Leiomodin-3-deficient mice display nemaline myopathy with fast-myofiber atrophy
Nemaline myopathy (NM) is one of the most common forms of congenital myopathy, and affects either fast myofibers, slow myofibers, or both. However, an animal model for congenital myopathy with fast-myofiber-specific atrophy is not available. Furthermore, mutations in the leiomodin-3 (LMOD3) gene hav...
Main Authors: | Lei Tian, Sheng Ding, Yun You, Tong-ruei Li, Yan Liu, Xiaohui Wu, Ling Sun, Tian Xu |
---|---|
Format: | Article |
Language: | English |
Published: |
The Company of Biologists
2015-06-01
|
Series: | Disease Models & Mechanisms |
Subjects: | |
Online Access: | http://dmm.biologists.org/content/8/6/635 |
Similar Items
-
Nemaline Myopathy: A Case Report
by: Adnan A. Mubaraki
Published: (2021-07-01) -
Nemaline myopathy: A report of four cases
by: Deepti A, et al.
Published: (2007-01-01) -
Nemaline Myopathy in Brazilian Patients: Molecular and Clinical Characterization
by: Juliana Gurgel-Giannetti, et al.
Published: (2022-10-01) -
Novel mutations in <it>NEB </it>cause abnormal nebulin expression and markedly impaired muscle force generation in severe nemaline myopathy
by: Lawlor Michael W, et al.
Published: (2011-06-01) -
Pharmacological Inhibition of Myostatin in a Mouse Model of Typical Nemaline Myopathy Increases Muscle Size and Force
by: Johan Lindqvist, et al.
Published: (2023-10-01)