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Jun Yoshimura

Showing results (1-10 of 52) with videos related to

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BMC Bioinformatics|December 2, 2009
siDirect 2.0: updated software for designing functional siRNA with reduced seed-dependent off-target effectYuki Naito, Jun Yoshimura, Shinichi Morishita, et al.
Journal of the Air & Waste Management Association (1995)|January 10, 2017
Development of the Simulation Model InPest for Prediction of the Indoor Behavior of PesticidesYoshihide Matoba, Jun Yoshimura, Jun-Ichi Ohnishi, et al.
Bioinformatics (Oxford, England)|June 6, 2009
UTGB toolkit for personalized genome browsersTaro L Saito, Jun Yoshimura, Shin Sasaki, et al.
Microbiome|August 29, 2019
Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gutYoshihiko Suzuki, Suguru Nishijima, Yoshikazu Furuta, et al.
Journal of the American Heart Association|June 15, 2024
Comparison of Endovascular Therapy and Open Surgical Revascularization in Patients With Acute Superior Mesenteric Artery Occlusion: A Large-Scale Analysis Based on the JROAD-DPC DatabaseDaiki Goto, Kenji Yanishi, Takaaki Ozawa, et al.
Internal Medicine (Tokyo, Japan)|December 10, 2019
A Novel de novo KIF1A Mutation in a Patient with Autism, Hyperactivity, Epilepsy, Sensory Disturbance, and Spastic ParaplegiaMasanori Kurihara, Hiroyuki Ishiura, Taro Bannai, et al.
International Heart Journal|February 2, 2025
Prognostic Factors After Bone Marrow-Derived Mononuclear Cell Implantation in No-Option Chronic Limb-Threatening Ischemia Patients with Atherosclerotic Lower Extremity Artery DiseaseHirofumi Kawamata, Kenji Yanishi, Jun Yoshimura, et al.
Human Mutation|June 3, 2020
Clinical and molecular genetic characterization of two female patients harboring the Xq27.3q28 deletion with different ratios of X chromosome inactivationKimiko Katoh, Kaori Aiba, Daisuke Fukushi, et al.
Journal of Human Genetics|September 13, 2020
Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese populationHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Nature Communications|November 30, 2017
Centromere evolution and CpG methylation during vertebrate speciationKazuki Ichikawa, Shingo Tomioka, Yuta Suzuki, et al.
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
BMC Bioinformatics|December 2, 2009
siDirect 2.0: updated software for designing functional siRNA with reduced seed-dependent off-target effectYuki Naito, Jun Yoshimura, Shinichi Morishita, et al.
Journal of the Air & Waste Management Association (1995)|January 10, 2017
Development of the Simulation Model InPest for Prediction of the Indoor Behavior of PesticidesYoshihide Matoba, Jun Yoshimura, Jun-Ichi Ohnishi, et al.
Bioinformatics (Oxford, England)|June 6, 2009
UTGB toolkit for personalized genome browsersTaro L Saito, Jun Yoshimura, Shin Sasaki, et al.
Microbiome|August 29, 2019
Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gutYoshihiko Suzuki, Suguru Nishijima, Yoshikazu Furuta, et al.
Journal of the American Heart Association|June 15, 2024
Comparison of Endovascular Therapy and Open Surgical Revascularization in Patients With Acute Superior Mesenteric Artery Occlusion: A Large-Scale Analysis Based on the JROAD-DPC DatabaseDaiki Goto, Kenji Yanishi, Takaaki Ozawa, et al.
Internal Medicine (Tokyo, Japan)|December 10, 2019
A Novel de novo KIF1A Mutation in a Patient with Autism, Hyperactivity, Epilepsy, Sensory Disturbance, and Spastic ParaplegiaMasanori Kurihara, Hiroyuki Ishiura, Taro Bannai, et al.
International Heart Journal|February 2, 2025
Prognostic Factors After Bone Marrow-Derived Mononuclear Cell Implantation in No-Option Chronic Limb-Threatening Ischemia Patients with Atherosclerotic Lower Extremity Artery DiseaseHirofumi Kawamata, Kenji Yanishi, Jun Yoshimura, et al.
Human Mutation|June 3, 2020
Clinical and molecular genetic characterization of two female patients harboring the Xq27.3q28 deletion with different ratios of X chromosome inactivationKimiko Katoh, Kaori Aiba, Daisuke Fukushi, et al.
Journal of Human Genetics|September 13, 2020
Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese populationHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Nature Communications|November 30, 2017
Centromere evolution and CpG methylation during vertebrate speciationKazuki Ichikawa, Shingo Tomioka, Yuta Suzuki, et al.
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