PMC Links for Gene (Select 65109) - PMC

María Isabel Tejada, Olatz Villate, Nekane Ibarluzea, Ana Belén de la Hoz, Cristina Martínez-Bouzas, Elena Beristain, Francisco Martínez, Michael J. Friez, Beatriz Sobrino, Francisco Barros

Front Genet. 2019; 10: 1074. Published online 2019 Oct 31. doi: 10.3389/fgene.2019.01074

PMCID:: PMC6836624

Abstract Article PDF–1.2M

Select item 56419134.

Dual function of UPF3B in early and late translation termination

Gabriele Neu‐Yilik, Etienne Raimondeau, Boris Eliseev, Lahari Yeramala, Beate Amthor, Aurélien Deniaud, Karine Huard, Kathrin Kerschgens, Matthias W Hentze, Christiane Schaffitzel, Andreas E Kulozik

EMBO J. 2017 Oct 16; 36(20): 2968–2986. Published online 2017 Sep 12. doi: 10.15252/embj.201797079

PMCID:: PMC5641913

Abstract Article PDF–5.2M

Select item 44459875.

Full UPF3B function is critical for neuronal differentiation of neural stem cells

Tahani Alrahbeni, Francesca Sartor, Jihan Anderson, Zosia Miedzybrodzka, Colin McCaig, Berndt Müller

Mol Brain. 2015; 8: 33. Published online 2015 May 27. doi: 10.1186/s13041-015-0122-1

PMCID:: PMC4445987

Abstract Article PDF–1.7M

Select item 42810196.

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

LS Nguyen, L Jolly, C Shoubridge, WK Chan, L Huang, F Laumonnier, M Raynaud, A Hackett, M Field, J Rodriguez, AK Srivastava, Y Lee, R Long, AM Addington, JL Rapoport, S Suren, CN Hahn, J Gamble, MF Wilkinson, MA Corbett, J Gecz

Mol Psychiatry. Author manuscript; available in PMC 2014 Dec 31.

Published in final edited form as: Mol Psychiatry. 2012 Nov; 17(11): 1103–1115. Published online 2011 Dec 20. doi: 10.1038/mp.2011.163

PMCID:: PMC4281019

Abstract Article PDF–1.3M

Select item 30244387.

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

AM Addington, J Gauthier, A Piton, FF Hamdan, A Raymond, N Gogtay, R Miller, J Tossell, J Bakalar, G Germain, P Gochman, R Long, JL Rapoport, GA Rouleau

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

Published in final edited form as: Mol Psychiatry. 2011 Mar; 16(3): 238–239. Published online 2010 May 18. doi: 10.1038/mp.2010.59

Correction in:: volume 17 on page 468

PMCID:: PMC3024438

Article PDF–151K

Select item 91086268.

Mammalian UPF3A and UPF3B can activate nonsense‐mediated mRNA decay independently of their exon junction complex binding

Zhongxia Yi, René M Arvola, Sean Myers, Corinne N Dilsavor, Rabab Abu Alhasan, Bayley N Carter, Robert D Patton, Ralf Bundschuh, Guramrit Singh

EMBO J. 2022 May; 41(10): e109202. Published online 2022 Apr 22. doi: 10.15252/embj.2021109202

PMCID:: PMC9108626

Abstract Article PDF–2.4M

Select item 91086199.

Human UPF3A and UPF3B enable fault‐tolerant activation of nonsense‐mediated mRNA decay

Damaris Wallmeroth, Jan‐Wilm Lackmann, Sabrina Kueckelmann, Janine Altmüller, Christoph Dieterich, Volker Boehm, Niels H Gehring

EMBO J. 2022 May; 41(10): e109191. Published online 2022 Apr 22. doi: 10.15252/embj.2021109191

PMCID:: PMC9108619

Abstract Article PDF–2.4M

Select item 589695710.

ICE1 promotes the link between splicing and nonsense-mediated mRNA decay

Thomas D Baird, Ken Chih-Chien Cheng, Yu-Chi Chen, Eugen Buehler, Scott E Martin, James Inglese, J Robert Hogg

eLife. 2018; 7: e33178. Published online 2018 Mar 12. doi: 10.7554/eLife.33178

PMCID:: PMC5896957

Abstract Article PDF–3.0M

Select item 287277011.

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

Patrick S Tarpey, F Lucy Raymond, Lam S Nguyen, Jayson Rodriguez, Anna Hackett, Lucianne Vandeleur, Raffaella Smith, Cheryl Shoubridge, Sarah Edkins, Claire Stevens, Sarah O'Meara, Calli Tofts, Syd Barthorpe, Gemma Buck, Jennifer Cole, Kelly Halliday, Katy Hills, David Jones, Tatiana Mironenko, Janet Perry, Jennifer Varian, Sofie West, Sara Widaa, John Teague, Ed Dicks, Adam Butler, Andrew Menzies, David Richardson, Andrew Jenkinson, Rebecca Shepherd, Keiran Raine, Jenny Moon, Yin Luo, Josep Parnau, Shambhu S Bhat, Alison Gardner, Mark Corbett, Doug Brooks, Paul Thomas, Emma Parkinson-Lawrence, Mary E Porteous, John P Warner, Tracy Sanderson, Pauline Pearson, Richard J Simensen, Cindy Skinner, George Hoganson, Duane Superneau, Richard Wooster, Martin Bobrow, Gillian Turner, Roger E Stevenson, Charles E Schwartz, P Andrew Futreal, Anand K Srivastava, Michael R Stratton, Jozef Gécz

Nat Genet. Author manuscript; available in PMC 2010 May 19.

Published in final edited form as: Nat Genet. 2007 Sep; 39(9): 1127–1133. Published online 2007 Aug 19. doi: 10.1038/ng2100

PMCID:: PMC2872770

Abstract Article PDF–1.5M

Select item 917795812.

Structures of nonsense-mediated mRNA decay factors UPF3B and UPF3A in complex with UPF2 reveal molecular basis for competitive binding and for neurodevelopmental disorder-causing mutation

Joshua C Bufton, Kyle T Powers, Jenn-Yeu A Szeto, Christine Toelzer, Imre Berger, Christiane Schaffitzel

Nucleic Acids Res. 2022 Jun 10; 50(10): 5934–5947. Published online 2022 May 31. doi: 10.1093/nar/gkac421

PMCID:: PMC9177958

Abstract Article PDF–2.7M

Select item 277974613.

Remodeling of the pioneer translation initiation complex involves translation and the karyopherin importin β

Hanae Sato, Lynne E. Maquat

Genes Dev. 2009 Nov 1; 23(21): 2537–2550. doi: 10.1101/gad.1817109

PMCID:: PMC2779746

Abstract Article PDF–915K

Select item 416017614.

Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene

Petcharat Leoyklang, Kanya Suphapeetiporn, Chalurmpon Srichomthong, Siraprapa Tongkobpetch, Stefanie Fietze, Heidi Dorward, Andrew R. Cullinane, William A. Gahl, Marjan Huizing, Vorasuk Shotelersuk

Hum Genet. Author manuscript; available in PMC 2014 Dec 1.

Published in final edited form as: Hum Genet. 2013 Dec; 132(12): 1383–1393. Published online 2013 Aug 8. doi: 10.1007/s00439-013-1345-9