Jian Zuo, PhD

Affiliations: 
Developmental Neurobiology St. Jude Children's Research Hospital, San Francisco, CA, United States 
Area:
Hearing
Google:
"Jian Zuo"
Mean distance: 17.13 (cluster 6)
 
Cross-listing: CSD Tree

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Publications

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Teitz T, Fang J, Goktug AN, et al. (2018) CDK2 inhibitors as candidate therapeutics for cisplatin- and noise-induced hearing loss. The Journal of Experimental Medicine
Walters BJ, Coak E, Dearman J, et al. (2017) In Vivo Interplay between p27(Kip1), GATA3, ATOH1, and POU4F3 Converts Non-sensory Cells to Hair Cells in Adult Mice. Cell Reports. 19: 307-320
Zhang J, Liu Z, Chang A, et al. (2016) Abnormal mRNA splicing but normal auditory brainstem response (ABR) in mice with the prestin (SLC26A5) IVS2-2A>G mutation. Mutation Research. 790: 1-7
Walters BJ, Diao S, Zheng F, et al. (2016) Corrigendum: Pseudo-immortalization of postnatal cochlear progenitor cells yields a scalable cell line capable of transcriptionally regulating mature hair cell genes. Scientific Reports. 6: 21708
Walters BJ, Diao S, Zheng F, et al. (2015) Pseudo-immortalization of postnatal cochlear progenitor cells yields a scalable cell line capable of transcriptionally regulating mature hair cell genes. Scientific Reports. 5: 17792
Iconaru LI, Ban D, Bharatham K, et al. (2015) Discovery of Small Molecules that Inhibit the Disordered Protein, p27(Kip1). Scientific Reports. 5: 15686
Yamashita T, Hakizimana P, Wu S, et al. (2015) Outer Hair Cell Lateral Wall Structure Constrains the Mobility of Plasma Membrane Proteins. Plos Genetics. 11: e1005500
Walters BJ, Yamashita T, Zuo J. (2015) Sox2-CreER mice are useful for fate mapping of mature, but not neonatal, cochlear supporting cells in hair cell regeneration studies. Scientific Reports. 5: 11621
Walters BJ, Zuo J. (2015) A Sox10(rtTA/+) Mouse Line Allows for Inducible Gene Expression in the Auditory and Balance Organs of the Inner Ear. Journal of the Association For Research in Otolaryngology : Jaro. 16: 331-45
Cai Q, Wang B, Coling D, et al. (2014) Reduction in noise-induced functional loss of the cochleae in mice with pre-existing cochlear dysfunction due to genetic interference of prestin. Plos One. 9: e113990
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