N. Shindoh

发表

Identification of a novel oncogenic mutation of FGFR4 in gastric cancer

T. Futami, T. Kawase, K. Mori, 2019, Scientific Reports.

ASP5878, a selective FGFR inhibitor, to treat FGFR3‐dependent urothelial cancer with or without chemoresistance

Tomoyuki Suzuki, M. Kameda, Tadashi Terasaka, 2017, Cancer science.

Single–minded and Down syndrome?

S. Antonarakis, S. Minoshima, N. Shimizu, 1995, Nature Genetics.

Mutations in G protein beta subunits promote transformation and kinase inhibitor resistance

B. Ebert, G. Adelmant, J. Marto, 2014, Nature Medicine.

Histone deacetylase inhibitors from microorganisms: the Astellas experience.

N. Shindoh, N. Inamura, Y. Masuoka, 2008, Progress in drug research. Fortschritte der Arzneimittelforschung. Progres des recherches pharmaceutiques.

The mammalian single-minded (SIM) gene: mouse cDNA structure and diencephalic expression indicate a candidate gene for Down syndrome.

N. Shimizu, K. Kawasaki, S. Minoshima, 1996, Genomics.

Abstract A227: Antitumor activities of ASP3026 against EML4-ALK-dependent tumor models.

H. Mano, M. Sasamata, N. Shindoh, 2011 .

Next-Generation cDNA Screening for Oncogene and Resistance Phenotypes

T. Sullivan, A. Lane, S. Rodig, 2012, PloS one.

ASP5878, a Novel Inhibitor of FGFR1, 2, 3, and 4, Inhibits the Growth of FGF19-Expressing Hepatocellular Carcinoma

Tomoyuki Suzuki, M. Kameda, Tadashi Terasaka, 2016, Molecular Cancer Therapeutics.

Cloning of a human homolog of the Drosophila minibrain/rat Dyrk gene from "the Down syndrome critical region" of chromosome 21.

N. Shimizu, S. Minoshima, J. Kudoh, 1996, Biochemical and biophysical research communications.

novel inhibitor of FGFR 1 , 2 , 3 , and 4 , inhibits the growth of FGF 19-expressing hepatocellular carcinoma

Tomoyuki Suzuki, M. Kameda, Tadashi Terasaka, 2016 .

YM753, a novel histone deacetylase inhibitor, exhibits antitumor activity with selective, sustained accumulation of acetylated histones in tumors in the WiDr xenograft model.

T. Sakai, M. Sasamata, Y. Sowa, 2008, International journal of oncology.

Three new cyclostellettamines, which inhibit histone deacetylase, from a marine sponge of the genus Xestospongia.

S. Matsunaga, N. Shindoh, N. Fusetani, 2004, Bioorganic & medicinal chemistry letters.

Azumamides A-E: histone deacetylase inhibitory cyclic tetrapeptides from the marine sponge Mycale izuensis.

A. Ganesan, S. Matsunaga, N. Shindoh, 2006, Angewandte Chemie.

Mutations in G protein beta subunits promote transformation and kinase inhibitor resistance

B. Ebert, G. Adelmant, J. Marto, 2014, Nature Medicine.

GNB1 Activating Mutations Promote Myeloid and Lymphoid Neoplasms Targetable By Combined PI3K/mTOR Inhibition

G. Adelmant, J. Marto, Kutlu G. Elpek, 2014 .

Azumamides A-E: histone deacetylase inhibitory cyclic tetrapeptides from the marine sponge Mycale izuensis.

A. Ganesan, S. Matsunaga, N. Shindoh, 2006, Angewandte Chemie.