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Shin-ichi Inoue

Showing results (81-90 of 93) with videos related to

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Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|September 2, 2016
Combinational approach using in situ hybridization targeting 23S ribosomal RNA genes and blood cultures for bacterial identification in patients with neutropenia and feverHideo Koh, Mizuki Aimoto, Akio Matsuhisa, et al.
Nature Metabolism|April 15, 2024
Nuclear receptor corepressors non-canonically drive glucocorticoid receptor-dependent activation of hepatic gluconeogenesisAmy K Hauck, Rashid Mehmood, Bryce J Carpenter, et al.
Bioorganic & Medicinal Chemistry|April 20, 2013
Lead optimization of 5-amino-6-(2,2-dimethyl-5-oxo-4-phenylpiperazin-1-yl)-4-hydroxyhexanamides to reduce a cardiac safety issue: discovery of DS-8108b, an orally active renin inhibitorYuji Nakamura, Teppei Fujimoto, Yasuyuki Ogawa, et al.
American Journal of Human Genetics|November 20, 2015
Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic ThrombocytopeniaTetsuya Niihori, Meri Ouchi-Uchiyama, Yoji Sasahara, et al.
American Journal of Human Genetics|May 28, 2019
Germline-Activating RRAS2 Mutations Cause Noonan SyndromeTetsuya Niihori, Koki Nagai, Atsushi Fujita, et al.
Molecular Medicine Reports|June 15, 2018
Amplification of bacterial genomic DNA from all ascitic fluids with a highly sensitive polymerase chain reactionHirayuki Enomoto, Shin-Ichi Inoue, Akio Matsuhisa, et al.
American Journal of Human Genetics|June 25, 2013
Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndromeYoko Aoki, Tetsuya Niihori, Toshihiro Banjo, et al.
Human Genetics|December 31, 2015
Spectrum of mutations and genotype-phenotype analysis in Noonan syndrome patients with RIT1 mutationsMasako Yaoita, Tetsuya Niihori, Seiji Mizuno, et al.
Iscience|March 28, 2024
Mitochondrial biogenesis in white adipose tissue mediated by JMJD1A-PGC-1 axis limits age-related metabolic diseaseRyo Ito, Shiyu Xie, Myagmar Tumenjargal, et al.
Nature Communications|December 3, 2021
Spatiotemporal dynamics of SETD5-containing NCoR-HDAC3 complex determines enhancer activation for adipogenesisYoshihiro Matsumura, Ryo Ito, Ayumu Yajima, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|September 2, 2016
Combinational approach using in situ hybridization targeting 23S ribosomal RNA genes and blood cultures for bacterial identification in patients with neutropenia and feverHideo Koh, Mizuki Aimoto, Akio Matsuhisa, et al.
Nature Metabolism|April 15, 2024
Nuclear receptor corepressors non-canonically drive glucocorticoid receptor-dependent activation of hepatic gluconeogenesisAmy K Hauck, Rashid Mehmood, Bryce J Carpenter, et al.
Bioorganic & Medicinal Chemistry|April 20, 2013
Lead optimization of 5-amino-6-(2,2-dimethyl-5-oxo-4-phenylpiperazin-1-yl)-4-hydroxyhexanamides to reduce a cardiac safety issue: discovery of DS-8108b, an orally active renin inhibitorYuji Nakamura, Teppei Fujimoto, Yasuyuki Ogawa, et al.
American Journal of Human Genetics|November 20, 2015
Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic ThrombocytopeniaTetsuya Niihori, Meri Ouchi-Uchiyama, Yoji Sasahara, et al.
American Journal of Human Genetics|May 28, 2019
Germline-Activating RRAS2 Mutations Cause Noonan SyndromeTetsuya Niihori, Koki Nagai, Atsushi Fujita, et al.
Molecular Medicine Reports|June 15, 2018
Amplification of bacterial genomic DNA from all ascitic fluids with a highly sensitive polymerase chain reactionHirayuki Enomoto, Shin-Ichi Inoue, Akio Matsuhisa, et al.
American Journal of Human Genetics|June 25, 2013
Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndromeYoko Aoki, Tetsuya Niihori, Toshihiro Banjo, et al.
Human Genetics|December 31, 2015
Spectrum of mutations and genotype-phenotype analysis in Noonan syndrome patients with RIT1 mutationsMasako Yaoita, Tetsuya Niihori, Seiji Mizuno, et al.
Iscience|March 28, 2024
Mitochondrial biogenesis in white adipose tissue mediated by JMJD1A-PGC-1 axis limits age-related metabolic diseaseRyo Ito, Shiyu Xie, Myagmar Tumenjargal, et al.
Nature Communications|December 3, 2021
Spatiotemporal dynamics of SETD5-containing NCoR-HDAC3 complex determines enhancer activation for adipogenesisYoshihiro Matsumura, Ryo Ito, Ayumu Yajima, et al.
Pageof 10