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THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia
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The phenotypes observed in Ehd1-null embryos resemble those of mutants with functional disruption of negative regulators of SHH signaling, including Rab23, Gpr161, Thm1, Ptch1, TULP3 and PKA.
“the phenotypes we observed resemble those of mutants with functional disruption of negative regulators of SHH signaling, including Rab23, Gpr161, Thm1, Ptch1, TULP3 and PKA”
From Endocytic recycling protein EHD1 regulates primary cilia morphogenesis and SHH signaling during neural tube development (2016) · cites this paper as [97]
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“First, in mice, mutations affecting the IFT dynein motor subunit, Dync2h1, show disruption of the Hedgehog activation pathway, whereas mutations in IFT-A subunits, including Ift122 and Thm1, show overactivation of the Shh pathway (16, 17).”
BackgroundBhattacharyya, S., Rainey, M. A., Arya, P., Mohapatra, B. C., Mushtaq, I., Dutta, S., George, M., Storck, M. D., McComb, R. D., Muirhead, D., et al. (2016) · Scientific Reports · doi:10.1038/srep20727 · Cited by 36
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Metadata
- Authors
- Tran, P. V., Haycraft, C. J., Besschetnova, T. Y., Turbe-Doan, A., Stottmann, R. W., Herron, B. J., Chesebro, A. L., Qiu, H., Scherz, P. J., Shah, J. V., Yoder, B. K., & Beier, D. R.
- Venue
- Nature Genetics
- Published
- 2008-03-09
- Volume
- 40
- Issue
- 4
- Pages
- 403-410
- ISSN
- 1061-4036
- 1546-1718
- Cited by
- 322
- References
- 6
- Language
- en
- Licence
- www.springer.com/tdm (tdm)
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