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MYO1H gene

Known as: FLJ37587, MYO1H, MYOSIN IH 
National Institutes of Health

Related topics

Related topics

1 relation
Myosin ATPase

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Genetic variants in ACTN3 and MYO1H are associated with sagittal and vertical craniofacial skeletal patterns.
2018
2018
Identification and Functional Studies of MYO1H for Mandibular Prognathism
Mandibular prognathism (MP) is regarded as a craniofacial deformity resulting from the combined effects of environmental and… 
2017
2017
Genetic polymorphisms underlying the skeletal Class III phenotype
Review
2017
Review
2017
Genetic Factors Involved in Mandibular Prognathism.
Mandibular prognathism is defined as an abnormal forward projection of the mandible beyond the standard relation to the cranial… 
2017
2017
Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction
Background Congenital central hypoventilation syndrome (CCHS) is a rare life-threatening disorder of respiratory and autonomic… 
2016
2016
Role of myosin 1H gene polymorphisms in mandibular retrognathism.
Highly Cited
2015
Highly Cited
2015
Candidate Gene Analyses of Skeletal Variation in Malocclusion
This study evaluated associations between craniofacial candidate genes and skeletal variation in patients with malocclusion… 
2013
2013
Myo1H GENE SINGLE NUCLEOTIDE POLYMORPHISM rs10850110 AND THE RISK OF MALOCCLUSION IN THE ROMANIAN POPULATION
Background. The Matrilin-1 gene is thought to be involved in the formation of the filamentous network of the cartilage's… 
Highly Cited
2012
Highly Cited
2012
Genetic variation in myosin 1H contributes to mandibular prognathism.
Highly Cited
2002
Highly Cited
2002
Myosin-I Isozymes in Neonatal Rodent Auditory and Vestibular Epithelia
Myosin isozymes are essential for hair cells, the sensory cells of the inner ear. Because a myosin-I subfamily member may mediate… 
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