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Items: 1 to 20 of 167

1.
Early onset hypertrophic cardiomyopathy mutations significantly increase the velocity, force, and actin-activated ATPase activity of human β-cardiac myosin
Arjun S. Adhikari, Kristina B. Kooiker, Saswata S. Sarkar, Chao Liu, Daniel Bernstein, James A. Spudich, Kathleen M. Ruppel
Cell Rep. Author manuscript; available in PMC 2024 May 11.
Published in final edited form as: Cell Rep. 2016 Dec 13; 17(11): 2857–2864. doi: 10.1016/j.celrep.2016.11.040
PMCID:
PMC11088367
AbstractArticlePDF–1.0M
2.
Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups: Insights From a New Zealand National Registry
Nikki J. Earle, Annika Winbo, Jackie Crawford, Miriam Wheeler, Rachael Stiles, Tom Donoghue, Martin K. Stiles, Ian Hayes, Luciana Marcondes, Andrew Martin, Jonathan R. Skinner
Circ Heart Fail. 2024 Mar; 17(3): e010970. Published online 2024 Mar 8. doi: 10.1161/CIRCHEARTFAILURE.123.010970
PMCID:
PMC10942243
AbstractArticlePDF–669K
3.
End-stage Hypertrophic Cardiomyopathy with Advanced Heart Failure in Patients Carrying MYH7 R453 Variants: A Case Series
Susumu Naito, Shuichiro Higo, Satoshi Kameda, Shou Ogawa, Tomoka Tabata, Yasuhiro Akazawa, Daisuke Nakamura, Kei Nakamoto, Fusako Sera, Yuki Kuramoto, Yoshihiro Asano, Shungo Hikoso, Shigeru Miyagawa, Yasushi Sakata
Intern Med. 2023 Nov 1; 62(21): 3167–3173. Published online 2023 Mar 22. doi: 10.2169/internalmedicine.1497-22
PMCID:
PMC10686745
AbstractArticlePDF–1.1M
4.
A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy
Niloofar Naderi, Neda Mohsen-Pour, Yalda Nilipour, Maryam Pourirahim, Majid Maleki, Samira Kalayinia
BMC Cardiovasc Disord. 2023; 23: 487. Published online 2023 Oct 4. doi: 10.1186/s12872-023-03538-8
PMCID:
PMC10552240
AbstractArticlePDF–2.2M
5.
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
6.
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
7.
MYH7基因突变致儿童肥厚型心肌病的研究进展
郑 奎, 刘 露, 张 英谦
Zhongguo Dang Dai Er Ke Za Zhi. 2023 Apr 15; 25(4): 425–430. Chinese. doi: 10.7499/j.issn.1008-8830.2211044
PMCID:
PMC10120347
AbstractArticlePDF–617K
8.
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
9.
Cardiomyocyte Apoptosis Is Associated with Contractile Dysfunction in Stem Cell Model of MYH7 E848G Hypertrophic Cardiomyopathy
Alexander M. Loiben, Wei-Ming Chien, Clayton E. Friedman, Leslie S.-L. Chao, Gerhard Weber, Alex Goldstein, Nathan J. Sniadecki, Charles E. Murry, Kai-Chun Yang
Int J Mol Sci. 2023 Mar; 24(5): 4909. Published online 2023 Mar 3. doi: 10.3390/ijms24054909
PMCID:
PMC10003263
AbstractArticlePDF–4.4M
10.
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
11.
A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy
Roman P. Myasnikov, Olga V. Kulikova, Alexey N. Meshkov, Anna A. Bukaeva, Anna V. Kiseleva, Alexandra I. Ershova, Anna V. Petukhova, Mikhail G. Divashuk, Evgenia D. Zotova, Evgeniia A. Sotnikova, Alexandra A. Abisheva, Alisa V. Muraveva, Sergey N. Koretskiy, Sergey V. Popov, Marina V. Utkina, Ekaterina A. Snigir, Sergey I. Mitrofanov, Ksenia D. Konureeva, Elena A. Mershina, Valentin E. Sinitsyn, Sergey M. Yudin, Oxana M. Drapkina
Genes (Basel) 2022 Oct; 13(10): 1750. Published online 2022 Sep 28. doi: 10.3390/genes13101750
PMCID:
PMC9602094
AbstractArticlePDF–2.3M
12.
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
13.
Genetic Association of Beta-Myosin Heavy-Chain Gene (MYH7) with Cardiac Dysfunction
Memoona Yousaf, Waqas Ahmed Khan, Khurrum Shahzad, Haq Nawaz Khan, Basharat Ali, Misbah Hussain, Fazli Rabbi Awan, Hamid Mustafa, Farah Nadia Sheikh
Genes (Basel) 2022 Sep; 13(9): 1554. Published online 2022 Aug 29. doi: 10.3390/genes13091554
PMCID:
PMC9498774
AbstractArticlePDF–497K
14.
HSF1 phosphorylation establishes an active chromatin state via the TRRAP–TIP60 complex and promotes tumorigenesis
Mitsuaki Fujimoto, Ryosuke Takii, Masaki Matsumoto, Mariko Okada, Keiich I. Nakayama, Ryuichiro Nakato, Katsunori Fujiki, Katsuhiko Shirahige, Akira Nakai
Nat Commun. 2022; 13: 4355. Published online 2022 Jul 29. doi: 10.1038/s41467-022-32034-4
PMCID:
PMC9338313
AbstractArticlePDF–2.8M
15.
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
16.
Tumor suppressor BAP1 nuclear import is governed by transportin-1
Tzu-Jing Yang, Tian-Neng Li, Rih-Sheng Huang, Max Yu-Chen Pan, Shu-Yu Lin, Steven Lin, Kuen-Phon Wu, Lily Hui-Ching Wang, Shang-Te Danny Hsu
J Cell Biol. 2022 Jun 6; 221(6): e202201094. Published online 2022 Apr 21. doi: 10.1083/jcb.202201094
PMCID:
PMC9036092
AbstractArticlePDF–4.0M
17.
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
18.
Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family
Peng Tu, Hairui Sun, Xiaohang Zhang, Qian Ran, Yihua He, Suzhen Ran
BMC Med Genomics. 2022; 15: 36. Published online 2022 Feb 24. doi: 10.1186/s12920-022-01186-z
PMCID:
PMC8876400
AbstractArticlePDF–1.1M
19.
Genotype-Phenotype Correlation in Hypertrophic Cardiomyopathy: New Variant p.Arg652Lys in MYH7
Guido Antoniutti, Fiama Giuliana Caimi-Martinez, Jorge Álvarez-Rubio, Paula Morlanes-Gracia, Jaume Pons-Llinares, Blanca Rodríguez-Picón, Elena Fortuny-Frau, Laura Torres-Juan, Damian Heine-Suner, Tomas Ripoll-Vera
Genes (Basel) 2022 Feb; 13(2): 320. Published online 2022 Feb 9. doi: 10.3390/genes13020320
PMCID:
PMC8872101
AbstractArticlePDF–927K
20.
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

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