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Items: 1 to 20 of 50

1.
α-myosin heavy chain lactylation maintains sarcomeric structure and function and alleviates the development of heart failure
Naijin Zhang, Ying Zhang, Jiaqi Xu, Pengbo Wang, Boquan Wu, Saien Lu, Xinxin Lu, Shilong You, Xinyue Huang, Mohan Li, Yuanming Zou, Mengke Liu, Yuanhui Zhao, Guozhe Sun, Wenbin Wang, Danxi Geng, Jingwei Liu, Liu Cao, Yingxian Sun
Cell Res. 2023 Sep; 33(9): 679–698. Published online 2023 Jul 13. doi: 10.1038/s41422-023-00844-w
PMCID:
PMC10474270
AbstractArticlePDF–14M
2.
Cross-Linking Mass Spectrometry Uncovers Interactions Between High-Density Lipoproteins and the SARS-CoV-2 Spike Glycoprotein
Sean A. Burnap, Ana Maria Ortega-Prieto, Jose M. Jimenez-Guardeño, Hashim Ali, Kaloyan Takov, Matthew Fish, Manu Shankar-Hari, Mauro Giacca, Michael H. Malim, Manuel Mayr
Mol Cell Proteomics. 2023 Aug; 22(8): 100600. Published online 2023 Jun 19. doi: 10.1016/j.mcpro.2023.100600
PMCID:
PMC10279469
AbstractArticlePDF–3.2M
3.
Multiplexed kinase interactome profiling quantifies cellular network activity and plasticity
Martin Golkowski, Andrea Lius, Tanmay Sapre, Ho-Tak Lau, Taylor Moreno, Dustin J. Maly, Shao-En Ong
Mol Cell. Author manuscript; available in PMC 2023 Apr 4.
Published in final edited form as: Mol Cell. 2023 Mar 2; 83(5): 803–818.e8. Published online 2023 Feb 2. doi: 10.1016/j.molcel.2023.01.015
PMCID:
PMC10072906
AbstractArticlePDF–4.2M
4.
Identification of the prognostic value of Th1/Th2 ratio and a novel prognostic signature in basal-like breast cancer
Yu Xiao, Yi Huang, Jianping Jiang, Yan Chen, Changyuan Wei
Hereditas. 2023; 160: 2. Published online 2023 Jan 25. doi: 10.1186/s41065-023-00265-0
PMCID:
PMC9875389
AbstractArticlePDF–4.4M
5.
Identification and functional analysis of variants of MYH6 gene promoter in isolated ventricular septal defects
Ji-Yang Zuo, Huan-Xin Chen, Zhi-Gang Liu, Qin Yang, Guo-Wei He
BMC Med Genomics. 2022; 15: 213. Published online 2022 Oct 8. doi: 10.1186/s12920-022-01365-y
PMCID:
PMC9548206
AbstractArticlePDF–1.8M
6.
Biophysical and functional study of CRL5Ozz, a muscle specific ubiquitin ligase complex
Yvan Campos, Amanda Nourse, Ajay Tanwar, Ravi Kalathur, Erik Bonten, Alessandra d’Azzo
Sci Rep. 2022; 12: 7820. Published online 2022 May 12. doi: 10.1038/s41598-022-10955-w
PMCID:
PMC9098882
AbstractArticlePDF–4.6M
7.
The Effect of the NFκB-USP9X-Cx43 Axis on the Dynamic Balance of Bone Formation/Degradation during Ossification of the Posterior Longitudinal Ligament of the Cervical Spine
Xiaoqiu Yuan, Yongfei Guo, Jilu Liu, Jingchuan Sun, Lei Shi, Jinhao Miao, Jiangang Shi, Yu Chen
Oxid Med Cell Longev. 2022; 2022: 1604932. Published online 2022 Mar 29. doi: 10.1155/2022/1604932
PMCID:
PMC8983240
AbstractArticlePDF–1.9M
8.
Identification of MYH6 as the potential gene for human ischaemic cardiomyopathy
Jian‐Hong Chen, Lei‐Li Wang, Lin Tao, Bin Qi, Yong Wang, Yu‐Jie Guo, Liu Miao
J Cell Mol Med. 2021 Nov; 25(22): 10736–10746. Published online 2021 Oct 26. doi: 10.1111/jcmm.17015
PMCID:
PMC8581323
AbstractArticlePDF–1.7M
9.
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
10.
Genetic Etiology of Left‐Sided Obstructive Heart Lesions: A Story in Development
Lauren E. Parker, Andrew P. Landstrom
J Am Heart Assoc. 2021 Jan 19; 10(2): e019006. Published online 2021 Jan 12. doi: 10.1161/JAHA.120.019006
PMCID:
PMC7955312
AbstractArticlePDF–503K
11.
Kinase Interaction Network Expands Functional and Disease Roles of Human Kinases
Marija Buljan, Rodolfo Ciuffa, Audrey van Drogen, Anton Vichalkovski, Martin Mehnert, George Rosenberger, Sohyon Lee, Markku Varjosalo, Lucia Espona Pernas, Vincent Spegg, Berend Snijder, Ruedi Aebersold, Matthias Gstaiger
Mol Cell. 2020 Aug 6; 79(3): 504–520.e9. doi: 10.1016/j.molcel.2020.07.001
PMCID:
PMC7427327
AbstractArticle
12.
TRIM6 promotes colorectal cancer cells proliferation and response to thiostrepton by TIS21/FoxM1
Shuier Zheng, Chenliang Zhou, Yonggang Wang, Hongtao Li, Yong Sun, Zan Shen
J Exp Clin Cancer Res. 2020; 39: 23. Published online 2020 Jan 28. doi: 10.1186/s13046-019-1504-5
Correction in:
J Exp Clin Cancer Res. 2022; 41: 221.
PMCID:
PMC6988281
AbstractArticlePDF–7.2M
13.
A comprehensive proteomics-based interaction screen that links DYRK1A to RNF169 and to the DNA damage response
Julia Roewenstrunk, Chiara Di Vona, Jie Chen, Eva Borras, Chao Dong, Krisztina Arató, Eduard Sabidó, Michael S. Y. Huen, Susana de la Luna
Sci Rep. 2019; 9: 6014. Published online 2019 Apr 12. doi: 10.1038/s41598-019-42445-x
PMCID:
PMC6461666
AbstractArticlePDF–3.3M
14.
High Throughput Chemical Screening Reveals Multiple Regulatory Proteins on FOXA1 in Breast Cancer Cell Lines
Shixiong Wang, Sachin Kumar Singh, Madhumohan R. Katika, Sandra Lopez-Aviles, Antoni Hurtado
Int J Mol Sci. 2018 Dec; 19(12): 4123. Published online 2018 Dec 19. doi: 10.3390/ijms19124123
PMCID:
PMC6321185
AbstractArticlePDF–2.8M
15.
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta
Thorsteinn Bjornsson, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, Gudmundur L Norddahl, Anna Helgadottir, Solveig Gretarsdottir, Audur Magnusdottir, Ragnar Danielsen, Emil L Sigurdsson, Berglind Adalsteinsdottir, Sverrir I Gunnarsson, Ingileif Jonsdottir, David O Arnar, Hrodmar Helgason, Tomas Gudbjartsson, Daniel F Gudbjartsson, Unnur Thorsteinsdottir, Hilma Holm, Kari Stefansson
Eur Heart J. 2018 Sep 7; 39(34): 3243–3249. Published online 2018 Mar 24. doi: 10.1093/eurheartj/ehy142
PMCID:
PMC6127890
AbstractArticlePDF–359K
16.
Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease
Ehsan Razmara, Masoud Garshasbi
BMC Cardiovasc Disord. 2018; 18: 137. Published online 2018 Jul 3. doi: 10.1186/s12872-018-0867-4
PMCID:
PMC6029398
AbstractArticlePDF–1.0M
17.
Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES)
Yong Liu, Yu Cao, Yaxiong Li, Dongyun Lei, Lin Li, Zong Liu Hou, Shen Han, Mingyao Meng, Jianlin Shi, Yayong Zhang, Yi Wang, Zhaoyi Niu, Yanhua Xie, Benshan Xiao, Yuanfei Wang, Xiao Li, Lirong Yang, Wenju Wang, Lihong Jiang
Med Sci Monit. 2018; 24: 1340–1358. Published online 2018 Mar 5. doi: 10.12659/MSM.908923
PMCID:
PMC5849354
AbstractArticlePDF–4.2M
18.
NDP52 activates nuclear myosin VI to enhance RNA polymerase II transcription
Natalia Fili, Yukti Hari-Gupta, Ália dos Santos, Alexander Cook, Simon Poland, Simon M. Ameer-Beg, Maddy Parsons, Christopher P. Toseland
Nat Commun. 2017; 8: 1871. Published online 2017 Nov 30. doi: 10.1038/s41467-017-02050-w
PMCID:
PMC5707354
AbstractArticlePDF–4.3M
19.
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah Morton, Steven R. DePalma, Xue Zeng, Hongjian Qi, Weni Chang, Michael C. Sierant, Wei-Chien Hung, Shozeb Haider, Junhui Zhang, James Knight, Robert D. Bjornson, Christopher Castaldi, Irina R. Tikhonoa, Kaya Bilguvar, Shrikant M. Mane, Stephan J. Sanders, Seema Mital, Mark Russell, William Gaynor, John Deanfield, Alessandro Giardini, George A. Porter, Jr., Deepak Srivastava, Cecelia W. Lo, Yufeng Shen, W. Scott Watkins, Mark Yandell, H. Joseph Yost, Martin Tristani-Firouzi, Jane W. Newburger, Amy E. Roberts, Richard Kim, Hongyu Zhao, Jonathan R. Kaltman, Elizabeth Goldmuntz, Wendy K. Chung, Jonathan G. Seidman, Bruce D. Gelb, Christine E. Seidman, Richard P. Lifton, Martina Brueckner
Nat Genet. Author manuscript; available in PMC 2018 Apr 9.
Published in final edited form as: Nat Genet. 2017 Nov; 49(11): 1593–1601. Published online 2017 Oct 9. doi: 10.1038/ng.3970
PMCID:
PMC5675000
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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