PMC Links for Gene (Select 304947) - PMC

Select item 64550341.

De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects

Anne Slavotinek, Maurizio Risolino, Marta Losa, Megan T Cho, Kristin G Monaghan, Dina Schneidman-Duhovny, Sarah Parisotto, Johanna C Herkert, Alexander P A Stegmann, Kathryn Miller, Natasha Shur, Jacqueline Chui, Eric Muller, Suzanne DeBrosse, Justin O Szot, Gavin Chapman, Nicholas S Pachter, David S Winlaw, Bryce A Mendelsohn, Joline Dalton, Kyriakie Sarafoglou, Peter I Karachunski, Jane M Lewis, Helio Pedro, Sally L Dunwoodie, Licia Selleri, Joseph Shieh

Hum Mol Genet. 2017 Dec 15; 26(24): 4849–4860. Published online 2017 Sep 22. doi: 10.1093/hmg/ddx363

PMCID:: PMC6455034

Abstract Article PDF–587K

Select item 2324162.

Meis proteins are major in vivo DNA binding partners for wild-type but not chimeric Pbx proteins.

C P Chang, Y Jacobs, T Nakamura, N A Jenkins, N G Copeland, M L Cleary

Mol Cell Biol. 1997 Oct; 17(10): 5679–5687. doi: 10.1128/mcb.17.10.5679

PMCID:: PMC232416

Summary PDF–921K

Select item 26330523.

Pbx/Meis Deficiencies Demonstrate Multigenetic Origins of Congenital Heart Disease

Kryn Stankunas, Ching Shang, Karen Y. Twu, Shih-Chu Kao, Nancy A. Jenkins, Neal G. Copeland, Mrinmoy Sanyal, Licia Selleri, Michael L. Cleary, Ching-Pin Chang

Circ Res. Author manuscript; available in PMC 2009 Sep 26.

Published in final edited form as: Circ Res. 2008 Sep 26; 103(7): 702–709. Published online 2008 Aug 21. doi: 10.1161/CIRCRESAHA.108.175489

PMCID:: PMC2633052

Abstract Article PDF–3.3M

Select item 29357964.

Activin Regulation of the Follicle-Stimulating Hormone β-Subunit Gene Involves Smads and the TALE Homeodomain Proteins Pbx1 and Prep1

JANICE S. BAILEY, NAAMA RAVE-HAREL, SHAUNA M. McGILLIVRAY, DJURDJICA COSS, PAMELA L. MELLON

Mol Endocrinol. Author manuscript; available in PMC 2010 Sep 8.

Published in final edited form as: Mol Endocrinol. 2004 May; 18(5): 1158–1170. Published online 2004 Feb 5. doi: 10.1210/me.2003-0442

PMCID:: PMC2935796

Abstract Article PDF–1.0M

Select item 25850845.

HOX cofactors expression and regulation in the human ovary

Takayo Ota, Haruka Asahina, Se-Hyung Park, Qing Huang, Takashi Minegishi, Nelly Auersperg, Peter CK Leung

Reprod Biol Endocrinol. 2008; 6: 49. Published online 2008 Oct 30. doi: 10.1186/1477-7827-6-49

PMCID:: PMC2585084

Abstract Article PDF–2.1M

Select item 5480076.

FOXC1 Transcriptional Regulatory Activity Is Impaired by PBX1 in a Filamin A-Mediated Manner

Fred B. Berry, Megan A. O'Neill, Miguel Coca-Prados, Michael A. Walter

Mol Cell Biol. 2005 Feb; 25(4): 1415–1424. doi: 10.1128/MCB.25.4.1415-1424.2005

PMCID:: PMC548007

Abstract Article PDF–550K

Select item 1647727.

Nonmuscle Myosin Promotes Cytoplasmic Localization of PBX

He Huang, Miltiadis Paliouras, Isabel Rambaldi, Paul Lasko, Mark Featherstone

Mol Cell Biol. 2003 May; 23(10): 3636–3645. doi: 10.1128/MCB.23.10.3636-3645.2003

PMCID:: PMC164772

Abstract Article PDF–1.1M

Select item 250528.

Meis1 and pKnox1 bind DNA cooperatively with Pbx1 utilizing an interaction surface disrupted in oncoprotein E2a-Pbx1

Paul S. Knoepfler, Katherine R. Calvo, Haiming Chen, Stylianos E. Antonarakis, Mark P. Kamps

Proc Natl Acad Sci U S A. 1997 Dec 23; 94(26): 14553–14558. doi: 10.1073/pnas.94.26.14553

PMCID:: PMC25052

Abstract Article PDF–372K

Select item 72068509.

Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease

Dimuthu Alankarage, Justin O Szot, Nick Pachter, Anne Slavotinek, Licia Selleri, Joseph T Shieh, David Winlaw, Eleni Giannoulatou, Gavin Chapman, Sally L Dunwoodie

Hum Mol Genet. 2020 May 8; 29(7): 1068–1082. Published online 2019 Oct 18. doi: 10.1093/hmg/ddz231

PMCID:: PMC7206850

Abstract Article PDF–1.5M

Select item 577995310.

Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma

Jinhui Wang, Daofei Qu, Jinghong An, Guoming Yuan, Yufu Liu

Mol Med Rep. 2017 Dec; 16(6): 8735–8746. Published online 2017 Oct 4. doi: 10.3892/mmr.2017.7711

PMCID:: PMC5779953

Abstract Article PDF–3.0M

Select item 159277111.

Hypomorphic Mutation of the TALE Gene Prep1 (pKnox1) Causes a Major Reduction of Pbx and Meis Proteins and a Pleiotropic Embryonic Phenotype

Elisabetta Ferretti, J. Carlos Villaescusa, Patrizia Di Rosa, Luis C. Fernandez-Diaz, Elena Longobardi, Roberta Mazzieri, Annarita Miccio, Nicola Micali, Licia Selleri, Giuliana Ferrari, Francesco Blasi

Mol Cell Biol. 2006 Aug; 26(15): 5650–5662. doi: 10.1128/MCB.00313-06

PMCID:: PMC1592771

Abstract Article PDF–1.3M

Select item 335650512.

Congenital Asplenia in Mice and Humans with Mutations in a Pbx/Nkx2-5/p15 Module

Matthew Koss, Alexandre Bolze, Andrea Brendolan, Matilde Saggese, Terence D. Capellini, Ekaterina Bojilova, Bertrand Boisson, Owen W.J. Prall, David Elliott, Mark Solloway, Elisa Lenti, Chisa Hidaka, Ching-Pin Chang, Nizar Mahlaoui, Richard P. Harvey, Jean-Laurent Casanova, Licia Selleri

Dev Cell. Author manuscript; available in PMC 2013 May 15.

Published in final edited form as: Dev Cell. 2012 May 15; 22(5): 913–926. Published online 2012 May 3. doi: 10.1016/j.devcel.2012.02.009

PMCID:: PMC3356505

Abstract Article PDF–6.8M

Select item 13924113.

Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

Mammalian Gene Collection (MGC) Program Team

Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899

PMCID:: PMC139241

Abstract Article PDF–118K

Select item 317805914.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

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