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Items: 4

1.
ESRP1 mutations cause hearing loss due to defects in alternative splicing that disrupt cochlear development
Alex M. Rohacek, Thomas W. Bebee, Richard K. Tilton, Caleb M. Radens, Chris McDermott-Roe, Natoya Peart, Maninder Kaur, Michael Zaykaner, Benjamin Cieply, Kiran Musunuru, Yoseph Barash, John A. Germiller, Ian D. Krantz, Russ P. Carstens, Douglas J. Epstein
Dev Cell. Author manuscript; available in PMC 2018 Nov 6.
Published in final edited form as: Dev Cell. 2017 Nov 6; 43(3): 318–331.e5. Published online 2017 Oct 26. doi: 10.1016/j.devcel.2017.09.026
PMCID:
PMC5687886
AbstractArticlePDF–2.4M
2.
Circulating primitive erythroblasts establish a functional, protein 4.1R-dependent cytoskeletal network prior to enucleating
Yu-Shan Huang, Luis F. Delgadillo, Kathryn H. Cyr, Paul D. Kingsley, Xiuli An, Kathleen E. McGrath, Narla Mohandas, John G. Conboy, Richard E. Waugh, Jiandi Wan, James Palis
Sci Rep. 2017; 7: 5164. Published online 2017 Jul 12. doi: 10.1038/s41598-017-05498-4
PMCID:
PMC5507979
AbstractArticlePDF–2.1M
3.
Protein 4.1R Influences Myogenin Protein Stability and Skeletal Muscle Differentiation
Shu-Ching Huang, Anyu Zhou, Dan T. Nguyen, Henry S. Zhang, Edward J. Benz, Jr.
J Biol Chem. 2016 Dec 2; 291(49): 25591–25607. Published online 2016 Oct 25. doi: 10.1074/jbc.M116.761296
PMCID:
PMC5207257
AbstractArticlePDF–2.9M
4.
Molecular cloning of protein 4.1, a major structural element of the human erythrocyte membrane skeleton.
J Conboy, Y W Kan, S B Shohet, N Mohandas
Proc Natl Acad Sci U S A. 1986 Dec; 83(24): 9512–9516. doi: 10.1073/pnas.83.24.9512
PMCID:
PMC387170
SummaryPage BrowsePDF–1.2M

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