| scholarly article | Q13442814 |
| P2093 | author name string | Flood JF | |
| King CD | |||
| Giddings SJ | |||
| Carnaghi LR | |||
| Harman KW | |||
| P2860 | cites work | Insulin II gene expression in rat central nervous system. | Q52222302 |
| Selective expression and developmental regulation of the ancestral rat insulin II gene in fetal liver. | Q52240260 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility | Q56524301 | ||
| Cell-specific expression controlled by the 5′-flanking region of insulin and chymotrypsin genes | Q59057041 | ||
| The structure and evolution of the two nonallelic rat preproinsulin genes | Q62397569 | ||
| Insulin receptors in embryo and extraembryonic membranes of early somite rat conceptus | Q68901106 | ||
| Epigenetic mechanisms underlying the imprinting of the mouse H19 gene | Q72094721 | ||
| Parental imprinting of the mouse H19 gene | Q22122365 | ||
| Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2 | Q31158518 | ||
| Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis | Q34056205 | ||
| Five mutant alleles of the insulin receptor gene in patients with genetic forms of insulin resistance | Q34256457 | ||
| Regulation of hepatic glycogen synthesis during fetal development: roles of hydrocortisone, insulin, and insulin receptors | Q34746883 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Differential expression of the two nonallelic proinsulin genes in the developing mouse embryo | Q36059091 | ||
| RNA-mediated gene duplication: the rat preproinsulin I gene is a functional retroposon | Q36892326 | ||
| Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene. | Q41979401 | ||
| Evolution of Insulin-Like Growth Factor II: Characterization of the Mouse IGF-II Gene and Identification of Two Pseudo-Exons | Q42615815 | ||
| Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region | Q44185908 | ||
| Proinsulin I and II gene expression in inbred mouse strains | Q45259590 | ||
| Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. | Q48125063 | ||
| Characterization of the two nonallelic genes encoding mouse preproinsulin | Q48370767 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 310-313 | |
| P577 | publication date | 1994-03-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting | |
| P478 | volume | 6 |
| Q71793991 | A chromatin model of IGF2/H19 imprinting |
| Q49057890 | A paternal-specific methylation imprint marks the alleles of the mouse H19 gene |
| Q38028387 | A survey of tissue-specific genomic imprinting in mammals |
| Q73666171 | Allelic expression of the putative tumor suppressor gene p73 in human fetal tissues and tumor specimens |
| Q35096694 | An extended domain of Kcnq1ot1 silencing revealed by an imprinted fluorescent reporter |
| Q37284686 | An imprinted GFP insertion reveals long-range epigenetic regulation in embryonic lineages |
| Q72161192 | An imprinted gene(s) for diabetes? |
| Q31147226 | Antisense transcripts with FANTOM2 clone set and their implications for gene regulation |
| Q28305462 | Association of IGF2 and H19 imprinting with choriocarcinoma development |
| Q33405733 | At least ten genes define the imprinted Dlk1-Dio3 cluster on mouse chromosome 12qF1 |
| Q35694446 | Central and peripheral autoantigen presentation in immune tolerance |
| Q41387004 | Chromatin structure and imprinting: developmental control of DNase-I sensitivity in the mouse insulin-like growth factor 2 gene. |
| Q35077074 | Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation. |
| Q41333669 | DNA methylation: biology and significance |
| Q28594495 | Defective haematopoiesis and vasculogenesis in transforming growth factor-β1 knock out mice |
| Q35211749 | Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. |
| Q46146329 | Deregulation of both imprinted and expressed alleles of the insulin–like growth factor 2 gene during β–cell tumorigenesis |
| Q35571341 | Detection of β cell death in diabetes using differentially methylated circulating DNA. |
| Q52214150 | Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes |
| Q28287765 | Disruption of imprinting caused by deletion of the H19 gene region in mice |
| Q74560571 | Effects of fibroblast growth factor 2 and insulin-like growth factor II on the development of parthenogenetic mouse embryos in vitro |
| Q36421376 | Epigenetic and phenotypic consequences of a truncation disrupting the imprinted domain on distal mouse chromosome 7. |
| Q43442385 | Expression of Ins1 and Ins2 genes in mouse fetal liver |
| Q30488150 | Generation of embryonic stem cells from mouse insulin I promoter-green fluorescent protein transgenic mice and characterization in a teratoma model |
| Q72639533 | Genetic mapping and systematic screening of mouse endogenously imprinted loci detected with restriction landmark genome scanning method (RLGS) |
| Q41099923 | Genetics of insulin-dependent diabetes mellitus |
| Q56903501 | Genetics of type 1 diabetes |
| Q36436558 | Genome-wide survey of imprinted genes |
| Q46005770 | Genomic deletion of an imprint maintenance element abolishes imprinting of both insulin-like growth factor II and H19. |
| Q33721384 | Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome |
| Q36436530 | Genomic imprinting in the placenta |
| Q37710386 | Genomic imprinting mechanisms in embryonic and extraembryonic mouse tissues |
| Q38298288 | Genomic imprinting of Mash2, a mouse gene required for trophoblast development |
| Q38291049 | Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse |
| Q35037387 | Genomic imprinting: could the chromatin structure be the driving force? |
| Q37362832 | Genomic imprinting: employing and avoiding epigenetic processes |
| Q33541538 | Genomic imprinting: implications for human disease |
| Q74243018 | Growth promoting effects of human placental lactogen during early organogenesis: a link to insulin-like growth factors |
| Q35814612 | High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes |
| Q35982840 | Hyper-Variability in Circulating Insulin, High Fat Feeding Outcomes, and Effects of Reducing Ins2 Dosage in Male Ins1-Null Mice in a Specific Pathogen-Free Facility |
| Q48060772 | Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M. |
| Q52211090 | Identification of genes showing altered expression in preimplantation and early postimplantation parthenogenetic embryos. |
| Q34994392 | Identification of novel imprinted genes in a genome-wide screen for maternal methylation. |
| Q35793734 | Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene |
| Q51046179 | Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies. |
| Q41066932 | Imprinted genes and regulation of gene expression by epigenetic inheritance. |
| Q36436584 | Imprinted genes and their role in human fetal growth. |
| Q26999035 | Imprinted silencing is extended over broad chromosomal domains in mouse extra-embryonic lineages |
| Q37543706 | Imprinting and extraembryonic tissues-mom takes control |
| Q34402875 | Imprinting and transgenerational modulation of gene expression; human growth as a model |
| Q40948397 | Imprinting of IGF2, insulin-dependent diabetes, immune function, and apoptosis: a hypothesis |
| Q33873823 | Improving the safety of embryo technologies: possible role of genomic imprinting |
| Q52196099 | Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus. |
| Q57384414 | Insulin is imprinted in the placenta of the marsupial, Macropus eugenii |
| Q43061716 | Insulin: a critical autoantigen and potential therapeutic agent in Type 1 diabetes |
| Q77618451 | Involvement of IGF2 and H19 imprinting in choriocarcinoma development |
| Q72890283 | Is human insulin imprinted? |
| Q24534306 | Isoform-specific imprinting of the human PEG1/MEST gene |
| Q52064363 | Knock-in of diphteria toxin A chain gene at Ins2 locus: effects on islet development and localization of Ins2 expression in the brain. |
| Q63916571 | Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome |
| Q40413626 | Mechanistic and developmental aspects of genetic imprinting in mammals |
| Q40337480 | Metabolic and genetic characterization of prediabetic states. Sequence of events leading to non-insulin-dependent diabetes mellitus |
| Q72007940 | Monoallelic expression of IGF2 at the human fetal/maternal boundary |
| Q24647321 | Mouse U2af1-rs1 is a neomorphic imprinted gene |
| Q33774256 | Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster |
| Q81152665 | Neonatal diabetes mellitus |
| Q41386996 | Non-insulin-dependent diabetes mellitus--a collision between thrifty genes and an affluent society |
| Q24672503 | Parent-of-origin effects in multiple endocrine neoplasia type 2B |
| Q40481212 | Parental imprinting effect at the INS-IGF2 diabetes susceptibility locus |
| Q46725382 | Parental imprinting of the Mas protooncogene in mouse |
| Q52174393 | Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation. |
| Q52197507 | Paternal repression of the imprinted mouse Igf2r locus occurs during implantation and is stable in all tissues of the post-implantation mouse embryo. |
| Q34634517 | Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse. |
| Q33523010 | Postnatal survival of mice with maternal duplication of distal chromosome 7 induced by a Igf2/H19 imprinting control region lacking insulator function |
| Q34510776 | Proinsulin in development: New roles for an ancient prohormone. |
| Q48569804 | Proliferation and differentiation of androgenetic cells in fetal mouse chimeras |
| Q36411455 | Selected imprinting of INS in the marsupial |
| Q33596180 | Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian Ascl2/Mash2-Igf2-H19 region |
| Q36065440 | Suppression of hyperinsulinaemia in growing female mice provides long-term protection against obesity |
| Q58201304 | Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus |
| Q35644181 | Testing parental imprinting in insulin-dependent diabetes mellitus by the marker-association-segregation-chi 2 method. |
| Q24318274 | The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis |
| Q48039596 | The Rasgrf1-repeat sequence (D9Ncvs53) maps between Mod1 and Rbp1 on mouse chromosome 9 and may define a putative imprinted region |
| Q33994222 | The absence of enhancer competition between Igf2 and H19 following transfer into differentiated cells |
| Q36081294 | The effect of parental imprinting on the INS-IGF2 locus of Korean type I diabetic patients |
| Q34580927 | The insulin gene in diabetes |
| Q37278762 | The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann region |
| Q73208039 | The mouse chromosome 7 distal imprinting domain maps to G-bands F4/F5 |
| Q35207966 | The potential role of gene duplications in the evolution of imprinting mechanisms |
| Q72017438 | The search for imprinted genes |
| Q35934507 | The structural H19 gene is required for transgene imprinting |
| Q72296658 | The use of restriction landmark genomic scanning to scan the mouse genome for endogenous loci with imprinted patterns of methylation |
| Q28207541 | Thioredoxin post-transcriptional regulation by H19 provides a new function to mRNA-like non-coding RNA |
| Q71441501 | Time of initiation and site of action of the mouse chromosome 11 imprinting effects |
| Q48652732 | Trim28 is required for epigenetic stability during mouse oocyte to embryo transition. |
| Q57751793 | U-P- What? |
| Q24311799 | UBE3A/E6-AP mutations cause Angelman syndrome |
| Q71989840 | Ubiquitous expression and imprinting of Snrpn in the mouse |
| Q36214949 | Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene |
| Q30856368 | Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines |
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