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Human Gene Therapy Methods
|
March 2, 2013
The chicken hypersensitivity site 4 core insulator blocks promoter interference in lentiviral vectors
Naoya Uchida, Hideki Hanawa, Motoko Yamamoto, et al.
Brain Research
|
March 15, 2011
Global gene transfer into the CNS across the BBB after neonatal systemic delivery of single-stranded AAV vectors
Noriko Miyake, Koichi Miyake, Motoko Yamamoto, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 19, 2009
Optimized lentiviral vector design improves titer and transgene expression of vectors containing the chicken beta-globin locus HS4 insulator element
Hideki Hanawa, Motoko Yamamoto, Huifen Zhao, et al.
Scientific Reports
|
October 16, 2021
Treatment of adult metachromatic leukodystrophy model mice using intrathecal administration of type 9 AAV vector encoding arylsulfatase A
Noriko Miyake, Koichi Miyake, Atsushi Sakai, et al.
Biochemical and Biophysical Research Communications
|
December 29, 2005
Mutations in p53 cDNA sequence introduced by retroviral vector
Su Su, Atsushi Watanabe, Motoko Yamamoto, et al.
Gene Therapy
|
October 11, 2021
A PCR-amplified transgene fragment flanked by a single copy of a truncated inverted terminal repeat for recombinant adeno-associated virus production prevents unnecessary plasmid DNA packaging
Kumi Adachi, Taro Tomono, Hironori Okada, et al.
The Journal of Gene Medicine
|
April 2, 2009
Global diffuse distribution in the brain and efficient gene delivery to the dorsal root ganglia by intrathecal injection of adeno-associated viral vector serotype 1
Naotaka Iwamoto, Atsushi Watanabe, Motoko Yamamoto, et al.
Scientific Reports
|
August 19, 2015
Enzyme replacement in the CSF to treat metachromatic leukodystrophy in mouse model using single intracerebroventricular injection of self-complementary AAV1 vector
Kohei Hironaka, Yoshiyuki Yamazaki, Yukihiko Hirai, et al.
Molecular Therapy. Methods & Clinical Development
|
July 7, 2022
Evaluation of parameters for efficient purification and long-term storage of herpes simplex virus-based vectors
Seiji Kuroda, Yoshitaka Miyagawa, Makoto Sukegawa, et al.
Molecular Therapy. Oncology
|
November 18, 2024
Mesenchymal stem cell origin contributes to the antitumor effect of oncolytic virus carriers
Makoto Sukegawa, Yoshitaka Miyagawa, Seiji Kuroda, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Human Gene Therapy Methods
|
March 2, 2013
The chicken hypersensitivity site 4 core insulator blocks promoter interference in lentiviral vectors
Naoya Uchida, Hideki Hanawa, Motoko Yamamoto, et al.
Brain Research
|
March 15, 2011
Global gene transfer into the CNS across the BBB after neonatal systemic delivery of single-stranded AAV vectors
Noriko Miyake, Koichi Miyake, Motoko Yamamoto, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 19, 2009
Optimized lentiviral vector design improves titer and transgene expression of vectors containing the chicken beta-globin locus HS4 insulator element
Hideki Hanawa, Motoko Yamamoto, Huifen Zhao, et al.
Scientific Reports
|
October 16, 2021
Treatment of adult metachromatic leukodystrophy model mice using intrathecal administration of type 9 AAV vector encoding arylsulfatase A
Noriko Miyake, Koichi Miyake, Atsushi Sakai, et al.
Biochemical and Biophysical Research Communications
|
December 29, 2005
Mutations in p53 cDNA sequence introduced by retroviral vector
Su Su, Atsushi Watanabe, Motoko Yamamoto, et al.
Gene Therapy
|
October 11, 2021
A PCR-amplified transgene fragment flanked by a single copy of a truncated inverted terminal repeat for recombinant adeno-associated virus production prevents unnecessary plasmid DNA packaging
Kumi Adachi, Taro Tomono, Hironori Okada, et al.
The Journal of Gene Medicine
|
April 2, 2009
Global diffuse distribution in the brain and efficient gene delivery to the dorsal root ganglia by intrathecal injection of adeno-associated viral vector serotype 1
Naotaka Iwamoto, Atsushi Watanabe, Motoko Yamamoto, et al.
Scientific Reports
|
August 19, 2015
Enzyme replacement in the CSF to treat metachromatic leukodystrophy in mouse model using single intracerebroventricular injection of self-complementary AAV1 vector
Kohei Hironaka, Yoshiyuki Yamazaki, Yukihiko Hirai, et al.
Molecular Therapy. Methods & Clinical Development
|
July 7, 2022
Evaluation of parameters for efficient purification and long-term storage of herpes simplex virus-based vectors
Seiji Kuroda, Yoshitaka Miyagawa, Makoto Sukegawa, et al.
Molecular Therapy. Oncology
|
November 18, 2024
Mesenchymal stem cell origin contributes to the antitumor effect of oncolytic virus carriers
Makoto Sukegawa, Yoshitaka Miyagawa, Seiji Kuroda, et al.
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of 2