PMC Links for Protein (Select 1756613217) - PMC

Select item 64538951.

TMCO1-mediated Ca²⁺ leak underlies osteoblast functions via CaMKII signaling

Jianwei Li, Caizhi Liu, Yuheng Li, Qiaoxia Zheng, Youjia Xu, Beibei Liu, Weijia Sun, Yuan Li, Shuhui Ji, Mingwei Liu, Jing Zhang, Dingsheng Zhao, Ruikai Du, Zizhong Liu, Guohui Zhong, Cuiwei Sun, Yanqing Wang, Jinping Song, Shu Zhang, Jun Qin, Shukuan Ling, Xianhua Wang, Yingxian Li

Nat Commun. 2019; 10: 1589. Published online 2019 Apr 8. doi: 10.1038/s41467-019-09653-5

PMCID:: PMC6453895

Abstract Article PDF–3.0M

Select item 51210912.

Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study (OHTS)

Todd E. Scheetz, Ben Faga, Lizette Ortega, Ben R. Roos, Mae O. Gordon, Michael A. Kass, Kai Wang, John H. Fingert

Ophthalmology. Author manuscript; available in PMC 2017 Dec 1.

Published in final edited form as: Ophthalmology. 2016 Dec; 123(12): 2527–2536. Published online 2016 Oct 1. doi: 10.1016/j.ophtha.2016.08.036

PMCID:: PMC5121091

Abstract Article PDF–1.2M

Select item 33429333.

Common Genetic Determinants of Intraocular Pressure and Primary Open-Angle Glaucoma

Leonieke M. E. van Koolwijk, Wishal D. Ramdas, M. Kamran Ikram, Nomdo M. Jansonius, Francesca Pasutto, Pirro G. Hysi, Stuart Macgregor, Sarah F. Janssen, Alex W. Hewitt, Ananth C. Viswanathan, Jacoline B. ten Brink, S. Mohsen Hosseini, Najaf Amin, Dominiek D. G. Despriet, Jacqueline J. M. Willemse-Assink, Rogier Kramer, Fernando Rivadeneira, Maksim Struchalin, Yurii S. Aulchenko, Nicole Weisschuh, Matthias Zenkel, Christian Y. Mardin, Eugen Gramer, Ulrich Welge-Lüssen, Grant W. Montgomery, Francis Carbonaro, Terri L. Young, The DCCT/EDIC Research Group, Céline Bellenguez, Peter McGuffin, Paul J. Foster, Fotis Topouzis, Paul Mitchell, Jie Jin Wang, Tien Y. Wong, Monika A. Czudowska, Albert Hofman, Andre G. Uitterlinden, Roger C. W. Wolfs, Paulus T. V. M. de Jong, Ben A. Oostra, Andrew D. Paterson, Wellcome Trust Case Control Consortium 2, David A. Mackey, Arthur A. B. Bergen, André Reis, Christopher J. Hammond, Johannes R. Vingerling, Hans G. Lemij, Caroline C. W. Klaver, Cornelia M. van Duijn

PLoS Genet. 2012 May; 8(5): e1002611. Published online 2012 May 3. doi: 10.1371/journal.pgen.1002611

PMCID:: PMC3342933

Abstract Article PDF–656K

Select item 28067764.

Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation

Baozhong Xin, Erik G. Puffenberger, Susan Turben, Haiyan Tan, Aimin Zhou, Heng Wang

Proc Natl Acad Sci U S A. 2010 Jan 5; 107(1): 258–263. Published online 2009 Dec 29. doi: 10.1073/pnas.0908457107

PMCID:: PMC2806776

Abstract Article PDF–1.0M

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