Protein sorting, targeting and trafficking in photoreceptor cells

Por Pearring, Jillian N., Salinas, Raquel Y., Baker, Sheila A., Arshavsky, Vadim Y.
Publicado em 2013

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

Por Pearring, Jillian N, Spencer, William J, Lieu, Eric C, Arshavsky, Vadim Y
Publicado no eLife (2015)

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

Por Pearring, Jillian N., Lieu, Eric C., Winter, Joan R., Baker, Sheila A., Arshavsky, Vadim Y.
Publicado em 2014

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

Por Pearring, Jillian N., Bojang, Pasano, Shen, Yin, Koike, Chieko, Furukawa, Takahisa, Nawy, Scott, Gregg, Ronald G.
Publicado em 2011

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

Por Salinas, Raquel Y., Pearring, Jillian N., Ding, Jin-Dong, Spencer, William J., Hao, Ying, Arshavsky, Vadim Y.
Publicado no 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...

Por Spencer, William J., Pearring, Jillian N., Salinas, Raquel Y., Loiselle, David R., Skiba, Nikolai P., Arshavsky, Vadim Y.
Publicado no Biochemistry (2016)

Dimerization deficiency of enigmatic retinitis pigmentosa-linked rhodopsin mutants

Por 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.
Publicado no Nat Commun (2016)

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

Por 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.
Publicado no PLoS Genet (2017)

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

Por 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
Publicado em 2009

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Por 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.
Publicado em 2012

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

Por 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.
Publicado em 2012

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

Por 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
Publicado no Am J Hum Genet (2015)