Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction - Wikidata - awgldk - TriplyDB

Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction

Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction

http://www.wikidata.org/entity/Q33911377

about

Autoimmune retinopathy Transscleral sustained vasohibin-1 delivery by a novel device suppressed experimentally-induced choroidal neovascularization Diagnosis of occult melanoma using transient receptor potential melastatin 1 (TRPM1) autoantibody testing: a novel approach.Acute progressive paravascular placoid neuroretinopathy with negative-type electroretinography in paraneoplastic retinopathy Autoantibodies in Melanoma-Associated Retinopathy Recognize an Epitope Conserved Between TRPM1 and TRPM3.B Cell Anomalies in Autoimmune Retinopathy (AIR)Paraneoplastic syndromes associated with lung cancer Autoantibody against transient receptor potential M1 cation channels of retinal ON bipolar cells in paraneoplastic vitelliform retinopathy.Serum TRPM1 autoantibodies from melanoma associated retinopathy patients enter retinal on-bipolar cells and attenuate the electroretinogram in mice Degeneration of retinal on bipolar cells induced by serum including autoantibody against TRPM1 in mouse model of paraneoplastic retinopathy Voriconazole, an antifungal triazol that causes visual side effects, is an inhibitor of TRPM1 and TRPM3 channels Differential function of Gγ13 in rod bipolar and ON cone bipolar cells.Serum Autoantibody Profiling of Patients with Paraneoplastic and Non-Paraneoplastic Autoimmune Retinopathy.Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.GCAP1, Rab6, and HSP27: Novel Autoantibody Targets in Cancer-Associated Retinopathy and Autoimmune Retinopathy.Lack of mGluR6-related cascade elements leads to retrograde trans-synaptic effects on rod photoreceptor synapses via matrix-associated proteins.TRPM channels: same ballpark, different players, and different rules in immunogenetics.The immunological basis of degenerative diseases of the eye.The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease.Genetic risk factors for insidious equine recurrent uveitis in Appaloosa horses.Choroidal atrophy in a patient with paraneoplastic retinopathy and anti-TRPM1 antibody Unilateral cancer-associated retinopathy: diagnosis, serology and treatment.Case of paraneoplastic retinopathy with retinal ON-bipolar cell dysfunction and subsequent resolution of ERGs.Autoimmune Retinopathy: Current Concepts and Practices (An American Ophthalmological Society Thesis).Are Anti-Retinal Autoantibodies a Cause or a Consequence of Retinal Degeneration in Autoimmune Retinopathies?

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Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction

http://www.wikidata.org/entity/Q33911377

description

2011 nî lūn-bûn

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2011 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2011 թվականի մայիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Identification of autoantibodi ...... th ON bipolar cell dysfunction

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Identification of autoantibodi ...... th ON bipolar cell dysfunction

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type

label

Identification of autoantibodi ...... th ON bipolar cell dysfunction

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Identification of autoantibodi ...... th ON bipolar cell dysfunction

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prefLabel

Identification of autoantibodi ...... th ON bipolar cell dysfunction

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Identification of autoantibodi ...... th ON bipolar cell dysfunction

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JOURNAL.PONE.0019911

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Identification of autoantibodi ...... th ON bipolar cell dysfunction

@en

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Grazyna Adamus

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Hiroko Terasaki

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Hiroshi Ohguro

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Mineo Kondo

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Naozumi Hashimoto

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Rikako Sanuki

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Shigeki Machida

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Shinji Ueno

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

Shuichi Yamamoto

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

Takahisa Furukawa

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P2860

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade

TRPM1 is required for the depolarizing light response in retinal ON-bipolar cells

SEREX identification of new tumor antigens linked to melanoma-associated retinopathy.

Melanoma-associated retinopathy: a paraneoplastic autoimmune complication

TRPM1 mutations are associated with the complete form of congenital stationary night blindness

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e19911

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scholarly article

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10.1371/JOURNAL.PONE.0019911

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21611200

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