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MYH9 wt Allele

Known as: Nonmuscle Myosin Heavy Chain II-A Gene, RP1-68O2.1, MHA 
Human MYH9 wild-type allele is located in the vicinity of 22q13.1 and is approximately 107 kb in length. This allele, which encodes myosin-9 protein… 
National Institutes of Health

Related topics

Related topics

9 relations
22q13.1Angiogenic ProcessCell MovementCytokinesis

Broader (1)

MYH9 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
PENGARUH SUPLEMENTASI ASAM LEMAK TIDAK JENUH GANDATERPROTEKSI DAN METIONIN HIDROKSI ANALOG TERHADAP PROTEIN, AMONIA DAN UREA DARAH KAMBING KACANG
Tujuan penelitian adalah untuk mengkaji pengaruh penambahan asam lemak tidak jenuh ganda terproteksi dan metionin hidroksi… 
2009
2009
Mutations in MYH9 exons 1, 16, 26, and 30 are infrequently found in Japanese patients with nonsyndromic deafness.
Mutations in MYH9 result in the autosomal dominant giant platelet disorders with leukocyte inclusion bodies with varying degrees… 
2006
2006
A Point Mutation in the SH1 Helix Alters Elasticity and Thermal Stability of Myosin II*
Movement generated by the myosin motor is generally thought to be driven by distortion of an elastic element within the myosin… 
2006
2006
Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: The use of public gene-targeted ES cell resources
Highly Cited
2004
Highly Cited
2004
Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO…
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