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

Ryosuke Ohsawa

Showing results (1-10 of 22) with videos related to

Pageof 3
Sort By:
Brain Research|May 10, 2007
Regulation of retinal cell fate specification by multiple transcription factorsRyosuke Ohsawa, Ryoichiro Kageyama
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 25, 2005
Mash1 and Math3 are required for development of branchiomotor neurons and maintenance of neural progenitorsRyosuke Ohsawa, Toshiyuki Ohtsuka, Ryoichiro Kageyama
Epigenetics & Chromatin|September 15, 2009
Epigenetic inheritance of an inducibly nucleosome-depleted promoter and its associated transcriptional state in the apparent absence of transcriptional activatorsRyosuke Ohsawa, Melissa Adkins, Jessica K Tyler
Frontiers in Genetics|August 23, 2013
At the intersection of non-coding transcription, DNA repair, chromatin structure, and cellular senescenceRyosuke Ohsawa, Ja-Hwan Seol, Jessica K Tyler
Experimental Cell Research|June 1, 2005
Roles of bHLH genes in neural stem cell differentiationRyoichiro Kageyama, Toshiyuki Ohtsuka, Jun Hatakeyama, et al.
Plos One|May 18, 2016
The Commercial Antibodies Widely Used to Measure H3 K56 Acetylation Are Non-Specific in Human and Drosophila CellsSangita Pal, Hillary Graves, Ryosuke Ohsawa, et al.
Journal of Human Genetics|May 27, 2020
The first Japanese case of primary familial brain calcification caused by an MYORG variantKodai Kume, Tadayuki Takata, Hiroyuki Morino, et al.
Journal of the Neurological Sciences|May 27, 2019
C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8Kodai Kume, Hiroyuki Morino, Osamu Komure, et al.
Molecular Endocrinology (Baltimore, Md.)|April 12, 2007
Hes1 and Hes5 control the progenitor pool, intermediate lobe specification, and posterior lobe formation in the pituitary developmentAya Kita, Itaru Imayoshi, Masato Hojo, et al.
Geriatrics & Gerontology International|October 13, 2018
Compound heterozygote mutations in the SIGMAR1 gene in an oldest-old patient with amyotrophic lateral sclerosisYuishin Izumi, Hiroyuki Morino, Ryosuke Miyamoto, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Brain Research|May 10, 2007
Regulation of retinal cell fate specification by multiple transcription factorsRyosuke Ohsawa, Ryoichiro Kageyama
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 25, 2005
Mash1 and Math3 are required for development of branchiomotor neurons and maintenance of neural progenitorsRyosuke Ohsawa, Toshiyuki Ohtsuka, Ryoichiro Kageyama
Epigenetics & Chromatin|September 15, 2009
Epigenetic inheritance of an inducibly nucleosome-depleted promoter and its associated transcriptional state in the apparent absence of transcriptional activatorsRyosuke Ohsawa, Melissa Adkins, Jessica K Tyler
Frontiers in Genetics|August 23, 2013
At the intersection of non-coding transcription, DNA repair, chromatin structure, and cellular senescenceRyosuke Ohsawa, Ja-Hwan Seol, Jessica K Tyler
Experimental Cell Research|June 1, 2005
Roles of bHLH genes in neural stem cell differentiationRyoichiro Kageyama, Toshiyuki Ohtsuka, Jun Hatakeyama, et al.
Plos One|May 18, 2016
The Commercial Antibodies Widely Used to Measure H3 K56 Acetylation Are Non-Specific in Human and Drosophila CellsSangita Pal, Hillary Graves, Ryosuke Ohsawa, et al.
Journal of Human Genetics|May 27, 2020
The first Japanese case of primary familial brain calcification caused by an MYORG variantKodai Kume, Tadayuki Takata, Hiroyuki Morino, et al.
Journal of the Neurological Sciences|May 27, 2019
C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8Kodai Kume, Hiroyuki Morino, Osamu Komure, et al.
Molecular Endocrinology (Baltimore, Md.)|April 12, 2007
Hes1 and Hes5 control the progenitor pool, intermediate lobe specification, and posterior lobe formation in the pituitary developmentAya Kita, Itaru Imayoshi, Masato Hojo, et al.
Geriatrics & Gerontology International|October 13, 2018
Compound heterozygote mutations in the SIGMAR1 gene in an oldest-old patient with amyotrophic lateral sclerosisYuishin Izumi, Hiroyuki Morino, Ryosuke Miyamoto, et al.
Pageof 3