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Intranuclear Rod Myopathy

Known as: Intranuclear Nemaline Rod Myopathy, Nemaline Myopathy with Exclusively Intranuclear Rods 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Myopathies, Nemaline

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Sexual role and HIV-1 set point viral load among men who have sex with men
Background: HIV-1 set point viral load (SPVL) is a highly variable trait that influences disease progression and transmission… Expand
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2017
2017
Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy.
Nemaline myopathy (NM) is a common form of congenital nondystrophic skeletal muscle disease characterized by muscular weakness of… Expand
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2017
2017
A Historical Taxonomy of Origin of Species Problems and Its Relevance to the Historiography of Evolutionary Thought
  • Koen Tanghe
  • Journal of the history of biology
  • 2017
    • Corpus ID: 3290594
Historians tend to speak of the problem of the origin of species or the species question, as if it were a monolithic problem. In… Expand
2016
2016
The Effects of Disease Models of Nuclear Actin Polymerization on the Nucleus
Actin plays a crucial role in regulating multiple processes within the nucleus, including transcription and chromatin… Expand
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2015
2015
Hypoxic ischemic encephalopathy in a case of intranuclear rod myopathy without any prenatal sentinel event
Intranuclear rod myopathy (IRM), a variant of nemaline myopathy, is characterized by the presence of nemaline bodies in myonuclei… Expand
Highly Cited
2007
Highly Cited
2007
Mechanisms underlying intranuclear rod formation.
Specific mutations within the alpha-skeletal actin gene (ACTA1) result in intranuclear rod myopathy (IRM), characterized by rod… Expand
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