| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1995PNAS...92..480T |
| P356 | DOI | 10.1073/PNAS.92.2.480 |
| P932 | PMC publication ID | 42764 |
| P698 | PubMed publication ID | 7831314 |
| P5875 | ResearchGate publication ID | 15368536 |
| P2093 | author name string | J H Thomas | |
| P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
| Genomic imprinting in mammalian development: a parental tug-of-war | Q28278146 | ||
| Ectopic expression of the H19 gene in mice causes prenatal lethality | Q28281671 | ||
| Role for DNA methylation in genomic imprinting | Q29618669 | ||
| Incidence of early loss of pregnancy | Q34177364 | ||
| Differential activity of maternally and paternally derived chromosome regions in mice | Q34198480 | ||
| Methylation and imprinting: from host defense to gene regulation? | Q34363070 | ||
| Allelotype of colorectal carcinomas | Q34461209 | ||
| Uniparental paternal disomy in a genetic cancer-predisposing syndrome | Q34535432 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Defects in a cell cycle checkpoint may be responsible for the genomic instability of cancer cells | Q35476763 | ||
| Delays in anaphase initiation occur in individual nuclei of the syncytial Drosophila embryo | Q37375667 | ||
| A cytogenetic study of spontaneous abortions with direct analysis of chorionic villi. | Q37634932 | ||
| Cytogenetic analysis of 1508 spontaneous abortions originating from south Slovakia | Q39232817 | ||
| Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region | Q44185908 | ||
| bcl-2 inhibits multiple forms of apoptosis but not negative selection in thymocytes | Q44192187 | ||
| The effect of in-vitro ageing on mouse sperm chromosomes | Q44842333 | ||
| Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method | Q48086267 | ||
| Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. | Q48125063 | ||
| Genomic imprinting--defusing the ovarian time bomb | Q49110236 | ||
| Relaxation of imprinted genes in human cancer. | Q52545355 | ||
| Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcoma. | Q52868711 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Factors affecting the observed number of young resulting from adjacent-2 disjunction in mice carrying a translocation | Q56049804 | ||
| Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour | Q59088779 | ||
| Radiation-induced interphase death of rat thymocytes is internally programmed (apoptosis) | Q68090652 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 480-482 | |
| P577 | publication date | 1995-01-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Genomic imprinting proposed as a surveillance mechanism for chromosome loss | |
| P478 | volume | 92 |
| Q28266696 | Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma |
| Q24676371 | B-chromosome evolution |
| Q27011914 | DNA demethylation and invasive cancer: implications for therapeutics |
| Q36049856 | DNA methylation and genetic instability in colorectal cancer cells |
| Q33733162 | DNA methylation in eukaryotic chromosome stability revisited: DNA methyltransferase in the management of DNA conformation space |
| Q37061792 | Epigenetics and colorectal cancer pathogenesis |
| Q36588877 | Genome-wide CpG island methylation and intergenic demethylation propensities vary among different tumor sites |
| Q36562187 | Genomic imprinting and dermatological disease |
| Q41175197 | Genomic imprinting in disorders of growth |
| Q55397342 | Hypomethylation of CpG sites and c-myc gene overexpression in hepatocellular carcinomas, but not hyperplastic nodules, induced by a choline-deficient L-amino acid-defined diet in rats. |
| Q33852775 | Imprinted genes as potential genetic and epigenetic toxicologic targets |
| Q38492613 | Maternal origin of a unique extra chromosome, der(9)(pter-->q13::q13-->q12:) in a girl with typical trisomy 9p syndrome |
| Q34378429 | Methylation and colorectal cancer |
| Q52535998 | Overall deregulation in gene expression as a novel indicator of tumor aggressiveness in colorectal cancer. |
| Q74219766 | Why do multiple deletions accumulate during progression in carcinomas? |
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