| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2002PNAS...99.7490F |
| P356 | DOI | 10.1073/PNAS.122039999 |
| P8608 | Fatcat ID | release_i6dphqti4jgotf3zqixs52zh2i |
| P3181 | OpenCitations bibliographic resource ID | 4061961 |
| P932 | PMC publication ID | 124258 |
| P698 | PubMed publication ID | 12032310 |
| P5875 | ResearchGate publication ID | 11340818 |
| P50 | author | Wolf Reik | Q15994704 |
| Lorraine Clark | Q64858601 | ||
| Anjana Saxena | Q77545530 | ||
| P2093 | author name string | Benjamin Tycko | |
| Chi-Ming Li | |||
| Dale Frank | |||
| Raymond Musalo | |||
| Thomas Ludwig | |||
| Weiwei Fortino | |||
| Wenxian Wang | |||
| P2860 | cites work | A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1: tissue-specific expression, chromosomal location, and parental imprinting | Q22010925 |
| The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis | Q24318274 | ||
| Signal-dependent membrane targeting by pleckstrin homology (PH) domains | Q24532099 | ||
| Genomic imprinting of a human apoptosis gene homologue, TSSC3 | Q28264509 | ||
| Genomic imprinting in mammalian development: a parental tug-of-war | Q28278146 | ||
| Disruption of imprinting caused by deletion of the H19 gene region in mice | Q28287765 | ||
| Essential role of Mash-2 in extraembryonic development | Q28508129 | ||
| Cooperation between the Cdk inhibitors p27(KIP1) and p57(KIP2) in the control of tissue growth and development | Q28512118 | ||
| Defects of the chorioallantoic placenta in mouse RXRalpha null fetuses | Q28587837 | ||
| Placental failure in mice lacking the homeobox gene Dlx3 | Q28591080 | ||
| Esx1 is an X-chromosome-imprinted regulator of placental development and fetal growth | Q28591932 | ||
| Role of insulin-like growth factors in embryonic and postnatal growth | Q29620034 | ||
| Beckwith-Wiedemann syndrome: imprinting in clusters revisited | Q33838090 | ||
| Genetic insights into trophoblast differentiation and placental morphogenesis | Q33954393 | ||
| Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes | Q35197831 | ||
| Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome | Q35209963 | ||
| Isolation and characterization of a novel trophoblast-specific cDNA in the mouse | Q36440030 | ||
| Genomic imprinting and the strange case of the insulin-like growth factor II receptor | Q37165552 | ||
| Genomic imprinting of Mash2, a mouse gene required for trophoblast development | Q38298288 | ||
| The pleckstrin homology and phosphotyrosine binding domains of insulin receptor substrate 1 mediate inhibition of apoptosis by insulin | Q39576638 | ||
| Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. | Q41066237 | ||
| Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice | Q42658164 | ||
| Lack of correlation between placenta and offspring size in mouse interspecific crosses | Q47258782 | ||
| Epigenetic instability in ES cells and cloned mice | Q48882976 | ||
| The sins of the fathers and mothers: genomic imprinting in mammalian development. | Q50532990 | ||
| Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12. | Q52164578 | ||
| Conditional mutagenesis in mice with heat shock promoter-driven cre transgenes. | Q52169941 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Placentomegaly in Cloned Mouse Concepti Caused by Expansion of the Spongiotrophoblast Layer1 | Q61984431 | ||
| Ultrastructural observations on the maturation of the placental labyrinth of the golden hamster (days 10 to 16 of gestation) | Q66964211 | ||
| GENETIC AND ENVIRONMENTAL EFFECTS ON FOETAL AND PLACENTAL GROWTH IN MICE | Q77221220 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Pleckstrin homology like domain, family A, member 2 | Q21986251 |
| P304 | page(s) | 7490-5 | |
| P577 | publication date | 2002-05-28 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Placental overgrowth in mice lacking the imprinted gene Ipl | |
| P478 | volume | 99 |
| Q34285755 | A genomic imprinting defect in mice traced to a single gene |
| Q34364011 | Aberrant growth and pattern formation in Peromyscus hybrid placental development |
| Q36324388 | Abnormal gene expression in regular and aggregated somatic cell nuclear transfer placentas |
| Q64889113 | 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. |
| Q37165888 | Acephalous lamb from an in vitro-produced sheep embryo |
| Q35320849 | Altered imprinted gene expression and methylation patterns in mid-gestation aborted cloned porcine fetuses and placentas |
| Q35754088 | Assisted reproduction causes placental maldevelopment and dysfunction linked to reduced fetal weight in mice. |
| Q33828515 | Autophagy and apoptosis: parent-of-origin genome-dependent mechanisms of cellular self-destruction |
| Q34442748 | BACs as tools for the study of genomic imprinting |
| Q38089794 | Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth |
| Q40462752 | Biallelic expression of Tssc4, Nap1l4, Phlda2 and Osbpl5 in adult cattle. |
| Q33285306 | Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. |
| Q33997704 | Characterisation of marsupial PHLDA2 reveals eutherian specific acquisition of imprinting |
| Q24647126 | Characterization of conserved and nonconserved imprinted genes in swine |
| Q35661043 | Cloning and transgenesis in mammals: implications for xenotransplantation |
| Q34409829 | Co-evolution of X-chromosome inactivation and imprinting in mammals |
| Q34979379 | Comparative anatomy of chromosomal domains with imprinted and non-imprinted allele-specific DNA methylation |
| Q36383223 | DNA methylation in the human placenta and fetal growth (review). |
| Q48798172 | Delta-like 1 homolog in Capra hircus: molecular characteristics, expression pattern and phylogeny |
| Q36166995 | Determinants of trophoblast lineage and cell subtype specification in the mouse placenta |
| Q33889437 | Developmental stage-specific imprinting of IPL in domestic pigs (Sus scrofa). |
| Q47701588 | Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation |
| Q28279818 | Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight |
| Q36311154 | Epigenetic modification is central to genome reprogramming in somatic cell nuclear transfer. |
| Q34734556 | Epigenetic regulation of placental endocrine lineages and complications of pregnancy |
| Q37801493 | Epigenetics and the placenta |
| Q50736910 | Establishment of a new diagnostic method for hydropic villi by using TSSC3 antibody. |
| Q54634225 | Expression and functional analysis of genes deregulated in mouse placental overgrowth models: Car2 and Ncam1. |
| Q59797945 | Fetal growth restriction in a genetic model of sporadic Beckwith-Wiedemann syndrome |
| Q36065882 | Genomic imprinting and epigenetic control of development |
| Q91596236 | Genomic imprinting and its effects on postnatal growth and adult metabolism |
| Q37715275 | Genomic imprinting in development, growth, behavior and stem cells |
| Q21145256 | Genomic imprinting in mammals: emerging themes and established theories |
| Q36436530 | Genomic imprinting in the placenta |
| Q37992688 | Health during pregnancy and beyond: Fetal trophoblast cells as chief co-ordinators of intrauterine growth and reproductive success |
| Q28510837 | Hectd1 is required for development of the junctional zone of the placenta |
| Q36166920 | Igf2 ligand dependency of Pten(+/-) developmental and tumour phenotypes in the mouse |
| Q36436584 | Imprinted genes and their role in human fetal growth. |
| Q36436588 | Imprinted genes in placental growth and obstetric disorders |
| Q90557455 | Imprinted genes influencing the quality of maternal care |
| Q28306944 | Imprinted genes, placental development and fetal growth |
| Q35043723 | Imprinting and disease |
| Q37543706 | Imprinting and extraembryonic tissues-mom takes control |
| Q41208500 | Increased dosage of the imprinted Ascl2 gene restrains two key endocrine lineages of the mouse Placenta |
| Q34241144 | Isolating the role of elevated Phlda2 in asymmetric late fetal growth restriction in mice |
| Q35943539 | Lentivirus-mediated PHLDA2 overexpression inhibits trophoblast proliferation, migration and invasion, and induces apoptosis |
| Q28506802 | Loss of Cited2 affects trophoblast formation and vascularization of the mouse placenta |
| Q35178408 | Loss of inherited genomic imprints in mice leads to severe disruption in placental lipid metabolism |
| Q33932918 | Male CD81 knockout genotype disrupts Mendelian distribution of offspring. |
| Q36510078 | Maternal DNA Methylation Regulates Early Trophoblast Development |
| Q56889416 | Maternal care boosted by paternal imprinting in mammals |
| Q35877833 | Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight |
| Q33789139 | Maternal psychosocial stress during pregnancy and placenta weight: evidence from a national cohort study |
| Q47172204 | Maternally-inherited Grb10 reduces placental size and efficiency |
| Q37391254 | Microarray analysis of prothrombin knockdown in zebrafish |
| Q52585697 | Molecular pathogenesis of pancreatic ductal adenocarcinoma: impact of passenger strand of pre-miR-148a on gene regulation. |
| Q36267711 | Nik-related kinase regulates trophoblast proliferation and placental development by modulating AKT phosphorylation |
| Q57230571 | Origin and characteristics of glycogen cells in the developing murine placenta |
| Q55118944 | PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice. |
| Q24309413 | PH domain-only protein PHLDA3 is a p53-regulated repressor of Akt |
| Q58738098 | PHLDA1, another PHLDA family protein that inhibits Akt |
| Q33767655 | PHLDA3 is a novel tumor suppressor of pancreatic neuroendocrine tumors |
| Q35737547 | Partial Loss of Genomic Imprinting Reveals Important Roles for Kcnq1 and Peg10 Imprinted Domains in Placental Development |
| Q28591355 | Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction |
| Q83004761 | Paternal age as a risk factor for low birthweight |
| Q37484070 | Paternally expressed, imprinted insulin-like growth factor-2 in chorionic villi correlates significantly with birth weight |
| Q33692490 | Phosphatidylinositol 3 kinase modulation of trophoblast cell differentiation |
| Q28206637 | Phosphoinositide binding by the pleckstrin homology domains of Ipl and Tih1 |
| Q59030457 | Piece of cake |
| Q28507167 | Plac1 (placenta-specific 1) is essential for normal placental and embryonic development |
| Q28384560 | Placental DNA hypomethylation in association with particulate air pollution in early life |
| Q30245567 | Placental Origins of Chronic Disease |
| Q47421227 | Pleckstrin homology-like domain family A, member 3 (PHLDA3) deficiency improves islets engraftment through the suppression of hypoxic damage |
| Q28513019 | Protocadherin 12 deficiency alters morphogenesis and transcriptional profile of the placenta |
| Q36436592 | Regulation of growth and metabolism by imprinted genes |
| Q35058363 | Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. |
| Q36852705 | Relationship between placental expression of the imprinted PHLDA2 gene, intrauterine skeletal growth and childhood bone mass |
| Q33575632 | Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome |
| Q24797256 | The Tnfrh1 (Tnfrsf23) gene is weakly imprinted in several organs and expressed at the trophoblast-decidua interface |
| Q36302091 | The cumulative effect of assisted reproduction procedures on placental development and epigenetic perturbations in a mouse model. |
| Q43704012 | The effect of paternal age on fetal birth outcomes |
| Q38848685 | The expression of the imprinted gene pleckstrin homology-like domain family A member 2 in placental tissues of preeclampsia and its effects on the proliferation, migration and invasion of trophoblast cells JEG-3. |
| Q33628787 | The importance of imprinting in the human placenta. |
| Q28593841 | The imprinted Phlda2 gene modulates a major endocrine compartment of the placenta to regulate placental demands for maternal resources |
| Q28512597 | The imprinted Phlda2 gene regulates extraembryonic energy stores |
| Q37278762 | The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann region |
| Q36466639 | The maternally expressed gene Tssc3 regulates the expression of MASH2 transcription factor in mouse trophoblast stem cells through the AKT-Sp1 signaling pathway |
| Q37284688 | The placental imprintome and imprinted gene function in the trophoblast glycogen cell lineage |
| Q28083223 | The role and interaction of imprinted genes in human fetal growth |
| Q28505544 | Transcriptional repressor erf determines extraembryonic ectoderm differentiation |
| Q33523184 | Transcriptomic profiling of bovine IVF embryos revealed candidate genes and pathways involved in early embryonic development |
| Q34705762 | Uncovering gene regulatory networks during mouse fetal germ cell development |
| Q38246516 | What does genetics tell us about imprinting and the placenta connection? |
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