| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1074/JBC.R400034200 |
| P698 | PubMed publication ID | 15561712 |
| P50 | author | Leena Bruckner-Tuderman | Q1812122 |
| P2093 | author name string | Peter Bruckner | |
| Claus-Werner Franzke | |||
| P2860 | cites work | Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells | Q22010370 |
| Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia | Q22010459 | ||
| Two-amino acid molecular switch in an epithelial morphogen that regulates binding to two distinct receptors | Q24290424 | ||
| CLAC: a novel Alzheimer amyloid plaque component derived from a transmembrane precursor, CLAC-P/collagen type XXV | Q24292980 | ||
| The type XIII collagen ectodomain is a 150-nm rod and capable of binding to fibronectin, nidogen-2, perlecan, and heparin | Q24294514 | ||
| Molecular evolution of olfactomedin | Q40856548 | ||
| Membrane protein secretases | Q41341215 | ||
| Type XIII collagen: a novel cell adhesion component present in a range of cell-matrix adhesions and in the intercalated discs between cardiac muscle cells | Q42054731 | ||
| Cleavage of BP180, a 180-kDa bullous pemphigoid antigen, yields a 120-kDa collagenous extracellular polypeptide | Q42453753 | ||
| Lack of cytosolic and transmembrane domains of type XIII collagen results in progressive myopathy | Q42856204 | ||
| A conserved postsynaptic transmembrane protein affecting neuromuscular signaling in Caenorhabditis elegans. | Q47069535 | ||
| X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein | Q24310290 | ||
| Structure of the human macrophage MARCO receptor and characterization of its bacteria-binding region | Q24310733 | ||
| Human macrophage scavenger receptors: primary structure, expression, and localization in atherosclerotic lesions | Q24556582 | ||
| Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia | Q24631099 | ||
| Crystal structure of a scavenger receptor cysteine-rich domain sheds light on an ancient superfamily | Q27617496 | ||
| Type XIII collagen is identified as a plasma membrane protein | Q28116601 | ||
| Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein | Q28213298 | ||
| Two forms of collagen XVII in keratinocytes. A full-length transmembrane protein and a soluble ectodomain | Q28283395 | ||
| Collagen XVII is destabilized by a glycine substitution mutation in the cell adhesion domain Col15 | Q28369420 | ||
| Type XXIII collagen, a new transmembrane collagen identified in metastatic tumor cells | Q28568589 | ||
| Distinct recognition of collagen subtypes by alpha(1)beta(1) and alpha(2)beta(1) integrins. Alpha(1)beta(1) mediates cell adhesion to type XIII collagen | Q28647122 | ||
| Shedding of Collagen XVII/BP180: STRUCTURAL MOTIFS INFLUENCE CLEAVAGE FROM CELL SURFACE | Q29013483 | ||
| Properties of the Collagen Type XVII Ectodomain: EVIDENCE FOR N- TO C-TERMINAL TRIPLE HELIX FOLDING | Q29013892 | ||
| Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa | Q33927237 | ||
| What are oligomerization domains good for? | Q34017790 | ||
| Characterization of recombinant soluble macrophage scavenger receptor MARCO. | Q34136893 | ||
| Type XIII collagen and some other transmembrane collagens contain two separate coiled-coil motifs, which may function as independent oligomerization domains | Q34209723 | ||
| Mechanisms of ectodermal organogenesis | Q34269035 | ||
| Collagens, modifying enzymes and their mutations in humans, flies and worms | Q34544297 | ||
| Multifunctional roles of macrophages in the development and progression of atherosclerosis in humans and experimental animals | Q35092592 | ||
| Keratinocytes from patients lacking collagen XVII display a migratory phenotype | Q35098451 | ||
| Collagenous transmembrane proteins: collagen XVII as a prototype | Q35205418 | ||
| Binding sites of amyloid beta-peptide in cell plasma membrane and implications for Alzheimer's disease | Q35668328 | ||
| The shed ectodomain of collagen XVII/BP180 is targeted by autoantibodies in different blistering skin diseases | Q35745439 | ||
| Molecular genetic studies of a human epidermal autoantigen (the 180-kD bullous pemphigoid antigen/BP180): identification of functionally important sequences within the BP180 molecule and evidence for an interaction between BP180 and alpha 6 integrin | Q36235763 | ||
| Amassin, an olfactomedin protein, mediates the massive intercellular adhesion of sea urchin coelomocytes | Q36324976 | ||
| The scavenger receptor MARCO is required for lung defense against pneumococcal pneumonia and inhaled particles | Q36399857 | ||
| Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain. | Q36880933 | ||
| Hemidesmosomes: molecular organization and their importance for cell adhesion and disease | Q37747227 | ||
| Abnormal adherence junctions in the heart and reduced angiogenesis in transgenic mice overexpressing mutant type XIII collagen. | Q39645757 | ||
| Transmembrane collagen XVII, an epithelial adhesion protein, is shed from the cell surface by ADAMs | Q39658973 | ||
| A short sequence in the N-terminal region is required for the trimerization of type XIII collagen and is conserved in other collagenous transmembrane proteins | Q40370857 | ||
| The shed ectodomain of type XIII collagen affects cell behaviour in a matrix-dependent manner | Q40581317 | ||
| Extracellular cleavage of bullous pemphigoid antigen 180/type XVII collagen and its involvement in hemidesmosomal disassembly | Q40645915 | ||
| The cell adhesion domain of type XVII collagen promotes integrin-mediated cell spreading by a novel mechanism | Q40784980 | ||
| Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A. | Q40816214 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | pathology | Q7208 |
| transmembrane protein | Q424204 | ||
| P304 | page(s) | 4005-4008 | |
| P577 | publication date | 2004-11-23 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Collagenous transmembrane proteins: recent insights into biology and pathology | |
| P478 | volume | 280 |
| Q37268563 | A role for anti-BP180 autoantibodies in chronic rhinosinusitis |
| Q34220757 | A role for collagen XXIII in cancer cell adhesion, anchorage-independence and metastasis |
| Q51076878 | Amino acid duplication in the coiled-coil structure of collagen XVII alters its maturation and trimerization causing mild junctional epidermolysis bullosa. |
| Q28390080 | Bacterial collagen-like proteins that form triple-helical structures |
| Q34016825 | Basement membranes in skin: unique matrix structures with diverse functions? |
| Q64252447 | Bullous Pemphigoid IgG Induces Cell Dysfunction and Enhances the Motility of Epidermal Keratinocytes via Rac1/Proteasome Activation |
| Q24328940 | CLAC binds to amyloid beta peptides through the positively charged amino acid cluster within the collagenous domain 1 and inhibits formation of amyloid fibrils |
| Q28588337 | Cleavage and oligomerization of gliomedin, a transmembrane collagen required for node of ranvier formation |
| Q42035825 | Coiled coils ensure the physiological ectodomain shedding of collagen XVII. |
| Q39333039 | Collagen XVII is expressed in malignant but not in benign melanocytic tumors and it can mediate antibody induced melanoma apoptosis |
| Q42449985 | Collagen XVII participates in keratinocyte adhesion to collagen IV, and in p38MAPK-dependent migration and cell signaling |
| Q38123486 | Collagen XVII: a shared antigen in neurodermatological interactions? |
| Q24623955 | Collagen XXIII, novel ligand for integrin alpha2beta1 in the epidermis |
| Q24610632 | Collagen structure and stability |
| Q24338828 | Collagens are functional, high affinity ligands for the inhibitory immune receptor LAIR-1 |
| Q38388575 | Correlations between prognosis and regional biomarker profiles in head and neck squamous cell carcinomas |
| Q36487760 | Current concepts of extracellular matrix |
| Q85771355 | Deletion of the major bullous pemphigoid epitope region of collagen XVII induces blistering, autoimmunization, and itching in mice |
| Q40154159 | Differential gene expression levels might explain association of LAIR2 polymorphisms with pemphigus |
| Q80177530 | Diversity of olfactomedin proteins in the sea urchin |
| Q35168077 | Dynamic interactions of epidermal collagen XVII with the extracellular matrix: laminin 332 as a major binding partner |
| Q36828014 | Expanding the lysyl hydroxylase toolbox: new insights into the localization and activities of lysyl hydroxylase 3 (LH3). |
| Q34530822 | Expression of type XXIII collagen mRNA and protein |
| Q28304833 | Extracellular phosphorylation of collagen XVII by ecto-casein kinase 2 inhibits ectodomain shedding |
| Q46064716 | Glycine substitution mutations cause intracellular accumulation of collagen XVII and affect its post-translational modifications |
| Q55428949 | Granzyme B is elevated in autoimmune blistering diseases and cleaves key anchoring proteins of the dermal-epidermal junction. |
| Q42134161 | Human bullous pemphigoid antigen 2 transgenic skin elicits specific IgG in wild-type mice |
| Q38005762 | Human pathogens utilize host extracellular matrix proteins laminin and collagen for adhesion and invasion of the host |
| Q79831909 | Humanization of autoantigen |
| Q37423979 | In epithelial cancers, aberrant COL17A1 promoter methylation predicts its misexpression and increased invasion. |
| Q37068010 | Increased Expression of Several Collagen Genes is Associated with Drug Resistance in Ovarian Cancer Cell Lines |
| Q87130792 | Itch, eosinophils, and autoimmunity: a novel murine model of bullous pemphigoid |
| Q34566125 | Lysyl hydroxylase 3 modifies lysine residues to facilitate oligomerization of mannan-binding lectin. |
| Q30369103 | Making recombinant extracellular matrix proteins. |
| Q38230276 | Molecular and cellular basis of scleroderma |
| Q36643333 | Molecular recognition in the assembly of collagens: terminal noncollagenous domains are key recognition modules in the formation of triple helical protomers. |
| Q39414522 | Neurological and psychiatric associations in bullous pemphigoid - more than skin deep? |
| Q38064788 | Overview of extracellular matrix |
| Q48906901 | Pigmentation and melanocyte supply to the epidermis depend on type XVII collagen |
| Q24622617 | Prolyl 4-hydroxylase |
| Q36119690 | Secreted gliomedin is a perinodal matrix component of peripheral nerves |
| Q28261785 | Shedding of collagen XVII ectodomain depends on plasma membrane microenvironment |
| Q37358108 | Shedding of collagen XVII/BP180 in skin depends on both ADAM10 and ADAM9. |
| Q34649929 | Shedding of collagen XXIII is mediated by furin and depends on the plasma membrane microenvironment |
| Q42124126 | Skin basement membrane: the foundation of epidermal integrity--BM functions and diverse roles of bridging molecules nidogen and perlecan |
| Q46543911 | Structural features and functional domains of amassin-1, a cell-binding olfactomedin protein |
| Q48624545 | Targeting of Cell Surface Proteolysis of Collagen XVII Impedes Squamous Cell Carcinoma Progression. |
| Q45878612 | Targeting of the hNC16A collagen domain to dendritic cells induces tolerance to human type XVII collagen |
| Q36526405 | The C-terminal peptide of chondroadherin modulates cellular activity by selectively binding to heparan sulfate chains. |
| Q38241803 | The Role of Collagens in Peripheral Nerve Myelination and Function. |
| Q36846125 | The bone morphogenetic protein 1/Tolloid-like metalloproteinases |
| Q37855335 | The collagen family |
| Q40009117 | The glycosyltransferase activities of lysyl hydroxylase 3 (LH3) in the extracellular space are important for cell growth and viability |
| Q85636068 | The missense mutation p.R1303Q in type XVII collagen underlies junctional epidermolysis bullosa resembling Kindler syndrome |
| Q40162042 | The role of disulfide bonds and alpha-helical coiled-coils in the biosynthesis of type XIII collagen and other collagenous transmembrane proteins |
| Q42128224 | Transient anti-CD40L co-stimulation blockade prevents immune responses against human bullous pemphigoid antigen 2: implications for gene therapy |
| Q55055900 | Transmembrane collagen XVII is a novel component of the glomerular filtration barrier. |
| Q42952272 | Zebrafish type XVII collagen: Gene structures, expression profiles, and morpholino “knock-down” phenotypes |
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