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Links from Nucleotide

Items: 4

1.
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability
Poh Hui Chia, Franklin Lei Zhong, Shinsuke Niwa, Carine Bonnard, Kagistia Hana Utami, Ruizhu Zeng, Hane Lee, Ascia Eskin, Stanley F Nelson, William H Xie, Samah Al-Tawalbeh, Mohammad El-Khateeb, Mohammad Shboul, Mahmoud A Pouladi, Mohammed Al-Raqad, Bruno Reversade
eLife. 2018; 7: e32451. Published online 2018 May 22. doi: 10.7554/eLife.32451
PMCID:
PMC5963920
AbstractArticlePDF–4.3M
2.
Ca2+/Calmodulin-Dependent Protein Kinase II (CaMKII) Increases Small-Conductance Ca2+-Activated K+ Current in Patients with Chronic Atrial Fibrillation
Xuehui Fan, Yiyan Yu, Huan Lan, Xianhong Ou, Lijie Yang, Tao Li, Jimin Cao, Xiaorong Zeng, Miaoling Li
Med Sci Monit. 2018; 24: 3011–3023. Published online 2018 May 8. doi: 10.12659/MSM.909684
PMCID:
PMC5963316
AbstractArticlePDF–1.2M
3.
Network analysis of UBE3A/E6AP-associated proteins provides connections to several distinct cellular processes
Gustavo Martínez-Noël, Katja Luck, Simone Kühnle, Alice Desbuleux, Patricia Szajner, Jeffrey T. Galligan, Diana Rodriguez, Leon Zheng, Kathleen Boyland, Flavian Leclere, Quan Zhong, David E. Hill, Marc Vidal, Peter M. Howley
J Mol Biol. Author manuscript; available in PMC 2019 Mar 30.
Published in final edited form as: J Mol Biol. 2018 Mar 30; 430(7): 1024–1050. Published online 2018 Feb 6. doi: 10.1016/j.jmb.2018.01.021
PMCID:
PMC5866790
AbstractArticlePDF–4.1M
4.
PKC epsilon-related kinase associates with and phosphorylates cytokeratin 8 and 18
J Cell Biol. 1992 May 1; 117(3): 583–593. doi: 10.1083/jcb.117.3.583
PMCID:
PMC2289443
SummaryPDF–1.7M

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