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

W Reik

Showing results (71-80 of 100) with videos related to

Pageof 10
Sort By:
The International Journal of Developmental Biology|April 13, 2000
Igf2 imprinting in development and diseaseW Reik, M Constancia, W Dean, et al.
Endocrinology|April 28, 1999
Overexpression of insulin-like growth factor-II in transgenic mice is associated with pancreatic islet cell hyperplasiaJ Petrik, J M Pell, E Arany, et al.
Current Biology : CB|May 10, 2000
Active demethylation of the paternal genome in the mouse zygoteJ Oswald, S Engemann, N Lane, et al.
Human Molecular Genetics|December 1, 1996
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathwayK W Brown, A J Villar, W Bickmore, et al.
Toxicology Letters|April 27, 2001
Genomic imprinting and cancer; new paradigms in the genetics of neoplasiaP N Schofield, J A Joyce, W K Lam, et al.
Genome Research|March 7, 2001
A dominant modifier of transgene methylation is mapped by QTL analysis to mouse chromosome 13P Valenza-Schaerly, B Pickard, J Walter, et al.
Human Molecular Genetics|August 1, 2000
Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouseM Paulsen, O El-Maarri, S Engemann, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|January 30, 1990
Developmental consequences of imprinting of parental chromosomes by DNA methylationM A Surani, N D Allen, S C Barton, et al.
Genes & Development|October 1, 1992
Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) geneH Sasaki, P A Jones, J R Chaillet, et al.
Journal of Medical Genetics|January 11, 2000
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndromeJ R Engel, A Smallwood, A Harper, et al.
Pageof 10

Showing results (71-80 of 100) with videos related to

Sort By:
Pageof 10
The International Journal of Developmental Biology|April 13, 2000
Igf2 imprinting in development and diseaseW Reik, M Constancia, W Dean, et al.
Endocrinology|April 28, 1999
Overexpression of insulin-like growth factor-II in transgenic mice is associated with pancreatic islet cell hyperplasiaJ Petrik, J M Pell, E Arany, et al.
Current Biology : CB|May 10, 2000
Active demethylation of the paternal genome in the mouse zygoteJ Oswald, S Engemann, N Lane, et al.
Human Molecular Genetics|December 1, 1996
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathwayK W Brown, A J Villar, W Bickmore, et al.
Toxicology Letters|April 27, 2001
Genomic imprinting and cancer; new paradigms in the genetics of neoplasiaP N Schofield, J A Joyce, W K Lam, et al.
Genome Research|March 7, 2001
A dominant modifier of transgene methylation is mapped by QTL analysis to mouse chromosome 13P Valenza-Schaerly, B Pickard, J Walter, et al.
Human Molecular Genetics|August 1, 2000
Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouseM Paulsen, O El-Maarri, S Engemann, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|January 30, 1990
Developmental consequences of imprinting of parental chromosomes by DNA methylationM A Surani, N D Allen, S C Barton, et al.
Genes & Development|October 1, 1992
Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) geneH Sasaki, P A Jones, J R Chaillet, et al.
Journal of Medical Genetics|January 11, 2000
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndromeJ R Engel, A Smallwood, A Harper, et al.
Pageof 10