LMOD3 gene

Known as: LEIOMODIN 3, LMOD3 
 
National Institutes of Health

Papers overview

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2018
2018
We describe the long-term follow-up of a patient with severe nemaline myopathy due to a novel homozygous mutation in the… (More)
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Review
2017
Review
2017
Cytoskeletal structures characterized by actin filaments with uniform lengths, including the thin filaments of striated muscles… (More)
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2016
2016
Leiomodin proteins, Lmod1, Lmod2 and Lmod3, are key regulators of the thin filament length in muscles. While Lmod1 is… (More)
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2015
2015
1.3 Name of the analysed genes or DNA/chromosome segments Slow muscle α-tropomyosin (TPM3) NEM1. Nebulin (NEB) NEM2. Skeletal… (More)
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2015
2015
Precise regulation of thin filament length is essential for optimal force generation during muscle contraction. The thin filament… (More)
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2015
2015
The sarcomeric tropomodulin (Tmod) isoforms Tmod1 and Tmod4 cap thin filament pointed ends and functionally interact with the… (More)
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2015
2015
Nemaline myopathy (NM) is one of the most common forms of congenital myopathy, and affects either fast myofibers, slow myofibers… (More)
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2014
2014
Nemaline myopathy (NM) is a congenital myopathy that can result in lethal muscle dysfunction and is thought to be a disease of… (More)
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