PMC Links for Nucleotide (Select 1519314740) - PMC

Select item 58509091.

Regulation of CNKSR2 protein stability by the HECT E3 ubiquitin ligase Smurf2, and its role in breast cancer progression

Diana David, Arun Surendran, Jissa V. Thulaseedharan, Asha S. Nair

BMC Cancer. 2018; 18: 284. Published online 2018 Mar 13. doi: 10.1186/s12885-018-4188-x

PMCID:: PMC5850909

Abstract Article PDF–7.4M

Select item 40063472.

The CNK2 Scaffold Interacts with Vilse/ARHGAP39 and Modulates Rac Cycling During Morphogenesis of Dendritic Spines

Junghwa Lim, Daniel A. Ritt, Ming Zhou, Deborah K. Morrison

Curr Biol. Author manuscript; available in PMC 2015 Mar 31.

Published in final edited form as: Curr Biol. 2014 Mar 31; 24(7): 786–792. Published online 2014 Mar 20. doi: 10.1016/j.cub.2014.02.036

PMCID:: PMC4006347

Abstract Article PDF–2.1M

Select item 28144153.

hKSR-2, a vitamin D–regulated gene, inhibits apoptosis in arabinocytosine-treated HL60 leukemia cells

Xuening Wang, Rahul Patel, George P. Studzinski

Mol Cancer Ther. Author manuscript; available in PMC 2010 Feb 1.

Published in final edited form as: Mol Cancer Ther. 2008 Sep; 7(9): 2798. doi: 10.1158/1535-7163.MCT-08-0276

PMCID:: PMC2814415

Abstract Article PDF–669K

Select item 22685464.

CNK and HYP form a discrete dimer by their SAM domains to mediate RAF kinase signaling

Thanashan Rajakulendran, Malha Sahmi, Igor Kurinov, Mike Tyers, Marc Therrien, Frank Sicheri

Proc Natl Acad Sci U S A. 2008 Feb 26; 105(8): 2836–2841. Published online 2008 Feb 19. doi: 10.1073/pnas.0709705105

PMCID:: PMC2268546

Abstract Article PDF–1018K

Select item 65365925.

Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy

Michelle Demos, Ilaria Guella, Conrado DeGuzman, Marna B. McKenzie, Sarah E. Buerki, Daniel M. Evans, Eric B. Toyota, Cyrus Boelman, Linda L. Huh, Anita Datta, Aspasia Michoulas, Kathryn Selby, Bruce H. Bjornson, Gabriella Horvath, Elena Lopez-Rangel, Clara D. M. van Karnebeek, Ramona Salvarinova, Erin Slade, Patrice Eydoux, Shelin Adam, Margot I. Van Allen, Tanya N. Nelson, Corneliu Bolbocean, Mary B. Connolly, Matthew J. Farrer

Front Neurol. 2019; 10: 434. Published online 2019 May 21. doi: 10.3389/fneur.2019.00434

PMCID:: PMC6536592

Abstract Article PDF–405K

Select item 62126096.

CNKSR2 mutation causes the X-linked epilepsy-aphasia syndrome: A case report and review of literature

Ying Sun, Yi-Dan Liu, Zhi-Feng Xu, Qing-Xia Kong, Yan-Ling Wang

World J Clin Cases. 2018 Oct 26; 6(12): 570–576. Published online 2018 Oct 26. doi: 10.12998/wjcc.v6.i12.570

PMCID:: PMC6212609

Abstract Article PDF–1.3M

Select item 37229457.

Analysis of the effects of rare variants on splicing identifies alterations in GABA_A receptor genes in autism spectrum disorder individuals

Amélie Piton, Loubna Jouan, Daniel Rochefort, Sylvia Dobrzeniecka, Karine Lachapelle, Patrick A Dion, Julie Gauthier, Guy A Rouleau

Eur J Hum Genet. 2013 Jul; 21(7): 749–756. Published online 2012 Nov 21. doi: 10.1038/ejhg.2012.243

PMCID:: PMC3722945

Abstract Article PDF–895K

Select item 31263368.

Deficiency of Sorting Nexin 27 (SNX27) Leads to Growth Retardation and Elevated Levels of N-Methyl-d-Aspartate Receptor 2C (NR2C)

Lei Cai, Li Shen Loo, Vadim Atlashkin, Brendon J. Hanson, Wanjin Hong

Mol Cell Biol. 2011 Apr; 31(8): 1734–1747. doi: 10.1128/MCB.01044-10

PMCID:: PMC3126336

Abstract Article PDF–3.6M

Select item 27149709.

Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes

Lane J. Jaeckle Santos, Chao Xing, Robert B. Barnes, Lesley C. Ades, Andre Megarbane, Christopher Vidal, Angela Xuereb, Patrick S. Tarpey, Raffaella Smith, Mahmoud Khazab, Cheryl Shoubridge, Michael Partington, Andrew Futreal, Michael R. Stratton, Jozef Gecz, Andrew R. Zinn

Hum Genet. Author manuscript; available in PMC 2009 Jul 24.

Published in final edited form as: Hum Genet. 2008 Jun; 123(5): 469–476. Published online 2008 Apr 11. doi: 10.1007/s00439-008-0498-4

PMCID:: PMC2714970

Abstract Article PDF–604K

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