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Oppositely imprinted genes p57(Kip2) and Igf2 interact in a mouse model for Beckwith–Wiedemann syndrome

Beckwith–Wiedemann syndrome (BWS) is a clinically variable disorder characterized by somatic overgrowth, macroglossia, abdominal wall defects, visceromegaly, and an increased susceptibility to childhood tumors. The disease has been linked to a large cluster of imprinted genes at human chromosome 11p...

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Bibliografske podrobnosti
izdano v:Genes Dev
Main Authors: Caspary, Tamara, Cleary, Michele A., Perlman, Elizabeth J., Zhang, Pumin, Elledge, Stephen J., Tilghman, Shirley M.
Format: Artigo
Jezik:Inglês
Izdano: Cold Spring Harbor Laboratory Press 1999
Teme:
Online dostop:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC317182/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10601037/
https://ncbi.nlm.nih.govhttps://doi.org/10.1101/gad.13.23.3115
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