The Imprinted Phlda2 Gene Regulates Extraembryonic Energy Stores

Por Tunster, S. J., Tycko, B., John, R. M.
Publicado em 2010

BACs as Tools for the Study of Genomic Imprinting

Por Tunster, S. J., Van De Pette, M., John, R. M.
Publicado em 2011

Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome

Por Tunster, Simon J., Van de Pette, Mathew, John, Rosalind M.
Publicado em 2011

Isolating the role of elevated Phlda2 in asymmetric late fetal growth restriction in mice

Por Tunster, Simon J., Van De Pette, Mathew, John, Rosalind M.
Publicado em 2014

The imprinted Phlda2 gene modulates a major endocrine compartment of the placenta to regulate placental demands for maternal resources

Por Tunster, S.J., Creeth, H.D.J., John, R.M.
Publicado no Dev Biol (2016)

Placental PHLDA2 expression is increased in cases of fetal growth restriction following reduced fetal movements

Por Janssen, Anna Bugge, Tunster, Simon J., Heazell, Alexander E. P., John, Rosalind M.
Publicado no BMC Med Genet (2016)

Increased dosage of the imprinted Ascl2 gene restrains two key endocrine lineages of the mouse Placenta

Por Tunster, S.J., McNamara, G.I., Creeth, H.D.J., John, R.M.
Publicado no Dev Biol (2016)

Cdkn1c (p57(Kip2)) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7

Por Andrews, Stuart C, Wood, Michelle D, Tunster, Simon J, Barton, Sheila C, Surani, M Azim, John, Rosalind M
Publicado em 2007

Placental expression of imprinted genes varies with sampling site and mode of delivery

Por Janssen, A.B., Tunster, S.J., Savory, N., Holmes, A., Beasley, J., Parveen, S.A.R., Penketh, R.J.A., John, R.M.
Publicado no Placenta (2015)

Maternal prenatal depression is associated with decreased placental expression of the imprinted gene PEG3

Por Janssen, A. B., Capron, L. E., O'Donnell, K., Tunster, S. J., Ramchandani, P. G., Heazell, A. E. P., Glover, V., John, R. M.
Publicado no Psychol Med (2016)

Cdkn1c Boosts the Development of Brown Adipose Tissue in a Murine Model of Silver Russell Syndrome

Por Van De Pette, Matthew, Tunster, Simon J., McNamara, Grainne I., Shelkovnikova, Tatyana, Millership, Steven, Benson, Lindsay, Peirson, Stuart, Christian, Mark, Vidal-Puig, Antonio, John, Rosalind M.
Publicado no PLoS Genet (2016)