Hiroshi Nakagawa

发表

Investigation of optimized high-density flip-chip interconnect design including micro Au bumps for 3-D stacked LSI packaging

Kohji Koshiji, Masahiro Aoyagi, Fumiki Kato, 2013, 2013 IEEE International 3D Systems Integration Conference (3DIC).

Setting the process parameters for the coating process in order to assure tablet appearance based on multivariate analysis of prior data.

Manabu Kano, Hidemi Minami, Hiroshi Nakagawa, 2016, International journal of pharmaceutics.

A New Strategy of High-Speed Screening and Quantitative Structure-Activity Relationship Analysis to Evaluate Human ATP-Binding Cassette Transporter ABCG2-Drug Interactions

Hiroyuki Hirano, Masako Osumi, Mami Konomi, 2006, Journal of Pharmacology and Experimental Therapeutics.

Oncogene-induced senescence is part of the tumorigenesis barrier imposed by DNA damage checkpoints

Dimitris Kletsas, Jiri Bartek, Frederic Tort, 2006, Nature.

Optical imaging of periostin enables early endoscopic detection and characterization of esophageal cancer in mice.

Umar Mahmood, Pedram Heidari, Timothy C Wang, 2013, Gastroenterology.

Molecular modeling of new camptothecin analogues to circumvent ABCG2-mediated drug resistance in cancer.

Hikaru Saito, Sachiko Aida-Hyugaji, Hiroshi Nakagawa, 2006, Cancer letters.

Telomerase induces immortalization of human esophageal keratinocytes without p16INK4a inactivation.

Hiroshi Nakagawa, A. Rustgi, H. Nakagawa, 2003, Molecular cancer research : MCR.

Ha-RasG12V induces senescence in primary and immortalized human esophageal keratinocytes with p53 dysfunction

Hiroshi Nakagawa, H. Nakagawa, T. Deramaudt, 2004, Oncogene.

Theoretical studies for molecular modeling of new camptothecin analogues

Minoru Sakurai, Umpei Nagashima, Sachiko Aida-Hyugaji, 2007 .

High-speed screening and QSAR analysis of human ATP-binding cassette transporter ABCB11 (bile salt export pump) to predict drug-induced intrahepatic cholestasis.

Hiroyuki Hirano, Hikaru Saito, Hiroshi Nakagawa, 2006, Molecular pharmaceutics.

EGFR-induced cell migration is mediated predominantly by the JAK-STAT pathway in primary esophageal keratinocytes.

Mark J. Bowser, Hiroshi Nakagawa, A. Rustgi, 2004, American journal of physiology. Gastrointestinal and liver physiology.