Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer - Wikidata - wikimedia - TriplyDB

Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

http://www.wikidata.org/entity/Q36553872

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Surgical and molecular pathology of pancreatic neoplasms Clinical Genetic Testing in Gastroenterology Is it time to split strategies to treat homologous recombinant deficiency in pancreas cancer?Lost in translation: returning germline genetic results in genome-scale cancer research Hereditary pancreatic cancer: related syndromes and clinical perspective.Germline mutations in Japanese familial pancreatic cancer patients.The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.MiR-377 inhibits the proliferation of pancreatic cancer by targeting Pim-3.Pancreatic cancer biology and genetics from an evolutionary perspective.Leveraging Mechanisms Governing Pancreatic Tumorigenesis To Reduce Pancreatic Cancer Mortality.Alterations of type II classical cadherin, cadherin-10 (CDH10), is associated with pancreatic ductal adenocarcinomas.Microenvironment in determining chemo-resistance in pancreatic cancer: Neighborhood matters.Early detection of pancreatic cancer: Where are we now and where are we going?Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.Prevalence of germline mutations in the spindle assembly checkpoint gene BUB1B in individuals with early-onset colorectal cancer.Lack of association between the pancreatitis risk allele CEL-HYB and pancreatic cancer.Phenotypic Heterogeneity of Circulating Tumor Cells Informs Clinical Decisions between AR Signaling Inhibitors and Taxanes in Metastatic Prostate Cancer.Associations between ABO blood groups and pancreatic ductal adenocarcinoma: influence on resection status and survival.ATM-deficiency increases genomic instability and metastatic potential in a mouse model of pancreatic cancer YTH domain family 2 orchestrates epithelial-mesenchymal transition/proliferation dichotomy in pancreatic cancer cells.Loss of DNA Damage Response in Neuroblastoma and Utility of a PARP Inhibitor.Exome-Wide Association Study of Pancreatic Cancer Risk.Integrated Genomic Characterization of Pancreatic Ductal Adenocarcinoma.Susceptibility of ATM-deficient pancreatic cancer cells to radiation.Prevalence of germ-line mutations in cancer genes among pancreatic cancer patients with a positive family history.The importance of a well-structured pancreatic screening program for familial and hereditary pancreatic cancer.Double germline mutations in APC and BRCA2 in an individual with a pancreatic tumor.Mutations in the pancreatic secretory enzymes CPA1 and CPB1 are associated with pancreatic cancer.Integrated analysis of tumor differentiation genes in pancreatic adenocarcinoma.Circulating Biomarkers to Identify Patients With Resectable Pancreatic Cancer.[Hereditary gastric and pancreatic cancer].Pancreatic Cancer: Molecular Characterization, Clonal Evolution and Cancer Stem Cells.Ethical concerns on sharing genomic data including patients' family members.Precision medicine meets the DNA damage response in pancreatic cancer.Glycoprotein biomarkers for the detection of pancreatic ductal adenocarcinoma.The Significance of Liquid Biopsy in Pancreatic Cancer Germline Variants and Risk for Pancreatic Cancer: A Systematic Review and Emerging Concepts Familial pancreatic cancer

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Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

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2015年の論文

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2015年论文

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Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

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Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

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Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

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Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

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Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

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Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

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Cancer Discovery

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Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

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Alexis L Norris

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Alison P Klein

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Alvin Makohon-Moore

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Alyssa L Smith

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Andrew D Rhim

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Anil K Rustgi

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Ann G Schwartz

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Christopher Douville

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Christopher L Wolfgang

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Elena Stoffel

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An integrated map of genetic variation from 1,092 human genomes

Cancer genome landscapes

Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes

Core signaling pathways in human pancreatic cancers revealed by global genomic analyses

dbSNP: the NCBI database of genetic variation

Mutation and cancer: statistical study of retinoblastoma

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene

BLAT--the BLAST-like alignment tool

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Evaluation of DNA from the Papanicolaou test to detect ovarian and endometrial cancers

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Ralph H. Hruban

Kenneth W Kinzler

Steven Gallinger

Christine A Iacobuzio-Donahue

Nicholas J Roberts

Michael Goggins

Bert Vogelstein

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2015-12-09T00:00:00Z

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26658419

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