| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1047075894 |
| P356 | DOI | 10.1038/364459A0 |
| P698 | PubMed publication ID | 8332218 |
| P2093 | author name string | Simon I | |
| Cedar H | |||
| Keshet I | |||
| Driscoll DJ | |||
| Nicholls RD | |||
| Brandeis M | |||
| Selig S | |||
| Kitsberg D | |||
| P2860 | cites work | Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 |
| Genetic analysis of genomic imprinting: An Imprintor-1 gene controls inactivation of the paternal copy of the mouse Tme locus | Q57406125 | ||
| Genomic imprinting and embryonal tumours | Q58992891 | ||
| Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour | Q59088779 | ||
| Report of the committee on the genetic constitution of chromosome 11 | Q59662132 | ||
| Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13 | Q67993243 | ||
| A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes | Q68019576 | ||
| A molecular genetic linkage map of mouse chromosome 7 | Q68166997 | ||
| Analysis of DNA replication during S-phase by means of dynamic chromosome banding at high resolution | Q68549870 | ||
| Replication asynchrony between homologs 15q11.2: cytogenetic evidence for genomic imprinting | Q70163316 | ||
| Correlation between X-chromosome inactivation and cell differentiation in female preimplantation mouse embryos | Q93613539 | ||
| Parental imprinting of the mouse H19 gene | Q22122365 | ||
| A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism | Q24320016 | ||
| Monoallelic expression of the human H19 gene | Q28184725 | ||
| Parental imprinting of the human H19 gene | Q28187996 | ||
| Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region | Q28208127 | ||
| High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones | Q28274183 | ||
| Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2 | Q31158518 | ||
| Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis | Q31165084 | ||
| Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites | Q34307556 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Mouse chromosome 7. | Q35675706 | ||
| Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse | Q36148677 | ||
| Isolation of the human insulin-like growth factor genes: insulin-like growth factor II and insulin genes are contiguous | Q36489597 | ||
| Polymorphic variants in human chromosome 15. | Q36656968 | ||
| Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides | Q37601020 | ||
| Differential imprinting and expression of maternal and paternal genomes | Q39569895 | ||
| Evolution of Insulin-Like Growth Factor II: Characterization of the Mouse IGF-II Gene and Identification of Two Pseudo-Exons | Q42615815 | ||
| Parental origin of chromosomes involved in the translocation t(9;22). | Q43592920 | ||
| Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region | Q44185908 | ||
| Replication timing of genes and middle repetitive sequences. | Q51233045 | ||
| Relaxation of imprinted genes in human cancer. | Q52545355 | ||
| A deletion of the human beta-globin locus activation region causes a major alteration in chromatin structure and replication across the entire beta-globin locus. | Q54314374 | ||
| Fluorescence and Giemsa banding studies of the allocyclic X chromosome in embryonic and adult mouse cells. | Q54386888 | ||
| Three mutant insulins in man | Q54498926 | ||
| P433 | issue | 6436 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 459-463 | |
| P577 | publication date | 1993-07-01 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Allele-specific replication timing of imprinted gene regions | |
| P478 | volume | 364 |
| Q24683678 | 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders |
| Q38302121 | A 330 kb CENP-A binding domain and altered replication timing at a human neocentromere. |
| Q34645636 | A genetic mechanism implicates chromosome 11 in schizophrenia and bipolar diseases |
| Q73131940 | A microsatellite map of the pink-eyed dilution (p) deletion complex in mouse chromosome 7 |
| Q63869173 | A role for common fragile site induction in amplification of human oncogenes |
| Q35601037 | A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes |
| Q33396014 | Aberrant allele-specific replication, independent of parental origin, in blood cells of cancer patients |
| Q71688471 | Absence of genomic imprinting at the DiGeorge locus |
| Q33913566 | Achieving singularity in mammalian odorant receptor gene choice |
| Q34337845 | Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region |
| Q88595593 | Allele-specific control of replication timing and genome organization during development |
| Q52549071 | Allele-specific replication associated with aneuploidy in blood cells of patients with hematologic malignancies. |
| Q41934469 | Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy |
| Q37393623 | Allelic inactivation of rDNA loci |
| Q34726828 | Allelic inactivation regulates olfactory receptor gene expression |
| Q34650812 | Allelic silencing at the tumor-suppressor locus 13q14.3 suggests an epigenetic tumor-suppressor mechanism |
| Q56418625 | Alterations in DNA Methylation: A Fundamental Aspect of Neoplasia |
| Q39242860 | Alterations in replication timing of cancer-related genes in malignant human breast cancer cells |
| Q34655383 | An epigenetic state associated with areas of gene duplication |
| Q81007603 | An isochore transition zone in the NF1 gene region is a conserved landmark of chromosome structure and function |
| Q41167757 | Are ABL and BCR imprinted? |
| Q36787330 | Asynchronous DNA replication between 15q11.2q12 homologs: cytogenetic evidence for maternal imprinting and delayed replication |
| Q59095417 | Asynchronous replication and allelic exclusion in the immune system |
| Q53462588 | Asynchronous replication dynamics of imprinted and non-imprinted chromosome regions in early mouse embryos. |
| Q78739434 | Asynchronous replication of biallelically expressed loci: a new phenomenon in Turner syndrome |
| Q40915347 | Asynchronous replication of imprinted genes is established in the gametes and maintained during development |
| Q41246983 | Asynchronous replication patterns of imprinted genes in triploid cells |
| Q35964571 | Asynchronous replication timing of imprinted loci is independent of DNA methylation, but consistent with differential subnuclear localization |
| Q36370610 | Biallelic germline transcription at the kappa immunoglobulin locus |
| Q61498079 | Bivalent 15 regularly associates with the sex vesicle in normal male meiosis |
| Q28292519 | Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient |
| Q30430861 | Bubble-chip analysis of human origin distributions demonstrates on a genomic scale significant clustering into zones and significant association with transcription |
| Q48352508 | Chromatin conformation of the H19 epigenetic mark |
| Q41387004 | Chromatin structure and imprinting: developmental control of DNase-I sensitivity in the mouse insulin-like growth factor 2 gene. |
| Q36846020 | Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation |
| Q33887777 | Competition--a common motif for the imprinting mechanism? |
| Q34327315 | Condensin II initiates sister chromatid resolution during S phase. |
| Q36745813 | Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting center |
| Q50671001 | Conserved synteny of mammalian imprinted genes in chicken, frog, and fish genomes. |
| Q48050158 | Consistent allelic loss on mouse chromosome 7 distal to tyrosinase in 4-nitroquinoline-1-oxide-induced oral cavity tumors with loss of heterozygosity at Ha-ras-1. |
| Q93064854 | Control of DNA replication timing in the 3D genome |
| Q34378421 | DNA methylation in genomic imprinting, development, and disease |
| Q35889273 | DNA replication analysis of FMR1, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late |
| Q74307721 | DNA replication origins: from sequence specificity to epigenetics |
| Q36553045 | DNA replication: the unbearable lightness of origins |
| Q34170680 | Demethylation and the establishment of kappa allelic exclusion |
| Q28363097 | Developmental regulation of DNA replication timing at the human beta globin locus. |
| Q33536540 | Developmental regulation of immune system gene rearrangement |
| Q85125710 | Diagnosis of Cryptic Chromosomal Syndromes by Fluorescence In Situ Hybridization (FISH) |
| Q37380861 | Differential replication and DNA elimination in the polytene chromosomes of Euplotes crassus |
| Q72345863 | Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution |
| Q34146198 | Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome |
| Q37518550 | Dynamic methylation adjustment and counting as part of imprinting mechanisms |
| Q34959586 | Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype |
| Q34637706 | Epigenetic regulation of monoallelic rearrangement (allelic exclusion) of antigen receptor genes |
| Q36958186 | Epigenetics and phenotypic variability: some interesting insights from birds |
| Q40494434 | Epigenetics: A new whiff of monoallelic expression |
| Q37268611 | Erasure and reestablishment of random allelic expression imbalance after epigenetic reprogramming |
| Q54611269 | Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli |
| Q41140340 | Expression of H19 does not influence the timing of replication of the Igf2/H19 imprinted region |
| Q71825351 | Factors affecting the timing and imprinting of replication on a mammalian chromosome |
| Q52220346 | Genetic imprinting in the mouse: implications for gene regulation. |
| Q41741395 | Genetics and developmental delay |
| Q72539974 | Genetics of Wilms' tumor: a blend of aberrant development and genomic imprinting |
| Q33721384 | Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome |
| Q41175197 | Genomic imprinting in disorders of growth |
| Q38298288 | Genomic imprinting of Mash2, a mouse gene required for trophoblast development |
| Q33987666 | Genomic imprinting, uniparental disomy and foetal growth |
| Q52218988 | Genomic imprinting. Imprinting with and without methylation. |
| Q35250186 | Genomic imprinting: a chromatin connection |
| Q33603375 | Genomic imprinting: concept and clinical consequences |
| 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 |
| Q36915079 | Global organization of replication time zones of the mouse genome |
| Q52208588 | H19 is imprinted in the choroid plexus and leptomeninges of the mouse foetus |
| Q35814612 | High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes |
| Q24644428 | High-resolution analysis of DNA replication domain organization across an R/G-band boundary |
| Q55036139 | Human cytogenetics: 46 chromosomes, 46 years and counting. |
| Q24532789 | Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons |
| Q24794612 | Imaging genome abnormalities in cancer research |
| Q51046179 | Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies. |
| Q52192434 | Imprinted expression of the Igf2r gene depends on an intronic CpG island. |
| Q41066932 | Imprinted genes and regulation of gene expression by epigenetic inheritance. |
| Q33852775 | Imprinted genes as potential genetic and epigenetic toxicologic targets |
| Q28237886 | Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method |
| Q48013064 | Imprinting in Prader-Willi and Angelman syndromes |
| Q41566242 | Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome |
| Q35889365 | Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes |
| Q34026945 | Imprinting: focusing on the center |
| Q72874155 | In and around SNRPN |
| Q33359714 | Independent recruitment of Igh alleles in V(D)J recombination |
| Q52178081 | Independent regulation of the two Pax5 alleles during B-cell development. |
| Q33678546 | Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studies. |
| Q34314269 | Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. |
| Q35099021 | Intermediate DNA methylation is a conserved signature of genome regulation |
| Q77534962 | Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability |
| Q38824303 | Maintenance of Epigenetic Information |
| Q34717494 | Mapping of DNA replication origins to noncoding genes of the X-inactivation center |
| Q24305283 | Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome |
| Q95811124 | Mechanisms and consequences of widespread random monoallelic expression |
| Q40575113 | Mechanisms of genomic imprinting in mammals |
| Q40413626 | Mechanistic and developmental aspects of genetic imprinting in mammals |
| Q37139251 | Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA. |
| Q37442282 | Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations. |
| Q34316722 | Minireview: Parthenogenesis in mammals |
| Q73467021 | Modified allelic replication in lymphocytes of patients with neurofibromatosis type 1 |
| Q44631120 | Modified order of allelic replication in lymphoma patients at different disease stages |
| Q41127747 | Molecular biology of Beckwith-Wiedemann syndrome |
| Q83305909 | Molecular cytogenetic characteristics of Down syndrome newborns |
| Q40496560 | Monoallelic expression and asynchronous replication of p120 catenin in mouse and human cells |
| Q41167673 | Multiple imprinted genes associated with Prader-Willi syndrome and location of an imprinting control element |
| Q33774256 | Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster |
| Q41044032 | Multiple roles for DNA methylation in gametic imprinting |
| Q28211002 | Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region |
| Q34276674 | Natural Selection and the Evolution of Genome Imprinting |
| Q33927035 | Natural selection and the function of genome imprinting: beyond the silenced minority |
| Q42558631 | New insights reveal complex mechanisms involved in genomic imprinting. |
| Q35446077 | Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion. |
| Q47911109 | Olfactory receptor gene regulation |
| Q34659444 | Parent-of-origin specific QTL--a possibility towards understanding reciprocal effects in chicken and the origin of imprinting |
| Q77777686 | Parental alleles of an imprinted mouse transgene replicate synchronously |
| Q48637146 | Parental chromosome-specific chromatin conformation in the imprinted U2af1-rs1 gene in the mouse. |
| Q40672445 | Parental imprinting of autosomal mammalian genes |
| Q35650825 | Position effect of human telomeric repeats on replication timing |
| Q51986573 | Profiling of DNA replication timing in unsynchronized cell populations. |
| Q77129209 | Promoter-specific insulin-like growth factor 2 gene imprinting in human fetal liver and hepatoblastoma |
| Q36465862 | Random and non-random monoallelic expression |
| Q33680613 | Random monoallelic expression: regulating gene expression one allele at a time |
| Q44542200 | Regulation of DNA replication timing |
| Q47911157 | Regulation of immunoglobulin light chain isotype expression |
| Q35042232 | Regulation of imprinting: A multi-tiered process |
| Q35038281 | Replicating by the clock |
| Q34041338 | Replication Timing Aberrations and Aneuploidy in Peripheral Blood Lymphocytes of Breast Cancer Patients |
| Q73711277 | Replication asynchrony increases in women at risk for aneuploid offspring |
| Q33963998 | Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability |
| Q78110976 | Replication pattern in cancer: asynchronous replication in multiple myeloma and in monoclonal gammopathy |
| Q37425974 | Replication profile of PCDH11X and PCDH11Y, a gene pair located in the non-pseudoautosomal homologous region Xq21.3/Yp11.2. |
| Q77454454 | Replication status as a possible marker for genomic instability in cells originating from genotypes with balanced rearrangements |
| Q43915901 | Replication status in leukocytes of treated and untreated patients with polycythemia vera and essential thrombocytosis |
| Q36952044 | Replication timing and transcriptional control: beyond cause and effect-part III. |
| Q74394515 | Replication timing properties within the mouse distal chromosome 7 imprinting cluster |
| Q36411455 | Selected imprinting of INS in the marsupial |
| Q33716524 | Sex-based differences in gene transmission and gene expression |
| Q33779051 | Single molecule analysis of DNA replication |
| Q93659262 | Slide Presentations |
| Q40924201 | Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease? |
| Q31955494 | Spatial and temporal dynamics of DNA replication sites in mammalian cells |
| Q41640473 | Structure and function of the human chromosome 15 imprinting center |
| Q48000452 | Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. |
| Q24610062 | The Air noncoding RNA: an imprinted cis-silencing transcript |
| 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 |
| Q35644289 | The fragile X premutation in carriers and its effect on mutation size in offspring |
| Q24677893 | The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome |
| Q24539032 | The imprinting mechanism of the Prader-Willi/Angelman regional control center |
| Q73918278 | The influence of cytogenetic aberrations on gene replication in chronic lymphocytic leukemia patients |
| Q24671994 | The odyssey of MeCP2 and parental imprinting |
| Q38007044 | The pain of social disconnection: examining the shared neural underpinnings of physical and social pain |
| Q99595515 | The physiological function of long-noncoding RNAs |
| Q24812133 | The replication timing program of the Chinese hamster beta-globin locus is established coincident with its repositioning near peripheral heterochromatin in early G1 phase |
| Q28292627 | The γ-aminobutyric acid receptor γ3 subunit gene (GABRG3) is tightly linked to the α5 subunit gene (GABRA5) on human chromosome 15q11–q13 and is transcribed in the same orientation |
| Q34126322 | Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus |
| Q41167741 | Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy? |
| Q36321358 | X chromosome choice occurs independently of asynchronous replication timing |
| Q43882805 | c-Myc initiates illegitimate replication of the ribonucleotide reductase R2 gene |
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