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Items: 1 to 20 of 60

1.
Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes
Anni A. Antikainen, Jani K. Haukka, Anmol Kumar, Anna Syreeni, Stefanie Hägg-Holmberg, Anni Ylinen, Elina Kilpeläinen, Anastasia Kytölä, Aarno Palotie, Jukka Putaala, Lena M. Thorn, Valma Harjutsalo, Per-Henrik Groop, Niina Sandholm, the FinnDiane Study Group
Sci Rep. 2024; 14: 13453. Published online 2024 Jun 11. doi: 10.1038/s41598-024-61840-7
PMCID:
PMC11166668
AbstractArticlePDF–4.0M
2.
Architecture of the human erythrocyte ankyrin-1 complex
F. Vallese, K. Kim, L.Y. Yen, J.D. Johnston, A.J. Noble, T. Calì, O.B. Clarke
Nat Struct Mol Biol. Author manuscript; available in PMC 2023 Jul 27.
Published in final edited form as: Nat Struct Mol Biol. 2022 Jul; 29(7): 706–718. Published online 2022 Jul 14. doi: 10.1038/s41594-022-00792-w
PMCID:
PMC10373098
AbstractArticlePDF–9.7M
3.
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing
Engin Demirdizen, Ruslan Al-Ali, Ashwin Narayanan, Xueyuan Sun, Julianna Patricia Varga, Bianca Steffl, Manuela Brom, Damir Krunic, Claudia Schmidt, Gabriele Schmidt, Felix Bestvater, Julian Taranda, Şevin Turcan
Neuro Oncol. 2023 Jun; 25(6): 1031–1043. Published online 2022 Nov 22. doi: 10.1093/neuonc/noac233
PMCID:
PMC10237422
AbstractArticlePDF–23M
4.
FBXO22 promotes leukemogenesis by targeting BACH1 in MLL-rearranged acute myeloid leukemia
Xiao-Na Zhu, Yu-Sheng Wei, Qian Yang, Hao-Ran Liu, Zhe Zhi, Di Zhu, Li Xia, Deng-Li Hong, Yun Yu, Guo-Qiang Chen
J Hematol Oncol. 2023; 16: 9. Published online 2023 Feb 11. doi: 10.1186/s13045-023-01400-0
PMCID:
PMC9922468
AbstractArticlePDF–4.9M
5.
De novo variations of ANK1 gene caused hereditary spherocytosis in two Chinese children by affecting pre-mRNA splicing
Yang Wang, Lan Huang, Yao Zhu, Xizhou An, Jiacheng Li, Jiangwei Zhen, Jie Yu
BMC Pediatr. 2023; 23: 23. Published online 2023 Jan 16. doi: 10.1186/s12887-022-03795-0
PMCID:
PMC9841706
AbstractArticlePDF–3.5M
6.
The SNP rs516946 Interacted in the Association of MetS with Dietary Iron among Chinese Males but Not Females
Zhenni Zhu, Zhengyuan Wang, Jiajie Zang, Ye Lu, Ziyi Xiao, Guangyong Zheng, Fan Wu
Nutrients. 2022 May; 14(10): 2024. Published online 2022 May 12. doi: 10.3390/nu14102024
PMCID:
PMC9147551
AbstractArticlePDF–898K
7.
Protein interaction landscapes revealed by advanced in vivo cross-linking–mass spectrometry
Andrew Wheat, Clinton Yu, Xiaorong Wang, Anthony M. Burke, Ilan E. Chemmama, Robyn M. Kaake, Peter Baker, Scott D. Rychnovsky, Jing Yang, Lan Huang
Proc Natl Acad Sci U S A. 2021 Aug 10; 118(32): e2023360118. Published online 2021 Aug 4. doi: 10.1073/pnas.2023360118
PMCID:
PMC8364181
AbstractArticlePDF–3.0M
8.
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
9.
Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis
Fei Xie, Lei Lei, Bin Cai, Lu Gan, Yu Gao, Xiaoying Liu, Lin Zhou, Jinjin Jiang
Mol Genet Genomic Med. 2021 Apr; 9(4): e1577. Published online 2021 Feb 23. doi: 10.1002/mgg3.1577
PMCID:
PMC8123760
AbstractArticlePDF–532K
10.
Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report
Senmao Chai, Rong Jiao, Xiaodong Sun, Pan Fu, Qiang Zhao, Ming Sang
BMC Med Genet. 2020; 21: 223. Published online 2020 Nov 13. doi: 10.1186/s12881-020-01161-4
PMCID:
PMC7666488
AbstractArticlePDF–1.0M
11.
ANK1和SPTB基因突变致遗传性球形红细胞增多症的临床特点及遗传学分析
龚 军, 贺 湘玲, 邹 润英, 陈 可可, 游 亚兰, 邹 惠, 田 鑫, 朱 呈光
Zhongguo Dang Dai Er Ke Za Zhi. 2019 Apr 25; 21(4): 370–374. Chinese. doi: 10.7499/j.issn.1008-8830.2019.04.013
PMCID:
PMC7389221
AbstractArticlePDF–1.9M
12.
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
13.
The Plasmodium falciparum MESA erythrocyte cytoskeleton-binding (MEC) motif binds to erythrocyte ankyrin
Geoffrey Kimiti Kilili, Bikash Shakya, Patrick T. Dolan, Ling Wang, Monica L. Husby, Robert V. Stahelin, Ernesto S. Nakayasu, Douglas J. LaCount
Mol Biochem Parasitol. Author manuscript; available in PMC 2020 Jul 1.
Published in final edited form as: Mol Biochem Parasitol. 2019 Jul; 231: 111189. Published online 2019 May 21. doi: 10.1016/j.molbiopara.2019.111189
PMCID:
PMC7020240
AbstractArticlePDF–1.0M
14.
Cytoplasmic Domain Mutations of the L1 Cell Adhesion Molecule Reduce L1–Ankyrin Interactions
Leila K. Needham, Karsten Thelen, Patricia F. Maness
J Neurosci. 2001 Mar 1; 21(5): 1490–1500. doi: 10.1523/JNEUROSCI.21-05-01490.2001
PMCID:
PMC6762935
AbstractArticlePDF–736K
15.
Two novel ANK1 loss‐of‐function mutations in Chinese families with hereditary spherocytosis
Lili Hao, Shanshan Li, Duan Ma, Shiyu Chen, Bowen Zhang, Deyong Xiao, Jin Zhang, Nan Jiang, Shayi Jiang, Jing Ma
J Cell Mol Med. 2019 Jun; 23(6): 4454–4463. Published online 2019 Apr 23. doi: 10.1111/jcmm.14343
PMCID:
PMC6533472
AbstractArticlePDF–1.0M
16.
BAP1 regulation of the key adaptor protein NCoR1 is critical for γ-globin gene repression
Lei Yu, Natee Jearawiriyapaisarn, Mary P. Lee, Tomonori Hosoya, Qingqing Wu, Greggory Myers, Kim-Chew Lim, Ryo Kurita, Yukio Nakamura, Anne B. Vojtek, Jean-François Rual, James Douglas Engel
Genes Dev. 2018 Dec 1; 32(23-24): 1537–1549. doi: 10.1101/gad.318436.118
PMCID:
PMC6295165
AbstractArticlePDF–3.5M
17.
VIRMA mediates preferential m6A mRNA methylation in 3′UTR and near stop codon and associates with alternative polyadenylation
Yanan Yue, Jun Liu, Xiaolong Cui, Jie Cao, Guanzheng Luo, Zezhou Zhang, Tao Cheng, Minsong Gao, Xiao Shu, Honghui Ma, Fengqin Wang, Xinxia Wang, Bin Shen, Yizhen Wang, Xinhua Feng, Chuan He, Jianzhao Liu
Cell Discov. 2018; 4: 10. Published online 2018 Feb 27. doi: 10.1038/s41421-018-0019-0
PMCID:
PMC5826926
AbstractArticlePDF–2.3M
18.
Airway expression of Transient Receptor Potential (TRP) Vanniloid-1 and Ankyrin-1 channels is not increased in patients with Idiopathic Pulmonary Fibrosis
Nicola-xan Hutchinson, Allen Gibbs, Amanda Tonks, Benjamin D. Hope-Gill
PLoS One. 2017; 12(11): e0187847. Published online 2017 Nov 17. doi: 10.1371/journal.pone.0187847
PMCID:
PMC5693416
AbstractArticlePDF–14M
19.
ANK1 Methylation Regulates Expression of MicroRNA-486-5p and Discriminates Lung tumors by Histology and Smoking Status
Mathewos Tessema, Christin M. Yingling, Maria A. Picchi, Guodong Wu, Tyrone Ryba, Yong Lin, Aaron O. Bungum, Eric S. Edell, Avrum Spira, Steven A. Belinsky
Cancer Lett. Author manuscript; available in PMC 2018 Dec 1.
Published in final edited form as: Cancer Lett. 2017 Dec 1; 410: 191–200. Published online 2017 Sep 29. doi: 10.1016/j.canlet.2017.09.038
PMCID:
PMC5675764
AbstractArticlePDF–1.2M
20.
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

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