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

Ohsuke Migita

Showing results (1-10 of 43) with videos related to

Pageof 5
Sort By:
Brain & Development|September 30, 2018
Reading disability due to an ocular motor disorder: A case of an adolescent girl with a previous diagnosis of dyslexiaTsunehiko Kurokami, Tatsuya Koeda, Ohsuke Migita, et al.
American Journal of Medical Genetics. Part A|March 17, 2009
Two distinctive classic genetic syndromes, 22q11.2 deletion syndrome and Angelman syndrome, occurring within the same familyRika Kosaki, Ohsuke Migita, Takao Takahashi, et al.
Clinical and Experimental Nephrology|May 19, 2025
The utility of urine specific gravity in combination with urinary qualitative protein testing for detecting abnormal proteinuriaMikako Hisamichi, Ohsuke Migita, Sachihiko Nobuoka, et al.
Reproductive Biomedicine Online|March 31, 2019
Analysis of chromosome microstructures in products of conception associated with recurrent miscarriageTaisuke Sato, Ohsuke Migita, Hiroka Hata, et al.
Human Genome Variation|May 20, 2022
A novel TP63 variant in a patient with ankyloblepharon-ectodermal defect-cleft lip/palate syndrome and Rapp-Hodgkin syndrome-like ectodermal dysplasiaAsuka Hori, Ohsuke Migita, Nobutaka Isogawa, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 27, 2021
Deleterious fibronectin type III-related gene variants may induce a spinal extradural arachnoid cyst: an exome sequencing study of identical twin casesTaijun Hana, Hideki Ogiwara, Ohsuke Migita, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|June 15, 2006
Determination of structure and transcriptional regulation of CYSLTR1 and an association study with asthma and rhinitisJian Zhang, Ohsuke Migita, Minori Koga, et al.
Human Genome Variation|October 30, 2021
A novel TAB2 mutation detected in a putative case of frontometaphyseal dysplasiaAsuka Hori, Ohsuke Migita, Rika Kawaguchi-Kawata, et al.
European Journal of Medical Genetics|September 14, 2019
A successful treatment of tadalafil in incontinentia pigmenti with pulmonary hypertensionMasanori Mizuno, Kentaro Aso, Yoshimitsu Tsuzuki, et al.
Human Mutation|October 23, 2012
Mechanisms of formation of structural variation in a fully sequenced human genomeAndy Wing Chun Pang, Ohsuke Migita, Jeffrey R Macdonald, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Brain & Development|September 30, 2018
Reading disability due to an ocular motor disorder: A case of an adolescent girl with a previous diagnosis of dyslexiaTsunehiko Kurokami, Tatsuya Koeda, Ohsuke Migita, et al.
American Journal of Medical Genetics. Part A|March 17, 2009
Two distinctive classic genetic syndromes, 22q11.2 deletion syndrome and Angelman syndrome, occurring within the same familyRika Kosaki, Ohsuke Migita, Takao Takahashi, et al.
Clinical and Experimental Nephrology|May 19, 2025
The utility of urine specific gravity in combination with urinary qualitative protein testing for detecting abnormal proteinuriaMikako Hisamichi, Ohsuke Migita, Sachihiko Nobuoka, et al.
Reproductive Biomedicine Online|March 31, 2019
Analysis of chromosome microstructures in products of conception associated with recurrent miscarriageTaisuke Sato, Ohsuke Migita, Hiroka Hata, et al.
Human Genome Variation|May 20, 2022
A novel TP63 variant in a patient with ankyloblepharon-ectodermal defect-cleft lip/palate syndrome and Rapp-Hodgkin syndrome-like ectodermal dysplasiaAsuka Hori, Ohsuke Migita, Nobutaka Isogawa, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 27, 2021
Deleterious fibronectin type III-related gene variants may induce a spinal extradural arachnoid cyst: an exome sequencing study of identical twin casesTaijun Hana, Hideki Ogiwara, Ohsuke Migita, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|June 15, 2006
Determination of structure and transcriptional regulation of CYSLTR1 and an association study with asthma and rhinitisJian Zhang, Ohsuke Migita, Minori Koga, et al.
Human Genome Variation|October 30, 2021
A novel TAB2 mutation detected in a putative case of frontometaphyseal dysplasiaAsuka Hori, Ohsuke Migita, Rika Kawaguchi-Kawata, et al.
European Journal of Medical Genetics|September 14, 2019
A successful treatment of tadalafil in incontinentia pigmenti with pulmonary hypertensionMasanori Mizuno, Kentaro Aso, Yoshimitsu Tsuzuki, et al.
Human Mutation|October 23, 2012
Mechanisms of formation of structural variation in a fully sequenced human genomeAndy Wing Chun Pang, Ohsuke Migita, Jeffrey R Macdonald, et al.
Pageof 5