Gene Ontology annotation through association of InterPro records with GO terms

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Gene Ontology annotation based on curation of intracellular localizations of expressed fusion proteins in living cells

Electronic Gene Ontology annotations created by ARBA machine learning models

Comparative sequence analysis of the complete human sarcomeric myosin heavy chain family: implications for functional diversity.

HGAL, a lymphoma prognostic biomarker, interacts with the cytoskeleton and mediates the effects of IL-6 on cell migration.

ZO-1 controls endothelial adherens junctions, cell-cell tension, angiogenesis, and barrier formation.

The myosin alkali light chain proteins and their genes.

Maximum velocity of shortening in relation to myosin isoform composition in single fibres from human skeletal muscles.

Role of myosins in phagosome formation

IgG:Leishmania surface:FCGR3A translocates from plasma membrane to the parasitophorous vacuole

Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene.

Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age.

Mutations and sequence variation in the human myosin heavy chain IIa gene (MYH2).

A Caenorhabditis elegans model of the myosin heavy chain IIa E706K [corrected] mutation.

Muscle cell and motor protein function in patients with a IIa myosin missense mutation (Glu-706 to Lys).

Functional diversity among a family of human skeletal muscle myosin motors.

Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations.

Myosinopathies: pathology and mechanisms.

MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12.

The superfast human extraocular myosin is kinetically distinct from the fast skeletal IIa, IIb, and IId isoforms.

Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations.

Myosin post-translational modifications and function in the presence of myopathy-linked truncating MYH2 mutations.

Human skeletal myopathy myosin mutations disrupt myosin head sequestration.

OpenScientist deep research report for human MYH2