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MYH15 gene

Known as: KIAA1000, MYH15, MYOSIN, HEAVY CHAIN 15 
National Institutes of Health

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Related topics

1 relation
MYH10 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Genetic basis of relapsing polychondritis revealed by family‐based whole‐exome sequencing
Genetic factors are believed to be implicated in the pathogenesis of relapsing polychondritis (RP). However, the molecular… 
2018
2018
Applying Two Different Bioinformatic Approaches to Discover Novel Genes Associated with Hereditary Hearing Loss via Whole-Exome Sequencing: ENDEAVOUR and HomozygosityMapper
Background: Hearing loss (HL) is a highly prevalent heterogeneous deficiency of sensory-neural system with involvement of several… 
Review
2018
Review
2018
AB0022 Family-based whole-exome sequencing reveals the genetic basis of relapsing polychondritis
  • Z. LinL. Gui J. Gu
  • Genomics, genetic basis of disease and antigen…
  • 2018
  • Corpus ID: 81965710
Background Relapsing polychondritis (RP) is a rare systemic disease, characterised by recurrent episodes of inflammation of… 
2015
2015
ПРОВЕРКА АССОЦИАЦИИ ОДНОНУКЛЕОТИДНЫХ ПОЛИМОРФИЗМОВ ГЕНОВ KIF6, PALLD, SNX19, MYH15, VAMP8 ГЕНЕТИЧЕСКОГО РИСКОМЕТРА ИШЕМИЧЕСКОЙ БОЛЕЗНИ СЕРДЦА С ВНЕЗАПНОЙ СЕРДЕЧНОЙ СМЕРТЬЮ
Aim. The study of mononucleotide polymorphisms associations rs20455 gene KIF6, rs7439293 gene PALLD, rs2298566 gene SNX19… 
2010
2010
Novel/ancient myosins in mammalian skeletal muscles: MYH7B and MYH15
Myosin, the molecular motor responsible for muscle contraction, exists in multiple forms which dictate muscle properties, such as… 
2010
2010
Novel / ancient myosins in mammalian skeletal muscles : MYH 7 B and MYH 15
Myosin, the molecular motor responsible for muscle contraction, exists in multiple forms which dictate muscle properties, such as… 
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