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W Reik

Showing results (81-90 of 100) with videos related to

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The EMBO Journal|July 4, 2001
An upstream repressor element plays a role in Igf2 imprintingS Eden, M Constancia, T Hashimshony, et al.
Human Molecular Genetics|September 1, 1997
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndromeJ A Joyce, W K Lam, D J Catchpoole, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 18, 1997
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and transT Forné, J Oswald, W Dean, et al.
Mechanisms of Development|May 4, 2001
Epigenetic targeting in the mouse zygote marks DNA for later methylation: a mechanism for maternal effects in developmentB Pickard, W Dean, S Engemann, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|February 27, 1993
The inheritance of germline-specific epigenetic modifications during developmentM A Surani, H Sasaki, A C Ferguson-Smith, et al.
Journal of Medical Genetics|May 1, 1997
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndromeD Catchpoole, W W Lam, D Valler, et al.
Placenta|March 1, 2006
Regulation of placental efficiency for nutrient transport by imprinted genesE Angiolini, A Fowden, P Coan, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|October 31, 1996
Nucleotide sequence of a 28-kb mouse genomic region comprising the imprinted Igf2 geneH Sasaki, K Shimozaki, M Zubair, et al.
The International Journal of Developmental Biology|January 1, 1996
Regulation of Igf2 imprinting in development and diseaseW Reik, L Bowden, M Constancia, et al.
Journal of Medical Genetics|April 25, 2000
Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndromeD Catchpoole, A V Smallwood, J A Joyce, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
The EMBO Journal|July 4, 2001
An upstream repressor element plays a role in Igf2 imprintingS Eden, M Constancia, T Hashimshony, et al.
Human Molecular Genetics|September 1, 1997
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndromeJ A Joyce, W K Lam, D J Catchpoole, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 18, 1997
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and transT Forné, J Oswald, W Dean, et al.
Mechanisms of Development|May 4, 2001
Epigenetic targeting in the mouse zygote marks DNA for later methylation: a mechanism for maternal effects in developmentB Pickard, W Dean, S Engemann, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|February 27, 1993
The inheritance of germline-specific epigenetic modifications during developmentM A Surani, H Sasaki, A C Ferguson-Smith, et al.
Journal of Medical Genetics|May 1, 1997
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndromeD Catchpoole, W W Lam, D Valler, et al.
Placenta|March 1, 2006
Regulation of placental efficiency for nutrient transport by imprinted genesE Angiolini, A Fowden, P Coan, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|October 31, 1996
Nucleotide sequence of a 28-kb mouse genomic region comprising the imprinted Igf2 geneH Sasaki, K Shimozaki, M Zubair, et al.
The International Journal of Developmental Biology|January 1, 1996
Regulation of Igf2 imprinting in development and diseaseW Reik, L Bowden, M Constancia, et al.
Journal of Medical Genetics|April 25, 2000
Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndromeD Catchpoole, A V Smallwood, J A Joyce, et al.
Pageof 10