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
Electronic Gene Ontology annotations created by ARBA machine learning models
DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation.
Elastic fibres in health and disease.
Three novel collagen VI chains, alpha4(VI), alpha5(VI), and alpha6(VI).
Proteomic analysis of human parotid gland exosomes by multidimensional protein identification technology (MudPIT).
Proteomics characterization of extracellular space components in the human aorta.
Proteomics analysis of cardiac extracellular matrix remodeling in a porcine model of ischemia/reperfusion injury.
Comparative proteomic analysis of supportive and unsupportive extracellular matrix substrates for human embryonic stem cell maintenance.
The expanded collagen VI family: new chains and new questions.
Proteomic analysis of cerebrospinal fluid extracellular vesicles: a comprehensive dataset.
Extracellular matrix signatures of human primary metastatic colon cancers and their metastases to liver.
Extracellular matrix remodelling in response to venous hypertension: proteomics of human varicose veins.
Glycoproteomics Reveals Decorin Peptides With Anti-Myostatin Activity in Human Atrial Fibrillation.
Comprehensive proteomic characterization of stem cell-derived extracellular matrices.
Proteomic characterization of human multiple myeloma bone marrow extracellular matrix.
Characterization of the Extracellular Matrix of Normal and Diseased Tissues Using Proteomics.
Collagen type VI degradation by MMP2,9,11
Dimerization of procollagen type VI
Tetramerization of procollagen VI
Procollagen triple helix formation
Formation of collagen networks
Collagen types III, IV, V, VI, VIII, IX, XVI bind integrins alpha1beta1 and alpha2beta1
DCN binds collagen I, II, III, VI fibrils
BGN binds Collagen types I, VI, (IX)
Interaction of NCAM1 with collagens
PDGF binds to extracellular matrix proteins
Collagen types VI, IX bind integrin alpha10beta1
Association of procollagen type VI
Sequence analysis of alpha 1(VI) and alpha 2(VI) chains of human type VI collagen reveals internal triplication of globular domains similar to the A domains of von Willebrand factor and two alpha 2(VI) chain variants that differ in the carboxy terminus.
Alternative splicing of the human alpha 2(VI) collagen gene generates multiple mRNA transcripts which predict three protein variants with distinct carboxyl termini.
Recombinant expression and structural and binding properties of alpha 1(VI) and alpha 2(VI) chains of human collagen type VI.
Expression of NG2 proteoglycan causes retention of type VI collagen on the cell surface.
The membrane-spanning proteoglycan NG2 binds to collagens V and VI through the central nonglobular domain of its core protein.
Molecular consequences of dominant Bethlem myopathy collagen VI mutations.
Hyperglycemic glucose concentrations up-regulate the expression of type VI collagen in vitro. Relevance to alterations of peripheral nerves in diabetes mellitus.
Developmental regulation of biglycan expression in muscle and tendon.
The full-ORF clone resource of the German cDNA Consortium.
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).