Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/KvLQT3> ?p ?o }
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- KvLQT3 abstract "Kv7.3 (KvLQT3) is a potassium channel protein coded for by the gene KCNQ3.It is associated with benign familial neonatal epilepsy.The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and one of two related proteins encoded by the KCNQ2 and KCNQ5 genes, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2).".
- KvLQT3 entrezgene "3786".
- KvLQT3 wikiPageID "11547974".
- KvLQT3 wikiPageLength "8437".
- KvLQT3 wikiPageOutDegree "9".
- KvLQT3 wikiPageRevisionID "678940087".
- KvLQT3 wikiPageWikiLink Benign_familial_neonatal_seizures.
- KvLQT3 wikiPageWikiLink Category:Ion_channels.
- KvLQT3 wikiPageWikiLink Category:Proteins.
- KvLQT3 wikiPageWikiLink Gene.
- KvLQT3 wikiPageWikiLink Ion_channel.
- KvLQT3 wikiPageWikiLink KCNQ5.
- KvLQT3 wikiPageWikiLink Potassium.
- KvLQT3 wikiPageWikiLink Protein.
- KvLQT3 wikiPageWikiLink Protein–protein_interaction.
- KvLQT3 wikiPageWikiLinkText "KCNQ3".
- KvLQT3 wikiPageWikiLinkText "KvLQT3".
- KvLQT3 requireManualInspection "no".
- KvLQT3 summaryText "The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and one of two related proteins encoded by the KCNQ2 and KCNQ5 genes, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 , also known as epilepsy, benign neonatal type 2 .".
- KvLQT3 updateCitations "yes".
- KvLQT3 updatePage "yes".
- KvLQT3 updateProteinBox "yes".
- KvLQT3 updateSummary "yes".
- KvLQT3 wikiPageUsesTemplate Template:Cite_journal.
- KvLQT3 wikiPageUsesTemplate Template:Ion_channels.
- KvLQT3 wikiPageUsesTemplate Template:Membrane-protein-stub.
- KvLQT3 wikiPageUsesTemplate Template:MeshName.
- KvLQT3 wikiPageUsesTemplate Template:NLM_content.
- KvLQT3 wikiPageUsesTemplate Template:PBB.
- KvLQT3 wikiPageUsesTemplate Template:PBB_Controls.
- KvLQT3 wikiPageUsesTemplate Template:PBB_Further_reading.
- KvLQT3 wikiPageUsesTemplate Template:PBB_Summary.
- KvLQT3 wikiPageUsesTemplate Template:Refbegin.
- KvLQT3 wikiPageUsesTemplate Template:Refend.
- KvLQT3 wikiPageUsesTemplate Template:Reflist.
- KvLQT3 subject Category:Ion_channels.
- KvLQT3 subject Category:Proteins.
- KvLQT3 hypernym Protein.
- KvLQT3 type Biomolecule.
- KvLQT3 type Protein.
- KvLQT3 type Biomolecule.
- KvLQT3 type Biophysic.
- KvLQT3 type Channel.
- KvLQT3 type Institute.
- KvLQT3 type Nutrient.
- KvLQT3 type Source.
- KvLQT3 type Thing.
- KvLQT3 type Q206229.
- KvLQT3 type Q8054.
- KvLQT3 comment "Kv7.3 (KvLQT3) is a potassium channel protein coded for by the gene KCNQ3.It is associated with benign familial neonatal epilepsy.The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and one of two related proteins encoded by the KCNQ2 and KCNQ5 genes, both integral membrane proteins.".
- KvLQT3 label "KvLQT3".
- KvLQT3 sameAs Q14914316.
- KvLQT3 sameAs m.02rhq2b.
- KvLQT3 sameAs Q14914316.
- KvLQT3 wasDerivedFrom KvLQT3?oldid=678940087.
- KvLQT3 isPrimaryTopicOf KvLQT3.