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Links from Protein

Items: 7

1.
Determination of basal phosphodiesterase activity in mouse rod photoreceptors with cGMP clamp
Teemu T. Turunen, Ari Koskelainen
Sci Rep. 2019; 9: 1183. Published online 2019 Feb 4. doi: 10.1038/s41598-018-37661-w
PMCID:
PMC6362171
ArticlePDF–2.8M
2.
Apo-Opsin Exists in Equilibrium Between a Predominant Inactive and a Rare Highly Active State
Shinya Sato, Beata Jastrzebska, Andreas Engel, Krzysztof Palczewski, Vladimir J. Kefalov
J Neurosci. 2019 Jan 9; 39(2): 212–223. doi: 10.1523/JNEUROSCI.1980-18.2018
PMCID:
PMC6325258
ArticlePDF–1.2M
3.
Investigating the Ca2+-dependent and Ca2+-independent mechanisms for mammalian cone light adaptation
Frans Vinberg, Vladimir J. Kefalov
Sci Rep. 2018; 8: 15864. Published online 2018 Oct 26. doi: 10.1038/s41598-018-34073-8
PMCID:
PMC6203770
ArticlePDF–2.6M
4.
Dominant Cone-Rod Dystrophy: A Mouse Model Generated by Gene Targeting of the GCAP1/Guca1a Gene
Prateek K. Buch, Marija Mihelec, Phillippa Cottrill, Susan E. Wilkie, Rachael A. Pearson, Yanai Duran, Emma L. West, Michel Michaelides, Robin R. Ali, David M. Hunt
PLoS One. 2011; 6(3): e18089. Published online 2011 Mar 28. doi: 10.1371/journal.pone.0018089
PMCID:
PMC3065489
ArticlePDF–960K
5.
Role of guanylate cyclase-activating proteins (GCAPs) in setting the flash sensitivity of rod photoreceptors
Ana Mendez, Marie E. Burns, Izabela Sokal, Alexander M. Dizhoor, Wolfgang Baehr, Krzysztof Palczewski, Denis A. Baylor, Jeannie Chen
Proc Natl Acad Sci U S A. 2001 Aug 14; 98(17): 9948–9953. Published online 2001 Aug 7. doi: 10.1073/pnas.171308998
PMCID:
PMC55558
ArticlePDF–339K
6.
Functional characterization of a novel GUCA1A missense mutation (D144G) in autosomal dominant cone dystrophy: A novel pathogenic GUCA1A variant in COD
Suzhen Tang, Yujun Xia, Yunhai Dai, Yaning Liu, Jingshuo Li, Xiaojing Pan, Peng Chen
Mol Vis. 2019; 25: 921–xxx. Published online 2019 Dec 31.
PMCID:
PMC6982429
ArticlePDF–4.8M
7.
GUCA1A mutation causes maculopathy in a five-generation family with a wide spectrum of severity
Xue Chen, Xunlun Sheng, Wenjuan Zhuang, Xiantao Sun, Guohua Liu, Xun Shi, Guofu Huang, Yan Mei, Yingjie Li, Xinyuan Pan, Yani Liu, Zili Li, Qingshun Zhao, Biao Yan, Chen Zhao
Genet Med. 2017 Aug; 19(8): 945–954. Published online 2017 Jan 26. doi: 10.1038/gim.2016.217
PMCID:
PMC5548935
ArticlePDF–1.6M

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