Protein sorting, targeting and trafficking in photoreceptor cells

Yazar: Pearring, Jillian N., Salinas, Raquel Y., Baker, Sheila A., Arshavsky, Vadim Y.
Baskı/Yayın Bilgisi 2013

Guanylate cyclase 1 relies on rhodopsin for intracellular stability and ciliary trafficking

Yazar: Pearring, Jillian N, Spencer, William J, Lieu, Eric C, Arshavsky, Vadim Y
Yayımlandı eLife (2015)

Photoreceptor discs: built like ectosomes

Yazar: Spencer, William J., Lewis, Tylor R., Pearring, Jillian N., Arshavsky, Vadim Y.
Yayımlandı Trends Cell Biol (2020)

R9AP targeting to rod outer segments is independent of rhodopsin and is guided by the SNARE homology domain

Yazar: Pearring, Jillian N., Lieu, Eric C., Winter, Joan R., Baker, Sheila A., Arshavsky, Vadim Y.
Baskı/Yayın Bilgisi 2014

A Role for Nyctalopin, a Small Leucine-Rich Repeat Protein, in Localizing the TRP Melastatin 1 Channel to Retinal Depolarizing Bipolar Cell Dendrites

Yazar: Pearring, Jillian N., Bojang, Pasano, Shen, Yin, Koike, Chieko, Furukawa, Takahisa, Nawy, Scott, Gregg, Ronald G.
Baskı/Yayın Bilgisi 2011

Photoreceptor discs form through peripherin-dependent suppression of ciliary ectosome release

Yazar: Salinas, Raquel Y., Pearring, Jillian N., Ding, Jin-Dong, Spencer, William J., Hao, Ying, Arshavsky, Vadim Y.
Yayımlandı J Cell Biol (2017)

Progressive Rod-Cone Degeneration (PRCD) Protein Requires N-Terminal S-Acylation and Rhodopsin Binding for Photoreceptor Outer Segment Localization and Maintaining Intracellular St...

Yazar: Spencer, William J., Pearring, Jillian N., Salinas, Raquel Y., Loiselle, David R., Skiba, Nikolai P., Arshavsky, Vadim Y.
Yayımlandı Biochemistry (2016)

The GARP Domain of the Rod CNG Channel's β1-Subunit Contains Distinct Sites for Outer Segment Targeting and Connecting to the Photoreceptor Disk Rim

Yazar: Pearring, Jillian N., Martínez-Márquez, Jorge, Willer, Jason R., Lieu, Eric C., Salinas, Raquel Y., Arshavsky, Vadim Y.
Yayımlandı J Neurosci (2021)

Dimerization deficiency of enigmatic retinitis pigmentosa-linked rhodopsin mutants

Yazar: Ploier, Birgit, Caro, Lydia N., Morizumi, Takefumi, Pandey, Kalpana, Pearring, Jillian N., Goren, Michael A., Finnemann, Silvia C., Graumann, Johannes, Arshavsky, Vadim Y., Dittman, Jeremy S., Ernst, Oliver P., Menon, Anant K.
Yayımlandı Nat Commun (2016)

Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration

Yazar: Pearring, Jillian N., San Agustin, Jovenal T., Lobanova, Ekaterina S., Gabriel, Christopher J., Lieu, Eric C., Monis, William J., Stuck, Michael W., Strittmatter, Lara, Jaber, Samer M., Arshavsky, Vadim Y., Pazour, Gregory J.
Yayımlandı PLoS Genet (2017)

Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

Yazar: van Genderen, Maria M., Bijveld, Mieke M.C., Claassen, Yvonne B., Florijn, Ralph J., Pearring, Jillian N., Meire, Francoise M., McCall, Maureen A., Riemslag, Frans C.C., Gregg, Ronald G., Bergen, Arthur A.B., Kamermans, Maarten
Baskı/Yayın Bilgisi 2009

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Yazar: Peachey, Neal S., Pearring, Jillian N., Bojang, Pasano, Hirschtritt, Matthew E., Sturgill-Short, Gwen, Ray, Thomas A., Furukawa, Takahisa, Koike, Chieko, Goldberg, Andrew F. X., Shen, Yin, McCall, Maureen A., Nawy, Scott, Nishina, Patsy M., Gregg, Ronald G.
Baskı/Yayın Bilgisi 2012

PRCD is essential for high-fidelity photoreceptor disc formation

Yazar: Spencer, William J., Ding, Jin-Dong, Lewis, Tylor R., Yu, Chen, Phan, Sebastien, Pearring, Jillian N., Kim, Keun-Young, Thor, Andrea, Mathew, Rose, Kalnitsky, Joan, Hao, Ying, Travis, Amanda M., Biswas, Sondip K., Lo, Woo-Kuen, Besharse, Joseph C., Ellisman, Mark H., Saban, Daniel R., Burns, Marie E., Arshavsky, Vadim Y.
Yayımlandı Proc Natl Acad Sci U S A (2019)

GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness

Yazar: Peachey, Neal S., Ray, Thomas A., Florijn, Ralph, Rowe, Lucy B., Sjoerdsma, Trijntje, Contreras-Alcantara, Susana, Baba, Kenkichi, Tosini, Gianluca, Pozdeyev, Nikita, Iuvone, P. Michael, Bojang, Pasano, Pearring, Jillian N., Simonsz, Huibert Jan, van Genderen, Maria, Birch, David G., Traboulsi, Elias I., Dorfman, Allison, Lopez, Irma, Ren, Huanan, Goldberg, Andrew F.X., Nishina, Patsy M., Lachapelle, Pierre, McCall, Maureen A., Koenekoop, Robert K., Bergen, Arthur A.B., Kamermans, Maarten, Gregg, Ronald G.
Baskı/Yayın Bilgisi 2012

De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome

Yazar: Burrage, Lindsay C., Charng, Wu-Lin, Eldomery, Mohammad K., Willer, Jason R., Davis, Erica E., Lugtenberg, Dorien, Zhu, Wenmiao, Leduc, Magalie S., Akdemir, Zeynep C., Azamian, Mahshid, Zapata, Gladys, Hernandez, Patricia P., Schoots, Jeroen, de Munnik, Sonja A., Roepman, Ronald, Pearring, Jillian N., Jhangiani, Shalini, Katsanis, Nicholas, Vissers, Lisenka E.L.M., Brunner, Han G., Beaudet, Arthur L., Rosenfeld, Jill A., Muzny, Donna M., Gibbs, Richard A., Eng, Christine M., Xia, Fan, Lalani, Seema R., Lupski, James R., Bongers, Ernie M.H.F., Yang, Yaping
Yayımlandı Am J Hum Genet (2015)