Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology von Wilson, Gabrielle R., Sim, Joe C.H., McLean, Catriona, Giannandrea, Maila, Galea, Charles A., Riseley, Jessica R., Stephenson, Sarah E.M., Fitzpatrick, Elizabeth, Haas, Stefan A., Pope, Kate, Hogan, Kirk J., Gregg, Ronald G., Bromhead, Catherine J., Wargowski, David S., Lawrence, Christopher H., James, Paul A., Churchyard, Andrew, Gao, Yujing, Phelan, Dean G., Gillies, Greta, Salce, Nicholas, Stanford, Lynn, Marsh, Ashley P.L., Mignogna, Maria L., Hayflick, Susan J., Leventer, Richard J., Delatycki, Martin B., Mellick, George D., Kalscheuer, Vera M., D’Adamo, Patrizia, Bahlo, Melanie, Amor, David J., Lockhart, Paul J.

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A Transient Receptor Potential-Like Channel Mediates Synaptic Transmission in Rod Bipolar Cells von Shen, Yin, Heimel, J. Alexander, Kamermans, Maarten, Peachey, Neal S, Gregg, Ronald G, Nawy, Scott

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

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Presynaptic Expression of LRIT3 Transsynaptically Organizes the Postsynaptic Glutamate Signaling Complex Containing TRPM1 von Hasan, Nazarul, Pangeni, Gobinda, Cobb, Catherine A, Ray, Thomas A, Nettesheim, Emily R, Ertel, Kristina J, Lipinski, Daniel M, McCall, Maureen A, Gregg, Ronald G

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GPR158/179 regulate G protein signaling by controlling localization and activity of the RGS7 complexes von Orlandi, Cesare, Posokhova, Ekaterina, Masuho, Ikuo, Ray, Thomas A, Hasan, Nazarul, Gregg, Ronald G, Martemyanov, Kirill A

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Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness von Scalabrino, Miranda L, Boye, Sanford L, Fransen, Kathryn M H, Noel, Jennifer M, Dyka, Frank M, Min, Seok Hong, Ruan, Qing, De Leeuw, Charles N, Simpson, Elizabeth M, Gregg, Ronald G, McCall, Maureen A, Peachey, Neal S, Boye, Shannon E

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Gain control by sparse, ultra-slow glycinergic synapses von Jain, Varsha, Hanson, Laura, Sethuramanujam, Santhosh, Michaels, Tracy, Gawley, Jerram, Gregg, Ronald G., Pyle, Ian, Zhang, Chi, Smith, Robert G., Berson, David, McCall, Maureen A., Awatramani, Gautam B.

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

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GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells von Ray, Thomas A, Heath, Kathryn M, Hasan, Nazarul, Noel, Jennifer M, Samuels, Ivy S, Martemyanov, Kirill A, Peachey, Neal S, McCall, Maureen A, Gregg, Ronald G

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Intermolecular Interaction between Anchoring Subunits Specify Subcellular Targeting and Function of RGS Proteins in Retina ON-Bipolar Neurons von Sarria, Ignacio, Orlandi, Cesare, McCall, Maureen A, Gregg, Ronald G, Martemyanov, Kirill A

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LRIT3 expression in cone photoreceptors restores post-synaptic bipolar cell signalplex assembly and partial function in Lrit3−/− mice von Gregg, Ronald G., Hasan, Nazarul, Borghuis, Bart G.

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Neuromuscular synaptic patterning requires the function of skeletal muscle dihydropyridine receptors von Lin, Weichun, Chen, Fujun, Liu, Yun, Sugiura, Yoshie, Allen, Paul D, Gregg, Ronald G

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Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cells von Dhingra, Anuradha, Fina, Marie E, Neinstein, Adam, Ramsey, David J, Xu, Ying, Fishman, Gerald A, Alexander, Kenneth R, Qian, Haohua, Peachey, Neal S, Gregg, Ronald G, Vardi, Noga

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rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA von Haud, Noémie, Kara, Firat, Diekmann, Simone, Henneke, Marco, Willer, Jason R., Hillwig, Melissa S., Gregg, Ronald G., MacIntosh, Gustavo C., Gärtner, Jutta, Alia, A., Hurlstone, Adam F. L., Moore, Melissa J.

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Comparisons of structural and functional abnormalities in mouse b-wave mutants von McCall, Maureen A., Gregg, Ronald G.

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Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma von Veth, Kerry N, Willer, Jason R, Collery, Ross F, Gray, Matthew P, Willer, Gregory B, Wagner, Daniel S, Mullins, Mary C, Udvadia, Ava J, Smith, Richard S, John, Simon W M, Gregg, Ronald G, Link, Brian A

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Anesthetic requirement is increased in redheads von LIEM, Edwin B, LIN, Chun-Ming, SULEMAN, Mohammad-Irfan, DOUFAS, Anthony G, GREGG, Ronald G, VEAUTHIER, Jacqueline M, LOYD, Gary, SESSLER, Daniel I

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Topological analysis of small leucine-rich repeat proteoglycan nyctalopin von Bojang, Jr, Pasano, Gregg, Ronald G

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Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylation von Song, Yuanquan, Willer, Jason R, Scherer, Paul C, Panzer, Jessica A, Kugath, Amy, Skordalakes, Emmanuel, Gregg, Ronald G, Willer, Gregory B, Balice-Gordon, Rita J

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Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation von Peachey, Neal S, Pearring, Jillian N, Bojang, Jr, 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

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