| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Sanjoy K Bhattacharya | |
| Neal S Peachey | |||
| John W Crabb | |||
| P2860 | cites work | ADAMTS-13 metalloprotease interacts with the endothelial cell-derived ultra-large von Willebrand factor | Q24303587 |
| The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment | Q24323040 | ||
| NMR structure of the LCCL domain and implications for DFNA9 deafness disorder | Q24535809 | ||
| Distribution and evolution of von Willebrand/integrin A domains: widely dispersed domains with roles in cell adhesion and elsewhere | Q24537227 | ||
| Subcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9 | Q24676750 | ||
| Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice | Q24795737 | ||
| Intraocular pressure in genetically distinct mice: an update and strain survey | Q24803197 | ||
| Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction | Q28117054 | ||
| High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene | Q28139351 | ||
| Bone morphogenetic protein-1 (BMP-1). Identification of the minimal domain structure for procollagen C-proteinase activity | Q28183257 | ||
| Paired basic/Furin-like proprotein convertase cleavage of Pro-BMP-1 in the trans-Golgi network | Q28183294 | ||
| Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9 | Q28205407 | ||
| Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families | Q28211584 | ||
| A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects | Q28296243 | ||
| Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening | Q28305893 | ||
| A novel developmentally regulated gene in lung mesenchyme: homology to a tumor-derived trypsin inhibitor | Q28570853 | ||
| Apoptin induces tumor-specific apoptosis as a globular multimer. | Q54533135 | ||
| Intracellular serine-protease zymogen, factor C, from horseshoe crab hemocytes. Its activation by synthetic lipid A analogues and acidic phospholipids | Q67925443 | ||
| Shear stress activation of platelet glycoprotein IIb/IIIa plus von Willebrand factor causes aggregation: filter blockage and the long bleeding time in von Willebrand's disease | Q68830553 | ||
| Quantitative analysis of 'plaque material' between ciliary muscle tips in normal- and glaucomatous eyes | Q69545714 | ||
| Intraocular pressure in inbred mouse strains | Q73013112 | ||
| Eyeing a new route along an old pathway | Q73570187 | ||
| Physical evidence that yeast frataxin is an iron storage protein | Q74143548 | ||
| Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice | Q74525489 | ||
| Cochlin deposits in the trabecular meshwork of the glaucomatous DBA/2J mouse | Q81700818 | ||
| A consensus tetrapeptide selected by phage display adopts the conformation of a dominant discontinuous epitope of a monoclonal anti-VWF antibody that inhibits the von Willebrand factor-collagen interaction | Q30961540 | ||
| Novel soluble molecule, Akhirin, is expressed in the embryonic chick eyes and exhibits heterophilic cell-adhesion activity | Q33212850 | ||
| Mouse genetics: a tool to help unlock the mechanisms of glaucoma | Q33799087 | ||
| Platelets have more than one binding site for von Willebrand factor | Q33821754 | ||
| The LCCL module | Q33916421 | ||
| VIT-1: the second member of a new branch of the von Willebrand factor A domain superfamily | Q33929394 | ||
| Evolution of von Willebrand factor A (VWA) domains | Q33929398 | ||
| Tachyplesin, a class of antimicrobial peptide from the hemocytes of the horseshoe crab (Tachypleus tridentatus). Isolation and chemical structure | Q34167677 | ||
| Type A modules: interacting domains found in several non-fibrillar collagens and in other extracellular matrix proteins | Q34358544 | ||
| Absolute on-line molecular mass analysis of basic fibroblast growth factor and its multimers by reversed-phase liquid chromatography with multi-angle laser light scattering detection | Q34393312 | ||
| Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork | Q34698962 | ||
| The role of the posterior ciliary body in the biosynthesis of vitreous humour. | Q34724462 | ||
| Development of new treatments for Parkinson's disease in transgenic animal models: a role for beta-synuclein | Q34995002 | ||
| Glaucoma: ocular Alzheimer's disease? | Q35212894 | ||
| Correlation between morphological and functional retinal impairment in patients affected by ocular hypertension, glaucoma, demyelinating optic neuritis and Alzheimer’s disease | Q35563013 | ||
| An evidence-based assessment of risk factors for the progression of ocular hypertension and glaucoma | Q35885791 | ||
| Risk assessment in the management of patients with ocular hypertension | Q35885890 | ||
| Reduction of type V collagen using a dominant-negative strategy alters the regulation of fibrillogenesis and results in the loss of corneal-specific fibril morphology | Q36237721 | ||
| Number of people with glaucoma worldwide | Q37320324 | ||
| Genetic segregation of brain gene expression identifies retinaldehyde binding protein 1 and syntaxin 12 as potential contributors to ethanol preference in mice | Q38342493 | ||
| Animal models of inner ear vascular disturbances | Q39731215 | ||
| Functional morphology of the trabecular meshwork in primate eyes | Q40827200 | ||
| Platelets and shear stress. | Q41090617 | ||
| Von Willebrand factor-dependent shear-induced platelet aggregation: basic mechanisms and clinical implications | Q41500697 | ||
| Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies | Q41574239 | ||
| Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice | Q42665432 | ||
| The alpha2beta1 integrin inhibitor rhodocetin binds to the A-domain of the integrin alpha2 subunit proximal to the collagen-binding site | Q43003242 | ||
| Retinal morphology and ERG response in the DBA/2NNia mouse model of angle-closure glaucoma | Q43592209 | ||
| Aspects of hydrodynamic shear regulating shear-induced platelet activation and self-association of von Willebrand factor in suspension | Q44232585 | ||
| Modification of ocular defects in mouse developmental glaucoma models by tyrosinase | Q44353964 | ||
| Quantitative analysis of retinal ganglion cell (RGC) loss in aging DBA/2NNia glaucomatous mice: comparison with RGC loss in aging C57/BL6 mice | Q44669093 | ||
| Identification of a novel Cochlin isoform in the perilymph: insights to Cochlin function and the pathogenesis of DFNA9. | Q44735348 | ||
| Ethanol preexposure increases ethanol self-administration in C57BL/6J and DBA/2J mice. | Q45176299 | ||
| Isolation and characterization of two domains of human von Willebrand factor that interact with fibrillar collagen types I and III. | Q45936667 | ||
| Optic nerve damage in mice with a targeted type I collagen mutation | Q46146096 | ||
| Genetics of age-related hearing loss in mice. IV. Cochlear pathology and hearing loss in 25 BXD recombinant inbred mouse strains | Q48439878 | ||
| Modulation of prepulse inhibition by an augmented acoustic environment in DBA/2J mice. | Q50493729 | ||
| DFNA9 is a progressive audiovestibular dysfunction with a microfibrillar deposit in the inner ear. | Q50495026 | ||
| Cochlin, a secreted von Willebrand factor type a domain-containing factor, is regulated by leukemia inhibitory factor in the uterus at the time of embryo implantation. | Q52096750 | ||
| Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice. | Q53726981 | ||
| Distribution of myocilin and extracellular matrix components in the juxtacanalicular tissue of human eyes. | Q53876452 | ||
| Importance of trabecular meshwork changes in the pathogenesis of primary open-angle glaucoma. | Q53899920 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 605-613 | |
| P577 | publication date | 2005-09-01 | |
| P1433 | published in | Visual neuroscience | Q969322 |
| P1476 | title | Cochlin and glaucoma: a mini-review | |
| P478 | volume | 22 |
| Q42181846 | Analysis of COCH and TNFA variants in East Indian primary open-angle glaucoma patients |
| Q35676399 | Anterior segment alterations and comparative aqueous humor proteomics in the buphthalmic rabbit (an American Ophthalmological Society thesis). |
| Q28078135 | Aqueous outflow - A continuum from trabecular meshwork to episcleral veins |
| Q37187107 | Cochlin expression in anterior segment organ culture models after TGFbeta2 treatment |
| Q36119792 | Cochlin in the eye: functional implications |
| Q34458951 | Identification of tissue-specific targeting peptide |
| Q36458667 | Increased expression of the WNT antagonist sFRP-1 in glaucoma elevates intraocular pressure |
| Q37206487 | Intraocular pressure elevation induces mitochondrial fission and triggers OPA1 release in glaucomatous optic nerve |
| Q37184094 | Memantine blocks mitochondrial OPA1 and cytochrome c release and subsequent apoptotic cell death in glaucomatous retina |
| Q38263876 | The Trabecular Meshwork: A Basic Review of Form and Function |
| Q45916238 | Ultrastructural analysis of the pigment dispersion syndrome in DBA/2J mice. |
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