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Institution

Nagoya City University

EducationNagoya, Japan
About: Nagoya City University is a education organization based out in Nagoya, Japan. It is known for research contribution in the topics: Cancer & Population. The organization has 9216 authors who have published 18519 publications receiving 458944 citations. The organization is also known as: Nagoya shiritsu daigaku.


Papers
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Journal ArticleDOI
04 Jun 2004-Science
TL;DR: Results suggest that EGFR mutations may predict sensitivity to gefitinib, and treatment with the EGFR kinase inhibitor gefitsinib causes tumor regression in some patients with NSCLC, more frequently in Japan.
Abstract: Receptor tyrosine kinase genes were sequenced in nonsmall cell lung cancer (NSCLC) and matched normal tissue. Somatic mutations of the epidermal growth factor receptor gene EGFR were found in 15 of 58 unselected tumors from Japan and 1 of 61 from the United States. Treatment with the EGFR kinase inhibitor gefitinib (Iressa) causes tumor regression in some patients with NSCLC, more frequently in Japan. EGFR mutations were found in additional lung cancer samples from U.S. patients who responded to gefitinib therapy and in a lung adenocarcinoma cell line that was hypersensitive to growth inhibition by gefitinib, but not in gefitinibinsensitive tumors or cell lines. These results suggest that EGFR mutations may predict sensitivity to gefitinib. Protein kinase activation by somatic mutation or

9,265 citations

Journal ArticleDOI
Takashi Matsumoto1, Jianzhong Wu1, Hiroyuki Kanamori1, Yuichi Katayose1  +262 moreInstitutions (25)
11 Aug 2005-Nature
TL;DR: A map-based, finished quality sequence that covers 95% of the 389 Mb rice genome, including virtually all of the euchromatin and two complete centromeres, and finds evidence for widespread and recurrent gene transfer from the organelles to the nuclear chromosomes.
Abstract: Rice, one of the world's most important food plants, has important syntenic relationships with the other cereal species and is a model plant for the grasses. Here we present a map-based, finished quality sequence that covers 95% of the 389 Mb genome, including virtually all of the euchromatin and two complete centromeres. A total of 37,544 non-transposable-element-related protein-coding genes were identified, of which 71% had a putative homologue in Arabidopsis. In a reciprocal analysis, 90% of the Arabidopsis proteins had a putative homologue in the predicted rice proteome. Twenty-nine per cent of the 37,544 predicted genes appear in clustered gene families. The number and classes of transposable elements found in the rice genome are consistent with the expansion of syntenic regions in the maize and sorghum genomes. We find evidence for widespread and recurrent gene transfer from the organelles to the nuclear chromosomes. The map-based sequence has proven useful for the identification of genes underlying agronomic traits. The additional single-nucleotide polymorphisms and simple sequence repeats identified in our study should accelerate improvements in rice production.

3,423 citations

Journal ArticleDOI
Rameen Beroukhim, Craig H. Mermel1, Craig H. Mermel2, Dale Porter3, Guo Wei2, Soumya Raychaudhuri2, Soumya Raychaudhuri4, Jerry Donovan3, Jordi Barretina2, Jordi Barretina1, Jesse S. Boehm2, Jennifer Dobson2, Jennifer Dobson1, Mitsuyoshi Urashima5, Kevin T. Mc Henry3, Reid M. Pinchback2, Azra H. Ligon4, Yoon Jae Cho6, Leila Haery2, Leila Haery1, Heidi Greulich, Michael R. Reich2, Wendy Winckler2, Michael S. Lawrence2, Barbara A. Weir1, Barbara A. Weir2, Kumiko E. Tanaka1, Kumiko E. Tanaka2, Derek Y. Chiang1, Derek Y. Chiang7, Derek Y. Chiang2, Adam J. Bass2, Adam J. Bass1, Adam J. Bass4, Alice Loo3, Carter Hoffman1, Carter Hoffman2, John R. Prensner2, John R. Prensner1, Ted Liefeld2, Qing Gao2, Derek Yecies1, Sabina Signoretti4, Sabina Signoretti1, Elizabeth A. Maher8, Frederic J. Kaye, Hidefumi Sasaki9, Joel E. Tepper7, Jonathan A. Fletcher4, Josep Tabernero10, José Baselga10, Ming-Sound Tsao11, Francesca Demichelis12, Mark A. Rubin12, Pasi A. Jänne1, Pasi A. Jänne4, Mark J. Daly2, Mark J. Daly1, Carmelo Nucera13, Ross L. Levine14, Benjamin L. Ebert1, Benjamin L. Ebert2, Benjamin L. Ebert4, Stacey Gabriel2, Anil K. Rustgi15, Cristina R. Antonescu14, Marc Ladanyi14, Anthony Letai1, Levi A. Garraway2, Levi A. Garraway1, Massimo Loda1, Massimo Loda4, David G. Beer16, Lawrence D. True17, Aikou Okamoto5, Scott L. Pomeroy6, Samuel Singer14, Todd R. Golub2, Todd R. Golub1, Todd R. Golub18, Eric S. Lander2, Eric S. Lander19, Eric S. Lander1, Gad Getz2, William R. Sellers3, Matthew Meyerson2, Matthew Meyerson1 
18 Feb 2010-Nature
TL;DR: It is demonstrated that cancer cells containing amplifications surrounding the MCL1 and BCL2L1 anti-apoptotic genes depend on the expression of these genes for survival, and a large majority of SCNAs identified in individual cancer types are present in several cancer types.
Abstract: A powerful way to discover key genes with causal roles in oncogenesis is to identify genomic regions that undergo frequent alteration in human cancers. Here we present high-resolution analyses of somatic copy-number alterations (SCNAs) from 3,131 cancer specimens, belonging largely to 26 histological types. We identify 158 regions of focal SCNA that are altered at significant frequency across several cancer types, of which 122 cannot be explained by the presence of a known cancer target gene located within these regions. Several gene families are enriched among these regions of focal SCNA, including the BCL2 family of apoptosis regulators and the NF-kappaBeta pathway. We show that cancer cells containing amplifications surrounding the MCL1 and BCL2L1 anti-apoptotic genes depend on the expression of these genes for survival. Finally, we demonstrate that a large majority of SCNAs identified in individual cancer types are present in several cancer types.

3,375 citations

Journal ArticleDOI
TL;DR: It is shown that the JFH1 genome replicates efficiently and supports secretion of viral particles after transfection into a human hepatoma cell line (Huh7) and provides a powerful tool for studying the viral life cycle and developing antiviral strategies.
Abstract: Hepatitis C virus (HCV) infection causes chronic liver diseases and is a global public health problem. Detailed analyses of HCV have been hampered by the lack of viral culture systems. Subgenomic replicons of the JFH1 genotype 2a strain cloned from an individual with fulminant hepatitis replicate efficiently in cell culture. Here we show that the JFH1 genome replicates efficiently and supports secretion of viral particles after transfection into a human hepatoma cell line (Huh7). Particles have a density of about 1.15–1.17 g/ml and a spherical morphology with an average diameter of about 55 nm. Secreted virus is infectious for Huh7 cells and infectivity can be neutralized by CD81-specific antibodies and by immunoglobulins from chronically infected individuals. The cell culture–generated HCV is infectious for chimpanzee. This system provides a powerful tool for studying the viral life cycle and developing antiviral strategies.

2,809 citations

Journal ArticleDOI
TL;DR: A genome-wide association study to null virological response (NVR) in the treatment of patients with hepatitis C virus (HCV) genotype 1 within a Japanese population is reported.
Abstract: Masashi Mizokami and colleagues report a genome-wide association study to hepatitis C treatment response in two Japanese cohorts. They report common variants at IL28B associated with sustained as well as null virologic response following pegylated interferon-alpha and ribavirin combined therapy.

2,097 citations


Authors

Showing all 9245 results

NameH-indexPapersCitations
Ronald C. Kessler2741332328983
Tien Yin Wong1601880131830
Joseph Lau140104899305
Ko Okumura134105767530
Gavin Andrews11282258486
Takashi Saito112104152937
Minoru Yoshida11178355767
James A. Blumenthal10647148607
Tamio Hayashi9879935281
Keitaro Matsuo9781837349
Tetsuo Nagano9649034267
Hironobu Sasano94120043414
Takashi Takahashi9187842082
Yoshito Ikada9148432434
Paul R. Sanberg8763529745
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202319
202264
2021957
2020826
2019737
2018702