Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork. - Wikidata - awgldk - TriplyDB

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

http://www.wikidata.org/entity/Q34698962

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Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change Cochlin induced TREK-1 co-expression and annexin A2 secretion: role in trabecular meshwork cell elongation and motility Surgery on the Trabecular Meshwork: Histopathological Evidence Extracellular matrix in the trabecular meshwork: intraocular pressure regulation and dysregulation in glaucoma Cochlin, intraocular pressure regulation and mechanosensing Current Awareness on Comparative and Functional Genomics Aqueous outflow - A continuum from trabecular meshwork to episcleral veins Cochlin produced by follicular dendritic cells promotes antibacterial innate immunity Disease gene candidates revealed by expression profiling of retinal ganglion cell development Cochlin expression in vestibular endorgans obtained from patients with Meniere's disease.Cochlin and glaucoma: a mini-review.Protein expression in human trabecular meshwork: downregulation of RhoGDI by dexamethasone in vitro.Preliminary quantitative proteomic characterization of glaucomatous rat retinal ganglion cells.Aberrant glycosylation in the human trabecular meshwork.Angiopoietin-like 7 secretion is induced by glaucoma stimuli and its concentration is elevated in glaucomatous aqueous humor.Interaction of cochlin and mechanosensitive channel TREK-1 in trabecular meshwork cells influences the regulation of intraocular pressure.Human trabecular meshwork sphingolipid and ceramide profiles and potential latent fungal commensalism Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in Usher syndrome type 1F.COCH transgene expression in cultured human trabecular meshwork cells and its effect on outflow facility in monkey organ cultured anterior segments.Self-complementary AAV virus (scAAV) safe and long-term gene transfer in the trabecular meshwork of living rats and monkeys.Evidence for a role of angiopoietin-like 7 (ANGPTL7) in extracellular matrix formation of the human trabecular meshwork: implications for glaucoma.Aqueous humor dynamics: a review A new classification of glaucomas The formation of cortical actin arrays in human trabecular meshwork cells in response to cytoskeletal disruption Mitochondrial genome analysis of primary open angle glaucoma patients Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.Quantitative proteomics: TGFβ₂ signaling in trabecular meshwork cells.Mapping molecular differences and extracellular matrix gene expression in segmental outflow pathways of the human ocular trabecular meshwork.Aqueous humor phospholipids of DBA/2J and DBA/2J-Gpnmb(+)/SjJ mice.Anterior segment alterations and comparative aqueous humor proteomics in the buphthalmic rabbit (an American Ophthalmological Society thesis).In vivo quantification of cochlin in glaucomatous DBA/2J mice using optical coherence tomography.Increased Endoplasmic Reticulum Stress in Human Glaucomatous Trabecular Meshwork Cells and Tissues.Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma.Aqueous outflow regulation: Optical coherence tomography implicates pressure-dependent tissue motion.Glaucoma related Proteomic Alterations in Human Retina Samples Cochlin in the eye: functional implications.Aqueous humor outflow: what do we know? Where will it lead us?Increased expression of the WNT antagonist sFRP-1 in glaucoma elevates intraocular pressure.Technical Brief: a novel strategy for enrichment of trabecular meshwork protease proteome.Targets of tyrosine nitration in diabetic rat retina.

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P2860

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

http://www.wikidata.org/entity/Q34698962

description

2004 nî lūn-bûn

@nan

2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2004年の論文

@ja

2004年論文

@yue

2004年論文

@zh-hant

2004年論文

@zh-hk

2004年論文

@zh-mo

2004年論文

@zh-tw

2004年论文

@wuu

name

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@ast

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@en

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@nl

type

label

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@ast

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@en

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@nl

prefLabel

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@ast

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@en

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@nl

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Journal of Biological Chemistry

P1476

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

@en

P2093

Cynthia C Morton

http://www.w3.org/2001/XMLSchema#string

Edward J Rockwood

http://www.w3.org/2001/XMLSchema#string

John S Crabb

http://www.w3.org/2001/XMLSchema#string

John W Crabb

http://www.w3.org/2001/XMLSchema#string

Nahid G Robertson

http://www.w3.org/2001/XMLSchema#string

Neal S Peachey

http://www.w3.org/2001/XMLSchema#string

Rachel W Kuchtey

http://www.w3.org/2001/XMLSchema#string

Sanjoy K Bhattacharya

http://www.w3.org/2001/XMLSchema#string

Scott D Smith

http://www.w3.org/2001/XMLSchema#string

Vera L Bonilha

http://www.w3.org/2001/XMLSchema#string

P2860

Subcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

Correlation between protein and mRNA abundance in yeast

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene

Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin

Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9

Gene expression profile of the human trabecular meshwork: NEIBank sequence tag analysis

Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9

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6080-6084

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10.1074/JBC.M411233200

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7

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280

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2004-12-03T00:00:00Z

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15579465

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1483217

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