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Emma Whitelaw

Showing results (51-60 of 65) with videos related to

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BMC Biology|April 11, 2015
The recently identified modifier of murine metastable epialleles, Rearranged L-Myc Fusion, is involved in maintaining epigenetic marks at CpG island shores and enhancersSarah K Harten, Harald Oey, Lauren M Bourke, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 25, 2011
A missense mutation in the transcription factor Foxo3a causes teratomas and oocyte abnormalities in miceN A Youngson, N Vickaryous, A van der Horst, et al.
Genomics|December 3, 2014
Identification of novel hypomorphic and null mutations in Klf1 derived from a genetic screen for modifiers of α-globin transgene variegationAnabel Sorolla, Michael R Tallack, Harald Oey, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2013
Reintroducing domesticated wild mice to sociality induces adaptive transgenerational effects on MUP expressionAdam C Nelson, Joseph W Cauceglia, Seth D Merkley, et al.
Blood Cells, Molecules & Diseases|October 9, 2012
ENU mutagenesis identifies the first mouse mutants reproducing human β-thalassemia at the genomic levelFiona C Brown, Nicholas Scott, Gerhard Rank, et al.
Nature Genetics|April 24, 2007
Modifiers of epigenetic reprogramming show paternal effects in the mouseSuyinn Chong, Nicola Vickaryous, Alyson Ashe, et al.
Nature Genetics|April 22, 2008
SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivationMarnie E Blewitt, Anne-Valerie Gendrel, Zhenyi Pang, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 3, 2013
No evidence for cumulative effects in a Dnmt3b hypomorph across multiple generationsNeil A Youngson, Trevor Epp, Amity R Roberts, et al.
Plos One|April 13, 2011
DNMT3L is a regulator of X chromosome compaction and post-meiotic gene transcriptionNatasha M Zamudio, Hamish S Scott, Katja Wolski, et al.
Human Molecular Genetics|January 10, 2012
Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathiesAlyson Ashe, Natalie C Butterfield, Liam Town, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
BMC Biology|April 11, 2015
The recently identified modifier of murine metastable epialleles, Rearranged L-Myc Fusion, is involved in maintaining epigenetic marks at CpG island shores and enhancersSarah K Harten, Harald Oey, Lauren M Bourke, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 25, 2011
A missense mutation in the transcription factor Foxo3a causes teratomas and oocyte abnormalities in miceN A Youngson, N Vickaryous, A van der Horst, et al.
Genomics|December 3, 2014
Identification of novel hypomorphic and null mutations in Klf1 derived from a genetic screen for modifiers of α-globin transgene variegationAnabel Sorolla, Michael R Tallack, Harald Oey, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2013
Reintroducing domesticated wild mice to sociality induces adaptive transgenerational effects on MUP expressionAdam C Nelson, Joseph W Cauceglia, Seth D Merkley, et al.
Blood Cells, Molecules & Diseases|October 9, 2012
ENU mutagenesis identifies the first mouse mutants reproducing human β-thalassemia at the genomic levelFiona C Brown, Nicholas Scott, Gerhard Rank, et al.
Nature Genetics|April 24, 2007
Modifiers of epigenetic reprogramming show paternal effects in the mouseSuyinn Chong, Nicola Vickaryous, Alyson Ashe, et al.
Nature Genetics|April 22, 2008
SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivationMarnie E Blewitt, Anne-Valerie Gendrel, Zhenyi Pang, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 3, 2013
No evidence for cumulative effects in a Dnmt3b hypomorph across multiple generationsNeil A Youngson, Trevor Epp, Amity R Roberts, et al.
Plos One|April 13, 2011
DNMT3L is a regulator of X chromosome compaction and post-meiotic gene transcriptionNatasha M Zamudio, Hamish S Scott, Katja Wolski, et al.
Human Molecular Genetics|January 10, 2012
Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathiesAlyson Ashe, Natalie C Butterfield, Liam Town, et al.
Pageof 7