PMC Links for OMIM (Select 605515) - PMC

Select item 53623621.

Whole-Exome Sequencing in the molecular diagnosis of individuals with congenital anomalies of kidney and urinary tract and identification of a new causative gene

Mir Reza Bekheirnia, Nasim Bekheirnia, Matthew N. Bainbridge, Shen Gu, Zeynep Hande Coban Akdemir, Tomek Gambin, Nicolette K. Janzen, Shalini N. Jhangiani, Donna M. Muzny, Mini Michael, Eileen D. Brewer, Ewa Elenberg, Arundhati S. Kale, Alyssa A. Riley, Sarah J. Swartz, Daryl A. Scott, Yaping Yang, Poyyapakkam R. Srivaths, Scott E. Wenderfer, Joann Bodurtha, Carolyn D. Applegate, Milen Velinov, Angela Myers, Lior Borovik, William J. Craigen, Neil A. Hanchard, Jill A. Rosenfeld, Richard Alan Lewis, Edmond T. Gonzales, Richard A. Gibbs, John W. Belmont, David R. Roth, Christine Eng, Michael C. Braun, James R. Lupski, Dolores J. Lamb

Genet Med. Author manuscript; available in PMC 2017 Apr 7.

Published in final edited form as: Genet Med. 2017 Apr; 19(4): 412–420. Published online 2016 Sep 22. doi: 10.1038/gim.2016.131

PMCID:: PMC5362362

Abstract Article PDF–270K

Select item 29874722.

Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency

Christopher W Carr, Daniel Moreno-De-Luca, Colette Parker, Holly H Zimmerman, Nikki Ledbetter, Christa Lese Martin, William B Dobyns, Omar A Abdul-Rahman

Eur J Hum Genet. 2010 Nov; 18(11): 1216–1220. Published online 2010 Jun 23. doi: 10.1038/ejhg.2010.96

PMCID:: PMC2987472

Abstract Article PDF–322K

Select item 29789543.

De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment

Fadi F. Hamdan, Hussein Daoud, Daniel Rochefort, Amélie Piton, Julie Gauthier, Mathieu Langlois, Gila Foomani, Sylvia Dobrzeniecka, Marie-Odile Krebs, Ridha Joober, Ronald G. Lafrenière, Jean-Claude Lacaille, Laurent Mottron, Pierre Drapeau, Miriam H. Beauchamp, Michael S. Phillips, Eric Fombonne, Guy A. Rouleau, Jacques L. Michaud

Am J Hum Genet. 2010 Nov 12; 87(5): 671–678. doi: 10.1016/j.ajhg.2010.09.017

PMCID:: PMC2978954

Abstract Article PDF–670K

Select item 28109844.

Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development

Xiaoming Feng, Gregory C. Ippolito, Lifeng Tian, Karla Wiehagen, Soyoung Oh, Arivazhagan Sambandam, Jessica Willen, Ralph M. Bunte, Shanna D. Maika, June V. Harriss, Andrew J. Caton, Avinash Bhandoola, Philip W. Tucker, Hui Hu

Blood. 2010 Jan 21; 115(3): 510–518. Prepublished online 2009 Nov 12. doi: 10.1182/blood-2009-07-232694

PMCID:: PMC2810984

Abstract Article

Select item 25971375.

Down-regulation of the forkhead transcription factor Foxp1 is required for monocyte differentiation and macrophage function

Can Shi, Masashi Sakuma, Toshifumi Mooroka, Alison Liscoe, Huiyun Gao, Kevin J. Croce, Arjun Sharma, David Kaplan, David R. Greaves, Yunmei Wang, Daniel I. Simon

Blood. 2008 Dec 1; 112(12): 4699–4711. Prepublished online 2008 Sep 17. doi: 10.1182/blood-2008-01-137018

PMCID:: PMC2597137

Abstract Article

Select item 25471256.

Coordinated Actions of the Forkhead Protein Foxp1 and Hox Proteins in the Columnar Organization of Spinal Motor Neurons

David L. Rousso, Zachary B. Gaber, Deneen Wellik, Edward E. Morrisey, Bennett G. Novitch

Neuron. Author manuscript; available in PMC 2009 Jul 31.

Published in final edited form as: Neuron. 2008 Jul 31; 59(2): 226–240. doi: 10.1016/j.neuron.2008.06.025

PMCID:: PMC2547125

Abstract Article PDF–6.9M

Select item 480287.

DNA-binding properties and secondary structural model of the hepatocyte nuclear factor 3/fork head domain.

C Li, P W Tucker

Proc Natl Acad Sci U S A. 1993 Dec 15; 90(24): 11583–11587. doi: 10.1073/pnas.90.24.11583

PMCID:: PMC48028

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