| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/NG0194-33 |
| P698 | PubMed publication ID | 8136831 |
| P50 | author | Yoshihide Hayashizaki | Q15055173 |
| P2093 | author name string | H Sugino | |
| M Muramatsu | |||
| Y Okazaki | |||
| K Hirose | |||
| N Sasaki | |||
| H Shibata | |||
| S Hirotsune | |||
| H Okuizumi | |||
| H Imoto | |||
| P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
| Cloning and intracellular localization of the U2 small nuclear ribonucleoprotein auxiliary factor small subunit | Q24293417 | ||
| A genomic scanning method for higher organisms using restriction sites as landmarks | Q24560146 | ||
| A comprehensive set of sequence analysis programs for the VAX | Q26778432 | ||
| Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region | Q28208127 | ||
| Restriction landmark genomic scanning method and its various applications | Q28263419 | ||
| A general method for isolation of high molecular weight DNA from eukaryotes | Q29618192 | ||
| A new method for constructing NotI linking and boundary libraries using a restriction trapper | Q33192387 | ||
| RI manager, a microcomputer program for analysis of data from recombinant inbred strains | Q33305406 | ||
| Enzymatic amplification of a Y chromosome repeat in a single blastomere allows identification of the sex of preimplantation mouse embryos | Q33601734 | ||
| Differential activity of maternally and paternally derived chromosome regions in mice | Q34198480 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Use of restriction enzymes to detect potential gene sequences in mammalian DNA. | Q35079757 | ||
| Differential imprinting and expression of maternal and paternal genomes | Q39569895 | ||
| Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region | Q44185908 | ||
| Genomic imprinting determines methylation of parental alleles in transgenic mice | Q44250721 | ||
| Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. | Q48125063 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Rare Bases in Animal DNA | Q59090587 | ||
| A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA | Q64441637 | ||
| A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression | Q67482957 | ||
| Parental legacy determines methylation and expression of an autosomal transgene: a molecular mechanism for parental imprinting | Q70191111 | ||
| Molecular cloning of polymorphic markers on RLGS gel using the spot target cloning method | Q72883426 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 33-40 | |
| P577 | publication date | 1994-01-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method | |
| P478 | volume | 6 |
| Q80094274 | A DNA microarray-based methylation-sensitive (MS)-AFLP hybridization method for genetic and epigenetic analyses |
| Q56783008 | A Genome-Wide Screen for Normally Methylated Human CpG Islands That Can Identify Novel Imprinted Genes |
| Q57591259 | A bird's eye view of global methylation |
| Q36452285 | A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2 |
| Q30830058 | A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes |
| Q36757273 | A model system to study genomic imprinting of human genes |
| Q28208083 | A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids |
| Q22009166 | A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region |
| Q53012214 | A novel strategy to identify maternal and paternal inheritance in the mouse |
| Q49057890 | A paternal-specific methylation imprint marks the alleles of the mouse H19 gene |
| Q24319782 | A protein related to splicing factor U2AF35 that interacts with U2AF65 and SR proteins in splicing of pre-mRNA |
| Q52879564 | A spot cloning method for restriction landmark genomic scanning. |
| Q28592430 | A tripartite paternally methylated region within the Gpr1-Zdbf2 imprinted domain on mouse chromosome 1 identified by meDIP-on-chip |
| Q36565229 | A unique downregulation of h2-calponin gene expression in Down syndrome: a possible attenuation mechanism for fetal survival by methylation at the CpG island in the trisomic chromosome 21. |
| Q33888431 | Aberrant CpG-island methylation has non-random and tumour-type-specific patterns. |
| Q41374924 | Accessibility to tissue-specific genes from methylation profiles of mouse brain genomic DNA. |
| Q24682438 | An AscI boundary library for the studies of genetic and epigenetic alterations in CpG islands |
| Q72296653 | An expanded system of restriction landmark genomic scanning (RLGS Ver. 1.8) |
| Q48611673 | Analyses of human gliomas by restriction landmark genomic scanning |
| 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 |
| Q35932331 | Base-resolution analyses of sequence and parent-of-origin dependent DNA methylation in the mouse genome |
| Q41387004 | Chromatin structure and imprinting: developmental control of DNase-I sensitivity in the mouse insulin-like growth factor 2 gene. |
| Q73793311 | Chromosome assignment of aberrant NotI restriction DNA fragments in primary hepatocellular carcinoma |
| Q40755201 | Combined restriction landmark genomic scanning and virtual genome scans identify a novel human homeobox gene, ALX3, that is hypermethylated in neuroblastoma |
| Q36669714 | Comparison of DNA methylation patterns among mouse cell lines by restriction landmark genomic scanning |
| Q31742998 | DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts |
| Q34375355 | DNA methylation and mammalian epigenetics |
| Q33733162 | DNA methylation in eukaryotic chromosome stability revisited: DNA methyltransferase in the management of DNA conformation space |
| Q41439642 | DNA methylation in genomic imprinting |
| Q33969187 | DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1. |
| Q74058992 | DNA methylation variation in cloned mice |
| Q41333669 | DNA methylation: biology and significance |
| Q46146329 | Deregulation of both imprinted and expressed alleles of the insulin–like growth factor 2 gene during β–cell tumorigenesis |
| Q52214150 | Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes |
| Q73764736 | Disruption of imprinted expression of U2afbp-rs/U2af1-rs1 gene in mouse parthenogenetic fetuses |
| Q36041771 | Dissecting DNA hypermethylation in cancer. |
| Q58042339 | Diversity of human U2AF splicing factors |
| Q53608718 | Epigenetic regulation of the imprinted U2af1-rs1 gene during retinoic acid-induced differentiation of embryonic stem cells. |
| Q37106588 | Epigenetics: application of virtual image restriction landmark genomic scanning (Vi-RLGS). |
| Q40579171 | Experimental embryological analysis of genetic imprinting in mouse development |
| Q52211093 | Expression of X-linked genes in androgenetic, gynogenetic, and normal mouse preimplantation embryos. |
| Q33425018 | Expression profile and transcription factor binding site exploration of imprinted genes in human and mouse |
| Q61693865 | Genetic conflicts and the evolutionary origin of genomic imprinting |
| Q72639533 | Genetic mapping and systematic screening of mouse endogenously imprinted loci detected with restriction landmark genome scanning method (RLGS) |
| Q40541321 | Genetic mapping of restriction landmark genomic scanning loci in the mouse |
| Q35761081 | Genetic variation detected by quantitative analysis of end-labeled genomic DNA fragments |
| Q34396556 | Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment |
| Q33841575 | Genome-wide prediction of imprinted murine genes |
| Q36436558 | Genome-wide survey of imprinted genes |
| Q33186874 | Genome‐Wide Analysis of Epigenetics in Cancer |
| Q48633313 | Genomic alterations in human glioma cell lines detected by restriction landmark genomic scanning |
| Q21145256 | Genomic imprinting in mammals: emerging themes and established theories |
| Q41587298 | Genomic imprinting in the brain |
| Q34771178 | Genomic imprinting proposed as a surveillance mechanism for chromosome loss |
| Q35037387 | Genomic imprinting: could the chromatin structure be the driving force? |
| Q33541538 | Genomic imprinting: implications for human disease |
| Q29616227 | Genomic imprinting: parental influence on the genome |
| Q28360366 | Global methylation profiling of lung cancer identifies novel methylated genes |
| 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 |
| Q34939534 | Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2. |
| Q41066932 | Imprinted genes and regulation of gene expression by epigenetic inheritance. |
| Q33852775 | Imprinted genes as potential genetic and epigenetic toxicologic targets |
| Q70972792 | Imprinted genes have few and small introns |
| Q37543706 | Imprinting and extraembryonic tissues-mom takes control |
| Q52187194 | Imprinting mechanisms in mammals. |
| Q77135814 | Improved restriction landmark cDNA scanning and its application to global analysis of genes regulated by nerve growth factor in PC12 cells |
| Q40442645 | Indirect gene diagnoses for complex (multifactorial) diseases-A review |
| Q33380291 | Inheritance and alteration of genome methylation in F1 hybrid rice |
| Q43872724 | Inhibition of histone deacetylases alters allelic chromatin conformation at the imprinted U2af1-rs1 locus in mouse embryonic stem cells |
| Q36556187 | Initiation binding repressor, a factor that binds to the transcription initiation site of the histone h5 gene, is a glycosylated member of a family of cell growth regulators [corrected] |
| Q77618451 | Involvement of IGF2 and H19 imprinting in choriocarcinoma development |
| Q72529317 | Localization of mouse imprinted gene U2af1-rs1 to A3.2-4 band of chromosome 11 by FISH |
| Q28603472 | Mammalian-specific genomic functions: Newly acquired traits generated by genomic imprinting and LTR retrotransposon-derived genes in mammals |
| Q40413626 | Mechanistic and developmental aspects of genetic imprinting in mammals |
| Q72164123 | Methylation imprinting was observed of mouse mo-2 macrosatellite on the pseudoautosomal region but not on chromosome 9 |
| Q28364163 | Methylation matters |
| Q72781919 | Methylation of the oestrogen receptor CpG island links ageing and neoplasia in human colon |
| Q42008490 | Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15 |
| Q48382320 | Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3. |
| Q41044032 | Multiple roles for DNA methylation in gametic imprinting |
| Q40695944 | Notl-Msell methylation-sensitive amplied fragment length polymorhism for DNA methylation analysis of human cancers |
| Q46134005 | Novel paternally expressed intergenic transcripts at the mouse Prader-Willi/Angelman Syndrome locus |
| Q48637146 | Parental chromosome-specific chromatin conformation in the imprinted U2af1-rs1 gene in the mouse. |
| Q40672445 | Parental imprinting of autosomal mammalian genes |
| Q34634517 | Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse. |
| Q33894408 | Programming and inheritance of parental DNA methylomes in mammals |
| Q28081962 | Programming and inheritance of parental DNA methylomes in vertebrates |
| Q41374914 | Quantitative and qualitative genetic variation in two-dimensional DNA gels of human lymphocytoid cell lines |
| Q52194011 | Requirement for protein synthesis during embryonic genome activation in mice. |
| Q39715337 | Restriction landmark cDNA scanning (RLCS): a novel cDNA display system using two-dimensional gel electrophoresis |
| Q83198247 | Restriction landmark genome scanning method using isoschizomers (MspI/HpaII) for DNA methylation analysis |
| Q45950867 | Restriction landmark genome scanning. |
| Q80093356 | Restriction landmark genomic scanning |
| Q36561256 | Screening for imprinted genes by allelic message display: identification of a paternally expressed gene impact on mouse chromosome 18 |
| Q33963896 | Successful computational prediction of novel imprinted genes from epigenomic features. |
| Q64929446 | Technical advances contribute to the study of genomic imprinting. |
| Q33530627 | The application of restriction landmark genome scanning method for surveillance of non-mendelian inheritance in f(1) hybrids |
| Q36283882 | The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins |
| Q34190554 | The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome |
| Q72017438 | The search for imprinted genes |
| Q72296658 | The use of restriction landmark genomic scanning to scan the mouse genome for endogenous loci with imprinted patterns of methylation |
| Q71441501 | Time of initiation and site of action of the mouse chromosome 11 imprinting effects |
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