Citations for
1PHLDA2
PHLDA2 gene polymorphisms and risk of HELLP syndrome and severe preeclampsia
Ding L, Blitz MJ, Wing DA, Epstein AJ, Gjessing HK, Wilson ML.
Pregnancy Hypertens. Jan;19:190-194. doi: 10.1016/j.preghy.2020.01.013. Epub 2020 Jan 28. 2020
2CDKN1C, IGF2, PHLDA2
Abundances of placental imprinted genes CDKN1C, PHLDA2 and IGF-2 are related to low birth weight and early catch-up growth in full-term infants born small for gestational age
Xing Y, Liu H, Cui Y, Wang X, Tong X.
PLoS One. Jun 13;14(6):e0218278. doi: 10.1371/journal.pone.0218278 2019
3IGF2, PHLDA2
Placental expression of PHLDA2 and IGF2 in selective intrauterine growth restriction in monozygotic twins.
Chen J, Pan S, Hang L, Zhong M, Yu Y.
Int J Clin Exp Pathol. Feb 1;11(2):876-881. 2018
4PHLDA2
Placental PHLDA2 expression is increased in cases of fetal growth restriction following reduced fetal movements.
Janssen AB, Tunster SJ, Heazell AE, John RM.
BMC Med Genet. Mar 5;17:17. doi: 10.1186/s12881-016-0279-1. 2016
5PHLDA2
The imprinted Phlda2 gene modulates a major endocrine compartment of the placenta to regulate placental demands for maternal resources.
Tunster SJ, Creeth HDJ, John RM.
Dev Biol. Jan 1;409(1):251-260. doi: 10.1016/j.ydbio.2015.10.015. Epub 2015 Oct 23. 2016
6PHLDA2
The significance of elevated placental PHLDA2 in human growth restricted pregnancies.
Jensen AB, Tunster SJ, John RM.
Placenta. Aug;35(8):528-32. doi: 10.1016/j.placenta.2014.04.018. Epub 2014 May 9. 2014
7PHLDA2
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight
Ishida M, Monk D, Duncan AJ, Abu-Amero S, Chong J, Ring SM, Pembrey ME, Hindmarsh PC, Whittaker JC, Stanier P, Moore GE.
Am J Hum Genet. Apr 6;90(4):715-9. doi: 10.1016/j.ajhg.2012.02.021. Epub 2012 Mar 22. 2012
8PHLDA2
Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight.
Apostolidou S, Abu-Amero S, O'Donoghue K, Frost J, Olafsdottir O, Chavele KM, Whittaker JC, Loughna P, Stanier P, Moore GE.
J Mol Med 85(4):379-87. Epub 2006 Dec 16. 2007
9DICER1, PHLDA2
Upregulation of PHLDA2 in Dicer knockdown HEK293 cells.
Tang KF, Wang Y, Wang P, Chen M, Chen Y, Hu HD, Hu P, Wang B, Yang W, Ren H.
Biochim Biophys Acta 1770(5):820-5. Epub 2007 Jan 17. 2007
10CDKN1C, H19, IGF2, KCNQ1OT1, SLC22A18, PHLDA2, BWS
Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development.
Weksberg R, Smith AC, Squire J, Sadowski P.
Hum Mol Genet 12 Spec No 1:R61-8. 2003
11PHLDA3, PHLDA2
Phosphoinositide binding by the pleckstrin homology domains of Ipl and Tih1.
Saxena A, Morozov P, Frank D, Musalo R, Lemmon MA, Skolnik EY, Tycko B.
J Biol Chem 277(51):49935-44. Epub 2002 Oct 8. 2002
12PHLDA2
Retention of imprinting of the human apoptosis-related gene TSSC3 in human brain tumors.
Muller S, van den Boom D, Zirkel D, Koster H, Berthold F, Schwab M, Westphal M, Zumkeller W.
Hum Mol Genet 9(5):757-63. 2000
13PHLDA3, PHLDA2
A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1: tissue-specific expression, chromosomal location, and parental imprinting.
Frank D, Mendelsohn CL, Ciccone E, Svensson K, Ohlsson R, Tycko B.
Mamm Genome 10(12):1150-9. 1999
14PHLDA2
Genomic imprinting of a human apoptosis gene homologue, TSSC3.
Lee MP, Feinberg AP.
Cancer Res 58(5):1052-6. 1998
15PHLDA2
The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis.
Qian N, Frank D, O'Keefe D, Dao D, Zhao L, Yuan L, Wang Q, Keating M, Walsh C, Tycko B.
Hum Mol Genet 6(12):2021-9. 1997
16ASCL2, BWS, CDKN1C, PHLDA2, KCNQ1, TSSC2, CD81, ST5, TSSC1
A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes.
Hu RJ, Lee MP, Connors TD, Johnson LA, Burn TC, Su K, Landes GM, Feinberg AP.
Genomics 46(1):9-17. 1997