Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Takahashi

Showing results (51-60 of 148) with videos related to

Pageof 15
Sort By:
Scientific Reports|July 6, 2013
Manumycin A corrects aberrant splicing of Clcn1 in myotonic dystrophy type 1 (DM1) miceKosuke Oana, Yoko Oma, Satoshi Suo, et al.
Frontiers in Cell and Developmental Biology|June 16, 2022
Mature Myotubes Generated From Human-Induced Pluripotent Stem Cells Without Forced Gene ExpressionKei Fujiwara, Risa Yamamoto, Tomoya Kubota, et al.
Journal of the Neurological Sciences|August 23, 2011
A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysisMakito Hirano, Yosuke Kokunai, Asami Nagai, et al.
Muscle & Nerve|April 7, 2009
New mutation of the Na channel in the severe form of potassium-aggravated myotoniaTomoya Kubota, Masanobu Kinoshita, Ryogen Sasaki, et al.
Neuromuscular Disorders : NMD|May 26, 2016
An elderly-onset limb girdle muscular dystrophy type 1B (LGMD1B) with pseudo-hypertrophy of paraspinal musclesMitsuru Furuta, Hisae Sumi-Akamaru, Masanori P Takahashi, et al.
Journal of Cell Science|May 5, 2005
Association of hnRNP S1 proteins with vimentin intermediate filaments in migrating cellsAkira Inoue, Takanori Watanabe, Kazunari Tominaga, et al.
Histochemistry|January 1, 1990
Immunohistochemical demonstration of nuclear S1 proteins in various cellsK P Takahashi, Y Higashi, T Uchimoto, et al.
Rinsho Shinkeigaku = Clinical Neurology|August 2, 2012
[A case of dysferlinopathy asymptomatic for 10 years after an episode of transient muscle weakness]Yoshito Kobayashi, Toshiaki Takahashi, Hisae Sumi, et al.
Human Molecular Genetics|December 16, 2024
Identification of ZNF850 as a novel CTG repeat expansion-related gene in myotonic dystrophy type 1 patient-derived iPSCsMasayoshi Kamon, Shuji Wakatsuki, Masayuki Nakamori, et al.
BMC Medical Ethics|August 25, 2016
Using digital technologies to engage with medical research: views of myotonic dystrophy patients in JapanVictoria Coathup, Harriet J A Teare, Jusaku Minari, et al.
Pageof 15

Showing results (51-60 of 148) with videos related to

Sort By:
Pageof 15
Scientific Reports|July 6, 2013
Manumycin A corrects aberrant splicing of Clcn1 in myotonic dystrophy type 1 (DM1) miceKosuke Oana, Yoko Oma, Satoshi Suo, et al.
Frontiers in Cell and Developmental Biology|June 16, 2022
Mature Myotubes Generated From Human-Induced Pluripotent Stem Cells Without Forced Gene ExpressionKei Fujiwara, Risa Yamamoto, Tomoya Kubota, et al.
Journal of the Neurological Sciences|August 23, 2011
A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysisMakito Hirano, Yosuke Kokunai, Asami Nagai, et al.
Muscle & Nerve|April 7, 2009
New mutation of the Na channel in the severe form of potassium-aggravated myotoniaTomoya Kubota, Masanobu Kinoshita, Ryogen Sasaki, et al.
Neuromuscular Disorders : NMD|May 26, 2016
An elderly-onset limb girdle muscular dystrophy type 1B (LGMD1B) with pseudo-hypertrophy of paraspinal musclesMitsuru Furuta, Hisae Sumi-Akamaru, Masanori P Takahashi, et al.
Journal of Cell Science|May 5, 2005
Association of hnRNP S1 proteins with vimentin intermediate filaments in migrating cellsAkira Inoue, Takanori Watanabe, Kazunari Tominaga, et al.
Histochemistry|January 1, 1990
Immunohistochemical demonstration of nuclear S1 proteins in various cellsK P Takahashi, Y Higashi, T Uchimoto, et al.
Rinsho Shinkeigaku = Clinical Neurology|August 2, 2012
[A case of dysferlinopathy asymptomatic for 10 years after an episode of transient muscle weakness]Yoshito Kobayashi, Toshiaki Takahashi, Hisae Sumi, et al.
Human Molecular Genetics|December 16, 2024
Identification of ZNF850 as a novel CTG repeat expansion-related gene in myotonic dystrophy type 1 patient-derived iPSCsMasayoshi Kamon, Shuji Wakatsuki, Masayuki Nakamori, et al.
BMC Medical Ethics|August 25, 2016
Using digital technologies to engage with medical research: views of myotonic dystrophy patients in JapanVictoria Coathup, Harriet J A Teare, Jusaku Minari, et al.
Pageof 15