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

I Hatada

Showing results (31-40 of 36) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 36 results.
Journal of Medical Genetics|July 29, 1999
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.
Nature Genetics|October 1, 1996
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndromeI Hatada, H Ohashi, Y Fukushima, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 1998
Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samplesC Schwienbacher, S Sabbioni, M Campi, et al.
Oncogene|January 13, 2006
Genome-wide profiling of promoter methylation in humanI Hatada, M Fukasawa, M Kimura, et al.
Human Genetics|October 28, 1997
New p57KIP2 mutations in Beckwith-Wiedemann syndromeI Hatada, A Nabetani, H Morisaki, et al.
Human Molecular Genetics|June 1, 1996
Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumorsI Hatada, J Inazawa, T Abe, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Journal of Medical Genetics|July 29, 1999
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.
Nature Genetics|October 1, 1996
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndromeI Hatada, H Ohashi, Y Fukushima, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 1998
Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samplesC Schwienbacher, S Sabbioni, M Campi, et al.
Oncogene|January 13, 2006
Genome-wide profiling of promoter methylation in humanI Hatada, M Fukasawa, M Kimura, et al.
Human Genetics|October 28, 1997
New p57KIP2 mutations in Beckwith-Wiedemann syndromeI Hatada, A Nabetani, H Morisaki, et al.
Human Molecular Genetics|June 1, 1996
Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumorsI Hatada, J Inazawa, T Abe, et al.
Pageof 4