PMC Links for OMIM (Select 107773) - PMC

Select item 68212391.

The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene

Gianna Carvalheira, Andrea M Malinverni, Mariana Moysés-Oliveira, Renata Ueta, Leonardo Cardili, Patrícia Monteagudo, Andreia L G Mathez, Ieda T Verreschi, Miguel A Maluf, Márcia E F Shida, Mila T C Leite, Diego Mazzotti, Maria Isabel Melaragno, Magnus R Dias-da-Silva

J Endocr Soc. 2019 Nov 1; 3(11): 2107–2113. Published online 2019 Aug 28. doi: 10.1210/js.2019-00241

Correction in:: J Endocr Soc. 2020 Mar 1; 4(3): bvaa022.

PMCID:: PMC6821239

Abstract Article PDF–1.1M

Select item 60533222.

Single cell analysis of early progenitor cells that build coronary arteries

Tianying Su, Geoff Stanley, Rahul Sinha, Gaetano D’Amato, Soumya Das, Siyeon Rhee, Andrew H. Chang, Aruna Poduri, Brian Raftrey, Thanh Theresa Dinh, Walter A. Roper, Guang Li, Kelsey E. Quinn, Kathleen M. Caron, Sean Wu, Lucile Miquerol, Eugene C. Butcher, Irving Weissman, Stephen Quake, Kristy Red-Horse

Nature. Author manuscript; available in PMC 2019 Jan 4.

Published in final edited form as: Nature. 2018 Jul; 559(7714): 356–362. Published online 2018 Jul 4. doi: 10.1038/s41586-018-0288-7

PMCID:: PMC6053322

Abstract Article PDF–5.1M

Select item 59852853.

Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children

Anu Bashamboo, Caroline Eozenou, Anne Jorgensen, Joelle Bignon-Topalovic, Jean-Pierre Siffroi, Capucine Hyon, Attila Tar, Péter Nagy, Janos Sólyom, Zita Halász, Annnabel Paye-Jaouen, Sophie Lambert, David Rodriguez-Buritica, Rita Bertalan, Laetitia Martinerie, Ewa Rajpert-De Meyts, John C. Achermann, Ken McElreavey

Am J Hum Genet. 2018 Mar 1; 102(3): 487–493. Published online 2018 Feb 22. doi: 10.1016/j.ajhg.2018.01.021

PMCID:: PMC5985285

Abstract Article PDF–1.3M

Select item 57138934.

Elimination of the male reproductive tract in the female embryo is actively promoted by COUP-TFII

Fei Zhao, Heather L. Franco, Karina F. Rodriguez, Paula R. Brown, Ming-Jer Tsai, Sophia Y. Tsai, Humphrey H.-C. Yao

Science. Author manuscript; available in PMC 2017 Dec 4.

Published in final edited form as: Science. 2017 Aug 18; 357(6352): 717–720. doi: 10.1126/science.aai9136

PMCID:: PMC5713893

Abstract Article PDF–1.4M

Select item 50031815.

De Novo Frameshift Mutation in COUP-TFII (NR2F2) in Human Congenital Diaphragmatic Hernia

Frances A. High, Pooja Bhayani, Jay M. Wilson, Carol J. Bult, Patricia K. Donahoe, Mauro Longoni

Am J Med Genet A. Author manuscript; available in PMC 2016 Sep 1.

Published in final edited form as: Am J Med Genet A. 2016 Sep; 170(9): 2457–2461. Published online 2016 Jul 1. doi: 10.1002/ajmg.a.37830

PMCID:: PMC5003181

Abstract Article PDF–362K

Select item 44107676.

Prevalence and penetrance of ZFPM2 mutations and deletions causing congenital diaphragmatic hernia

M. Longoni, M.K. Russell, F.A. High, K. Darvishi, F.I. Maalouf, A. Kashani, A.A. Tracy, C.M. Coletti, M. Loscertales, K. Lage, K.G. Ackerman, S.A. Woods, C. Ward-Melver, D. Andrews, C. Lee, B.R. Pober, P.K. Donahoe

Clin Genet. Author manuscript; available in PMC 2015 Apr 27.

Published in final edited form as: Clin Genet. 2015 Apr; 87(4): 362–367. Published online 2014 Apr 26. doi: 10.1111/cge.12395

PMCID:: PMC4410767

Abstract Article PDF–558K

Select item 40223467.

COUP-TFII inhibits TGF-β-induced growth barrier to promote prostate tumorigenesis

Jun Qin, San-Pin Wu, Chad J. Creighton, Fangyan Dai, Xin Xie, Chiang-Min Cheng, Anna Frolov, Gustavo Ayala, Xia Lin, Xin-Hua Feng, Michael M. Ittmann, Shaw-Jenq Tsai, Ming-Jer Tsai, Sophia Y. Tsai

Nature. Author manuscript; available in PMC 2014 May 15.

Published in final edited form as: Nature. 2013 Jan 10; 493(7431): 236–240. Published online 2012 Nov 28. doi: 10.1038/nature11674

PMCID:: PMC4022346

Abstract Article PDF–1.4M

Select item 39805098.

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

Saeed Al Turki, Ashok K. Manickaraj, Catherine L. Mercer, Sebastian S. Gerety, Marc-Phillip Hitz, Sarah Lindsay, Lisa C.A. D’Alessandro, G. Jawahar Swaminathan, Jamie Bentham, Anne-Karin Arndt, Jacoba Low, Jeroen Breckpot, Marc Gewillig, Bernard Thienpont, Hashim Abdul-Khaliq, Christine Harnack, Kirstin Hoff, Hans-Heiner Kramer, Stephan Schubert, Reiner Siebert, Okan Toka, Catherine Cosgrove, Hugh Watkins, Anneke M. Lucassen, Ita M. O’Kelly, Anthony P. Salmon, Frances A. Bu’Lock, Javier Granados-Riveron, Kerry Setchfield, Chris Thornborough, J. David Brook, Barbara Mulder, Sabine Klaassen, Shoumo Bhattacharya, Koen Devriendt, David F. FitzPatrick, UK10K Consortium, David I. Wilson, Seema Mital, Matthew E. Hurles

Am J Hum Genet. 2014 Apr 3; 94(4): 574–585. doi: 10.1016/j.ajhg.2014.03.007

Correction in:: Am J Hum Genet. 2014 Jul 3; 95(1): 126.

Correction in:: Am J Hum Genet. 2016 Mar 3; 98(3): 592.

PMCID:: PMC3980509

Abstract Article PDF–2.4M

Select item 28276849.

COUP-TFs regulate eye development by controlling factors essential for optic vesicle morphogenesis

Ke Tang, Xin Xie, Joo-In Park, Milan Jamrich, Sophia Tsai, Ming-Jer Tsai

Development. 2010 Mar 1; 137(5): 725–734. doi: 10.1242/dev.040568

PMCID:: PMC2827684

Abstract Article

Select item 281935610.

Isolation of a Novel Family of C₂H₂ Zinc Finger Proteins Implicated in Transcriptional Repression Mediated by Chicken Ovalbumin Upstream Promoter Transcription Factor (COUP-TF) Orphan Nuclear Receptors

Dorina Avram, Andrew Fields, Karen Pretty On Top, Daniel J. Nevrivy, Jane E. Ishmael, Mark Leid

J Biol Chem. Author manuscript; available in PMC 2010 Feb 10.

Published in final edited form as: J Biol Chem. 2000 Apr 7; 275(14): 10315. doi: 10.1074/jbc.275.14.10315

PMCID:: PMC2819356

Abstract Article PDF–1.0M

Select item 185105911.

Deletion of the orphan nuclear receptor COUP-TFII in uterus leads to placental deficiency

Fabrice G. Petit, Soazik P. Jamin, Isao Kurihara, Richard R. Behringer, Francesco J. DeMayo, Ming-Jer Tsai, Sophia Y. Tsai

Proc Natl Acad Sci U S A. 2007 Apr 10; 104(15): 6293–6298. Published online 2007 Apr 2. doi: 10.1073/pnas.0702039104

Correction in:: Proc Natl Acad Sci U S A. 2007 Jun 5; 104(23): 9911.

PMCID:: PMC1851059

Abstract Article PDF–3.3M

Select item 128344912.

Mouse lacking COUP-TFII as an animal model of Bochdalek-type congenital diaphragmatic hernia

Li-Ru You, Norio Takamoto, Cheng-Tai Yu, Toshiya Tanaka, Tatsuhiko Kodama, Francesco J. DeMayo, Sophia Y. Tsai, Ming-Jer Tsai

Proc Natl Acad Sci U S A. 2005 Nov 8; 102(45): 16351–16356. Published online 2005 Oct 26. doi: 10.1073/pnas.0507832102

PMCID:: PMC1283449

Abstract Article PDF–798K

Select item 119937613.

Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization

M. Klaassens, M. van Dooren, H. J. Eussen, H. Douben, A. T. den Dekker, C. Lee, P. K. Donahoe, R. J. Galjaard, N. Goemaere, R. R. de Krijger, C. Wouters, J. Wauters, B. A. Oostra, D. Tibboel, A. de Klein

Am J Hum Genet. 2005 May; 76(5): 877–882. Published online 2005 Mar 4. doi: 10.1086/429842

PMCID:: PMC1199376

Abstract Article PDF–582K

Select item 35971814.

Synergistic interactions between transcription factors control expression of the apolipoprotein AI gene in liver cells.

R L Widom, J A Ladias, S Kouidou, S K Karathanasis

Mol Cell Biol. 1991 Feb; 11(2): 677–687. doi: 10.1128/mcb.11.2.677

PMCID:: PMC359718

Summary Page Browse PDF–2.6M

Select item 31663715.

The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development

Fred A. Pereira, Yuhong Qiu, Ge Zhou, Ming-Jer Tsai, Sophia Y. Tsai

Genes Dev. 1999 Apr 15; 13(8): 1037–1049. doi: 10.1101/gad.13.8.1037

PMCID:: PMC316637

Abstract Article PDF–3.8M

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