Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
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 immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Combined Automated Annotation using Multiple IEA Methods
Identification of putative mammalian D-lactate dehydrogenase enzymes.
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy.
Decreased interactions of mutant muscle LIM protein (MLP) with N-RAP and alpha-actinin and their implication for hypertrophic cardiomyopathy.
Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy.
Muscle lim protein isoform negatively regulates striated muscle actin dynamics and differentiation.
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Muscle LIM protein, a novel essential regulator of myogenesis, promotes myogenic differentiation.
Muscle LIM protein promotes myogenesis by enhancing the activity of MyoD.
Muscle LIM protein interacts with cofilin 2 and regulates F-actin dynamics in cardiac and skeletal muscle.
Human muscle LIM protein dimerizes along the actin cytoskeleton and cross-links actin filaments.
MLP and CARP are linked to chronic PKCĪ± signalling in dilated cardiomyopathy.
Chronic phospholamban-sarcoplasmic reticulum calcium ATPase interaction is the critical calcium cycling defect in dilated cardiomyopathy.