| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/HMG/6.12.2021 |
| P698 | PubMed publication ID | 9328465 |
| P50 | author | Colum Walsh | Q62740262 |
| P2093 | author name string | Q Wang | |
| L Zhao | |||
| D Frank | |||
| B Tycko | |||
| L Yuan | |||
| N Qian | |||
| D Dao | |||
| D O'Keefe | |||
| M Keating | |||
| P2860 | cites work | Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting | Q48084682 |
| Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies. | Q51046179 | ||
| Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. | Q52196602 | ||
| Relaxation of imprinted genes in human cancer. | Q52545355 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome | Q70765937 | ||
| Imprinted genes have few and small introns | Q70972792 | ||
| Parental genomic imprinting of the human IGF2 gene | Q72222239 | ||
| Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour | Q72703028 | ||
| Epigenetic lesions at the H19 locus in Wilms' tumour patients | Q72703033 | ||
| Parental imprinting of the mouse H19 gene | Q22122365 | ||
| Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias | Q24311437 | ||
| A novel L23-related gene 40 kb downstream of the imprinted H19 gene is biallelically expressed in mid-fetal and adult human tissues | Q24314602 | ||
| Monoallelic expression of the human H19 gene | Q28184725 | ||
| 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 | ||
| A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues | Q28297029 | ||
| Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. | Q34314269 | ||
| The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts. | Q34428055 | ||
| Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor | Q34572727 | ||
| DNA methylation: evolution of a bacterial immune function into a regulator of gene expression and genome structure in higher eukaryotes | Q37581127 | ||
| Sex, maps, and imprinting | Q37623659 | ||
| Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse | Q38291049 | ||
| Genomic imprinting of Mash2, a mouse gene required for trophoblast development | Q38298288 | ||
| Polymorphisms in the human apolipoprotein-J/clusterin gene: ethnic variation and distribution in Alzheimer's disease | Q38352857 | ||
| Parental imprinting of autosomal mammalian genes | Q40672445 | ||
| Creation of genomic methylation patterns | Q40986760 | ||
| Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors | Q41178952 | ||
| Allele-specific replication timing of imprinted gene regions | Q41541045 | ||
| An extended region of biallelic gene expression and rodent-human synteny downstream of the imprinted H19 gene on chromosome 11p15.5. | Q42646441 | ||
| Parental imprinting of the Mas protooncogene in mouse | Q46725382 | ||
| Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M. | Q48060772 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | apoptotic process | Q14599311 |
| Pleckstrin homology like domain family A member 2 | Q21122517 | ||
| P304 | page(s) | 2021-2029 | |
| P577 | publication date | 1997-11-01 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis | |
| P478 | volume | 6 |
| Q22009166 | A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region |
| Q35096694 | An extended domain of Kcnq1ot1 silencing revealed by an imprinted fluorescent reporter |
| Q31147226 | Antisense transcripts with FANTOM2 clone set and their implications for gene regulation |
| 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. |
| Q47818769 | C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5. |
| 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 |
| Q35077074 | Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation. |
| Q34241318 | Death the Fas way: regulation and pathophysiology of CD95 and its ligand |
| Q33889437 | Developmental stage-specific imprinting of IPL in domestic pigs (Sus scrofa). |
| Q42658164 | Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice |
| Q35806688 | Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region |
| Q36421376 | Epigenetic and phenotypic consequences of a truncation disrupting the imprinted domain on distal mouse chromosome 7. |
| Q34734556 | Epigenetic regulation of placental endocrine lineages and complications of pregnancy |
| Q36499262 | Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine |
| Q28505485 | Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome |
| Q36976941 | Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas |
| Q28289659 | Genes affecting the cell cycle, growth, maintenance, and drug sensitivity are preferentially regulated by anti-HER2 antibody through phosphatidylinositol 3-kinase-AKT signaling |
| Q33875930 | Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways |
| Q39573980 | Genome-wide assessment of imprinted expression in human cells |
| Q77809556 | Genomic imprinting and cancer |
| Q33721384 | Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome |
| Q35037387 | Genomic imprinting: could the chromatin structure be the driving force? |
| Q33541538 | Genomic imprinting: implications for human disease |
| Q35814612 | High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes |
| Q74133538 | Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios |
| Q42661390 | Hypoxia influences expression profile of Pleckstrin homology-like domain, family A, member 2 in Indian catfish, Clarias batrachus (Linnaeus, 1758): a new candidate gene for hypoxia tolerance in fish |
| Q39741184 | Identification of Hodgkin and Reed-Sternberg cell-specific genes by gene expression profiling |
| Q51803860 | Identification of a putative transcriptome signature common to neuroblastoma and neural crest cells. |
| Q37543706 | Imprinting and extraembryonic tissues-mom takes control |
| Q24291248 | Inhibition of protein synthesis by the T cell receptor-inducible human TDAG51 gene product |
| Q41759014 | Insulin-like growth factor 2 and overgrowth: molecular biology and clinical implications |
| 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 |
| Q24684284 | Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting |
| 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 |
| Q33774256 | Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster |
| Q37445958 | New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain |
| Q52624229 | PHLDA2 is an imprinted gene in cattle. |
| Q36648088 | Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction |
| 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 |
| Q24530568 | Placental overgrowth in mice lacking the imprinted gene Ipl |
| Q39709920 | Quantitative proteomics analysis reveals molecular networks regulated by epidermal growth factor receptor level in head and neck cancer. |
| Q28589840 | Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1 |
| Q34303375 | Regulation of T-cell death-associated gene 51 (TDAG51) expression in human T-cells. |
| 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 |
| Q36748462 | Structure and sequence of the human fast skeletal troponin T (TNNT3) gene: insight into the evolution of the gene and the origin of the developmentally regulated isoforms. |
| Q48000452 | Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. |
| Q24746223 | TDAG51 is not essential for Fas/CD95 regulation and apoptosis in vivo |
| Q45130742 | TIMP1 and SERPIN-A overexpression and TFF3 and CRABP1 underexpression as biomarkers for papillary thyroid carcinoma. |
| Q39345500 | TSSC3 overexpression reduces stemness and induces apoptosis of osteosarcoma tumor-initiating cells |
| 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. |
| Q29617273 | The history of cancer epigenetics |
| 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 |
| Q36466639 | The maternally expressed gene Tssc3 regulates the expression of MASH2 transcription factor in mouse trophoblast stem cells through the AKT-Sp1 signaling pathway |
| Q27007861 | The origin and evolution of genomic imprinting and viviparity in mammals |
| Q37284688 | The placental imprintome and imprinted gene function in the trophoblast glycogen cell lineage |
| Q81512924 | Thioredoxin-interacting protein (txnip) is a glucocorticoid-regulated primary response gene involved in mediating glucocorticoid-induced apoptosis |
| Q58789746 | Transcription factor ASCL2 is required for development of the glycogen trophoblast cell lineage |
| Q24681580 | Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples |
| Q33523184 | Transcriptomic profiling of bovine IVF embryos revealed candidate genes and pathways involved in early embryonic development |
| Q36392021 | Two distinct mechanisms of silencing by the KvDMR1 imprinting control region |
| Q28138506 | Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting |
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