In utero growth restriction is the failure of a fetus to achieve its genetic growth potential during gestation. Elevated expression of the maternally expressed imprinted gene PHLDA2, has been reported in the human placenta of growth restricted pregnancies. A mouse modelling this alteration has been generated and also displays fetal growth restriction suggesting that increased expression of PHLDA2 is not an effect but rather a cause of growth restriction in human pregnancies. Here we review the current data linking PHLDA2 to growth restriction and the data from human and animal model studies suggesting that placental PHLDA2 expression may be responsive to environmental stimuli such as maternal lifestyle. Further investigation is warranted in...
The maternally expressed/paternally silenced genes Phlda2 (a.k.a. Ipl/Tssc3), Slc22a1l, Cdkn1c, Kcnq...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
Genomic imprinting, an epigenetic phenomenon that causes the expression of a small set of genes in a...
Pleckstrin homology-like domain family A member 2 (PHLDA2) is a maternally expressed imprinted gene ...
Background Maternal perception of reduced fetal movements (RFM) is associated with increased risk...
Pleckstrin homology-like domain family A member 2 (PHLDA2) is a maternally expressed imprinted gene ...
Pleckstrin homology-like domain family A member 2 (PHLDA2) is a maternally expressed imprinted gene ...
The identification of genes that regulate fetal growth will help establish the reasons for intrauter...
Alterations in expression of the imprinted gene PHLDA2 are linked to low birth weight in both humans...
Alterations in expression of the imprinted gene PHLDA2 are linked to low birth weight in both humans...
AbstractAlterations in expression of the imprinted gene PHLDA2 are linked to low birth weight in bot...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
The maternally expressed/paternally silenced genes Phlda2 (a.k.a. Ipl/Tssc3), Slc22a1l, Cdkn1c, Kcnq...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
Genomic imprinting, an epigenetic phenomenon that causes the expression of a small set of genes in a...
Pleckstrin homology-like domain family A member 2 (PHLDA2) is a maternally expressed imprinted gene ...
Background Maternal perception of reduced fetal movements (RFM) is associated with increased risk...
Pleckstrin homology-like domain family A member 2 (PHLDA2) is a maternally expressed imprinted gene ...
Pleckstrin homology-like domain family A member 2 (PHLDA2) is a maternally expressed imprinted gene ...
The identification of genes that regulate fetal growth will help establish the reasons for intrauter...
Alterations in expression of the imprinted gene PHLDA2 are linked to low birth weight in both humans...
Alterations in expression of the imprinted gene PHLDA2 are linked to low birth weight in both humans...
AbstractAlterations in expression of the imprinted gene PHLDA2 are linked to low birth weight in bot...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
The maternally expressed/paternally silenced genes Phlda2 (a.k.a. Ipl/Tssc3), Slc22a1l, Cdkn1c, Kcnq...
A small fraction of mammalian genes exhibit parent-of-origin specific monoallelic expression. They a...
Genomic imprinting, an epigenetic phenomenon that causes the expression of a small set of genes in a...