| scholarly article | Q13442814 |
| P2093 | author name string | Matteson PG | |
| Tilghman SM | |||
| Schmidt JV | |||
| Jones BK | |||
| Guan XJ | |||
| P2860 | cites work | Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation. | Q52174393 |
| Imprinted expression of the Igf2r gene depends on an intronic CpG island. | Q52192434 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Mouse fetal antigen 1 (mFA1), the circulating gene product of mdlk, pref-1 and SCP-1: isolation, characterization and biology | Q71707989 | ||
| Genetics of mouse growth | Q77684683 | ||
| Protein structure of fetal antigen 1 (FA1). A novel circulating human epidermal-growth-factor-like protein expressed in neuroendocrine tumors and its relation to the gene products of dlk and pG2 | Q24322471 | ||
| dlk, a putative mammalian homeotic gene differentially expressed in small cell lung carcinoma and neuroendocrine tumor cell line | Q28115743 | ||
| Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction | Q28131789 | ||
| The protein CTCF is required for the enhancer blocking activity of vertebrate insulators | Q28142800 | ||
| Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene | Q28145754 | ||
| CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus | Q28145756 | ||
| Pref-1, a protein containing EGF-like repeats, inhibits adipocyte differentiation | Q28269495 | ||
| Studies on the isolation, structural analysis and tissue localization of fetal antigen 1 and its relation to a human adrenal-specific cDNA, pG2 | Q28269567 | ||
| Disruption of imprinting caused by deletion of the H19 gene region in mice | Q28287765 | ||
| An enhancer deletion affects both H19 and Igf2 expression | Q28288348 | ||
| The mouse Gtl2 gene is differentially expressed during embryonic development, encodes multiple alternatively spliced transcripts, and may act as an RNA | Q28594499 | ||
| Role for DNA methylation in genomic imprinting | Q29618669 | ||
| Maternal uniparental disomy for chromosome 14 | Q33597323 | ||
| Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster | Q33774256 | ||
| Competition--a common motif for the imprinting mechanism? | Q33887777 | ||
| Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q. | Q33897694 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier. | Q35196696 | ||
| Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. | Q35211749 | ||
| Hematopoietic activity of a stromal cell transmembrane protein containing epidermal growth factor-like repeat motifs | Q36108691 | ||
| Screening for imprinted genes by allelic message display: identification of a paternally expressed gene impact on mouse chromosome 18 | Q36561256 | ||
| Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern | Q36585144 | ||
| Growth hormone and prolactin stimulate the expression of rat preadipocyte factor-1/delta-like protein in pancreatic islets: molecular cloning and expression pattern during development and growth of the endocrine pancreas. | Q36879578 | ||
| Modulated expression of the epidermal growth factor-like homeotic protein dlk influences stromal-cell-pre-B-cell interactions, stromal cell adipogenesis, and pre-B-cell interleukin-7 requirements | Q39575878 | ||
| Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis | Q40413201 | ||
| Genomic imprinting is disrupted in interspecific Peromyscus hybrids | Q48003531 | ||
| The sins of the fathers and mothers: genomic imprinting in mammalian development. | Q50532990 | ||
| Gtl2lacZ, an insertional mutation on mouse chromosome 12 with parental origin-dependent phenotype. | Q50994637 | ||
| P433 | issue | 16 | |
| P304 | page(s) | 1997-2002 | |
| P577 | publication date | 2000-08-01 | |
| P1433 | published in | Genes & Development | Q1524533 |
| P1476 | title | The Dlk1 and Gtl2 genes are linked and reciprocally imprinted | |
| P478 | volume | 14 |
| Q37496222 | A large imprinted microRNA gene cluster at the mouse Dlk1-Gtl2 domain |
| Q24322379 | A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints |
| Q35221526 | A survey for novel imprinted genes in the mouse placenta by mRNA-seq |
| Q34022185 | Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells |
| Q28585506 | Activation of paternally expressed genes and perinatal death caused by deletion of the Gtl2 gene |
| Q35645900 | Allele-specific histone modifications regulate expression of the Dlk1-Gtl2 imprinted domain |
| Q48110067 | Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32. |
| Q37291298 | An emerging role for long non-coding RNA dysregulation in neurological disorders |
| Q33712659 | Analysis of DNA methylation acquisition at the imprinted Dlk1 locus reveals asymmetry at CpG dyads |
| Q34277546 | Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting |
| Q35024139 | Astrocyte elevated gene-1 and c-Myc cooperate to promote hepatocarcinogenesis in mice |
| Q33405733 | At least ten genes define the imprinted Dlk1-Dio3 cluster on mouse chromosome 12qF1 |
| Q34442748 | BACs as tools for the study of genomic imprinting |
| Q48711067 | BEGAIN: a novel imprinted gene that generates paternally expressed transcripts in a tissue- and promoter-specific manner in sheep |
| Q33288477 | Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets |
| Q57908927 | Comparative phylogenetic analysis reveals multiple non-imprinted isoforms of opossum Dlk1 |
| Q40415818 | Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region. |
| Q49325078 | Comprehensive analysis of mRNA-lncRNA co-expression profile revealing crucial role of imprinted gene cluster DLK1-MEG3 in chordoma |
| Q35142587 | Concomitant downregulation of the imprinted genes DLK1 and MEG3 at 14q32.2 by epigenetic mechanisms in urothelial carcinoma |
| Q36605372 | Conditional deletions refine the embryonic requirement for Dlk1. |
| Q81146048 | Conservation of genomic imprinting at the XIST, IGF2, and GTL2 loci in the bovine |
| Q45820635 | DLK1 promotes neurogenesis of human and mouse pluripotent stem cell-derived neural progenitors via modulating Notch and BMP signalling |
| Q34526596 | DLK1/PREF1 regulates nutrient metabolism and protects from steatosis. |
| Q53701712 | DNA methylation of imprinted gene control regions in the regression of low-grade cervical lesions. |
| Q41054929 | Decreased expression of MEG3 contributes to retinoblastoma progression and affects retinoblastoma cell growth by regulating the activity of Wnt/β-catenin pathway |
| Q35161000 | Deleting maternal Gtl2 leads to growth enhancement and decreased expression of stem cell markers in teratoma |
| Q48798172 | Delta-like 1 homolog in Capra hircus: molecular characteristics, expression pattern and phylogeny |
| Q36579049 | Dlk1 is a negative regulator of emerging hematopoietic stem and progenitor cells. |
| Q33760580 | Dlk1 is necessary for proper skeletal muscle development and regeneration |
| Q64101590 | Dlk1-Mediated Temporal Regulation of Notch Signaling Is Required for Differentiation of Alveolar Type II to Type I Cells during Repair |
| Q35070932 | Ectodomain shedding of preadipocyte factor 1 (Pref-1) by tumor necrosis factor alpha converting enzyme (TACE) and inhibition of adipocyte differentiation |
| Q40441171 | Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour |
| Q35985459 | Establishment of paternal allele-specific DNA methylation at the imprinted mouse Gtl2 locus |
| Q36814408 | Expression of DLK1 Gene in the Bone Marrow Cells of Patients with Myelodysplastic Syndromes and Its Clinical Significance |
| Q24802429 | Expression of PEG11 and PEG11AS transcripts in normal and callipyge sheep |
| Q37730219 | Fetus-derived DLK1 is required for maternal metabolic adaptations to pregnancy and is associated with fetal growth restriction |
| Q34958754 | Gatm, a creatine synthesis enzyme, is imprinted in mouse placenta |
| Q27312725 | Gene dosage effects of the imprinted delta-like homologue 1 (dlk1/pref1) in development: implications for the evolution of imprinting |
| Q38041107 | Genes contributing to genetic variation of muscling in sheep |
| Q33841575 | Genome-wide prediction of imprinted murine genes |
| Q34128597 | Genome-wide profiling of the microRNA-mRNA regulatory network in skeletal muscle with aging |
| Q24796472 | Genomic analysis of early murine mammary gland development using novel probe-level algorithms |
| Q37274038 | Genomic imprinting is variably lost during reprogramming of mouse iPS cells |
| Q36421141 | Genomic imprinting of Dopa decarboxylase in heart and reciprocal allelic expression with neighboring Grb10. |
| Q24619515 | Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8 |
| Q36192047 | Identification of imprinting regulators at the Meg3 differentially methylated region |
| Q35805932 | Identification of the single base change causing the callipyge muscle hypertrophy phenotype, the only known example of polar overdominance in mammals. |
| Q33768928 | Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type. |
| Q33622341 | Imprinted genes: identification by chromosome rearrangements and post-genomic strategies |
| Q51864579 | Imprinting analysis of porcine DIO3 gene in two fetal stages and association analysis with carcass and meat quality traits. |
| Q48140497 | Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors |
| Q34837133 | Inhibition of adipogenesis and development of glucose intolerance by soluble preadipocyte factor-1 (Pref-1). |
| Q28730015 | Localizing transcriptional regulatory elements at the mouse Dlk1 locus |
| Q41676843 | Long non-coding RNA MEG3 inhibits the proliferation and metastasis of oral squamous cell carcinoma by regulating the WNT/β-catenin signaling pathway |
| Q38065895 | Long non-coding RNAs and p53 regulation. |
| Q26991873 | Long noncoding RNAs: past, present, and future |
| Q33259112 | Loss of imprinting at the Dlk1-Gtl2 locus caused by insertional mutagenesis in the Gtl2 5' region |
| Q35549396 | Maternal and zygotic Zfp57 modulate NOTCH signaling in cardiac development |
| Q24623420 | Maternally expressed gene 3 (MEG3) noncoding ribonucleic acid: isoform structure, expression, and functions |
| Q28115872 | Maternally expressed gene 3, an imprinted noncoding RNA gene, is associated with meningioma pathogenesis and progression |
| Q41640900 | Methods of epigenome editing for probing the function of genomic imprinting |
| Q34284044 | Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity |
| Q59798126 | MicroRNA and Long Non-coding RNA Regulation in Skeletal Muscle From Growth to Old Age Shows Striking Dysregulation of the Callipyge Locus |
| Q34656513 | Microarray analysis of novel candidate genes responsible for glucose-stimulated insulin secretion in mouse pancreatic β cell line MIN6. |
| Q37418152 | Minireview: Pref-1: role in adipogenesis and mesenchymal cell fate |
| Q81327078 | Monoallelic expression of the protease inhibitor gene in humans, sheep, and cattle |
| Q33925224 | Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation |
| Q42815739 | Only the large soluble form of preadipocyte factor-1 (Pref-1), but not the small soluble and membrane forms, inhibits adipocyte differentiation: role of alternative splicing |
| Q35629832 | Overexpression of Pref-1 in pancreatic islet β-cells in mice causes hyperinsulinemia with increased islet mass and insulin secretion |
| Q49962283 | Overexpression of microRNAs from the Gtl2-Rian locus contributes to postnatal death in mice. |
| Q42013208 | PBX1 is dispensable for neural commitment of RA-treated murine ES cells |
| Q47821601 | Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. |
| Q33380215 | Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation |
| Q35910690 | Peromyscus as a Mammalian epigenetic model |
| Q36876889 | Pituitary phenotypes of mice lacking the notch signalling ligand delta-like 1 homologue. |
| Q80561361 | Polar overdominant inheritance of a DLK1 polymorphism is associated with growth and fatness in pigs |
| Q35177835 | Postnatal loss of Dlk1 imprinting in stem cells and niche astrocytes regulates neurogenesis |
| Q35676240 | Pref-1 (preadipocyte factor 1) activates the MEK/extracellular signal-regulated kinase pathway to inhibit adipocyte differentiation |
| Q36977026 | Pref-1, a gatekeeper of adipogenesis |
| Q64118326 | RNA-seq of Isolated Chromaffin Cells Highlights the Role of Sex-Linked and Imprinted Genes in Adrenal Medulla Development |
| Q35161545 | Reduced DNA methylation at the PEG3 DMR and KvDMR1 loci in children exposed to alcohol in utero: a South African Fetal Alcohol Syndrome cohort study |
| Q33649662 | Regulation of Mammalian Gene Dosage by Long Noncoding RNAs |
| Q34074322 | Restoration of Dlk1 and Rtl1 is necessary but insufficient to rescue lethality in intergenic differentially methylated region (IG-DMR)-deficient mice |
| Q26801268 | Role of DNA methylation in renal cell carcinoma |
| Q40068949 | Role of preadipocyte factor 1 in adipocyte differentiation |
| Q35267816 | Roles for genomic imprinting and the zygotic genome in placental development. |
| Q51947093 | Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12). |
| Q40004705 | Spatiotemporal expression pattern of Mirg, an imprinted non-coding gene, during mouse embryogenesis |
| Q64929446 | Technical advances contribute to the study of genomic imprinting. |
| Q39818991 | The Begain gene marks the centromeric boundary of the imprinted region on mouse chromosome 12. |
| Q57161236 | The Dysregulation of the - Locus in Islets From Patients With Type 2 Diabetes Is Mimicked by Targeted Epimutation of Its Promoter With TALE-DNMT Constructs |
| Q33828371 | The Missing lnc(RNA) between the pancreatic β-cell and diabetes |
| Q33761870 | The function of non-coding RNAs in genomic imprinting |
| Q28271675 | The microRNAs within the DLK1-DIO3 genomic region: involvement in disease pathogenesis |
| Q37537864 | The pancreatic β cell and type 1 diabetes: innocent bystander or active participant? |
| Q33389173 | Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain |
| Q43011700 | Transcriptomic and genomic analysis of human hepatocellular carcinomas and hepatoblastomas |
| Q38246516 | What does genetics tell us about imprinting and the placenta connection? |
Search more.