SAM1 domain of SASH1 harbors distinctive structural heterogeneity
Author:
Funder
National Institutes of Health
University of Colorado Boulder
University of Colorado Cancer Center
Publisher
Elsevier BV
Subject
Structural Biology
Reference50 articles.
1. Five novel mutations in SASH1 contribute to lentiginous phenotypes in Japanese families;Araki;Pigment Cell Melanoma Res.,2021
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3. Burgess, J.T., Bolderson, E., Adams, M.N., Duijf, P.H.G., Zhang, S.-D., Gray, S.G., Wright, G., Richard, D.J., O’byrne, K.J., 2020. SASH1 is a prognostic indicator and potential therapeutic target in non-small cell lung cancer. Nature Scientific Reports 10, 18605. https://doi.org/10.1038/s41598-020-75625-1.
4. The SAM domain of mouse SAMHD1 is critical for its activation and regulation;Buzovetsky;Nat Commun,2018
5. Novel missense mutation of SASH1 in a Chinese family with dyschromatosis universalis hereditaria;Cao;BMC Med Genomics,2021
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