Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("MEYERSON, Matthew")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 77

  • Page / 4
Export

Selection :

  • and

Telomerase activation, cellular immortalization and cancer : GENETICS OF CANCERHAHN, William C; MEYERSON, Matthew.Annals of medicine (Helsinki). 2001, Vol 33, Num 2, pp 123-129, issn 0785-3890Article

ROS1 Rearrangements in Lung Cancer: A New Genomic Subset of Lung AdenocarcinomaJANNE, Pasi A; MEYERSON, Matthew.Journal of clinical oncology. 2012, Vol 30, Num 8, pp 878-879, issn 0732-183X, 2 p.Article

Advances in understanding cancer genomes through second-generation sequencingMEYERSON, Matthew; GABRIEL, Stacey; GETZ, Gad et al.Nature reviews. Genetics (Print). 2010, Vol 11, Num 10, pp 685-696, issn 1471-0056, 12 p.Article

Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative PotentialSOLIMINI, Nicole L; QIKAI XU; BEROUKHIM, Rameen et al.Science (Washington, D.C.). 2012, Vol 337, Num 6090, pp 104-109, issn 0036-8075, 6 p.Article

SF3B1 and Other Novel Cancer Genes in Chronic Lymphocytic LeukemiaLILI WANG; LAWRENCE, Michael S; WANDI ZHANG et al.The New England journal of medicine. 2011, Vol 365, Num 26, pp 2497-2506, issn 0028-4793, 10 p.Article

In Situ Evidence of KRAS Amplification and Association With Increased p21 Levels in Non-Small Cell Lung CarcinomaWAGNER, Patrick L; PERNER, Sven; RICKMAN, David S et al.American journal of clinical pathology. 2009, Vol 132, Num 4, pp 500-505, issn 0002-9173, 6 p.Article

SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomasBASS, Adam J; WATANABE, Hideo; RAMOS, Alex H et al.Nature genetics. 2009, Vol 41, Num 11, pp 1238-1242, issn 1061-4036, 5 p.Article

HER-2/neu expression is associated with high tumor cell proliferation and aggressive phenotype in a population based patient series of endometrial carcinomasENGELSEN, Ingeborg B; STEFANSSON, Ingunn M; BEROUKHIM, Rameen et al.International journal of oncology. 2008, Vol 32, Num 2, pp 307-316, issn 1019-6439, 10 p.Article

A rapid and sensitive enzymatic method for epidermal growth factor receptor mutation screeningJÄNNE, Pasi A; BORRAS, Ana M; DISTEL, Robert J et al.Clinical cancer research. 2006, Vol 12, Num 3, pp 751-758, issn 1078-0432, 8 p., 1Article

Genomic approaches to lung cancerTHOMAS, Roman K; WEIR, Barbara; MEYERSON, Matthew et al.Clinical cancer research. 2006, Vol 12, Num 14, issn 1078-0432, 4384s-4391s, 2Conference Paper

Interlaboratory comparability study of cancer gene expression analysis using oligonucleotide microarraysDOBBIN, Kevin K; BEER, David G; MINNA, John D et al.Clinical cancer research. 2005, Vol 11, Num 2, pp 565-572, issn 1078-0432, 8 p., 1Article

Medulloblastoma exome sequencing uncovers subtype―specific somatic mutationsPUGH, Trevor J; DILHAN WEERARATNE, Shyamal; GREULICH, Heidi et al.Nature (London). 2012, Vol 488, Num 7409, pp 106-110, issn 0028-0836, 5 p.Article

Glioblastoma-Derived Epidermal Growth Factor Receptor Carboxyl-Terminal Deletion Mutants Are Transforming and Are Sensitive to EGFR-Directed TherapiesCHO, Jeonghee; PASTORINO, Sandra; KWON, Jihyun et al.Cancer research (Chicago, Ill.). 2011, Vol 71, Num 24, pp 7587-7596, issn 0008-5472, 10 p.Article

Prognostic and Predictive Gene Signature for Adjuvant Chemotherapy in Resected Non-Small-Cell Lung CancerZHU, Chang-Qi; DING, Keyue; PINTILIE, Melania et al.Journal of clinical oncology. 2010, Vol 28, Num 29, pp 4417-4424, issn 0732-183X, 8 p.Article

Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1BARBIE, David A; TAMAYO, Pablo; FRÖHLING, Stefan et al.Nature (London). 2009, Vol 462, Num 7269, pp 108-112, issn 0028-0836, 5 p.Article

High-throughput sequence analysis of the tyrosine kinome in acute myeloid leukemia. CommentaryCROSS, Nicholas C. P; LORIAUX, Marc M; BERGER, Roland et al.Blood. 2008, Vol 111, Num 9, issn 0006-4971, 4428, 4788-4796 [10 p.]Article

Homozygous deletions and chromosome amplifications in human lung carcinomas revealed by single nucleotide polymorphism array analysisXIAOJUN ZHAO; WEIR, Barbara A; SUGARBAKER, David et al.Cancer research (Baltimore). 2005, Vol 65, Num 13, pp 5561-5570, issn 0008-5472, 10 p.Article

Loss of heterozygosity and its correlation with expression profiles in subclasses of invasive breast cancersWANG, Zhigang C; MING LIN; IGLEHART, James D et al.Cancer research (Baltimore). 2004, Vol 64, Num 1, pp 64-71, issn 0008-5472, 8 p.Article

Missense mutations of the BRAF gene in human lung adenocarcinomaNAOKI, Katsuhiko; CHEN, Tzu-Hsiu; RICHARDS, William G et al.Cancer research (Baltimore). 2002, Vol 62, Num 23, pp 7001-7003, issn 0008-5472, 3 p.Article

Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arraysLINDBLAD-TOH, Kerstin; TANENBAUM, David M; LANDER, Eric S et al.Nature biotechnology. 2000, Vol 18, Num 9, pp 1001-1005, issn 1087-0156Article

Integrative and Comparative Genomic Analysis of Lung Squamous Cell Carcinomas in East Asian PatientsYOUNGWOOK KIM; HAMMERMAN, Peter S; LAWRENCE, Michael S et al.Journal of clinical oncology. 2014, Vol 32, Num 2, pp 121-128, issn 0732-183X, 8 p.Article

Kinase Domain Activation of FGFR2 Yields High-Grade Lung Adenocarcinoma Sensitive to a Pan-FGFR Inhibitor in a Mouse Model of NSCLCTCHAICHA, Jeremy H; AKBAY, Esra A; HAMMERMAN, Peter S et al.Cancer research (Chicago, Ill.). 2014, Vol 74, Num 17, pp 4676-4684, issn 0008-5472, 9 p.Article

Integrative Radiogenomic Profiling of Squamous Cell Lung CancerABAZEED, Mohamed E; ADAMS, Drew J; MESIROV, Jill P et al.Cancer research (Chicago, Ill.). 2013, Vol 73, Num 20, pp 6289-6298, issn 0008-5472, 10 p.Article

Gastrointestinal Adenocarcinomas of the Esophagus, Stomach, and Colon Exhibit Distinct Patterns of Genome Instability and OncogenesisDULAK, Austin M; SCHUMACHER, Steven E; TABERNERO, Josep et al.Cancer research (Chicago, Ill.). 2012, Vol 72, Num 17, pp 4383-4393, issn 0008-5472, 11 p.Article

Melanoma genome sequencing reveals frequent PREX2 mutationsBERGER, Michael F; HODIS, Eran; HAILEI ZHANG et al.Nature (London). 2012, Vol 485, Num 7399, pp 502-506, issn 0028-0836, 5 p.Article

  • Page / 4