Ville Mustonen,et al. The repertoire of mutational signatures in human cancer , 2018, Nature.
[9] T. Iwakuma,et al. Regulators of Oncogenic Mutant TP53 Gain of Function , 2018, Cancers.
[10] Young Kee Shin,et al. Loss of Tumor Suppressor Gene Function in Human Cancer: An Overview , 2018, Cellular Physiology and Biochemistry.
[11] J. Cadet,et al. Formation of UV-induced DNA damage contributing to skin cancer development , 2018, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.
[12] Marek Kimmel,et al. Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples , 2018, BMC Bioinformatics.
[13] B. Schuster-Böckler,et al. Mutational signature distribution varies with DNA replication timing and strand asymmetry , 2018, Genome Biology.
[14] D. Phillips. Mutational spectra and mutational signatures: Insights into cancer aetiology and mechanisms of DNA damage and repair , 2018, DNA repair.
[15] C. Yeang,et al. Explaining cancer type specific mutations with transcriptomic and epigenomic features in normal tissues , 2018, Scientific Reports.
[16] P. Lønning,et al. Patterns of genomic evolution in advanced melanoma , 2018, Nature Communications.
[17] Marcos Díaz-Gay,et al. Mutational Signatures in Cancer (MuSiCa): a web application to implement mutational signatures analysis in cancer samples , 2018, BMC Bioinformatics.
[18] Carol J. Bult,et al. The Mouseion at the JAXlibrary , 2022 .
[19] Chuang Tan,et al. Universal Patterns of Selection in Cancer and Somatic Tissues , 2018, Cell.
[20] Seon-Young Kim,et al. Variability in Chromatin Architecture and Associated DNA Repair at Genomic Positions Containing Somatic Mutations. , 2017, Cancer research.
[21] P. Hainaut,et al. Somatic TP53 Mutations in the Era of Genome Sequencing. , 2016, Cold Spring Harbor perspectives in medicine.
[22] Akash Kumar,et al. Mutational Heterogeneity in Cancer , 2016 .
[23] Zigang Dong,et al. Implications of Genetic and Epigenetic Alterations of CDKN2A (p16INK4a) in Cancer , 2016, EBioMedicine.
[24] E. Birney,et al. The topography of mutational processes in breast cancer genomes , 2016, Nature Communications.
[25] P. Pauwels,et al. TP53 and MDM2 genetic alterations in non-small cell lung cancer: Evaluating their prognostic and predictive value. , 2016, Critical reviews in oncology/hematology.
[26] Martin H. Schaefer,et al. Cell type-specific properties and environment shape tissue specificity of cancer genes , 2016, Scientific Reports.
[27] P. Hsieh,et al. DNA mismatch repair and the DNA damage response. , 2016, DNA repair.
[28] C. Thompson,et al. The Emerging Hallmarks of Cancer Metabolism. , 2016, Cell metabolism.
[29] J. L. Bose. Chemical and UV Mutagenesis. , 2016, Methods in molecular biology.
[30] Matthew J. Davis,et al. Exome sequencing identifies recurrent somatic RAC 1 mutations in melanoma , 2016 .
[31] P. Campbell,et al. Somatic mutation in cancer and normal cells , 2015, Science.
[32] S. Ariyan,et al. Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas , 2015, Nature Genetics.
[33] Nam Huh,et al. Phylogenetic analyses of melanoma reveal complex patterns of metastatic dissemination , 2015, Proceedings of the National Academy of Sciences.
[34] Nam Huh,et al. Exome sequencing of desmoplastic melanoma identifies recurrent NFKBIE promoter mutations and diverse activating mutations in the MAPK pathway , 2015, Nature Genetics.
[35] Z. Bebők,et al. Decoding mechanisms by which silent codon changes influence protein biogenesis and function. , 2015, The international journal of biochemistry & cell biology.
[36] M. Stratton,et al. High burden and pervasive positive selection of somatic mutations in normal human skin , 2015, Science.
[37] J. Robert. MAP Kinase Pathway , 2015 .
[38] R. Melamed,et al. FBXW7 mutations in melanoma and a new therapeutic paradigm. , 2014, Journal of the National Cancer Institute.
[39] Dennis C. Friedrich,et al. MAP kinase pathway alterations in BRAF-mutant melanoma patients with acquired resistance to combined RAF/MEK inhibition. , 2014, Cancer discovery.
[40] P. Meltzer,et al. The exomes of the NCI-60 panel: a genomic resource for cancer biology and systems pharmacology. , 2013, Cancer research.
[41] Steven A. Roberts,et al. Mutational heterogeneity in cancer and the search for new cancer genes , 2014 .
[42] M. Stratton,et al. Deciphering Signatures of Mutational Processes Operative in Human Cancer , 2013, Cell reports.
[43] Junfeng Xia,et al. BRAF(L597) mutations in melanoma are associated with sensitivity to MEK inhibitors. , 2012, Cancer discovery.
[44] M. Marinus,et al. DNA Mismatch Repair , 2012, EcoSal Plus.
[45] A. Sivachenko,et al. A Landscape of Driver Mutations in Melanoma , 2012, Cell.
[46] Matthew J. Davis,et al. Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma , 2012, Nature Genetics.
[47] A. Ashworth,et al. Genomic characterisation of acral melanoma cell lines , 2012, Pigment cell & melanoma research.
[48] T. Fennell,et al. Melanoma genome sequencing reveals frequent PREX2 mutations , 2012, Nature.
[49] C. V. Jongeneel,et al. Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma , 2011, Nature Genetics.
[50] L. Samson,et al. Balancing repair and tolerance of DNA damage caused by alkylating agents , 2012, Nature Reviews Cancer.
[51] C. Cole,et al. COSMIC: the catalogue of somatic mutations in cancer , 2011, Genome Biology.
[52] S. Davis,et al. Exome sequencing identifies GRIN2A as frequently mutated in melanoma , 2011, Nature Genetics.
[53] G. Kristiansen,et al. Tumorigenesis and Neoplastic Progression The Androgen-Regulated Calcium-Activated Nucleotidase 1 ( CANT 1 ) Is Commonly Overexpressed in Prostate Cancer and Is Tumor-Biologically Relevant in Vitro , 2011 .
[54] D. Hanahan,et al. Hallmarks of Cancer: The Next Generation , 2011, Cell.
[55] T. Ono,et al. The mechanisms of UV mutagenesis. , 2011, Journal of radiation research.
[56] Tom Royce,et al. A comprehensive catalogue of somatic mutations from a human cancer genome , 2010, Nature.
[57] Mingming Jia,et al. COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer , 2009, Nucleic Acids Res..
[58] R. Millikan,et al. CDKN2A germline mutations in individuals with cutaneous malignant melanoma. , 2007, The Journal of investigative dermatology.
[59] R. Millikan,et al. The Prevalence of CDKN2A Germ-Line Mutations and Relative Risk for Cutaneous Malignant Melanoma: An International Population-Based Study , 2006, Cancer Epidemiology Biomarkers & Prevention.
[60] R. Millikan,et al. The Prevalence of CDKN 2 A GermLine Mutations and Relative Risk for Cutaneous Malignant Melanoma : An International Population-Based Study , 2006 .
[61] R. Millikan,et al. Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample. , 2005, Journal of the National Cancer Institute.
[62] M. Raponi,et al. Synonymous mutations in CFTR exon 12 affect splicing and are not neutral in evolution. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[63] Luciano Milanesi,et al. From Context-Dependence of Mutations to Molecular Mechanisms of Mutagenesis , 2004, Pacific Symposium on Biocomputing.
[64] P. Vineis. Cancer as an evolutionary process at the cell level: an epidemiological perspective. , 2003, Carcinogenesis.
[65] William D. Foulkes,et al. The CDKN2A (p16) Gene and Human Cancer , 1997, Molecular medicine.
[66] R. L. Dusenbery,et al. Drosophila mutations at the mei-9 and mus(2)201 loci which block excision of thymine dimers also block induction of unscheduled DNA synthesis by methyl methanesulfonate, ethyl methanesulfonate, N-methyl-N-nitrosourea, UV light and X-rays. , 1983, Mutation research.
[67] D. Kuckein. [Computed tomography in cases of pancreas neoplasms (author's transl)]. , 1980, Rontgen-Blatter; Zeitschrift fur Rontgen-Technik und medizinisch-wissenschaftliche Photographie.
[68] R. Kaplan. Electiveness of photorepair, influence of dark-repair on shape of dose-response curves, and high-dose decline, in UV-induced colour mutations of Serratia. , 1978, Mutation research.