Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Yaoliang Tang"'
Autor:
Satoshi Kawaguchi, Bruno Moukette, Marisa N. Sepúlveda, Taiki Hayasaka, Tatsuya Aonuma, Angela K. Haskell, Jessica Mah, Suthat Liangpunsakul, Yaoliang Tang, Simon J. Conway, Il-man Kim
Publikováno v:
Cell Death and Disease, Vol 14, Iss 7, Pp 1-13 (2023)
Abstract MicroRNA-150 (miR-150) is conserved between rodents and humans, is significantly downregulated during heart failure (HF), and correlates with patient outcomes. We previously reported that miR-150 is protective during myocardial infarction (M
Externí odkaz:
https://doaj.org/article/be44d7e74dae4911ad37d1fbfb21d92e
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 15, p 12463 (2023)
The gene dystrophin is responsible for Duchenne muscular dystrophy (DMD), a grave X-linked recessive ailment that results in respiratory and cardiac failure. As the expression of dystrophin in muscle stem cells (MuSCs) is a topic of debate, there exi
Externí odkaz:
https://doaj.org/article/badb7089d66049dc8c26ba6107c92ba3
Autor:
Satoshi Kawaguchi, Bruno Moukette, Taiki Hayasaka, Angela K. Haskell, Jessica Mah, Marisa N. Sepúlveda, Yaoliang Tang, Il-man Kim
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 10, Iss 4, p 166 (2023)
Noncoding RNAs (ncRNAs) play fundamental roles in cardiac development and cardiovascular diseases (CVDs), which are a major cause of morbidity and mortality. With advances in RNA sequencing technology, the focus of recent research has transitioned fr
Externí odkaz:
https://doaj.org/article/0f74e9acc9794fa6a493df8ef9e3cd91
Publikováno v:
Biology, Vol 12, Iss 3, p 422 (2023)
Introduction: Duchenne muscular dystrophy (DMD) is a severe X-linked recessive disorder caused by mutations in the dystrophin gene, which leads to heart and respiratory failure. Despite the critical impact of DMD on endothelial cells (ECs), there is
Externí odkaz:
https://doaj.org/article/74e04f6255ff403fb10d1fdc241e92c8
Autor:
Haitao Zhang, Yan Shen, Il-man Kim, Yutao Liu, Jingwen Cai, Adam E. Berman, Kent R. Nilsson, Neal L. Weintraub, Yaoliang Tang
Publikováno v:
Cells, Vol 12, Iss 6, p 875 (2023)
Clinical trials have shown that electric stimulation (ELSM) using either cardiac resynchronization therapy (CRT) or cardiac contractility modulation (CCM) approaches is an effective treatment for patients with moderate to severe heart failure, but th
Externí odkaz:
https://doaj.org/article/13413d90958c4ce5ae439a89c83d029c
Publikováno v:
Cells, Vol 12, Iss 6, p 892 (2023)
Duchenne muscular dystrophy is an X-linked recessive disease caused by mutations in dystrophin proteins that lead to heart failure and respiratory failure. Dystrophin (DMD) is not only expressed in cardiomyocytes and skeletal muscle cells, but also i
Externí odkaz:
https://doaj.org/article/27ed66b2c6a34d15aea24d00be08618d
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Externí odkaz:
https://doaj.org/article/9930cbb8425547a3b76ca425f632cdcc
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 18, Iss , Pp 765-773 (2020)
Duchenne muscular dystrophy (DMD) is a progressive myopathic disease caused by mutations in the gene encoding dystrophin protein that eventually leads to the exhaustion of myogenic progenitor cells (MPC). Autologous induced pluripotent stem cells (iP
Externí odkaz:
https://doaj.org/article/0105e12a1b094eb0bc5c0a06ab4bcc70
Autor:
Tatsuya Aonuma, Bruno Moukette, Satoshi Kawaguchi, Nipuni P. Barupala, Marisa N. Sepúlveda, Christopher Corr, Yaoliang Tang, Suthat Liangpunsakul, R. Mark Payne, Monte S. Willis, Il-man Kim
Publikováno v:
JCI Insight, Vol 6, Iss 18 (2021)
MicroRNA-150 (miR-150) is downregulated in patients with multiple cardiovascular diseases and in diverse mouse models of heart failure (HF). miR-150 is significantly associated with HF severity and outcome in humans. We previously reported that miR-1
Externí odkaz:
https://doaj.org/article/b19319eb3d6643b781ba5acb4ed11b68
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Elderly patients are more susceptible to ischemic injury. N6-methyladenosine (m6A) modification is the most abundant reversible epitranscriptomic modification in mammalian RNA and plays a vital role in many biological processes. However, it is unclea
Externí odkaz:
https://doaj.org/article/bd7921471f3a420a8485786cb6315a89