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Results: 1 to 20 of 160

1.

Heterotrimeric Kinesin-2 (KIF3) Mediates Transition Zone and Axoneme Formation of Mouse Photoreceptors.

Jiang L, Wei Y, Ronquillo CC, Marc RE, Yoder BK, Frederick JM, Baehr W.

J Biol Chem. 2015 Mar 30. pii: jbc.M115.638437. [Epub ahead of print]

2.

Domain Organization and Conformational Plasticity of the G Protein Effector, PDE6.

Zhang Z, He F, Constantine R, Baker ML, Baehr W, Schmid MF, Wensel TG, Agosto MA.

J Biol Chem. 2015 Mar 25. pii: jbc.M115.647636. [Epub ahead of print]

3.

Ca(2+) and Ca(2+)-interlocked membrane guanylate cyclase signal modulation of neuronal and cardiovascular signal transduction.

Sharma RK, Baehr W, Makino CL, Duda T.

Front Mol Neurosci. 2015 Mar 6;8:7. doi: 10.3389/fnmol.2015.00007. eCollection 2015. No abstract available.

4.

Retinal cone photoreceptors require phosducin-like protein 1 for G protein complex assembly and signaling.

Tracy CM, Kolesnikov AV, Blake DR, Chen CK, Baehr W, Kefalov VJ, Willardson BM.

PLoS One. 2015 Feb 6;10(2):e0117129. doi: 10.1371/journal.pone.0117129. eCollection 2015.

5.

Membrane protein transport in photoreceptors: the function of PDEδ: the Proctor lecture.

Baehr W.

Invest Ophthalmol Vis Sci. 2014 Dec 30;55(12):8653-66. doi: 10.1167/iovs.14-16066.

PMID:
25550383
6.

Mistrafficking of prenylated proteins causes retinitis pigmentosa 2.

Zhang H, Hanke-Gogokhia C, Jiang L, Li X, Wang P, Gerstner CD, Frederick JM, Yang Z, Baehr W.

FASEB J. 2015 Mar;29(3):932-42. doi: 10.1096/fj.14-257915. Epub 2014 Nov 24.

PMID:
25422369
7.

Inactivity of human β,β-carotene-9',10'-dioxygenase (BCO2) underlies retinal accumulation of the human macular carotenoid pigment.

Li B, Vachali PP, Gorusupudi A, Shen Z, Sharifzadeh H, Besch BM, Nelson K, Horvath MM, Frederick JM, Baehr W, Bernstein PS.

Proc Natl Acad Sci U S A. 2014 Jul 15;111(28):10173-8. doi: 10.1073/pnas.1402526111. Epub 2014 Jun 30.

8.

FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression.

Owen LA, Morrison MA, Ahn J, Woo SJ, Sato H, Robinson R, Morgan DJ, Zacharaki F, Simeonova M, Uehara H, Chakravarthy U, Hogg RE, Ambati BK, Kotoula M, Baehr W, Haider NB, Silvestri G, Miller JW, Tsironi EE, Farrer LA, Kim IK, Park KH, DeAngelis MM.

Invest Ophthalmol Vis Sci. 2014 May 8;55(6):3543-54. doi: 10.1167/iovs.14-14047.

9.

Centrin 2 is required for mouse olfactory ciliary trafficking and development of ependymal cilia planar polarity.

Ying G, Avasthi P, Irwin M, Gerstner CD, Frederick JM, Lucero MT, Baehr W.

J Neurosci. 2014 Apr 30;34(18):6377-88. doi: 10.1523/JNEUROSCI.0067-14.2014.

10.

RNA interference gene therapy in dominant retinitis pigmentosa and cone-rod dystrophy mouse models caused by GCAP1 mutations.

Jiang L, Frederick JM, Baehr W.

Front Mol Neurosci. 2014 Apr 7;7:25. doi: 10.3389/fnmol.2014.00025. eCollection 2014. Review.

11.

Unc119 gene deletion partially rescues the GRK1 transport defect of Pde6d (- /-) cones.

Zhang H, Frederick JM, Baehr W.

Adv Exp Med Biol. 2014;801:487-93. doi: 10.1007/978-1-4614-3209-8_62.

12.

Suppressing thyroid hormone signaling preserves cone photoreceptors in mouse models of retinal degeneration.

Ma H, Thapa A, Morris L, Redmond TM, Baehr W, Ding XQ.

Proc Natl Acad Sci U S A. 2014 Mar 4;111(9):3602-7. doi: 10.1073/pnas.1317041111. Epub 2014 Feb 18.

13.

A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated INPP5E protein to the primary cilium.

Thomas S, Wright KJ, Le Corre S, Micalizzi A, Romani M, Abhyankar A, Saada J, Perrault I, Amiel J, Litzler J, Filhol E, Elkhartoufi N, Kwong M, Casanova JL, Boddaert N, Baehr W, Lyonnet S, Munnich A, Burglen L, Chassaing N, Encha-Ravazi F, Vekemans M, Gleeson JG, Valente EM, Jackson PK, Drummond IA, Saunier S, Attié-Bitach T.

Hum Mutat. 2014 Jan;35(1):137-46.

14.

cGMP accumulation causes photoreceptor degeneration in CNG channel deficiency: evidence of cGMP cytotoxicity independently of enhanced CNG channel function.

Xu J, Morris L, Thapa A, Ma H, Michalakis S, Biel M, Baehr W, Peshenko IV, Dizhoor AM, Ding XQ.

J Neurosci. 2013 Sep 11;33(37):14939-48. doi: 10.1523/JNEUROSCI.0909-13.2013.

15.

Photoreceptor avascular privilege is shielded by soluble VEGF receptor-1.

Luo L, Uehara H, Zhang X, Das SK, Olsen T, Holt D, Simonis JM, Jackman K, Singh N, Miya TR, Huang W, Ahmed F, Bastos-Carvalho A, Le YZ, Mamalis C, Chiodo VA, Hauswirth WW, Baffi J, Lacal PM, Orecchia A, Ferrara N, Gao G, Young-Hee K, Fu Y, Owen L, Albuquerque R, Baehr W, Thomas K, Li DY, Chalam KV, Shibuya M, Grisanti S, Wilson DJ, Ambati J, Ambati BK.

Elife. 2013 Jun 18;2:e00324. doi: 10.7554/eLife.00324.

16.

Germline deletion of Cetn1 causes infertility in male mice.

Avasthi P, Scheel JF, Ying G, Frederick JM, Baehr W, Wolfrum U.

J Cell Sci. 2013 Jul 15;126(Pt 14):3204-13. doi: 10.1242/jcs.128587. Epub 2013 May 2.

17.

Phosducin-like protein 1 is essential for G-protein assembly and signaling in retinal rod photoreceptors.

Lai CW, Kolesnikov AV, Frederick JM, Blake DR, Jiang L, Stewart JS, Chen CK, Barrow JR, Baehr W, Kefalov VJ, Willardson BM.

J Neurosci. 2013 May 1;33(18):7941-51. doi: 10.1523/JNEUROSCI.5001-12.2013.

18.

RNAi-mediated gene suppression in a GCAP1(L151F) cone-rod dystrophy mouse model.

Jiang L, Li TZ, Boye SE, Hauswirth WW, Frederick JM, Baehr W.

PLoS One. 2013;8(3):e57676. doi: 10.1371/journal.pone.0057676. Epub 2013 Mar 5.

19.

AAV-mediated gene therapy in the guanylate cyclase (RetGC1/RetGC2) double knockout mouse model of Leber congenital amaurosis.

Boye SL, Peshenko IV, Huang WC, Min SH, McDoom I, Kay CN, Liu X, Dyka FM, Foster TC, Umino Y, Karan S, Jacobson SG, Baehr W, Dizhoor A, Hauswirth WW, Boye SE.

Hum Gene Ther. 2013 Feb;24(2):189-202. doi: 10.1089/hum.2012.193.

20.

Retina ciliopathies: from genes to mechanisms and treatment.

Khanna H, Baehr W.

Vision Res. 2012 Dec 15;75:1. doi: 10.1016/j.visres.2012.11.007. No abstract available.

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