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Items: 1 to 20 of 23

1.
Silencing PEX26 as an unconventional mode to kill drug-resistant cancer cells and forestall drug resistance
Michael S. Dahabieh, Fan Huang, Christophe Goncalves, Raúl Ernesto Flores González, Sathyen Prabhu, Alicia Bolt, Erminia Di Pietro, Elie Khoury, John Heath, Zi Yi Xu, Joelle Rémy-Sarrazin, Koren K. Mann, Alexandre Orthwein, François-Michel Boisvert, Nancy Braverman, Wilson H. Miller, Sonia V. del Rincón
Autophagy. 2022; 18(3): 540–558. Published online 2021 Jun 21. doi: 10.1080/15548627.2021.1936932
PMCID:
PMC9037551
AbstractArticlePDF–4.7M
2.
A newly identified mutation in the PEX26 gene is associated with a milder form of Zellweger spectrum disorder
Akemi J. Tanaka, Kanji Okumoto, Shigehiko Tamura, Yuichi Abe, Yoel Hirsch, Liyong Deng, Joseph Ekstein, Wendy K. Chung, Yukio Fujiki
Cold Spring Harb Mol Case Stud. 2019 Feb; 5(1): a003483. doi: 10.1101/mcs.a003483
PMCID:
PMC6371744
AbstractArticlePDF–12M
3.
Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation
Naomi Matsumoto, Shigehiko Tamura, Satomi Furuki, Non Miyata, Ann Moser, Nobuyuki Shimozawa, Hugo W. Moser, Yasuyuki Suzuki, Naomi Kondo, Yukio Fujiki
Am J Hum Genet. 2003 Aug; 73(2): 233–246. Published online 2003 Jul 8. doi: 10.1086/377004
PMCID:
PMC1180364
AbstractArticlePDF–691K
4.
Alternative Splicing Suggests Extended Function of PEX26 in Peroxisome Biogenesis
Sabine Weller, Ivelisse Cajigas, James Morrell, Cassandra Obie, Gary Steel, Stephen J. Gould, David Valle
Am J Hum Genet. 2005 Jun; 76(6): 987–1007. Published online 2005 Apr 27. doi: 10.1086/430637
PMCID:
PMC1196456
AbstractArticlePDF–7.9M
5.
Expanding the clinical and genetic spectrum of Heimler syndrome
Feng-Juan Gao, Fang-Yuan Hu, Ping Xu, Yu-He Qi, Jian-Kang Li, Yong-Jin Zhang, Fang Chen, Qing Chang, Fang Song, Si-Mai Shen, Ge-Zhi Xu, Ji-Hong Wu
Orphanet J Rare Dis. 2019; 14: 290. Published online 2019 Dec 12. doi: 10.1186/s13023-019-1243-x
PMCID:
PMC6909578
AbstractArticlePDF–2.1M
6.
AAA Peroxins and Their Recruiter Pex26p Modulate the Interactions of Peroxins Involved in Peroxisomal Protein Import
Shigehiko Tamura, Naomi Matsumoto, Ryota Takeba, Yukio Fujiki
J Biol Chem. 2014 Aug 29; 289(35): 24336–24346. Published online 2014 Jul 11. doi: 10.1074/jbc.M114.588038
PMCID:
PMC4148862
AbstractArticlePDF–959K
7.
Conserved targeting information in mammalian and fungal peroxisomal tail-anchored proteins
Judith Buentzel, Fabio Vilardi, Amelie Lotz-Havla, Jutta Gärtner, Sven Thoms
Sci Rep. 2015; 5: 17420. Published online 2015 Dec 2. doi: 10.1038/srep17420
PMCID:
PMC4667187
AbstractArticlePDF–1.0M
8.
Identification of Novel Mutations and Sequence Variation in the Zellweger Syndrome Spectrum of Peroxisome Biogenesis Disorders
Wing Yan Yik, Steven J. Steinberg, Ann B. Moser, Hugo W. Moser, Joseph G. Hacia
Hum Mutat. Author manuscript; available in PMC 2009 Mar 2.
Published in final edited form as: Hum Mutat. 2009 Mar; 30(3): E467–E480. doi: 10.1002/humu.20932
PMCID:
PMC2649967
AbstractArticlePDF–853K
9.
Chemically monoubiquitinated PEX5 binds to the components of the peroxisomal docking and export machinery
Vera Hagmann, Stefanie Sommer, Patrick Fabian, Jan Bierlmeier, Nadine van Treel, Henning D. Mootz, Dirk Schwarzer, Jorge E. Azevedo, Gabriele Dodt
Sci Rep. 2018; 8: 16014. Published online 2018 Oct 30. doi: 10.1038/s41598-018-34200-5
PMCID:
PMC6207756
AbstractArticlePDF–1.7M
10.
Tail-anchored PEX26 targets peroxisomes via a PEX19-dependent and TRC40-independent class I pathway
Yuichi Yagita, Takahide Hiromasa, Yukio Fujiki
J Cell Biol. 2013 Mar 4; 200(5): 651–666. doi: 10.1083/jcb.201211077
PMCID:
PMC3587837
AbstractArticlePDF–3.4M
11.
The peroxisomal receptor Pex19p forms a helical mPTS recognition domain
Nicole Schueller, Simon J Holton, Krisztian Fodor, Morlin Milewski, Petr Konarev, Will A Stanley, Janina Wolf, Ralf Erdmann, Wolfgang Schliebs, Young-Hwa Song, Matthias Wilmanns
EMBO J. 2010 Aug 4; 29(15): 2491–2500. Published online 2010 Jun 8. doi: 10.1038/emboj.2010.115
PMCID:
PMC2928687
AbstractArticlePDF–1.3M
12.
Regulation of ETAA1-mediated ATR activation couples DNA replication fidelity and genome stability
Divya Achuthankutty, Roshan Singh Thakur, Peter Haahr, Saskia Hoffmann, Alexandros P. Drainas, Anna H. Bizard, Joachim Weischenfeldt, Ian D. Hickson, Niels Mailand
J Cell Biol. 2019 Dec 2; 218(12): 3943–3953. Published online 2019 Oct 15. doi: 10.1083/jcb.201905064
PMCID:
PMC6891097
AbstractArticlePDF–2.7M
13.
N6-methyladenosine on mRNA facilitates a phase-separated nuclear body that suppresses myeloid leukemic differentiation
Yuanming Cheng, Wei Xie, Brian F Pickering, Karen L Chu, Angela M Savino, Xuejing Yang, Hanzhi Luo, Diu TT Nguyen, Shanlan Mo, Ersilia Barin, Anthony Velleca, Thomas Rohwetter, Dinshaw J Patel, Samie R Jaffrey, Michael G Kharas
Cancer Cell. Author manuscript; available in PMC 2022 Jul 12.
Published in final edited form as: Cancer Cell. 2021 Jul 12; 39(7): 958–972.e8. Published online 2021 May 27. doi: 10.1016/j.ccell.2021.04.017
PMCID:
PMC8282764
AbstractArticlePDF–3.4M
14.
A genome annotation-driven approach to cloning the human ORFeome
John E Collins, Charmain L Wright, Carol A Edwards, Matthew P Davis, James A Grinham, Charlotte G Cole, Melanie E Goward, Begoña Aguado, Meera Mallya, Younes Mokrab, Elizabeth J Huckle, David M Beare, Ian Dunham
Genome Biol. 2004; 5(10): R84. Published online 2004 Sep 30. doi: 10.1186/gb-2004-5-10-r84
PMCID:
PMC545604
AbstractArticlePDF–762K
15.
Widespread expansion of protein interaction capabilities by alternative splicing
Xinping Yang, Jasmin Coulombe-Huntington, Shuli Kang, Gloria M. Sheynkman, Tong Hao, Aaron Richardson, Song Sun, Fan Yang, Yun A. Shen, Ryan R. Murray, Kerstin Spirohn, Bridget E. Begg, Miquel Duran-Frigola, Andrew MacWilliams, Samuel J. Pevzner, Quan Zhong, Shelly A. Wanamaker, Stanley Tam, Lila Ghamsari, Nidhi Sahni, Song Yi, Maria D. Rodriguez, Dawit Balcha, Guihong Tan, Michael Costanzo, Brenda Andrews, Charles Boone, Xianghong J. Zhou, Kourosh Salehi-Ashtiani, Benoit Charloteaux, Alyce A. Chen, Michael A. Calderwood, Patrick Aloy, Frederick P. Roth, David E. Hill, Lilia M. Iakoucheva, Yu Xia, Marc Vidal
Cell. Author manuscript; available in PMC 2017 Feb 11.
Published in final edited form as: Cell. 2016 Feb 11; 164(4): 805–817. doi: 10.1016/j.cell.2016.01.029
PMCID:
PMC4882190
AbstractArticlePDF–1.9M
16.
The STUbL RNF4 regulates protein group SUMOylation by targeting the SUMO conjugation machinery
Ramesh Kumar, Román González-Prieto, Zhenyu Xiao, Matty Verlaan-de Vries, Alfred C. O. Vertegaal
Nat Commun. 2017; 8: 1809. Published online 2017 Nov 27. doi: 10.1038/s41467-017-01900-x
PMCID:
PMC5703878
AbstractArticlePDF–3.7M
17.
Sequence Comparison of Human and Mouse Genes Reveals a Homologous Block Structure in the Promoter Regions
Yutaka Suzuki, Riu Yamashita, Matsuyuki Shirota, Yuta Sakakibara, Joe Chiba, Junko Mizushima-Sugano, Kenta Nakai, Sumio Sugano
Genome Res. 2004 Sep; 14(9): 1711–1718. doi: 10.1101/gr.2435604
PMCID:
PMC515316
AbstractArticlePDF–181K
18.
Ubiquitin-mediated proteolysis of HuR by heat shock
Kotb Abdelmohsen, Subramanya Srikantan, Xiaoling Yang, Ashish Lal, Hyeon Ho Kim, Yuki Kuwano, Stefanie Galban, Kevin G Becker, Davida Kamara, Rafael de Cabo, Myriam Gorospe
EMBO J. 2009 May 6; 28(9): 1271–1282. Published online 2009 Mar 26. doi: 10.1038/emboj.2009.67
PMCID:
PMC2683047
AbstractArticlePDF–1.4M
19.
Diversification of transcriptional modulation: Large-scale identification and characterization of putative alternative promoters of human genes
Kouichi Kimura, Ai Wakamatsu, Yutaka Suzuki, Toshio Ota, Tetsuo Nishikawa, Riu Yamashita, Jun-ichi Yamamoto, Mitsuo Sekine, Katsuki Tsuritani, Hiroyuki Wakaguri, Shizuko Ishii, Tomoyasu Sugiyama, Kaoru Saito, Yuko Isono, Ryotaro Irie, Norihiro Kushida, Takahiro Yoneyama, Rie Otsuka, Katsuhiro Kanda, Takahide Yokoi, Hiroshi Kondo, Masako Wagatsuma, Katsuji Murakawa, Shinichi Ishida, Tadashi Ishibashi, Asako Takahashi-Fujii, Tomoo Tanase, Keiichi Nagai, Hisashi Kikuchi, Kenta Nakai, Takao Isogai, Sumio Sugano
Genome Res. 2006 Jan; 16(1): 55–65. doi: 10.1101/gr.4039406
PMCID:
PMC1356129
AbstractArticlePDF–438K
20.
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

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