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

Toshiyuki Maeda

Showing results (51-60 of 54) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 54 results.
European Journal of Human Genetics : EJHG|March 15, 2013
Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndromeKen Higashimoto, Toshiyuki Maeda, Junichiro Okada, et al.
BMC Cancer|December 31, 2013
Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastomaJanette Mareska Rumbajan, Toshiyuki Maeda, Ryota Souzaki, et al.
Epilepsia|February 27, 2016
De novo GABRA1 mutations in Ohtahara and West syndromesHirofumi Kodera, Chihiro Ohba, Mitsuhiro Kato, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2014
Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutationsToshiyuki Maeda, Ken Higashimoto, Kosuke Jozaki, et al.
Pageof 6

Showing results (51-60 of 54) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 54 results.
European Journal of Human Genetics : EJHG|March 15, 2013
Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndromeKen Higashimoto, Toshiyuki Maeda, Junichiro Okada, et al.
BMC Cancer|December 31, 2013
Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastomaJanette Mareska Rumbajan, Toshiyuki Maeda, Ryota Souzaki, et al.
Epilepsia|February 27, 2016
De novo GABRA1 mutations in Ohtahara and West syndromesHirofumi Kodera, Chihiro Ohba, Mitsuhiro Kato, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2014
Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutationsToshiyuki Maeda, Ken Higashimoto, Kosuke Jozaki, et al.
Pageof 6