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Title: Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour
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Nature Genetics [1061-4036] Steenman, Marja J. C. yr:1994


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1. Jurkiewicz, D. "A novelIGF2/H19domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family." American journal of medical genetics. Part A 173.1 (2017): 72-78. Link to Full Text for this item Link to SFX for this item
2. Hashimoto, K. "Loss of H19 imprinting and up-regulation of H19 and SNRPN in a case with malignant mixed Müllerian tumor of the uterus." Human pathology (1997): 862-5. Link to Full Text for this item Link to SFX for this item
3. SUTCLIFFE, J S S. "DELETIONS OF A DIFFERENTIALLY METHYLATED CPG ISLAND AT THE SNRPN GENE DEFINE A PUTATIVE IMPRINTING CONTROL REGION." Nature genetics 8.1 (1994): 52-58. Link to Full Text for this item Link to SFX for this item
4. Zhang, Michael e. "Long noncoding RNA-mediated intrachromosomal interactions promote imprinting at the Kcnq1 locus." The Journal of cell biology 204.1 (2014): 61-75. Link to Full Text for this item Link to SFX for this item
5. Dugimont, T. "The H19 TATA-less promoter is efficiently repressed by wild-type tumor suppressor gene product p53." Oncogene 16.18 (1998): 2395-401. Link to Full Text for this item Link to SFX for this item
6. Gray, T A A. "An imprinted, mammalian bicistronic transcript encodes two independent proteins." Proceedings of the National Academy of Sciences of the United States of America 96.10 (1999): 5616-21. Link to Full Text for this item Link to SFX for this item
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8. Kanduri, C. "Long noncoding RNAs: Lessons from genomic imprinting." Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms 1859.1 (2016): 102-111. Link to SFX for this item
9. Himeda, Charis L. "Myogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy associated DUX4 gene." Molecular and cellular biology 34.11 (2014): 1942-55. Link to Full Text for this item Link to SFX for this item
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11. Saitoh, S. "Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome." American journal of human genetics 66.6 (2000): 1958-1962. Link to Full Text for this item Link to SFX for this item
12. Gray, T A A. "Concerted regulation and molecular evolution of the duplicated SNRPB'/B and SNRPN loci." Nucleic acids research 27.23 (1999): 4577-4584. Link to Full Text for this item Link to SFX for this item
13. Kopf, E. "The effect of retinoic acid on the activation of the human H19 promoter by a 3' downstream region." FEBS letters 432.3 (1998): 123-7. Link to Full Text for this item Link to SFX for this item
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16. Gardner, R J J. "An imprinted locus associated with transient neonatal diabetes mellitus." Human Molecular Genetics 9.4 (2000): 589-96. Link to SFX for this item
17. Felsenfeld, G. "Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene." Nature 405.6785 (2000): 482-5. Link to Full Text for this item Link to SFX for this item
18. Orr, Harry T T. "Trinucleotide repeat disorders." Annual review of neuroscience 30.1 (2007): 575-621. Link to Full Text for this item Link to SFX for this item
19. Smith, Adam C C. "Beckwith-Wiedemann syndrome." American journal of medical genetics. Part C, Seminars in medical genetics 137.1 (2005): 12-23. Link to Full Text for this item Link to SFX for this item
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