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Items: 1 to 20 of 31

1.
NR2E3 loss disrupts photoreceptor cell maturation and fate in human organoid models of retinal development
Nathaniel K. Mullin, Laura R. Bohrer, Andrew P. Voigt, Lola P. Lozano, Allison T. Wright, Vera L. Bonilha, Robert F. Mullins, Edwin M. Stone, Budd A. Tucker
J Clin Invest. 2024 Jun 3; 134(11): e173892. Published online 2024 Apr 23. doi: 10.1172/JCI173892
PMCID:
PMC11142732
AbstractArticlePDF–16M
2.
Clinical and Genetic Features of NR2E3-Associated Retinopathy: A Report of Eight Families with a Longitudinal Study and Literature Review
Sainan Xiao, Zhen Yi, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Ping Lian, Wenmin Sun, Panfeng Wang, Lin Lu, Qingjiong Zhang
Genes (Basel) 2023 Aug; 14(8): 1525. Published online 2023 Jul 26. doi: 10.3390/genes14081525
PMCID:
PMC10454055
AbstractArticlePDF–4.1M
3.
Nuclear Receptor Subfamily 2 Group E Member 3 (NR2E3): Role in Retinal Development and Disease
Maria Toms, Natasha Ward, Mariya Moosajee
Genes (Basel) 2023 Jul; 14(7): 1325. Published online 2023 Jun 23. doi: 10.3390/genes14071325
PMCID:
PMC10379133
AbstractArticlePDF–4.4M
4.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
5.
Novel Pathogenic Sequence Variants in NR2E3 and Clinical Findings in Three Patients
Saoud Al-khuzaei, Suzanne Broadgate, Stephanie Halford, Jasleen K. Jolly, Morag Shanks, Penny Clouston, Susan M. Downes
Genes (Basel) 2020 Nov; 11(11): 1288. Published online 2020 Oct 29. doi: 10.3390/genes11111288
PMCID:
PMC7716234
AbstractArticlePDF–2.8M
6.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M
7.
The Rod Photoreceptor-Specific Nuclear Receptor Nr2e3 Represses Transcription of Multiple Cone-Specific Genes
Jichao Chen, Amir Rattner, Jeremy Nathans
J Neurosci. 2005 Jan 5; 25(1): 118–129. doi: 10.1523/JNEUROSCI.3571-04.2005
PMCID:
PMC6725199
AbstractArticlePDF–1003K
8.
Antisense Oligonucleotide-Based Downregulation of the G56R Pathogenic Variant Causing NR2E3-Associated Autosomal Dominant Retinitis Pigmentosa
Sarah Naessens, Laurien Ruysschaert, Steve Lefever, Frauke Coppieters, Elfride De Baere
Genes (Basel) 2019 May; 10(5): 363. Published online 2019 May 10. doi: 10.3390/genes10050363
PMCID:
PMC6562693
AbstractArticlePDF–1.7M
9.
Loss of NR2E3 represses AHR by LSD1 reprogramming, is associated with poor prognosis in liver cancer
Tilak Khanal, Kwangmin Choi, Yuet-Kin Leung, Jiang Wang, Dasom Kim, Vinothini Janakiram, Sung-Gook Cho, Alvaro Puga, Shuk-Mei Ho, Kyounghyun Kim
Sci Rep. 2017; 7: 10662. Published online 2017 Sep 6. doi: 10.1038/s41598-017-11106-2
PMCID:
PMC5587550
AbstractArticlePDF–2.1M
10.
Heterodimers of photoreceptor-specific nuclear receptor (PNR/NR2E3) and peroxisome proliferator-activated receptor-γ (PPARγ) are disrupted by retinal disease-associated mutations
Joel Fulton, Bismoy Mazumder, Jonathan B Whitchurch, Cintia J Monteiro, Hilary M Collins, Chun M Chan, Maria P Clemente, Miguel Hernandez-Quiles, Elizabeth A Stewart, Winfried M Amoaku, Paula M Moran, Nigel P Mongan, Jenny L Persson, Simak Ali, David M Heery
Cell Death Dis. 2017 Mar; 8(3): e2677. Published online 2017 Mar 16. doi: 10.1038/cddis.2017.98
PMCID:
PMC5386588
AbstractArticlePDF–1.1M
11.
Differential dimerization of variants linked to enhanced S-Cone Sensitivity Syndrome (ESCS) located in the NR2E3 ligand-binding domain
Désirée von Alpen, H. Viet Tran, Nicolas Guex, Giulia Venturini, Francis L. Munier, Daniel F. Schorderet, Neena B. Haider, Pascal Escher
Hum Mutat. Author manuscript; available in PMC 2016 Sep 7.
Published in final edited form as: Hum Mutat. 2015 Jun; 36(6): 599–610. Published online 2015 Apr 27. doi: 10.1002/humu.22775
PMCID:
PMC5014385
AbstractArticlePDF–1.4M
12.
Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases
Fiona Blanco-Kelly, María García Hoyos, Miguel Angel Lopez Martinez, Maria Isabel Lopez-Molina, Rosa Riveiro-Alvarez, Patricia Fernandez-San Jose, Almudena Avila-Fernandez, Marta Corton, Jose M. Millan, Blanca García Sandoval, Carmen Ayuso
PLoS One. 2016; 11(2): e0149473. Published online 2016 Feb 24. doi: 10.1371/journal.pone.0149473
PMCID:
PMC4766102
AbstractArticlePDF–5.1M
13.
Deregulation of NR2E3, an orphan nuclear receptor, by benzo(a)pyrene-induced oxidative stress is associated with histone modification status change of the estrogen receptor gene promoter
Tilak Khnal, Dasom Kim, Abby Johnson, Divaker Choubey, Kyounghyun Kim
Toxicol Lett. Author manuscript; available in PMC 2016 Sep 17.
Published in final edited form as: Toxicol Lett. 2015 Sep 17; 237(3): 228–236. Published online 2015 Jul 3. doi: 10.1016/j.toxlet.2015.06.1708
PMCID:
PMC4524348
AbstractArticlePDF–876K
14.
IL-13Rα2 mediates PNR-induced migration and metastasis in ERα-negative breast cancer
Z Zhao, L Wang, W Xu
Oncogene. Author manuscript; available in PMC 2015 Mar 20.
Published in final edited form as: Oncogene. 2015 Mar 19; 34(12): 1596–1607. Published online 2014 Apr 21. doi: 10.1038/onc.2014.53
PMCID:
PMC4321963
AbstractArticlePDF–2.3M
15.
Disruption of the human cone photoreceptor mosaic from a defect in NR2E3 transcription factor function in young adults
Sung Pyo Park, In Hwan Hong, Stephen H. Tsang, Winston Lee, Jason Horowitz, Suzanne Yzer, Rando Allikmets, Stanley Chang
Graefes Arch Clin Exp Ophthalmol. Author manuscript; available in PMC 2015 Jan 12.
Published in final edited form as: Graefes Arch Clin Exp Ophthalmol. 2013 Oct; 251(10): 2299–2309. Published online 2013 Apr 19. doi: 10.1007/s00417-013-2296-5
PMCID:
PMC4291322
AbstractArticlePDF–4.1M
16.
A novel mutation in the NR2E3 gene associated with Goldmann-Favre syndrome and vasoproliferative tumor of the retina
George J. Manayath, Prasanthi Namburi, Sundaresan Periasamy, Jeevan A. Kale, Venkatapathy Narendran, Anuradha Ganesh
Mol Vis. 2014; 20: 724–731. Published online 2014 May 29.
PMCID:
PMC4039415
AbstractArticlePDF–1.2M
17.
A signature motif mediating selective interactions of BCL11A with the NR2E/F subfamily of orphan nuclear receptors
Chun Ming Chan, Joel Fulton, Cristina Montiel-Duarte, Hilary M. Collins, Neetu Bharti, Frances R. Wadelin, Paula M. Moran, Nigel P. Mongan, David M. Heery
Nucleic Acids Res. 2013 Nov; 41(21): 9663–9679. Published online 2013 Aug 23. doi: 10.1093/nar/gkt761
PMCID:
PMC3834829
AbstractArticlePDF–3.7M
18.
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in a same family
Pascal Escher, Peter Gouras, Raphaël Roduit, Leila Tiab, Sylvain Bolay, Tania Delarive, Shiming Chen, Chih-Cheng Tsai, Masanori Hayashi, Jana Zernant, Joanna E. Merriam, Nicolas Mermod, Rando Allikmets, Francis L. Munier, Daniel F. Schorderet
Hum Mutat. Author manuscript; available in PMC 2013 May 20.
Published in final edited form as: Hum Mutat. 2009 Mar; 30(3): 342–351. doi: 10.1002/humu.20858
PMCID:
PMC3658139
AbstractArticlePDF–1.8M
19.
Reconstruction of nuclear receptor network reveals that NR2E3 is a novel upstream regulator of ESR1 in breast cancer
Yun-Yong Park, Kyounghyun Kim, Sang-Bae Kim, Bryan T Hennessy, Soo Mi Kim, Eun Sung Park, Jae Yun Lim, Jane Li, Yiling Lu, Ana Maria Gonzalez-Angulo, Woojin Jeong, Gordon B Mills, Stephen Safe, Ju-Seog Lee
EMBO Mol Med. 2012 Jan; 4(1): 52–67. doi: 10.1002/emmm.201100187
PMCID:
PMC3376834
AbstractArticlePDF–9.4M
20.
Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa
Chitra Kannabiran, Hardeep Singh, Nishika Sahini, Subhadra Jalali, Gayathri Mohan
Mol Vis. 2012; 18: 1165–1174. Published online 2012 May 4.
PMCID:
PMC3351411
AbstractArticlePDF–4.5M

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