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Items: 1 to 50 of 115

1.

Presynaptic Expression of LRIT3 Transsynaptically Organizes the Postsynaptic Glutamate Signaling Complex Containing TRPM1.

Hasan N, Pangeni G, Cobb CA, Ray TA, Nettesheim ER, Ertel KJ, Lipinski DM, McCall MA, Gregg RG.

Cell Rep. 2019 Jun 11;27(11):3107-3116.e3. doi: 10.1016/j.celrep.2019.05.056.

2.

A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function.

Peachey NS, Hasan N, FitzMaurice B, Burrill S, Pangeni G, Karst SY, Reinholdt L, Berry ML, Strobel M, Gregg RG, McCall MA, Chang B.

J Neurophysiol. 2017 Aug 1;118(2):845-854. doi: 10.1152/jn.00888.2016. Epub 2017 May 10.

3.

A novel transgenic mouse model of lysosomal storage disorder.

Ortiz-Miranda S, Ji R, Jurczyk A, Aryee KE, Mo S, Fletcher T, Shaffer SA, Greiner DL, Bortell R, Gregg RG, Cheng A, Hennings LJ, Rittenhouse AR.

Am J Physiol Gastrointest Liver Physiol. 2016 Nov 1;311(5):G903-G919. doi: 10.1152/ajpgi.00313.2015. Epub 2016 Sep 22.

4.

CACNA1S expression in mouse retina: Novel isoforms and antibody cross-reactivity with GPR179.

Hasan N, Ray TA, Gregg RG.

Vis Neurosci. 2016 Jan;33:E009. doi: 10.1017/S0952523816000055.

5.

Intermolecular Interaction between Anchoring Subunits Specify Subcellular Targeting and Function of RGS Proteins in Retina ON-Bipolar Neurons.

Sarria I, Orlandi C, McCall MA, Gregg RG, Martemyanov KA.

J Neurosci. 2016 Mar 9;36(10):2915-25. doi: 10.1523/JNEUROSCI.3833-15.2016.

6.

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.

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.

Hum Mol Genet. 2015 Nov 1;24(21):6229-39. doi: 10.1093/hmg/ddv341. Epub 2015 Aug 26.

7.

Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness.

Qian H, Ji R, Gregg RG, Peachey NS.

Vis Neurosci. 2015 Jan;32:E004. doi: 10.1017/S0952523815000012.

8.

pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability.

Carmean V, Yonkers MA, Tellez MB, Willer JR, Willer GB, Gregg RG, Geisler R, Neuhauss SC, Ribera AB.

J Neurophysiol. 2015 Aug;114(2):1146-57. doi: 10.1152/jn.00355.2015. Epub 2015 Jul 1.

9.

Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.

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, James PA, Churchyard A, Gao Y, Phelan DG, Gillies G, Salce N, Stanford L, Marsh AP, Mignogna ML, Hayflick SJ, Leventer RJ, Delatycki MB, Mellick GD, Kalscheuer VM, D'Adamo P, Bahlo M, Amor DJ, Lockhart PJ.

Am J Hum Genet. 2014 Dec 4;95(6):729-35. doi: 10.1016/j.ajhg.2014.10.015. Epub 2014 Nov 26.

10.

GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells.

Ray TA, Heath KM, Hasan N, Noel JM, Samuels IS, Martemyanov KA, Peachey NS, McCall MA, Gregg RG.

J Neurosci. 2014 Apr 30;34(18):6334-43. doi: 10.1523/JNEUROSCI.4044-13.2014.

11.

Presence of the Gpr179(nob5) allele in a C3H-derived transgenic mouse.

Balmer J, Ji R, Ray TA, Selber F, Gassmann M, Peachey NS, Gregg RG, Enzmann V.

Mol Vis. 2013 Dec 31;19:2615-25. eCollection 2013.

12.

Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse model.

Klooster J, van Genderen MM, Yu M, Florijn RJ, Riemslag FC, Bergen AA, Gregg RG, Peachey NS, Kamermans M.

Invest Ophthalmol Vis Sci. 2013 Oct 23;54(10):6973-81. doi: 10.1167/iovs.13-12293.

13.

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.

Peachey NS, Pearring JN, Bojang P Jr, Hirschtritt ME, Sturgill-Short G, Ray TA, Furukawa T, Koike C, Goldberg AF, Shen Y, McCall MA, Nawy S, Nishina PM, Gregg RG.

J Neurophysiol. 2012 Nov;108(9):2442-51. doi: 10.1152/jn.00137.2012. Epub 2012 Aug 15.

14.

Proteomic and UTR analyses of a rapidly evolving hypervariable family of vertebrate pheromones.

Wilburn DB, Bowen KE, Gregg RG, Cai J, Feldhoff PW, Houck LD, Feldhoff RC.

Evolution. 2012 Jul;66(7):2227-39. doi: 10.1111/j.1558-5646.2011.01572.x. Epub 2012 Feb 17.

PMID:
22759298
15.

GPR158/179 regulate G protein signaling by controlling localization and activity of the RGS7 complexes.

Orlandi C, Posokhova E, Masuho I, Ray TA, Hasan N, Gregg RG, Martemyanov KA.

J Cell Biol. 2012 Jun 11;197(6):711-9. doi: 10.1083/jcb.201202123.

16.

Topological analysis of small leucine-rich repeat proteoglycan nyctalopin.

Bojang P Jr, Gregg RG.

PLoS One. 2012;7(4):e33137. doi: 10.1371/journal.pone.0033137. Epub 2012 Apr 2.

17.

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.

Peachey NS, Ray TA, Florijn R, Rowe LB, Sjoerdsma T, Contreras-Alcantara S, Baba K, Tosini G, Pozdeyev N, Iuvone PM, Bojang P Jr, Pearring JN, Simonsz HJ, van Genderen M, Birch DG, Traboulsi EI, Dorfman A, Lopez I, Ren H, Goldberg AF, Nishina PM, Lachapelle P, McCall MA, Koenekoop RK, Bergen AA, Kamermans M, Gregg RG.

Am J Hum Genet. 2012 Feb 10;90(2):331-9. doi: 10.1016/j.ajhg.2011.12.006.

18.

Distribution of voltage gated calcium channel β subunits in the mouse retina.

Ball SL, McEnery MW, Yunker AM, Shin HS, Gregg RG.

Brain Res. 2011 Sep 15;1412:1-8. doi: 10.1016/j.brainres.2011.07.033. Epub 2011 Jul 23.

19.

A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites.

Pearring JN, Bojang P Jr, Shen Y, Koike C, Furukawa T, Nawy S, Gregg RG.

J Neurosci. 2011 Jul 6;31(27):10060-6. doi: 10.1523/JNEUROSCI.1014-11.2011.

20.

Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eye.

Murphy TR, Vihtelic TS, Ile KE, Watson CT, Willer GB, Gregg RG, Bankaitis VA, Hyde DR.

Exp Eye Res. 2011 Oct;93(4):460-74. doi: 10.1016/j.exer.2011.06.010. Epub 2011 Jun 23.

21.

Loss of Lrp2 in zebrafish disrupts pronephric tubular clearance but not forebrain development.

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.

Dev Dyn. 2011 Jun;240(6):1567-77. doi: 10.1002/dvdy.22624. Epub 2011 Mar 31.

22.

Neuromuscular synaptic patterning requires the function of skeletal muscle dihydropyridine receptors.

Chen F, Liu Y, Sugiura Y, Allen PD, Gregg RG, Lin W.

Nat Neurosci. 2011 May;14(5):570-7. doi: 10.1038/nn.2792. Epub 2011 Mar 27.

23.

Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cells.

Dhingra A, Fina ME, Neinstein A, Ramsey DJ, Xu Y, Fishman GA, Alexander KR, Qian H, Peachey NS, Gregg RG, Vardi N.

J Neurosci. 2011 Mar 16;31(11):3962-7. doi: 10.1523/JNEUROSCI.6007-10.2011.

24.

Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma.

Veth KN, Willer JR, Collery RF, Gray MP, Willer GB, Wagner DS, Mullins MC, Udvadia AJ, Smith RS, John SW, Gregg RG, Link BA.

PLoS Genet. 2011 Feb;7(2):e1001310. doi: 10.1371/journal.pgen.1001310. Epub 2011 Feb 17.

25.

The loss of vacuolar protein sorting 11 (vps11) causes retinal pathogenesis in a vertebrate model of syndromic albinism.

Thomas JL, Vihtelic TS, denDekker AD, Willer G, Luo X, Murphy TR, Gregg RG, Hyde DR, Thummel R.

Invest Ophthalmol Vis Sci. 2011 May 11;52(6):3119-28. doi: 10.1167/iovs.10-5957.

26.

rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA.

Haud N, Kara F, Diekmann S, Henneke M, Willer JR, Hillwig MS, Gregg RG, Macintosh GC, Gärtner J, Alia A, Hurlstone AF.

Proc Natl Acad Sci U S A. 2011 Jan 18;108(3):1099-103. doi: 10.1073/pnas.1009811107. Epub 2011 Jan 3.

27.

Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylation.

Song Y, Willer JR, Scherer PC, Panzer JA, Kugath A, Skordalakes E, Gregg RG, Willer GB, Balice-Gordon RJ.

PLoS One. 2010 Oct 29;5(10):e13743. doi: 10.1371/journal.pone.0013743.

28.

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.

Pani AM, Hobart HH, Morris CA, Mervis CB, Bray-Ward P, Kimberley KW, Rios CM, Clark RC, Gulbronson MD, Gowans GC, Gregg RG.

PLoS One. 2010 Aug 31;5(8):e12349. doi: 10.1371/journal.pone.0012349.

29.

Alpha 1 antitrypsin deficiency alleles are associated with joint dislocation and scoliosis in Williams syndrome.

Morris CA, Pani AM, Mervis CB, Rios CM, Kistler DJ, Gregg RG.

Am J Med Genet C Semin Med Genet. 2010 May 15;154C(2):299-306. doi: 10.1002/ajmg.c.30265.

30.

Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome.

Hobart HH, Morris CA, Mervis CB, Pani AM, Kistler DJ, Rios CM, Kimberley KW, Gregg RG, Bray-Ward P.

Am J Med Genet C Semin Med Genet. 2010 May 15;154C(2):220-8. doi: 10.1002/ajmg.c.30258.

31.

Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD).

Song Y, Selak MA, Watson CT, Coutts C, Scherer PC, Panzer JA, Gibbs S, Scott MO, Willer G, Gregg RG, Ali DW, Bennett MJ, Balice-Gordon RJ.

PLoS One. 2009 Dec 17;4(12):e8329. doi: 10.1371/journal.pone.0008329.

32.

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.

van Genderen MM, Bijveld MM, Claassen YB, Florijn RJ, Pearring JN, Meire FM, McCall MA, Riemslag FC, Gregg RG, Bergen AA, Kamermans M.

Am J Hum Genet. 2009 Nov;85(5):730-6. doi: 10.1016/j.ajhg.2009.10.012. Epub 2009 Nov 5.

33.

Muscle contractions guide rohon-beard peripheral sensory axons.

Paulus JD, Willer GB, Willer JR, Gregg RG, Halloran MC.

J Neurosci. 2009 Oct 21;29(42):13190-201. doi: 10.1523/JNEUROSCI.2179-09.2009.

34.

The Ca2+ channel subunit beta2 regulates Ca2+ channel abundance and function in inner hair cells and is required for hearing.

Neef J, Gehrt A, Bulankina AV, Meyer AC, Riedel D, Gregg RG, Strenzke N, Moser T.

J Neurosci. 2009 Aug 26;29(34):10730-40. doi: 10.1523/JNEUROSCI.1577-09.2009.

35.

Genetic variations associated with red hair color and fear of dental pain, anxiety regarding dental care and avoidance of dental care.

Binkley CJ, Beacham A, Neace W, Gregg RG, Liem EB, Sessler DI.

J Am Dent Assoc. 2009 Jul;140(7):896-905.

36.

A transient receptor potential-like channel mediates synaptic transmission in rod bipolar cells.

Shen Y, Heimel JA, Kamermans M, Peachey NS, Gregg RG, Nawy S.

J Neurosci. 2009 May 13;29(19):6088-93. doi: 10.1523/JNEUROSCI.0132-09.2009.

37.

Evolutionary shifts in courtship pheromone composition revealed by EST analysis of plethodontid salamander mental glands.

Kiemnec-Tyburczy KM, Watts RA, Gregg RG, von Borstel D, Arnold SJ.

Gene. 2009 Mar 1;432(1-2):75-81. doi: 10.1016/j.gene.2008.11.007. Epub 2008 Nov 21.

PMID:
19084057
38.

Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.

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, Naggert JK, Troy JB, Pinto LH, Nishina PM, McCall MA.

J Physiol. 2008 Sep 15;586(18):4409-24. doi: 10.1113/jphysiol.2008.157289. Epub 2008 Aug 7.

39.

Comparisons of structural and functional abnormalities in mouse b-wave mutants.

McCall MA, Gregg RG.

J Physiol. 2008 Sep 15;586(18):4385-92. doi: 10.1113/jphysiol.2008.159327. Epub 2008 Jul 24. Review.

40.

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

Marshall CR, Young EJ, Pani AM, Freckmann ML, Lacassie Y, Howald C, Fitzgerald KK, Peippo M, Morris CA, Shane K, Priolo M, Morimoto M, Kondo I, Manguoglu E, Berker-Karauzum S, Edery P, Hobart HH, Mervis CB, Zuffardi O, Reymond A, Kaplan P, Tassabehji M, Gregg RG, Scherer SW, Osborne LR.

Am J Hum Genet. 2008 Jul;83(1):106-11. doi: 10.1016/j.ajhg.2008.06.001. Epub 2008 Jun 19.

41.

Zebrafish blowout provides genetic evidence for Patched1-mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye.

Lee J, Willer JR, Willer GB, Smith K, Gregg RG, Gross JM.

Dev Biol. 2008 Jul 1;319(1):10-22. doi: 10.1016/j.ydbio.2008.03.035. Epub 2008 Apr 4.

42.

Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness.

Gregg RG, Kamermans M, Klooster J, Lukasiewicz PD, Peachey NS, Vessey KA, McCall MA.

J Neurophysiol. 2007 Nov;98(5):3023-33. Epub 2007 Sep 19.

43.

Plethodontid modulating factor, a hypervariable salamander courtship pheromone in the three-finger protein superfamily.

Palmer CA, Hollis DM, Watts RA, Houck LD, McCall MA, Gregg RG, Feldhoff PW, Feldhoff RC, Arnold SJ.

FEBS J. 2007 May;274(9):2300-10. Epub 2007 Apr 5.

44.

In vivo development of retinal ON-bipolar cell axonal terminals visualized in nyx::MYFP transgenic zebrafish.

Schroeter EH, Wong RO, Gregg RG.

Vis Neurosci. 2006 Sep-Oct;23(5):833-43.

PMID:
17020638
45.

Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish.

Semina EV, Bosenko DV, Zinkevich NC, Soules KA, Hyde DR, Vihtelic TS, Willer GB, Gregg RG, Link BA.

Dev Biol. 2006 Nov 1;299(1):63-77. Epub 2006 Jul 12.

46.

The light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1).

Marmorstein LY, Wu J, McLaughlin P, Yocom J, Karl MO, Neussert R, Wimmers S, Stanton JB, Gregg RG, Strauss O, Peachey NS, Marmorstein AD.

J Gen Physiol. 2006 May;127(5):577-89.

47.

Failure to maintain eye-specific segregation in nob, a mutant with abnormally patterned retinal activity.

Demas J, Sagdullaev BT, Green E, Jaubert-Miazza L, McCall MA, Gregg RG, Wong RO, Guido W.

Neuron. 2006 Apr 20;50(2):247-59.

48.

The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.

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, Vessey KA, Gregg RG.

Vis Neurosci. 2006 Jan-Feb;23(1):11-24.

49.

Lineage-specific differences in evolutionary mode in a salamander courtship pheromone.

Palmer CA, Watts RA, Gregg RG, McCall MA, Houck LD, Highton R, Arnold SJ.

Mol Biol Evol. 2005 Nov;22(11):2243-56. Epub 2005 Jul 20.

PMID:
16033988
50.

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