PMC Links for Nucleotide (Select 1677529933) - PMC

Select item 61871301.

ASTN2 modulates synaptic strength by trafficking and degradation of surface proteins

Hourinaz Behesti, Taylor R. Fore, Peter Wu, Zachi Horn, Mary Leppert, Court Hull, Mary E. Hatten

Proc Natl Acad Sci U S A. 2018 Oct 9; 115(41): E9717–E9726. Published online 2018 Sep 21. doi: 10.1073/pnas.1809382115

PMCID:: PMC6187130

Select item 48924352.

Structure of astrotactin-2: a conserved vertebrate-specific and perforin-like membrane protein involved in neuronal development

Tao Ni, Karl Harlos, Robert Gilbert

Open Biol. 2016 May; 6(5): 160053. Published online 2016 May 4. doi: 10.1098/rsob.160053

PMCID:: PMC4892435

Abstract Article PDF–1.1M

Select item 46890373.

iCLIP identifies novel roles for SAFB1 in regulating RNA processing and neuronal function

Caroline Rivers, Jalilah Idris, Helen Scott, Mark Rogers, Youn-Bok Lee, Jessica Gaunt, Leonidas Phylactou, Tomaz Curk, Colin Campbell, Jernej Ule, Michael Norman, James B. Uney

BMC Biol. 2015; 13: 111. Published online 2015 Dec 22. doi: 10.1186/s12915-015-0220-7

PMCID:: PMC4689037

Abstract Article PDF–2.7M

Select item 33025764.

Genome-wide association study of smoking behaviors in COPD patients

Mateusz Siedlinski, Michael H. Cho, Per Bakke, Amund Gulsvik, David A. Lomas, Wayne Anderson, Xiangyang Kong, Stephen I. Rennard, Terri H. Beaty, John E. Hokanson, James D. Crapo, Edwin K. Silverman, the COPDGene and ECLIPSE Investigators

Thorax. Author manuscript; available in PMC 2012 Oct 1.

Published in final edited form as: Thorax. 2011 Oct; 66(10): 894–902. Published online 2011 Jun 16. doi: 10.1136/thoraxjnl-2011-200154

PMCID:: PMC3302576

Abstract Article PDF–1.2M

Select item 28911635.

Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs

Daniel E. Adkins, Karolina Åberg, Joseph L. McClay, József Bukszár, Zhongming Zhao, Peilin Jia, T. Scott Stroup, Diana Perkins, Joseph P. McEvoy, Jeffrey A. Lieberman, Patrick F. Sullivan, Edwin J.C.G. van den Oord

Mol Psychiatry. Author manuscript; available in PMC 2011 Sep 1.

Published in final edited form as: Mol Psychiatry. 2011 Mar; 16(3): 321–332. Published online 2010 Mar 2. doi: 10.1038/mp.2010.14

PMCID:: PMC2891163

Abstract Article PDF–491K

Select item 25619366.

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

Terry Vrijenhoek, Jacobine E. Buizer-Voskamp, Inge van der Stelt, Eric Strengman, Genetic Risk and Outcome in Psychosis (GROUP) Consortium, Chiara Sabatti, Ad Geurts van Kessel, Han G. Brunner, Roel A. Ophoff, Joris A. Veltman

Am J Hum Genet. 2008 Oct 10; 83(4): 504–510. Published online 2008 Oct 3. doi: 10.1016/j.ajhg.2008.09.011

PMCID:: PMC2561936

Abstract Article PDF–698K

Select item 39901737.

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

Anath C. Lionel, Kristiina Tammimies, Andrea K. Vaags, Jill A. Rosenfeld, Joo Wook Ahn, Daniele Merico, Abdul Noor, Cassandra K. Runke, Vamsee K. Pillalamarri, Melissa T. Carter, Matthew J. Gazzellone, Bhooma Thiruvahindrapuram, Christina Fagerberg, Lone W. Laulund, Giovanna Pellecchia, Sylvia Lamoureux, Charu Deshpande, Jill Clayton-Smith, Ann C. White, Susan Leather, John Trounce, H. Melanie Bedford, Eli Hatchwell, Peggy S. Eis, Ryan K.C. Yuen, Susan Walker, Mohammed Uddin, Michael T. Geraghty, Sarah M. Nikkel, Eva M. Tomiak, Bridget A. Fernandez, Noam Soreni, Jennifer Crosbie, Paul D. Arnold, Russell J. Schachar, Wendy Roberts, Andrew D. Paterson, Joyce So, Peter Szatmari, Christina Chrysler, Marc Woodbury-Smith, R. Brian Lowry, Lonnie Zwaigenbaum, Divya Mandyam, John Wei, Jeffrey R. MacDonald, Jennifer L. Howe, Thomas Nalpathamkalam, Zhuozhi Wang, Daniel Tolson, David S. Cobb, Timothy M. Wilks, Mark J. Sorensen, Patricia I. Bader, Yu An, Bai-Lin Wu, Sebastiano Antonino Musumeci, Corrado Romano, Diana Postorivo, Anna M. Nardone, Matteo Della Monica, Gioacchino Scarano, Leonardo Zoccante, Francesca Novara, Orsetta Zuffardi, Roberto Ciccone, Vincenzo Antona, Massimo Carella, Leopoldo Zelante, Pietro Cavalli, Carlo Poggiani, Ugo Cavallari, Bob Argiropoulos, Judy Chernos, Charlotte Brasch-Andersen, Marsha Speevak, Marco Fichera, Caroline Mackie Ogilvie, Yiping Shen, Jennelle C. Hodge, Michael E. Talkowski, Dimitri J. Stavropoulos, Christian R. Marshall, Stephen W. Scherer

Hum Mol Genet. 2014 May 15; 23(10): 2752–2768. Published online 2013 Dec 30. doi: 10.1093/hmg/ddt669

PMCID:: PMC3990173

Abstract Article PDF–952K

Select item 38654058.

Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta

James A Poulter, Walid El-Sayed, Roger C Shore, Jennifer Kirkham, Chris F Inglehearn, Alan J Mighell

Eur J Hum Genet. 2014 Jan; 22(1): 132–135. Published online 2013 May 1. doi: 10.1038/ejhg.2013.76

PMCID:: PMC3865405

Abstract Article PDF–459K

Select item 36777039.

BIODOSIMETRY ON SMALL BLOOD VOLUME USING GENE EXPRESSION ASSAY

Muriel Brengues, Brigitte Paap, Michael Bittner, Sally Amundson, Bruce Seligmann, Ronald Korn, Ralf Lenigk, Frederic Zenhausern

Health Phys. Author manuscript; available in PMC 2013 Jun 10.

Published in final edited form as: Health Phys. 2010 Feb; 98(2): 179–185. doi: 10.1097/01.HP.0000346706.44253.5c

PMCID:: PMC3677703

Abstract Article PDF–3.1M

Select item 247863910.

Development of gene expression signatures for practical radiation biodosimetry

Sunirmal Paul, Sally A. Amundson

Int J Radiat Oncol Biol Phys. Author manuscript; available in PMC 2009 Jul 15.

Published in final edited form as: Int J Radiat Oncol Biol Phys. 2008 Jul 15; 71(4): 1236–1244. doi: 10.1016/j.ijrobp.2008.03.043

PMCID:: PMC2478639

Abstract Article PDF–463K

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