Zobrazeno 1 - 10
of 561
pro vyhledávání: '"Tropomyosin 3 (TPM3)"'
Autor:
Lambert, Matthias R.1,2 (AUTHOR) Matthias.lambert@childrens.harvard.edu, Gussoni, Emanuela1,2,3 (AUTHOR)
Publikováno v:
Skeletal Muscle. 11/7/2023, Vol. 13 Issue 1, p1-18. 18p.
Autor:
Matthias R. Lambert, Emanuela Gussoni
Publikováno v:
Skeletal Muscle, Vol 13, Iss 1, Pp 1-18 (2023)
Abstract The tropomyosin genes (TPM1-4) contribute to the functional diversity of skeletal muscle fibers. Since its discovery in 1988, the TPM3 gene has been recognized as an indispensable regulator of muscle contraction in slow muscle fibers. Recent
Externí odkaz:
https://doaj.org/article/b84bc009df984d0481b3726d61a9edce
Publikováno v:
Genes and Diseases, Vol 8, Iss 5, Pp 715-720 (2021)
According to existing reports, mutations in the slow tropomyosin gene (TPM3) may lead to congenital fiber-type disproportion (CFTD), nemaline myopathy (NM) and cap myopathy (CD). They are all congenital myopathies and are associated with clinical, pa
Externí odkaz:
https://doaj.org/article/f022ad9bfeb44a069769a2478a803d2c
Akademický článek
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Akademický článek
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Publikováno v:
Bioengineered. 13:8581-8592
The molecular etiology of esophageal squamous cell carcinoma (ESCC) has not been fully elucidated. Understanding the molecular mechanisms and finding new therapeutic targets for ESCC are of crucial importance. PolyC-RNA-binding protein 1 (PCBP1) is a
Publikováno v:
Journal of the Korean Neurological Association. 37:174-177
Autor:
Xu H; Department of Orthopedic, Chongqing Children's Hospital, Chongqing Medical University, No. 136 of Zhong Shan Er Lu, Chongqing, 400014, PR China., Liu H; Department of Orthopedic, Chongqing Children's Hospital, Chongqing Medical University, No. 136 of Zhong Shan Er Lu, Chongqing, 400014, PR China., Chen T; Department of Orthopedic, Chongqing Children's Hospital, Chongqing Medical University, No. 136 of Zhong Shan Er Lu, Chongqing, 400014, PR China., Song B; Department of Orthopedic, Chongqing Children's Hospital, Chongqing Medical University, No. 136 of Zhong Shan Er Lu, Chongqing, 400014, PR China., Zhu J; Department of Pathology, Chongqing Children's Hospital, Chongqing Medical University, No. 136 of Zhong Shan Er Lu, Chongqing, 400014, PR China., Liu X; Department of Orthopedic, Chongqing Children's Hospital, Chongqing Medical University, No. 136 of Zhong Shan Er Lu, Chongqing, 400014, PR China.; Molecular Oncology Laboratory, Department of Orthopaedic Surgery, The University of Chicago Medical Center, Chicago, IL 60637, USA., Li M; Department of Orthopedic, Chongqing Children's Hospital, Chongqing Medical University, No. 136 of Zhong Shan Er Lu, Chongqing, 400014, PR China., Luo C; Department of Orthopedic, Chongqing Children's Hospital, Chongqing Medical University, No. 136 of Zhong Shan Er Lu, Chongqing, 400014, PR China.
Publikováno v:
Genes & diseases [Genes Dis] 2020 Jan 25; Vol. 8 (5), pp. 715-720. Date of Electronic Publication: 2020 Jan 25 (Print Publication: 2021).
Publikováno v:
Genes & Diseases
Genes and Diseases, Vol 8, Iss 5, Pp 715-720 (2021)
Genes and Diseases, Vol 8, Iss 5, Pp 715-720 (2021)
According to existing reports, mutations in the slow tropomyosin gene (TPM3) may lead to congenital fiber-type disproportion (CFTD), nemaline myopathy (NM) and cap myopathy (CD). They are all congenital myopathies and are associated with clinical, pa
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.