Terry Watnick

University of Maryland School of Medicine, Baltimore, MD, United States 
"Terry Watnick"

I trained in Craig Montell's lab as a post doc 1999-2003

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Hofherr A, Seger C, Fitzpatrick F, et al. (2018) The mitochondrial transporter SLC25A25 links ciliary TRPP2 signaling and cellular metabolism. Plos Biology. 16: e2005651
Cai J, Song X, Wang W, et al. (2018) A RhoA-YAP-c-Myc signaling axis promotes the development of polycystic kidney disease. Genes & Development
Lin CC, Kurashige M, Liu Y, et al. (2018) A cleavage product of Polycystin-1 is a mitochondrial matrix protein that affects mitochondria morphology and function when heterologously expressed. Scientific Reports. 8: 2743
Kaimori JY, Lin CC, Outeda P, et al. (2017) NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology. Scientific Reports. 7: 7733
Outeda P, Menezes L, Hartung EA, et al. (2017) A novel model of autosomal recessive polycystic kidney questions the role of the fibrocystin C-terminus in disease mechanism. Kidney International
Porath B, Gainullin VG, Cornec-Le Gall E, et al. (2016) Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease. American Journal of Human Genetics. 98: 1193-1207
Kim S, Nie H, Nesin V, et al. (2016) The polycystin complex mediates Wnt/Ca(2+) signalling. Nature Cell Biology
Perrone RD, Malek AM, Watnick T. (2015) Vascular complications in autosomal dominant polycystic kidney disease. Nature Reviews. Nephrology
Chapman AB, Devuyst O, Eckardt KU, et al. (2015) Autosomal-dominant polycystic kidney disease (ADPKD): Executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference Kidney International. 88: 17-27
Kim H, Xu H, Yao Q, et al. (2014) Ciliary membrane proteins traffic through the Golgi via a Rabep1/GGA1/Arl3-dependent mechanism. Nature Communications. 5: 5482
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