Yi-Chun Hsiao, PhD - Publications

Affiliations: 
Genentech, Inc., San Francisco, CA, United States 

9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Hsiao YC, Muñoz-Estrada J, Tuz K, Ferland RJ. The transition zone protein AHI1 regulates neuronal ciliary trafficking of MCHR1 and its downstream signaling pathway. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 33741721 DOI: 10.1523/JNEUROSCI.2993-20.2021  0.705
2018 Heger K, Wickliffe KE, Ndoja A, Zhang J, Murthy A, Dugger DL, Maltzman A, de Sousa E Melo F, Hung J, Zeng Y, Verschueren E, Kirkpatrick DS, Vucic D, Lee WP, Roose-Girma M, ... ... Hsiao YC, et al. OTULIN limits cell death and inflammation by deubiquitinating LUBAC. Nature. PMID 29950720 DOI: 10.1038/S41586-018-0256-2  0.325
2018 Huang CS, Oberbeck N, Hsiao YC, Liu P, Johnson AR, Dixit VM, Hymowitz SG. Crystal Structure of Ripk4 Reveals Dimerization-Dependent Kinase Activity. Structure (London, England : 1993). PMID 29706531 DOI: 10.1016/J.Str.2018.04.002  0.366
2013 Tuz K, Hsiao YC, Juárez O, Shi B, Harmon EY, Phelps IG, Lennartz MR, Glass IA, Doherty D, Ferland RJ. The Joubert syndrome-associated missense mutation (V443D) in the Abelson-helper integration site 1 (AHI1) protein alters its localization and protein-protein interactions. The Journal of Biological Chemistry. 288: 13676-94. PMID 23532844 DOI: 10.1074/Jbc.M112.420786  0.687
2012 Hsiao YC, Tuz K, Ferland RJ. Trafficking in and to the primary cilium. Cilia. 1: 4. PMID 23351793 DOI: 10.1186/2046-2530-1-4  0.755
2010 Westfall JE, Hoyt C, Liu Q, Hsiao YC, Pierce EA, Page-McCaw PS, Ferland RJ. Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 8759-68. PMID 20592197 DOI: 10.1523/Jneurosci.5229-09.2010  0.679
2009 Hsiao YC, Tong ZJ, Westfall JE, Ault JG, Page-McCaw PS, Ferland RJ. Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking. Human Molecular Genetics. 18: 3926-41. PMID 19625297 DOI: 10.1093/Hmg/Ddp335  0.712
2009 Ferland RJ, Batiz LF, Neal J, Lian G, Bundock E, Lu J, Hsiao YC, Diamond R, Mei D, Banham AH, Brown PJ, Vanderburg CR, Joseph J, Hecht JL, Folkerth R, et al. Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia. Human Molecular Genetics. 18: 497-516. PMID 18996916 DOI: 10.1093/Hmg/Ddn377  0.764
2008 Doering JE, Kane K, Hsiao YC, Yao C, Shi B, Slowik AD, Dhagat B, Scott DD, Ault JG, Page-McCaw PS, Ferland RJ. Species differences in the expression of Ahi1, a protein implicated in the neurodevelopmental disorder Joubert syndrome, with preferential accumulation to stigmoid bodies. The Journal of Comparative Neurology. 511: 238-56. PMID 18785627 DOI: 10.1002/Cne.21824  0.527
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