U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO Profiles

Items: 1 to 20 of 51

1.
Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms
Hui Zhang, Jian Gao, Hanjun Wang, Mengli Liu, Shuangshuang Lu, Hongen Xu, Wenxue Tang, Guoxi Zheng
BMC Med Genomics. 2024; 17: 89. Published online 2024 Apr 16. doi: 10.1186/s12920-024-01858-y
PMCID:
PMC11020176
AbstractArticlePDF–1.5M
2.
The Eyes Absent family members EYA4 and EYA1 promote PLK1 activation and successful mitosis through tyrosine dephosphorylation
Christopher B. Nelson, Samuel Rogers, Kaushik Roychoudhury, Yaw Sing Tan, Caroline J. Atkinson, Alexander P. Sobinoff, Christopher G. Tomlinson, Anton Hsu, Robert Lu, Eloise Dray, Michelle Haber, Jamie I. Fletcher, Anthony J. Cesare, Rashmi S. Hegde, Hilda A. Pickett
Nat Commun. 2024; 15: 1385. Published online 2024 Feb 15. doi: 10.1038/s41467-024-45683-4
PMCID:
PMC10869800
AbstractArticlePDF–9.3M
3.
鳃-耳-肾综合征家系EYA1基因一个新的外显子重复变异
李 隽, 赵 培伟, 夏 志杰, 姚 薇, 魏 幼华, 郝 丽丽, 夏 忠芳, 何 学莲
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021 Jul 5; 35(7): 607–612. Chinese. doi: 10.13201/j.issn.2096-7993.2021.07.007
PMCID:
PMC10127898
AbstractArticlePDF–5.8M
4.
A monoallelic variant in EYA1 is associated with Branchio‐Otic syndrome in a Malian family
Abdoulaye Yalcouyé, Oumou Traoré, Salimata Diarra, Isabelle Schrauwen, Kevin Esoh, Magda Kamila Kadlubowska, Thashi Bharadwaj, Samuel Mawuli Adadey, Mohamed Kéita, Cheick O. Guinto, Suzanne M. Leal, Guida Landouré, Ambroise Wonkam
Mol Genet Genomic Med. 2022 Jul; 10(7): e1995. Published online 2022 Jun 14. doi: 10.1002/mgg3.1995
PMCID:
PMC9266589
AbstractArticlePDF–2.0M
5.
Phenotype–genotype correlation in patients with typical and atypical branchio-oto-renal syndrome
Masatsugu Masuda, Ayako Kanno, Kiyomitsu Nara, Hideki Mutai, Naoya Morisada, Kazumoto Iijima, Noriko Morimoto, Atsuko Nakano, Tomoko Sugiuchi, Yasuhide Okamoto, Sawako Masuda, Sayaka Katsunuma, Kaoru Ogawa, Tatsuo Matsunaga
Sci Rep. 2022; 12: 969. Published online 2022 Jan 19. doi: 10.1038/s41598-022-04885-w
PMCID:
PMC8770796
AbstractArticlePDF–1.5M
6.
Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration
Stephane Bourgeois, Daniel F. Carr, Crispin O. Musumba, Alexander Penrose, Celestine Esume, Andrew P. Morris, Andrea L. Jorgensen, J. Eunice Zhang, D. Mark Pritchard, Panos Deloukas, Munir Pirmohamed
EBioMedicine. 2021 Dec; 74: 103728. Published online 2021 Dec 2. doi: 10.1016/j.ebiom.2021.103728
PMCID:
PMC8646165
AbstractArticlePDF–1013K
7.
The deubiquitinase OTUB1 fosters papillary thyroid carcinoma growth through EYA1 stabilization
Peiyi Xie, Qing Chao, Jiuang Mao, Yue Liu, Jiayu Fang, Jing Xie, Jing Zhen, Yongqi Ding, Bidong Fu, Yun Ke, Da Huang
J Cell Mol Med. 2021 Dec; 25(23): 10980–10989. Published online 2021 Nov 12. doi: 10.1111/jcmm.17020
PMCID:
PMC8642681
AbstractArticlePDF–1.5M
8.
Two naturally derived small molecules disrupt the sineoculis homeobox homolog 1–eyes absent homolog 1 (SIX1–EYA1) interaction to inhibit colorectal cancer cell growth
Jing Wu, Bin Huang, Hong-Bo He, Wen-Zhu Lu, Wei-Guo Wang, Hong Liu
Chin Med J (Engl) 2021 Oct 5; 134(19): 2340–2352. Published online 2021 Sep 23. doi: 10.1097/CM9.0000000000001736
PMCID:
PMC8509980
AbstractArticlePDF–1.9M
9.
The Eyes Absent proteins in development and in developmental disorders
Upendra Kumar Soni, Kaushik Roychoudhury, Rashmi S. Hegde
Biochem Soc Trans. 2021 Jun 30; 49(3): 1397–1408. Published online 2021 Jul 1. doi: 10.1042/BST20201302
PMCID:
PMC8286820
AbstractArticlePDF–2.1M
10.
A mutation of EYA1 gene in a Chinese Han family with Branchio-Oto syndrome
Rui Han, Yan Xia, Zhijuan Liu, Shuang Wu, Erdengqieqieke Ye, Ling Duan, Jianbing Ding, Xiaolin La
Medicine (Baltimore) 2021 Jun 25; 100(25): e24691. Published online 2021 Jun 25. doi: 10.1097/MD.0000000000024691
PMCID:
PMC8238333
AbstractArticlePDF–963K
11.
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
12.
The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases
Kaushik Roychoudhury, Rashmi S. Hegde
Int J Mol Sci. 2021 Apr; 22(8): 3925. Published online 2021 Apr 10. doi: 10.3390/ijms22083925
PMCID:
PMC8069645
AbstractArticlePDF–1.7M
13.
Blocking PPARγ interaction facilitates Nur77 interdiction of fatty acid uptake and suppresses breast cancer progression
Peng-bo Yang, Pei-pei Hou, Fu-yuan Liu, Wen-bin Hong, Hang-zi Chen, Xiao-yu Sun, Peng Li, Yi Zhang, Cui-yu Ju, Li-juan Luo, Sheng-fu Wu, Jia-xin Zhou, Zhi-jing Wang, Jian-ping He, Li Li, Tong-Jin Zhao, Xianming Deng, Tianwei Lin, Qiao Wu
Proc Natl Acad Sci U S A. 2020 Nov 3; 117(44): 27412–27422. Published online 2020 Oct 21. doi: 10.1073/pnas.2002997117
PMCID:
PMC7959534
AbstractArticlePDF–3.1M
14.
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
15.
Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei
Domenico Fasci, Hugo van Ingen, Richard A. Scheltema, Albert J. R. Heck
Mol Cell Proteomics. 2018 Oct; 17(10): 2018–2033. Published online 2018 Jul 18. doi: 10.1074/mcp.RA118.000924
PMCID:
PMC6166682
AbstractArticlePDF–3.8M
16.
A novel mutation in EYA1 in a Chinese family with Branchio-oto-renal syndrome
Yan-gong Wang, Shu-ping Sun, Yi-ling Qiu, Qing-he Xing, Wei Lu
BMC Med Genet. 2018; 19: 139. Published online 2018 Aug 7. doi: 10.1186/s12881-018-0653-2
PMCID:
PMC6081847
AbstractArticlePDF–1.1M
17.
A de novo and novel mutation in the EYA1 gene in a Chinese child with branchio-oto-renal syndrome
Guomin Li, Qian Shen, Li Sun, Haimei Liu, Yu An, Hong Xu
Intractable Rare Dis Res. 2018 Feb; 7(1): 42–45. doi: 10.5582/irdr.2017.01075
PMCID:
PMC5849624
AbstractArticlePDF–418K
18.
A Human Tyrosine Phosphatase Interactome Mapped by Proteomic Profiling
Parveen Kumar, Prathyusha Munnangi, KVS Rammohan Chowdary, Varun J. Shah, Swapnil R. Shinde, Nanci R. Kolli, Rachita R. Halehalli, Hampapathalu A. Nagarajaram, Subbareddy Maddika
J Proteome Res. 2017 Aug 4; 16(8): 2789–2801. Published online 2017 Jul 4. doi: 10.1021/acs.jproteome.7b00065
PMCID:
PMC5548413
AbstractArticlePDF–5.2M
19.
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper
Nature. Author manuscript; available in PMC 2017 Nov 17.
Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366
PMCID:
PMC5531611
AbstractArticlePDF–2.7M
20.
Novel EYA1 Variants Causing Branchio-Oto-Renal Syndrome
Kyle D. Klingbeil, Christopher M. Greenland, Selcuk Arslan, Arianne Llamos Paneque, Hakan Gurkan, Selma Demir Ulusal, Reza Maroofian, Andrea Carrera-Gonzalez, Stefany Montufar-Armendariz, Rosario Paredes, Nursel Elcioglu, Ibis Menendez, Mahdiyeh Behnam, Joseph Foster, II, Shengru Guo, Sebastian Escarfuller, Filiz Basak Cengiz, Duygu Duman, Guney Bademci, Mustafa Tekin
Int J Pediatr Otorhinolaryngol. Author manuscript; available in PMC 2018 Jul 1.
Published in final edited form as: Int J Pediatr Otorhinolaryngol. 2017 Jul; 98: 59–63. Published online 2017 Apr 26. doi: 10.1016/j.ijporl.2017.04.037
PMCID:
PMC5516569
AbstractArticlePDF–222K

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

You are here: NCBI > Literature > PubMed Central (PMC)
Support Center