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BMC Bioinformatics
|
December 2, 2009
siDirect 2.0: updated software for designing functional siRNA with reduced seed-dependent off-target effect
Yuki 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 Pesticides
Yoshihide Matoba, Jun Yoshimura, Jun-Ichi Ohnishi, et al.
Bioinformatics (Oxford, England)
|
June 6, 2009
UTGB toolkit for personalized genome browsers
Taro L Saito, Jun Yoshimura, Shin Sasaki, et al.
Microbiome
|
August 29, 2019
Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gut
Yoshihiko 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 Database
Daiki 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 Paraplegia
Masanori 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 Disease
Hirofumi 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 inactivation
Kimiko 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 population
Hiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Nature Communications
|
November 30, 2017
Centromere evolution and CpG methylation during vertebrate speciation
Kazuki Ichikawa, Shingo Tomioka, Yuta Suzuki, et al.
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Showing results (1-10 of 52) with videos related to
Sort By:
Page
of 6
BMC Bioinformatics
|
December 2, 2009
siDirect 2.0: updated software for designing functional siRNA with reduced seed-dependent off-target effect
Yuki 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 Pesticides
Yoshihide Matoba, Jun Yoshimura, Jun-Ichi Ohnishi, et al.
Bioinformatics (Oxford, England)
|
June 6, 2009
UTGB toolkit for personalized genome browsers
Taro L Saito, Jun Yoshimura, Shin Sasaki, et al.
Microbiome
|
August 29, 2019
Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gut
Yoshihiko 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 Database
Daiki 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 Paraplegia
Masanori 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 Disease
Hirofumi 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 inactivation
Kimiko 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 population
Hiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Nature Communications
|
November 30, 2017
Centromere evolution and CpG methylation during vertebrate speciation
Kazuki Ichikawa, Shingo Tomioka, Yuta Suzuki, et al.
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of 6