| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0165-4608(96)00221-X |
| P698 | PubMed publication ID | 9062579 |
| P2093 | author name string | T Matsuda | |
| T Arima | |||
| N Takagi | |||
| N Wake | |||
| P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
| Monoallelic expression of the human H19 gene | Q28184725 | ||
| Parental imprinting of the human H19 gene | Q28187996 | ||
| Establishment of functional imprinting of the H19 gene in human developing placentae | Q28297145 | ||
| Isolation and characterization of rat and human glyceraldehyde-3-phosphate dehydrogenase cDNAs: genomic complexity and molecular evolution of the gene | Q28776291 | ||
| The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. | Q34059933 | ||
| Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse | Q34088761 | ||
| Parental-origin-specific epigenetic modification of the mouse H19 gene | Q34363043 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| A new imprinted gene cloned by a methylation-sensitive genome scanning method | Q35017116 | ||
| Polymerase chain reaction (PCR) for detection of APal polymorphism at the insulin like growth factor II gene (IGF2) | Q35801824 | ||
| Genomic imprinting of Mash2, a mouse gene required for trophoblast development | Q38298288 | ||
| Androgenetic origin of hydatidiform mole | Q41973808 | ||
| Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region | Q44185908 | ||
| Parental imprinting of the Mas protooncogene in mouse | Q46725382 | ||
| Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting | Q48084682 | ||
| Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method | Q48086267 | ||
| A paternal-specific methylation imprint marks the alleles of the mouse H19 gene | Q49057890 | ||
| Non-random inactivation of X chromosome in the rat yolk sac | Q50889386 | ||
| Relaxation of imprinted genes in human cancer. | Q52545355 | ||
| A newly established human gestational choriocarcinoma cell line and its characterization | Q52831341 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Mechanism of origin of complete hydatidiform moles | Q59060743 | ||
| Tumour-suppressor activity of H19 RNA | Q59071440 | ||
| Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour | Q59088779 | ||
| Androgenesis as a Cause of Hydatidiform Mole 2 | Q67277974 | ||
| Cytologic evidence for preferential inactivation of the paternally derived X chromosome in XX mouse blastocysts | Q67326172 | ||
| IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome | Q70765937 | ||
| Transcribed dinucleotide repeat polymorphism in the IGF2 gene | Q71996217 | ||
| Parental genomic imprinting of the human IGF2 gene | Q72222239 | ||
| TaqI and RsaI polymorphisms in the H19 gene (D11S813E) | Q72228845 | ||
| Genetic origin of malignant trophoblastic neoplasms | Q72399743 | ||
| Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour | Q72703028 | ||
| Epigenetic lesions at the H19 locus in Wilms' tumour patients | Q72703033 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | choriocarcinoma | Q1076481 |
| P304 | page(s) | 39-47 | |
| P577 | publication date | 1997-01-01 | |
| P1433 | published in | Cancer Genetics and Cytogenetics | Q15753061 |
| P1476 | title | Association of IGF2 and H19 imprinting with choriocarcinoma development | |
| P478 | volume | 93 |
| Q73153544 | Altered imprinting, promoter usage, and expression of insulin-like growth factor-II gene in gestational trophoblastic diseases |
| Q36562166 | CUDR promotes liver cancer stem cell growth through upregulating TERT and C-Myc |
| Q51894988 | Characteristics of peri‐implantation porcine concepti population and maternal milieu influence the transcriptome profile |
| Q38466353 | Comparative genomic hybridization studies in hydatidiform moles and choriocarcinoma: amplification of 7q21-q31 and loss of 8p12-p21 in choriocarcinoma. |
| Q39024684 | Down-regulation of ncRAN, a long non-coding RNA, contributes to colorectal cancer cell migration and invasion and predicts poor overall survival for colorectal cancer patients |
| Q50736910 | Establishment of a new diagnostic method for hydropic villi by using TSSC3 antibody. |
| Q33199277 | GTT1/StarD7, a novel phosphatidylcholine transfer protein-like highly expressed in gestational trophoblastic tumour: cloning and characterization |
| Q35582563 | Genetics and molecular markers in gestational trophoblastic disease with special reference to their clinical application |
| Q33541538 | Genomic imprinting: implications for human disease |
| Q46525173 | Hedgehog signaling induces osteosarcoma development through Yap1 and H19 overexpression. |
| Q99552114 | Increased Expression Level of Long Noncoding RNA H19 in Plasma of Patients with Myocardial Infarction |
| Q50504586 | LncRNA H19-mediated mouse cleft palate induced by all-trans retinoic acid. |
| Q36790436 | Long non-coding RNA in cancer |
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| Q37831991 | Molecular mechanisms of genomic imprinting and clinical implications for cancer |
| Q30054218 | NECC1, a candidate choriocarcinoma suppressor gene that encodes a homeodomain consensus motif☆☆Sequence data from this article have been deposited with the DDBJ/EMBL/GenBank Data Libraries under Accession No. AB059410 |
| Q34605730 | Non-Coding RNAs: Functional Aspects and Diagnostic Utility in Oncology |
| Q89148846 | Non-coding RNAs in pancreatic cancer: challenges and opportunities for clinical application |
| Q37414363 | Pathogenesis of choriocarcinoma: clinical, genetic and stem cell perspectives |
| Q35789796 | Promoter hypermethylation of multiple genes in hydatidiform mole and choriocarcinoma |
| Q33541952 | Recent advances in gestational trophoblastic disease |
| Q28215769 | Renal cell carcinoma-associated G250 methylation and expression: in vivo and in vitro studies |
| Q34995156 | The functional role of long non-coding RNA in human carcinomas |
| Q38045210 | The long non-coding RNAs, a new cancer diagnostic and therapeutic gold mine |
| Q35847774 | deepBase v2.0: identification, expression, evolution and function of small RNAs, LncRNAs and circular RNAs from deep-sequencing data |
| Q36544748 | miR675 upregulates long noncoding RNA H19 through activating EGR1 in human liver cancer |
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