PMC Links for GEO Profiles (Select 131501487) - PMC

Select item 87381391.

Structural mechanisms of assembly, permeation, gating, and pharmacology of native human rod CNG channel

Jing Xue, Yan Han, Weizhong Zeng, Youxing Jiang

Neuron. Author manuscript; available in PMC 2023 Jan 5.

Published in final edited form as: Neuron. 2022 Jan 5; 110(1): 86–95.e5. Published online 2021 Oct 25. doi: 10.1016/j.neuron.2021.10.006

PMCID:: PMC8738139

Abstract Article PDF–2.5M

Select item 81650302.

Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome

Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi

Cell. Author manuscript; available in PMC 2022 May 27.

Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011

PMCID:: PMC8165030

Abstract Article PDF–2.2M

Select item 79071213.

A case of retinitis pigmentosa homozygous for a rare CNGA1 causal variant

Kohei Saito, Norimoto Gotoh, Inyeop Kang, Toshio Shimada, Takeshi Usui, Chikashi Terao

Sci Rep. 2021; 11: 4681. Published online 2021 Feb 25. doi: 10.1038/s41598-021-84098-9

PMCID:: PMC7907121

Abstract Article PDF–1.2M

Select item 74113324.

Identification of a novel homozygous variant in the CNGA1 gene in a Chinese family with autosomal recessive retinitis pigmentosa

Le Wang, Tongdan Zou, Yongqiong Lin, Ling Li, Peng Zhang, Bo Gong, Jilong Hao, Houbin Zhang

Mol Med Rep. 2020 Sep; 22(3): 2516–2520. Published online 2020 Jul 10. doi: 10.3892/mmr.2020.11331

PMCID:: PMC7411332

Abstract Article PDF–457K

Select item 65756605.

Human rod photoreceptor cGMP-gated channel: amino acid sequence, gene structure, and functional expression

RS Dhallan, JP Macke, RL Eddy, TB Shows, RR Reed, KW Yau, J Nathans

J Neurosci. 1992 Aug 1; 12(8): 3248–3256. doi: 10.1523/JNEUROSCI.12-08-03248.1992

PMCID:: PMC6575660

Abstract PDF–1.9M

Select item 49389716.

Novel compound heterozygous mutations in CNGA1in a Chinese family affected with autosomal recessive retinitis pigmentosa by targeted sequencing

Min Wang, Dekang Gan, Xin Huang, Gezhi Xu

BMC Ophthalmol. 2016; 16: 101. Published online 2016 Jul 8. doi: 10.1186/s12886-016-0281-6

PMCID:: PMC4938971

Abstract Article PDF–837K

Select item 47252447.

Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family

Xin Jin, Ling-Hui Qu, Bao-Ke Hou, Hai-Wei Xu, Xiao-Hong Meng, Chi-Pui Pang, Zheng-Qin Yin

Biosci Rep. 2016 Feb; 36(1): e00289. Published online 2016 Jan 22. doi: 10.1042/BSR20150131

PMCID:: PMC4725244

Abstract Article PDF–866K

Select item 41825608.

Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa

Satoshi Katagiri, Masakazu Akahori, Yuri Sergeev, Kazutoshi Yoshitake, Kazuho Ikeo, Masaaki Furuno, Takaaki Hayashi, Mineo Kondo, Shinji Ueno, Kazushige Tsunoda, Kei Shinoda, Kazuki Kuniyoshi, Yohinori Tsurusaki, Naomichi Matsumoto, Hiroshi Tsuneoka, Takeshi Iwata

PLoS One. 2014; 9(9): e108721. Published online 2014 Sep 30. doi: 10.1371/journal.pone.0108721