H19 and Igf2 – enhancing the confusion?
- 1 January 2003
- journal article
- review article
- Published by Elsevier in Trends in Genetics
- Vol. 19 (1) , 17-23
- https://doi.org/10.1016/s0168-9525(02)00004-5
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Placental-specific IGF-II is a major modulator of placental and fetal growthNature, 2002
- Analysis of Sequence Upstream of the Endogenous H19 Gene Reveals Elements Both Essential and Dispensable for ImprintingMolecular and Cellular Biology, 2002
- Regulatory Mechanisms at the MouseIgf2/H19 LocusMolecular and Cellular Biology, 2001
- Elucidation of the Minimal Sequence Required to Imprint H19 TransgenesGenomics, 2001
- Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19Nature Genetics, 2000
- Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element.Genes & Development, 1997
- Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathwayHuman Molecular Genetics, 1996
- An enhancer deletion affects both H19 and Igf2 expression.Genes & Development, 1995
- Disruption of imprinting caused by deletion of the H19 gene region in miceNature, 1995
- A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targetingNature, 1990