H19 | Encyclopedia MDPI

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Liu, D. H19. Encyclopedia. Available online: https://encyclopedia.pub/entry/3831 (accessed on 27 September 2026).

Liu D. H19. Encyclopedia. Available at: https://encyclopedia.pub/entry/3831. Accessed September 27, 2026.

Liu, Dean. "H19" Encyclopedia, https://encyclopedia.pub/entry/3831 (accessed September 27, 2026).

Liu, D. (2020, December 22). H19. In Encyclopedia. https://encyclopedia.pub/entry/3831

Liu, Dean. "H19." Encyclopedia. Web. 22 December, 2020.

H19

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H19, imprinted maternally expressed transcript

genes

References

Abu-Amero S, Monk D, Frost J, Preece M, Stanier P, Moore GE. The geneticaetiology of Silver-Russell syndrome. J Med Genet. 2008 Apr;45(4):193-9. Epub2007 Dec 21. Review.
Al-Hussain T, Ali A, Akhtar M. Wilms tumor: an update. Adv Anat Pathol. 2014May;21(3):166-73. doi: 10.1097/PAP.0000000000000017. Review.
Cai X, Cullen BR. The imprinted H19 noncoding RNA is a primary microRNAprecursor. RNA. 2007 Mar;13(3):313-6. Epub 2007 Jan 19.
Dome JS, Huff V. Wilms Tumor Predisposition. 2003 Dec 19 [updated 2016 Oct20]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K,Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University ofWashington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK1294/
Eggermann T, Eggermann K, Schönherr N. Growth retardation versus overgrowth:Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome.Trends Genet. 2008 Apr;24(4):195-204. doi: 10.1016/j.tig.2008.01.003. Epub 2008Mar 7. Review.
Gabory A, Jammes H, Dandolo L. The H19 locus: role of an imprinted non-coding RNA in growth and development. Bioessays. 2010 Jun;32(6):473-80. doi:10.1002/bies.200900170. Review.
MacFarland SP, Duffy KA, Bhatti TR, Bagatell R, Balamuth NJ, Brodeur GM,Ganguly A, Mattei PA, Surrey LF, Balis FM, Kalish JM. Diagnosis ofBeckwith-Wiedemann syndrome in children presenting with Wilms tumor. PediatrBlood Cancer. 2018 Oct;65(10):e27296. doi: 10.1002/pbc.27296. Epub 2018 Jun 22.
Nativio R, Sparago A, Ito Y, Weksberg R, Riccio A, Murrell A. Disruption ofgenomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemannsyndrome and Silver-Russell syndrome. Hum Mol Genet. 2011 Apr 1;20(7):1363-74.doi: 10.1093/hmg/ddr018. Epub 2011 Jan 31.
Sparago A, Cerrato F, Vernucci M, Ferrero GB, Silengo MC, Riccio A.Microdeletions in the human H19 DMR result in loss of IGF2 imprinting andBeckwith-Wiedemann syndrome. Nat Genet. 2004 Sep;36(9):958-60. Epub 2004 Aug 15.
Tian F, Yourek G, Shi X, Yang Y. The development of Wilms tumor: from WT1 and microRNA to animal models. Biochim Biophys Acta. 2014 Aug;1846(1):180-7. doi:10.1016/j.bbcan.2014.07.003. Epub 2014 Jul 11. Review.

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Subjects: Genetics & Heredity

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