PMC Links for Gene (Select 362021) - PMC

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Items: 11

Select item 36577501.

A truncating mutation in GPSM2 is associated with recessive nonsyndromic hearing loss

Kemal O. Yariz, Tom Walsh, Hatice Akay, Duygu Duman, Adil Cinar Akkaynak, Mary-Claire King, Mustafa Tekin

Clin Genet. Author manuscript; available in PMC 2013 May 20.

Published in final edited form as: Clin Genet. 2012 Mar; 81(3): 289–293. Published online 2011 Mar 15. doi: 10.1111/j.1399-0004.2011.01654.x

PMCID:: PMC3657750

Abstract Article PDF–1.0M

Select item 33702712.

GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome

Dan Doherty, Albert E. Chudley, Gail Coghlan, Gisele E. Ishak, A. Micheil Innes, Edmond G. Lemire, R. Curtis Rogers, Aizeddin A. Mhanni, Ian G. Phelps, Steven J.M. Jones, Shing H. Zhan, Anthony P. Fejes, Hashem Shahin, Moien Kanaan, Hatice Akay, Mustafa Tekin, FORGE Canada Consortium, Barbara Triggs-Raine, Teresa Zelinski

Am J Hum Genet. 2012 Jun 8; 90(6): 1088–1093. doi: 10.1016/j.ajhg.2012.04.008

Correction in:: Am J Hum Genet. 2012 Jul 13; 91(1): 209.

PMCID:: PMC3370271

Abstract Article PDF–494K

Select item 34812803.

Crystal Structures of the Scaffolding Protein LGN Reveal the General Mechanism by Which GoLoco Binding Motifs Inhibit the Release of GDP from Gα_i

Min Jia, Jianchao Li, Jinwei Zhu, Wenyu Wen, Mingjie Zhang, Wenning Wang

J Biol Chem. 2012 Oct 26; 287(44): 36766–36776. Published online 2012 Sep 5. doi: 10.1074/jbc.M112.391607

PMCID:: PMC3481280

Abstract Article PDF–3.5M

Select item 31584604.

Structures of the LGN/mInsc and LGN/NuMA complexes suggest distinct functions of the Par3/mInsc/LGN and Gαi/LGN/NuMA pathways in asymmetric cell division

Jinwei Zhu, Wenyu Wen, Zhen Zheng, Yuan Shang, Zhiyi Wei, Zhuoni Xiao, Zhu Pan, Quansheng Du, Wenning Wang, Mingjie Zhang

Mol Cell. Author manuscript; available in PMC 2012 Aug 5.

Published in final edited form as: Mol Cell. 2011 Aug 5; 43(3): 418–431. doi: 10.1016/j.molcel.2011.07.011

PMCID:: PMC3158460

Abstract Article PDF–4.4M

Select item 28967765.

Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82

Tom Walsh, Hashem Shahin, Tal Elkan-Miller, Ming K. Lee, Anne M. Thornton, Wendy Roeb, Amal Abu Rayyan, Suheir Loulus, Karen B. Avraham, Mary-Claire King, Moien Kanaan

Am J Hum Genet. 2010 Jul 9; 87(1): 90–94. doi: 10.1016/j.ajhg.2010.05.010