Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Yongxin Mu"'
Publikováno v:
Thrombosis Journal, Vol 20, Iss 1, Pp 1-8 (2022)
Abstract Background This study aimed to analyze the role of circular RNA ciRs-126 in hypoxia/reoxygenation cardiac injury (H/R). Methods Expression of ciRs-126 and miR-21 in plasma samples from patients with H/R and healthy controls was determined by
Externí odkaz:
https://doaj.org/article/50dc1bd4a21b4245acec20658dfd4947
Autor:
John Scott, Sonal Thakar, Ye Mao, Huaping Qin, Helen Hejran, Su-Yee Lee, Ting Yu, Olga Klezovitch, Hongqiang Cheng, Yongxin Mu, Sourav Ghosh, Valeri Vasioukhin, Yimin Zou
Publikováno v:
iScience, Vol 20, Iss , Pp 25-41 (2019)
Summary: Normal synapse formation is fundamental to brain function. We show here that an apical-basal polarity (A-BP) protein, Lgl1, is present in the postsynaptic density and negatively regulates glutamatergic synapse numbers by antagonizing the aty
Externí odkaz:
https://doaj.org/article/4db09dab8cfd40ea8a63fac71f1df9eb
Publikováno v:
PLoS Genetics, Vol 16, Iss 4, p e1008730 (2020)
O-linked N-acetylglucosamine (GlcNAc) transferase (OGT) is the only enzyme catalyzing O-GlcNAcylation. Although it has been shown that OGT plays an essential role in maintaining postnatal heart function, its role in heart development remains unknown.
Externí odkaz:
https://doaj.org/article/d6d9c9f401734777af729cf91bdea453
Autor:
Yongxin Mu, Ran Jing, Angela K. Peter, Stephan Lange, Lizhu Lin, Jianlin Zhang, Kunfu Ouyang, Xi Fang, Jennifer Veevers, Xinmin Zhou, Sylvia M. Evans, Hongqiang Cheng, Ju Chen
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 4, Iss 5, Pp n/a-n/a (2015)
Background The striated muscle Z‐line, a multiprotein complex at the boundary between sarcomeres, plays an integral role in maintaining striated muscle structure and function. Multiple Z‐line‐associated proteins have been identified and shown t
Externí odkaz:
https://doaj.org/article/0e7a2cd50c6b4e12bb31552ec8fce900
Autor:
Yingjie Liu, Ruiwu Wang, Bo Sun, Tao Mi, Jingqun Zhang, Yongxin Mu, Ju Chen, Michael J Bround, James D Johnson, Anne M Gillis, S R Wayne Chen
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e95615 (2014)
A large genomic deletion in human cardiac ryanodine receptor (RYR2) gene has been detected in a number of unrelated families with various clinical phenotypes, including catecholaminergic polymorphic ventricular tachycardia (CPVT). This genomic deleti
Externí odkaz:
https://doaj.org/article/95a9089f39734c29969e44187d689695
Autor:
Bo Sun, Mingke Ni, Shanshan Tian, Wenting Guo, Shitian Cai, Mads T. Sondergaard, Yongxiang Chen, Yongxin Mu, John P. Estillore, Ruiwu Wang, Ju Chen, Michael T. Overgaard, Michael Fill, Josefina Ramos‐Franco, Mette Nyegaard, Sui Rong Wayne Chen
Publikováno v:
Sun, B, Ni, M, Tian, S, Guo, W, Cai, S, Sondergaard, M T, Chen, Y, Mu, Y, Estillore, J P, Wang, R, Chen, J, Overgaard, M T, Fill, M, Ramos-Franco, J, Nyegaard, M & Wayne Chen, S R 2022, ' A gain-of-function mutation in the ITPR1 gating domain causes male infertility in mice ', Journal of Cellular Physiology, vol. 237, no. 8, pp. 3305-3316 . https://doi.org/10.1002/jcp.30783
Sun, B, Ni, M, Tian, S, Guo, W, Cai, S, Sondergaard, M T, Chen, Y, Mu, Y, Estillore, J P, Wang, R, Chen, J, Overgaard, M T, Fill, M, Ramos-Franco, J, Nyegaard, M & Wayne Chen, S R 2022, ' A gain-of-function mutation in the ITPR1 gating domain causes male infertility in mice ', Journal of cellular physiology, vol. 237, no. 8, pp. 3305-3316 . https://doi.org/10.1002/jcp.30783
Sun, B, Ni, M, Tian, S, Guo, W, Cai, S, Sondergaard, M T, Chen, Y, Mu, Y, Estillore, J P, Wang, R, Chen, J, Overgaard, M T, Fill, M, Ramos-Franco, J, Nyegaard, M & Wayne Chen, S R 2022, ' A gain-of-function mutation in the ITPR1 gating domain causes male infertility in mice ', Journal of cellular physiology, vol. 237, no. 8, pp. 3305-3316 . https://doi.org/10.1002/jcp.30783
Inositol 1,4,5-trisphosphate receptor 1 (ITPR1) is an intracellular Ca2+ release channel critical for numerous cellular processes. Despite its ubiquitous physiological significance, ITPR1 mutations have thus far been linked to primarily movement diso
Publikováno v:
Theranostics. 12(11)
Autor:
Olga Klezovitch, Hongqiang Cheng, Ting Yu, Huaping Qin, Sourav Ghosh, Ye Mao, Sonal Thakar, Yongxin Mu, Valeri Vasioukhin, Su-Yee Lee, Yimin Zou, Helen Hejran, John W. Scott
Publikováno v:
iScience
iScience, Vol 20, Iss, Pp 25-41 (2019)
iScience, Vol 20, Iss, Pp 25-41 (2019)
Summary Normal synapse formation is fundamental to brain function. We show here that an apical-basal polarity (A-BP) protein, Lgl1, is present in the postsynaptic density and negatively regulates glutamatergic synapse numbers by antagonizing the atyp
Publikováno v:
Oxidative Medicine and Cellular Longevity
Oxidative Medicine and Cellular Longevity, Vol 2020 (2020)
Oxidative Medicine and Cellular Longevity, Vol 2020 (2020)
Since both O-GlcNAcylation and autophagy sense intracellular nutrient level, the alteration of those two pathways plays substantial roles in the progression of heart failure. Hence, determining the relationship between O-GlcNAcylation and autophagy i
Publikováno v:
PLoS Genetics, Vol 16, Iss 4, p e1008730 (2020)
PLoS Genetics
PLoS genetics, vol 16, iss 4
PLoS Genetics
PLoS genetics, vol 16, iss 4
O-linked N-acetylglucosamine (GlcNAc) transferase (OGT) is the only enzyme catalyzing O-GlcNAcylation. Although it has been shown that OGT plays an essential role in maintaining postnatal heart function, its role in heart development remains unknown.