GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000052
Gene Ontology annotation based on curation of immunofluorescence data
GO_REF:0000107
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
GO_REF:0000117
Electronic Gene Ontology annotations created by ARBA machine learning models
PMID:10037815
Combining SSH and cDNA microarrays for rapid identification of differentially expressed genes.
PMID:15846844
Proteomic profiling of cellular proteins interacting with the hepatitis C virus core protein.
PMID:16000376
Specific interaction of the actin-binding domain of dystrophin with intermediate filaments containing keratin 19.
PMID:16189514
Towards a proteome-scale map of the human protein-protein interaction network.
PMID:19185580
The microRNA-30 family is required for vertebrate hepatobiliary development.
PMID:19199708
Proteomic analysis of human parotid gland exosomes by multidimensional protein identification technology (MudPIT).
PMID:20080707
EGF potentiated oncogenesis requires a tissue transglutaminase-dependent signaling pathway leading to Src activation.
PMID:23377137
Expression of caspase-14 and keratin-19 in the human epidermis and appendages during fetal skin development.
PMID:2448790
Sequence of the human 40-kDa keratin reveals an unusual structure with very high sequence identity to the corresponding bovine keratin.
PMID:25416956
A proteome-scale map of the human interactome network.
PMID:25910212
Widespread macromolecular interaction perturbations in human genetic disorders.
PMID:26871637
Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.
PMID:29892012
An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders.
PMID:31515488
Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.
PMID:32296183
A reference map of the human binary protein interactome.
PMID:32814053
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Reactome:R-HSA-6805546
Keratin type I binds keratin type II
Reactome:R-HSA-6805573
Keratin type I/type II heterodimers form tetramers
Reactome:R-HSA-6806610
Keratin filament formation
Reactome:R-HSA-6806613
Keratin tetramers bind to form unit length filaments
Reactome:R-HSA-6806629
Formation of tonofilament bundles
Reactome:R-HSA-6809393
Keratin filaments bind cell-cell adhesion complexes
Reactome:R-HSA-6809663
Formation of hair keratin fibres
Reactome:R-HSA-6810357
Fillagrin and keratin intermediate filaments polymerize forming a network
Reactome:R-HSA-6810937
Lamellar bodies bind the early cornified envelope
Reactome:R-HSA-6811539
Reinforcement of the Cornified Envelope
Reactome:R-HSA-6814298
Late envelope proteins bind cornified envelope:CDSN
Reactome:R-HSA-6814387
CASP14 cleaves filaggrin
Reactome:R-HSA-6814734
CDSN binds the cornified envelope
Reactome:R-HSA-6814764
Plasma membrane resorption
Reactome:R-HSA-8942224
Filaggrin binds Keratin tonofilament:Desmosome
PMID:17971417
Absence of keratin 19 in mice causes skeletal myopathy with mitochondrial and sarcolemmal reorganization.
PMID:21209367
Physiology, structure, and susceptibility to injury of skeletal muscle in mice lacking keratin 19-based and desmin-based intermediate filaments.
PMID:22287836
Influences of desmin and keratin 19 on passive biomechanical properties of mouse skeletal muscle.
PMID:27345400
KRT19 directly interacts with β-catenin/RAC1 complex to regulate NUMB-dependent NOTCH signaling pathway and breast cancer properties.
PMID:30650643
Opposing Regulation of Cancer Properties via KRT19-Mediated Differential Modulation of Wnt/β-Catenin/Notch Signaling in Breast and Colon Cancers.
PMID:31601969
Keratin 19 regulates cell cycle pathway and sensitivity of breast cancer cells to CDK inhibitors.
file:human/KRT19/KRT19-uniprot.txt
UniProt entry P08727 (KRT19_HUMAN)
file:human/KRT19/KRT19-deep-research-falcon.md
Falcon deep research report on human KRT19