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Stem Cell Reports
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August 25, 2023
Dual CRISPR-Cas3 system for inducing multi-exon skipping in DMD patient-derived iPSCs
Yuto Kita, Yuya Okuzaki, Youichi Naoe, et al.
Experimental Hematology
|
May 30, 2015
Targeted gene correction of RUNX1 in induced pluripotent stem cells derived from familial platelet disorder with propensity to myeloid malignancy restores normal megakaryopoiesis
Hiromitsu Iizuka, Yuki Kagoya, Keisuke Kataoka, et al.
Journal of Neuromuscular Diseases
|
July 23, 2025
Report on the rare disease consortium Japan inaugural symposium - July 18, 2023, shonan health innovation park, Japan
Toshifumi Yokota, Naoto Inukai, Hiroyuki Shibasaki, et al.
Stem Cell Reports
|
April 2, 2021
Characterization of hiPSC-Derived Muscle Progenitors Reveals Distinctive Markers for Myogenic Cell Purification Toward Cell Therapy
Minas Nalbandian, Mingming Zhao, Mitsuru Sasaki-Honda, et al.
Stem Cell Reports
|
December 10, 2013
Direct comparison of autologous and allogeneic transplantation of iPSC-derived neural cells in the brain of a non-human primate
Asuka Morizane, Daisuke Doi, Tetsuhiro Kikuchi, et al.
Cells
|
October 23, 2021
Contractile Activity of Myotubes Derived from Human Induced Pluripotent Stem Cells: A Model of Duchenne Muscular Dystrophy
Kantaro Yoshioka, Akira Ito, Masanobu Horie, et al.
Journal of Bioscience and Bioengineering
|
October 20, 2005
Production of anti-prion scFv-Fc fusion proteins by recombinant animal cells
Ken-Ichiro Ono, Masamichi Kamihira, Yuko Kuga, et al.
Stem Cell Reports
|
March 12, 2021
Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein
Akihiro Kagita, Mandy S Y Lung, Huaigeng Xu, et al.
Stem Cell Reports
|
September 26, 2014
Focal transplantation of human iPSC-derived glial-rich neural progenitors improves lifespan of ALS mice
Takayuki Kondo, Misato Funayama, Kayoko Tsukita, et al.
Regenerative Therapy
|
September 29, 2021
Development of alternative gene transfer techniques for <i>ex vivo</i> and <i>in vivo</i> gene therapy in a canine model
Masashi Noda, Kohei Tatsumi, Hideto Matsui, et al.
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Search research articles
Search
Showing results (51-60 of 95) with videos related to
Sort By:
Page
of 10
Stem Cell Reports
|
August 25, 2023
Dual CRISPR-Cas3 system for inducing multi-exon skipping in DMD patient-derived iPSCs
Yuto Kita, Yuya Okuzaki, Youichi Naoe, et al.
Experimental Hematology
|
May 30, 2015
Targeted gene correction of RUNX1 in induced pluripotent stem cells derived from familial platelet disorder with propensity to myeloid malignancy restores normal megakaryopoiesis
Hiromitsu Iizuka, Yuki Kagoya, Keisuke Kataoka, et al.
Journal of Neuromuscular Diseases
|
July 23, 2025
Report on the rare disease consortium Japan inaugural symposium - July 18, 2023, shonan health innovation park, Japan
Toshifumi Yokota, Naoto Inukai, Hiroyuki Shibasaki, et al.
Stem Cell Reports
|
April 2, 2021
Characterization of hiPSC-Derived Muscle Progenitors Reveals Distinctive Markers for Myogenic Cell Purification Toward Cell Therapy
Minas Nalbandian, Mingming Zhao, Mitsuru Sasaki-Honda, et al.
Stem Cell Reports
|
December 10, 2013
Direct comparison of autologous and allogeneic transplantation of iPSC-derived neural cells in the brain of a non-human primate
Asuka Morizane, Daisuke Doi, Tetsuhiro Kikuchi, et al.
Cells
|
October 23, 2021
Contractile Activity of Myotubes Derived from Human Induced Pluripotent Stem Cells: A Model of Duchenne Muscular Dystrophy
Kantaro Yoshioka, Akira Ito, Masanobu Horie, et al.
Journal of Bioscience and Bioengineering
|
October 20, 2005
Production of anti-prion scFv-Fc fusion proteins by recombinant animal cells
Ken-Ichiro Ono, Masamichi Kamihira, Yuko Kuga, et al.
Stem Cell Reports
|
March 12, 2021
Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein
Akihiro Kagita, Mandy S Y Lung, Huaigeng Xu, et al.
Stem Cell Reports
|
September 26, 2014
Focal transplantation of human iPSC-derived glial-rich neural progenitors improves lifespan of ALS mice
Takayuki Kondo, Misato Funayama, Kayoko Tsukita, et al.
Regenerative Therapy
|
September 29, 2021
Development of alternative gene transfer techniques for <i>ex vivo</i> and <i>in vivo</i> gene therapy in a canine model
Masashi Noda, Kohei Tatsumi, Hideto Matsui, et al.
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