Search research articles
Contact Us
Filters
Showing results (61-70 of 100) with videos related to
Page
of 10
Sort By:
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 Om
R Feil, P A Baldacci, E Tarttelin, et al.
Cloning and Stem Cells
|
October 26, 2002
Nucleus replacement in Mammalian oocytes
J 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 domain
W 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 embryo
W Reik, I Römer, S C Barton, et al.
Human Molecular Genetics
|
August 1, 1994
Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome
W Reik, K W Brown, R E Slatter, et al.
The EMBO Journal
|
March 1, 1996
Instability of long inverted repeats within mouse transgenes
A 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 imprinting
S Engemann, M Strödicke, M Paulsen, et al.
Nature
|
June 30, 1988
Transgenes as probes for active chromosomal domains in mouse development
N 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 clusters
W 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 phenotypes
W Dean, L Bowden, A Aitchison, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 100) with videos related to
Sort By:
Page
of 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 Om
R Feil, P A Baldacci, E Tarttelin, et al.
Cloning and Stem Cells
|
October 26, 2002
Nucleus replacement in Mammalian oocytes
J 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 domain
W 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 embryo
W Reik, I Römer, S C Barton, et al.
Human Molecular Genetics
|
August 1, 1994
Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome
W Reik, K W Brown, R E Slatter, et al.
The EMBO Journal
|
March 1, 1996
Instability of long inverted repeats within mouse transgenes
A 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 imprinting
S Engemann, M Strödicke, M Paulsen, et al.
Nature
|
June 30, 1988
Transgenes as probes for active chromosomal domains in mouse development
N 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 clusters
W 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 phenotypes
W Dean, L Bowden, A Aitchison, et al.
Page
of 10