N. Arimura

发表

Sterol Regulatory Element-binding Protein-2 Interacts with Hepatocyte Nuclear Factor-4 to Enhance Sterol Isomerase Gene Expression in Hepatocytes*

J. Inoue, H. Shimano, T. Horiba, 2003, Journal of Biological Chemistry.

Perilipin-Mediated Lipid Droplet Formation in Adipocytes Promotes Sterol Regulatory Element-Binding Protein-1 Processing and Triacylglyceride Accumulation

J. Inoue, R. Sato, I. Ichi, 2013, PloS one.

Anti-sortilin1 Antibody Up-Regulates Progranulin via Sortilin1 Down-Regulation

Shuji Sato, Yuri Hori, Dnyaneshwar Warude, 2020, Frontiers in Neuroscience.

The Peroxisome Proliferator-activated Receptor γ Regulates Expression of the Perilipin Gene in Adipocytes*

T. Horiba, R. Sato, M. Imagawa, 2004, Journal of Biological Chemistry.

Cholesterol-functionalized DNA/RNA heteroduplexes cross the blood–brain barrier and knock down genes in the rodent CNS

F. Rigo, T. Ishii, T. Uchihara, 2021, Nature Biotechnology.

Design, Synthesis, and Evaluation of (4 R)-1-{3-[2-(18F)Fluoro-4-methylpyridin-3-yl]phenyl}-4-[4-(1,3-thiazol-2-ylcarbonyl)piperazin-1-yl]pyrrolidin-2-one ([18F]T-401) as a Novel Positron-Emission Tomography Imaging Agent for Monoacylglycerol Lipase.

Ming-Rong Zhang, J. Maeda, Yuji Nagai, 2019, Journal of medicinal chemistry.

A new class of non-thiazolidinedione, non-carboxylic-acid-based highly selective peroxisome proliferator-activated receptor (PPAR) γ agonists: design and synthesis of benzylpyrazole acylsulfonamides.

Toshimasa Tanaka, Biching Sang, C. Mol, 2012, Bioorganic & medicinal chemistry.

Design and Synthesis of Novel Spiro Derivatives as Potent and Reversible Monoacylglycerol Lipase (MAGL) Inhibitors: Bioisosteric Transformation from 3-Oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl Moiety.

L. Qin, S. Gay, D. Dougan, 2021, Journal of medicinal chemistry.

Design, Synthesis, and Evaluation of Piperazinyl Pyrrolidin-2-ones as a Novel Series of Reversible Monoacylglycerol Lipase Inhibitors.

M. Fushimi, S. Sogabe, Kazunobu Aoyama, 2018, Journal of medicinal chemistry.

[Diacylglycerol acyltransferase].

N. Arimura, R. Sato, M. Shimizu, 2001, Nihon rinsho. Japanese journal of clinical medicine.

Structure-activity relationships and key structural feature of pyridyloxybenzene-acylsulfonamides as new, potent, and selective peroxisome proliferator-activated receptor (PPAR) γ Agonists.

Toshimasa Tanaka, Biching Sang, C. Mol, 2012, Bioorganic & medicinal chemistry.

Discovery of a Novel Series of Potent, Selective, Orally Available, and Brain-Penetrable C1s Inhibitors for Modulation of the Complement Pathway

C.-H. Chen, Kenjiro Sato, D. Dougan, 2023, Journal of medicinal chemistry.

A new class of non-thiazolidinedione, non-carboxylic-acid-based highly selective peroxisome proliferator-activated receptor (PPAR) γ agonists: design and synthesis of benzylpyrazole acylsulfonamides.

Toshimasa Tanaka, Biching Sang, C. Mol, 2012, Bioorganic & medicinal chemistry.