| Year |
Citation |
Score |
| 2023 |
Gregg RG, Hasan N, Borghuis BG. LRIT3 expression in cone photoreceptors restores post-synaptic bipolar cell signalplex assembly and partial function in mice. Iscience. 26: 106499. PMID 37091241 DOI: 10.1016/j.isci.2023.106499 |
0.304 |
|
| 2019 |
Hasan N, Pangeni G, Cobb CA, Ray TA, Nettesheim ER, Ertel KJ, Lipinski DM, McCall MA, Gregg RG. Presynaptic Expression of LRIT3 Transsynaptically Organizes the Postsynaptic Glutamate Signaling Complex Containing TRPM1. Cell Reports. 27: 3107-3116.e3. PMID 31189098 DOI: 10.1016/J.Celrep.2019.05.056 |
0.345 |
|
| 2017 |
Peachey NS, Hasan N, FitzMaurice B, Burrill S, Pangeni G, Karst SY, Reinholdt L, Berry ML, Strobel M, Gregg RG, McCall MA, Chang B. A MISSENSE MUTATION IN GRM6 REDUCES BUT DOES NOT ELIMINATE MGLUR6 EXPRESSION OR ROD DEPOLARIZING BIPOLAR CELL FUNCTION. Journal of Neurophysiology. jn.00888.2016. PMID 28490646 DOI: 10.1152/Jn.00888.2016 |
0.45 |
|
| 2016 |
Ortiz-Miranda S, Ji R, Jurczyk A, Aryee KE, Mo S, Fletcher T, Shaffer SA, Greiner DL, Bortell R, Gregg R, Cheng A, Hennings LJ, Rittenhouse AR. A Novel Transgenic Mouse Model of Lysosomal Storage Disorder. American Journal of Physiology. Gastrointestinal and Liver Physiology. ajpgi.00313.2015. PMID 27659423 DOI: 10.1152/Ajpgi.00313.2015 |
0.32 |
|
| 2016 |
Hasan N, Ray TA, Gregg RG. CACNA1S expression in mouse retina: Novel isoforms and antibody cross-reactivity with GPR179. Visual Neuroscience. 33: E009. PMID 27471951 DOI: 10.1017/S0952523816000055 |
0.428 |
|
| 2016 |
Sarria I, Orlandi C, McCall MA, Gregg RG, Martemyanov KA. Intermolecular Interaction between Anchoring Subunits Specify Subcellular Targeting and Function of RGS Proteins in Retina ON-Bipolar Neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 2915-25. PMID 26961947 DOI: 10.1523/Jneurosci.3833-15.2016 |
0.363 |
|
| 2015 |
Scalabrino ML, Boye SL, Fransen KM, Noel JM, Dyka FM, Min SH, Ruan Q, De Leeuw CN, Simpson EM, Gregg RG, McCall MA, Peachey NS, Boye SE. 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. Human Molecular Genetics. PMID 26310623 DOI: 10.1093/Hmg/Ddv341 |
0.436 |
|
| 2015 |
Qian H, Ji R, Gregg RG, Peachey NS. Identification of a new mutant allele, Grm6 nob7, for complete congenital stationary night blindness. Visual Neuroscience. 32: E004. PMID 26241901 DOI: 10.1017/S0952523815000012 |
0.41 |
|
| 2015 |
Carmean V, Yonkers MA, Tellez MB, Willer JR, Willer GB, Gregg RG, Geisler R, Neuhauss SC, Ribera AB. pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability. Journal of Neurophysiology. 114: 1146-57. PMID 26133798 DOI: 10.1152/Jn.00355.2015 |
0.359 |
|
| 2015 |
White ML, Boye SL, Dyka FM, Fransen KM, de Leeuw CN, Simpson EM, Gregg RG, McCall MA, Peachey NS, Boye SE. 498. Optimization of rAAV Targets ON Bipolar Cells and Rescues the nobnyx Mouse Model of X-Linked Congenital Stationary Night Blindness Molecular Therapy. 23: S199. DOI: 10.1016/S1525-0016(16)34107-7 |
0.359 |
|
| 2014 |
Wilson GR, Sim JC, McLean C, Giannandrea M, Galea CA, Riseley JR, Stephenson SE, Fitzpatrick E, Haas SA, Pope K, Hogan KJ, Gregg RG, Bromhead CJ, Wargowski DS, Lawrence CH, et al. Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology. American Journal of Human Genetics. 95: 729-35. PMID 25434005 DOI: 10.1016/J.Ajhg.2014.10.015 |
0.325 |
|
| 2014 |
Ray TA, Heath KM, Hasan N, Noel JM, Samuels IS, Martemyanov KA, Peachey NS, McCall MA, Gregg RG. GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 6334-43. PMID 24790204 DOI: 10.1523/Jneurosci.4044-13.2014 |
0.422 |
|
| 2013 |
Klooster J, van Genderen MM, Yu M, Florijn RJ, Riemslag FC, Bergen AA, Gregg RG, Peachey NS, Kamermans M. Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse model. Investigative Ophthalmology & Visual Science. 54: 6973-81. PMID 24084093 DOI: 10.1167/Iovs.13-12293 |
0.438 |
|
| 2013 |
Daly CM, Willer J, Gregg R, Gross JM. snow white, a zebrafish model of Hermansky-Pudlak Syndrome type 5. Genetics. 195: 481-94. PMID 23893484 DOI: 10.1534/Genetics.113.154898 |
0.394 |
|
| 2012 |
Peachey NS, Pearring JN, Bojang P, Hirschtritt ME, Sturgill-Short G, Ray TA, Furukawa T, Koike C, Goldberg AF, Shen Y, McCall MA, Nawy S, Nishina PM, Gregg RG. Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation. Journal of Neurophysiology. 108: 2442-51. PMID 22896717 DOI: 10.1152/Jn.00137.2012 |
0.456 |
|
| 2012 |
Wilburn DB, Bowen KE, Gregg RG, Cai J, Feldhoff PW, Houck LD, Feldhoff RC. Proteomic and UTR analyses of a rapidly evolving hypervariable family of vertebrate pheromones Evolution. 66: 2227-2239. PMID 22759298 DOI: 10.1111/J.1558-5646.2011.01572.X |
0.307 |
|
| 2012 |
Bojang P, Gregg RG. Topological analysis of small leucine-rich repeat proteoglycan nyctalopin. Plos One. 7: e33137. PMID 22485138 DOI: 10.1371/Journal.Pone.0033137 |
0.367 |
|
| 2012 |
Peachey NS, Ray TA, Florijn R, Rowe LB, Sjoerdsma T, Contreras-Alcantara S, Baba K, Tosini G, Pozdeyev N, Iuvone PM, Bojang P, Pearring JN, Simonsz HJ, van Genderen M, Birch DG, ... ... Gregg RG, et al. GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness. American Journal of Human Genetics. 90: 331-9. PMID 22325362 DOI: 10.1016/J.Ajhg.2011.12.006 |
0.45 |
|
| 2011 |
Ball SL, McEnery MW, Yunker AM, Shin HS, Gregg RG. Distribution of voltage gated calcium channel β subunits in the mouse retina. Brain Research. 1412: 1-8. PMID 21831364 DOI: 10.1016/J.Brainres.2011.07.033 |
0.368 |
|
| 2011 |
Pearring JN, Bojang P, Shen Y, Koike C, Furukawa T, Nawy S, Gregg RG. A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 10060-6. PMID 21734298 DOI: 10.1523/Jneurosci.1014-11.2011 |
0.398 |
|
| 2011 |
Murphy TR, Vihtelic TS, Ile KE, Watson CT, Willer GB, Gregg RG, Bankaitis VA, Hyde DR. Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eye. Experimental Eye Research. 93: 460-74. PMID 21722635 DOI: 10.1016/J.Exer.2011.06.010 |
0.409 |
|
| 2011 |
Kur E, Christa A, Veth KN, Gajera CR, Andrade-Navarro MA, Zhang J, Willer JR, Gregg RG, Abdelilah-Seyfried S, Bachmann S, Link BA, Hammes A, Willnow TE. Loss of Lrp2 in zebrafish disrupts pronephric tubular clearance but not forebrain development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 240: 1567-77. PMID 21455927 DOI: 10.1002/Dvdy.22624 |
0.301 |
|
| 2011 |
Chen F, Liu Y, Sugiura Y, Allen PD, Gregg RG, Lin W. Neuromuscular synaptic patterning requires the function of skeletal muscle dihydropyridine receptors. Nature Neuroscience. 14: 570-7. PMID 21441923 DOI: 10.1038/Nn.2792 |
0.301 |
|
| 2011 |
Dhingra A, Fina ME, Neinstein A, Ramsey DJ, Xu Y, Fishman GA, Alexander KR, Qian H, Peachey NS, Gregg RG, Vardi N. Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 3962-7. PMID 21411639 DOI: 10.1523/Jneurosci.6007-10.2011 |
0.401 |
|
| 2011 |
Veth KN, Willer JR, Collery RF, Gray MP, Willer GB, Wagner DS, Mullins MC, Udvadia AJ, Smith RS, John SW, Gregg RG, Link BA. Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma. Plos Genetics. 7: e1001310. PMID 21379331 DOI: 10.1371/Journal.Pgen.1001310 |
0.404 |
|
| 2011 |
Thomas JL, Vihtelic TS, denDekker AD, Willer G, Luo X, Murphy TR, Gregg RG, Hyde DR, Thummel R. The loss of vacuolar protein sorting 11 (vps11) causes retinal pathogenesis in a vertebrate model of syndromic albinism. Investigative Ophthalmology & Visual Science. 52: 3119-28. PMID 21330665 DOI: 10.1167/Iovs.10-5957 |
0.417 |
|
| 2010 |
Song Y, Willer JR, Scherer PC, Panzer JA, Kugath A, Skordalakes E, Gregg RG, Willer GB, Balice-Gordon RJ. Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylation. Plos One. 5: e13743. PMID 21060795 DOI: 10.1371/Journal.Pone.0013743 |
0.353 |
|
| 2009 |
van Genderen MM, Bijveld MM, Claassen YB, Florijn RJ, Pearring JN, Meire FM, McCall MA, Riemslag FC, Gregg RG, Bergen AA, Kamermans M. Mutations in TRPM1 are a common cause of complete congenital stationary night blindness. American Journal of Human Genetics. 85: 730-6. PMID 19896109 DOI: 10.1016/J.Ajhg.2009.10.012 |
0.344 |
|
| 2009 |
Neef J, Gehrt A, Bulankina AV, Meyer AC, Riedel D, Gregg RG, Strenzke N, Moser T. The Ca2+ channel subunit beta2 regulates Ca2+ channel abundance and function in inner hair cells and is required for hearing. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 10730-40. PMID 19710324 DOI: 10.1523/Jneurosci.1577-09.2009 |
0.315 |
|
| 2009 |
Shen Y, Heimel JA, Kamermans M, Peachey NS, Gregg RG, Nawy S. A transient receptor potential-like channel mediates synaptic transmission in rod bipolar cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 6088-93. PMID 19439586 DOI: 10.1523/Jneurosci.0132-09.2009 |
0.384 |
|
| 2008 |
Maddox DM, Vessey KA, Yarbrough GL, Invergo BM, Cantrell DR, Inayat S, Balannik V, Hicks WL, Hawes NL, Byers S, Smith RS, Hurd R, Howell D, Gregg RG, Chang B, et al. Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses. The Journal of Physiology. 586: 4409-24. PMID 18687716 DOI: 10.1113/Jphysiol.2008.157289 |
0.421 |
|
| 2008 |
McCall MA, Gregg RG. Comparisons of structural and functional abnormalities in mouse b-wave mutants. The Journal of Physiology. 586: 4385-92. PMID 18653656 DOI: 10.1113/Jphysiol.2008.159327 |
0.393 |
|
| 2008 |
Lee J, Willer JR, Willer GB, Smith K, Gregg RG, Gross JM. Zebrafish blowout provides genetic evidence for Patched1-mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye. Developmental Biology. 319: 10-22. PMID 18479681 DOI: 10.1016/J.Ydbio.2008.03.035 |
0.34 |
|
| 2007 |
Gregg RG, Kamermans M, Klooster J, Lukasiewicz PD, Peachey NS, Vessey KA, McCall MA. Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness. Journal of Neurophysiology. 98: 3023-33. PMID 17881478 DOI: 10.1152/Jn.00608.2007 |
0.452 |
|
| 2006 |
Schroeter EH, Wong RO, Gregg RG. In vivo development of retinal ON-bipolar cell axonal terminals visualized in nyx::MYFP transgenic zebrafish. Visual Neuroscience. 23: 833-43. PMID 17020638 DOI: 10.1017/S0952523806230219 |
0.336 |
|
| 2006 |
Semina EV, Bosenko DV, Zinkevich NC, Soules KA, Hyde DR, Vihtelic TS, Willer GB, Gregg RG, Link BA. Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish. Developmental Biology. 299: 63-77. PMID 16973147 DOI: 10.1016/J.Ydbio.2006.07.005 |
0.376 |
|
| 2006 |
Marmorstein LY, Wu J, McLaughlin P, Yocom J, Karl MO, Neussert R, Wimmers S, Stanton JB, Gregg RG, Strauss O, Peachey NS, Marmorstein AD. The light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1). The Journal of General Physiology. 127: 577-89. PMID 16636205 DOI: 10.1085/Jgp.200509473 |
0.356 |
|
| 2006 |
Demas J, Sagdullaev BT, Green E, Jaubert-Miazza L, McCall MA, Gregg RG, Wong RO, Guido W. Failure to maintain eye-specific segregation in nob, a mutant with abnormally patterned retinal activity. Neuron. 50: 247-59. PMID 16630836 DOI: 10.1016/J.Neuron.2006.03.033 |
0.366 |
|
| 2006 |
Chang B, Heckenlively JR, Bayley PR, Brecha NC, Davisson MT, Hawes NL, Hirano AA, Hurd RE, Ikeda A, Johnson BA, McCall MA, Morgans CW, Nusinowitz S, Peachey NS, Rice DS, ... ... Gregg RG, et al. The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses. Visual Neuroscience. 23: 11-24. PMID 16597347 DOI: 10.1017/S095252380623102X |
0.468 |
|
| 2005 |
Willer GB, Lee VM, Gregg RG, Link BA. Analysis of the Zebrafish perplexed mutation reveals tissue-specific roles for de novo pyrimidine synthesis during development. Genetics. 170: 1827-37. PMID 15937129 DOI: 10.1534/Genetics.105.041608 |
0.394 |
|
| 2003 |
Ball SL, Pardue MT, McCall MA, Gregg RG, Peachey NS. Immunohistochemical analysis of the outer plexiform layer in the nob mouse shows no abnormalities. Visual Neuroscience. 20: 267-72. PMID 14570248 DOI: 10.1017/S0952523803203059 |
0.423 |
|
| 2003 |
Gregg RG, Willer GB, Fadool JM, Dowling JE, Link BA. Positional cloning of the young mutation identifies an essential role for the Brahma chromatin remodeling complex in mediating retinal cell differentiation. Proceedings of the National Academy of Sciences of the United States of America. 100: 6535-40. PMID 12748389 DOI: 10.1073/Pnas.0631813100 |
0.423 |
|
| 2003 |
Gregg RG, Mukhopadhyay S, Candille SI, Ball SL, Pardue MT, McCall MA, Peachey NS. Identification of the gene and the mutation responsible for the mouse nob phenotype. Investigative Ophthalmology & Visual Science. 44: 378-84. PMID 12506099 DOI: 10.1167/Iovs.02-0501 |
0.601 |
|
| 2003 |
Arikkath J, Chen CC, Ahern C, Allamand V, Flanagan JD, Coronado R, Gregg RG, Campbell KP. Gamma 1 subunit interactions within the skeletal muscle L-type voltage-gated calcium channels. The Journal of Biological Chemistry. 278: 1212-9. PMID 12409298 DOI: 10.1074/Jbc.M208689200 |
0.316 |
|
| 2002 |
Ball SL, Gregg RG. Using mutant mice to study the role of voltage-gated calcium channels in the retina. Advances in Experimental Medicine and Biology. 514: 439-50. PMID 12596937 DOI: 10.1007/978-1-4615-0121-3_26 |
0.454 |
|
| 2002 |
Read DS, McCall MA, Gregg RG. Absence of voltage-dependent calcium channels delays photoreceptor degeneration in rd mice. Experimental Eye Research. 75: 415-20. PMID 12387789 DOI: 10.1006/Exer.2002.2034 |
0.634 |
|
| 2002 |
McCall MA, Lukasiewicz PD, Gregg RG, Peachey NS. Elimination of the ρ1 Subunit Abolishes GABACReceptor Expression and Alters Visual Processing in the Mouse Retina The Journal of Neuroscience. 22: 4163-4174. DOI: 10.1523/Jneurosci.22-10-04163.2002 |
0.355 |
|
| 2001 |
Ahern CA, Powers PA, Biddlecome GH, Roethe L, Vallejo P, Mortenson L, Strube C, Campbell KP, Coronado R, Gregg RG. Modulation of L-type Ca2+ current but not activation of Ca2+ release by the gamma1 subunit of the dihydropyridine receptor of skeletal muscle. Bmc Physiology. 1: 8. PMID 11495636 DOI: 10.1186/1472-6793-1-8 |
0.349 |
|
| 1999 |
Hogan K, Gregg RG, Powers PA. Structure and alternative splicing of the gene encoding the human β1 subunit of voltage dependent calcium channels Neuroscience Letters. 277: 111-114. PMID 10624822 DOI: 10.1016/S0304-3940(99)00851-4 |
0.315 |
|
| 1999 |
Beurg M, Ahern CA, Vallejo P, Conklin MW, Powers PA, Gregg RG, Coronado R. Involvement of the carboxy-terminus region of the dihydropyridine receptor β1a subunit in excitation-contraction coupling of skeletal muscle Biophysical Journal. 77: 2953-2967. PMID 10585919 DOI: 10.1016/S0006-3495(99)77128-6 |
0.367 |
|
| 1999 |
Beurg M, Sukhareva M, Ahern CA, Conklin MW, Perez-Reyes E, Powers PA, Gregg RG, Coronado R. Differential regulation of skeletal muscle L-type Ca2+ current and excitation-contraction coupling by the dihydropyridine receptor beta subunit. Biophysical Journal. 76: 1744-56. PMID 10096875 DOI: 10.1016/S0006-3495(99)77336-4 |
0.365 |
|
| 1999 |
Conklin MW, Powers P, Gregg RG, Coronado R. Ca2+ sparks in embryonic mouse skeletal muscle selectively deficient in dihydropyridine receptor α(1s) β(1a) subunits Biophysical Journal. 76: 657-669. PMID 9929471 DOI: 10.1016/S0006-3495(99)77233-4 |
0.321 |
|
| 1998 |
Strube C, Beurg M, Sukhareva M, Ahern CA, Powell JA, Powers PA, Gregg RG, Coronado R. Molecular origin of the L-type Ca2+ current of skeletal muscle myotubes selectively deficient in dihydropyridine receptor β(1a) subunit Biophysical Journal. 75: 207-217. PMID 9649380 DOI: 10.1016/S0006-3495(98)77507-1 |
0.351 |
|
| 1994 |
Powers PA, Scherer SW, Tsui LC, Gregg RG, Hogan K. Localization of the Gene Encoding the α2/δ Subunit (CACNL2A) of the Human Skeletal Muscle Voltage-Dependent Ca2+ Channel to Chromosome 7q21-q22 by Somatic Cell Hybrid Analysis Genomics. 19: 192-193. PMID 8188232 DOI: 10.1006/Geno.1994.1044 |
0.344 |
|
| 1994 |
Jurkat-Rott K, Lehmann-Horn F, Elbaz A, Heine R, Gregg RG, Hogan K, Powers PA, Lapie P, Vale-Santos JE, Weissenbach J, Fontaine B. A calcium channel mutation causing hypokalemic periodic paralysis Human Molecular Genetics. 3: 1415-1419. PMID 7987325 DOI: 10.1093/Hmg/3.8.1415 |
0.395 |
|
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