PMC Links for Nucleotide (Select 1814781254) - PMC

Select item 50279021.

Whole genome association analysis of treatment response in obsessive-compulsive disorder

H Qin, JF Samuels, Y Wang, Y Zhu, MA Grados, MA Riddle, BD Greenberg, JA Knowles, AJ Fyer, JT McCracken, DL Murphy, SA Rasmussen, BA Cullen, J Piacentini, D Geller, SE Stewart, D Pauls, OJ Bienvenu, FS Goes, B Maher, AE Pulver, D Valle, C Lange, M Mattheisen, NC McLaughlin, K-Y Liang, EL Nurmi, KD Askland, G Nestadt, YY Shugart

Mol Psychiatry. Author manuscript; available in PMC 2016 Sep 19.

Published in final edited form as: Mol Psychiatry. 2016 Feb; 21(2): 270–276. Published online 2015 Mar 31. doi: 10.1038/mp.2015.32

PMCID:: PMC5027902

Abstract Article PDF–378K

Select item 38219722.

The Hedgehog processing pathway is required for NSCLC growth and survival

Jezabel Rodriguez-Blanco, Neal S. Schilling, Robert Tokhunts, Camilla Giambelli, Jun Long, Dennis Liang Fei, Samer Singh, Kendall E. Black, Zhiqiang Wang, Fabrizio Galimberti, Pablo A. Bejarano, Sharon Elliot, Marilyn K. Glassberg, Dao M. Nguyen, William W. Lockwood, Wan L. Lam, Ethan Dmitrovsky, Anthony J. Capobianco, David J. Robbins

Oncogene. Author manuscript; available in PMC 2014 May 2.

Published in final edited form as: Oncogene. 2013 May 2; 32(18): 10.1038/onc.2012.243. Published online 2012 Jun 25. doi: 10.1038/onc.2012.243

PMCID:: PMC3821972

Abstract Article PDF–3.1M

Select item 37975303.

Characterization of the Chromosome 1q41q42.12 region, and the Candidate Gene DISP1, in Patients with CDH

Sibel Kantarci, Kate G Ackerman, Meaghan N Russell, Mauro Longoni, Carrie Sougnez, Kristin M Noonan, Eli Hatchwell, Xiaoyun Zhang, Rafael Pieretti Vanmarcke, Kwame Anyane-Yeboa, Paul Dickman, Jay Wilson, Patricia K Donahoe, Barbara R Pober

Am J Med Genet A. Author manuscript; available in PMC 2013 Oct 16.

Published in final edited form as: Am J Med Genet A. 2010 Oct; 0(10): 2493–2504. doi: 10.1002/ajmg.a.33618

PMCID:: PMC3797530

Abstract Article PDF–1.3M

Select item 27748494.

Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans

Erich Roessler, Yong Ma, Maia V. Ouspenskaia, Felicitas Lacbawan, Claude Bendavid, Christèle Dubourg, Philip A. Beachy, Maximilian Muenke

Hum Genet. Author manuscript; available in PMC 2009 Nov 9.

Published in final edited form as: Hum Genet. 2009 May; 125(4): 393–400. Published online 2009 Jan 31. doi: 10.1007/s00439-009-0628-7

PMCID:: PMC2774849

Abstract Article PDF–1.3M

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