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Cell Stem Cell
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January 21, 2020
Tissue-Engineered Vascular Grafts with Advanced Mechanical Strength from Human iPSCs
Jiesi Luo, Lingfeng Qin, Liping Zhao, et al.
Clinical Science (London, England : 1979)
|
February 20, 2019
<i>MiR-33a</i> is a therapeutic target in SPG4-related hereditary spastic paraplegia human neurons
Fumiko Nakazeki, Itaru Tsuge, Takahiro Horie, et al.
Biochemical and Biophysical Research Communications
|
February 21, 2018
Human AK2 links intracellular bioenergetic redistribution to the fate of hematopoietic progenitors
Koichi Oshima, Norikazu Saiki, Michihiro Tanaka, et al.
Nature Communications
|
March 15, 2020
Extracellular nanovesicles for packaging of CRISPR-Cas9 protein and sgRNA to induce therapeutic exon skipping
Peter Gee, Mandy S Y Lung, Yuya Okuzaki, et al.
Science Translational Medicine
|
May 26, 2017
The Src/c-Abl pathway is a potential therapeutic target in amyotrophic lateral sclerosis
Keiko Imamura, Yuishin Izumi, Akira Watanabe, et al.
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of 10
Search research articles
Search
Showing results (91-100 of 95) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 95 results.
Cell Stem Cell
|
January 21, 2020
Tissue-Engineered Vascular Grafts with Advanced Mechanical Strength from Human iPSCs
Jiesi Luo, Lingfeng Qin, Liping Zhao, et al.
Clinical Science (London, England : 1979)
|
February 20, 2019
<i>MiR-33a</i> is a therapeutic target in SPG4-related hereditary spastic paraplegia human neurons
Fumiko Nakazeki, Itaru Tsuge, Takahiro Horie, et al.
Biochemical and Biophysical Research Communications
|
February 21, 2018
Human AK2 links intracellular bioenergetic redistribution to the fate of hematopoietic progenitors
Koichi Oshima, Norikazu Saiki, Michihiro Tanaka, et al.
Nature Communications
|
March 15, 2020
Extracellular nanovesicles for packaging of CRISPR-Cas9 protein and sgRNA to induce therapeutic exon skipping
Peter Gee, Mandy S Y Lung, Yuya Okuzaki, et al.
Science Translational Medicine
|
May 26, 2017
The Src/c-Abl pathway is a potential therapeutic target in amyotrophic lateral sclerosis
Keiko Imamura, Yuishin Izumi, Akira Watanabe, et al.
Page
of 10