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W Reik

Showing results (61-70 of 100) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 1, 1995
Cbx-rs2 (M31), a mouse homolog of the Drosophila Heterochromatin protein 1 gene, maps to distal chromosome 11 and is nonallelic to OmR Feil, P A Baldacci, E Tarttelin, et al.
Cloning and Stem Cells|October 26, 2002
Nucleus replacement in Mammalian oocytesJ Fulka, P Loi, Helena Fulka, et al.
Human Molecular Genetics|December 1, 1995
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domainW Reik, K W Brown, H Schneid, et al.
Development (Cambridge, England)|November 1, 1993
Adult phenotype in the mouse can be affected by epigenetic events in the early embryoW Reik, I Römer, S C Barton, et al.
Human Molecular Genetics|August 1, 1994
Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndromeW Reik, K W Brown, R E Slatter, et al.
The EMBO Journal|March 1, 1996
Instability of long inverted repeats within mouse transgenesA Collick, J Drew, J Penberth, et al.
Human Molecular Genetics|November 7, 2000
Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprintingS Engemann, M Strödicke, M Paulsen, et al.
Nature|June 30, 1988
Transgenes as probes for active chromosomal domains in mouse developmentN D Allen, D G Cran, S C Barton, et al.
Cold Spring Harbor Symposia on Quantitative Biology|August 25, 2005
Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clustersW Reik, A Murrell, A Lewis, et al.
Development (Cambridge, England)|May 19, 1998
Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypesW Dean, L Bowden, A Aitchison, et al.
Pageof 10

Showing results (61-70 of 100) with videos related to

Sort By:
Pageof 10
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 1, 1995
Cbx-rs2 (M31), a mouse homolog of the Drosophila Heterochromatin protein 1 gene, maps to distal chromosome 11 and is nonallelic to OmR Feil, P A Baldacci, E Tarttelin, et al.
Cloning and Stem Cells|October 26, 2002
Nucleus replacement in Mammalian oocytesJ Fulka, P Loi, Helena Fulka, et al.
Human Molecular Genetics|December 1, 1995
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domainW Reik, K W Brown, H Schneid, et al.
Development (Cambridge, England)|November 1, 1993
Adult phenotype in the mouse can be affected by epigenetic events in the early embryoW Reik, I Römer, S C Barton, et al.
Human Molecular Genetics|August 1, 1994
Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndromeW Reik, K W Brown, R E Slatter, et al.
The EMBO Journal|March 1, 1996
Instability of long inverted repeats within mouse transgenesA Collick, J Drew, J Penberth, et al.
Human Molecular Genetics|November 7, 2000
Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprintingS Engemann, M Strödicke, M Paulsen, et al.
Nature|June 30, 1988
Transgenes as probes for active chromosomal domains in mouse developmentN D Allen, D G Cran, S C Barton, et al.
Cold Spring Harbor Symposia on Quantitative Biology|August 25, 2005
Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clustersW Reik, A Murrell, A Lewis, et al.
Development (Cambridge, England)|May 19, 1998
Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypesW Dean, L Bowden, A Aitchison, et al.
Pageof 10