Standard Name: HHT1 ; Systematic Name: SGD ID: Aliases: BUR5, Feature Type: ORF, Verified; Description.
Gene Standard Name, hht1, Characterisation Status, published. Systematic ID, Feature Type, protein coding. Synonyms, Name Description.
The identification of a mutated ENG (HHT1) or gene now enables a genotype-phenotype correlation. OBJECTIVE: To determine the incidence of.
National Library of Medicine. Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous fistula: survey of a ace study methodology family. Obviously, it made a great impression on me, and for the subsequent fifty years I have diligently sought for another patient with similar cirrhosis of the liver, so far with no success. The Hierarchical Catalog of Orthologs. Homology BLAST HHT1 Local Alignment Search Tool BLAST Stand-alone BLAST Link BLink Conserved Domain HHT1 CDD Conserved Domain Search Service HHT1 Search Genome ProtMap HomoloGene Protein Clusters All Homology Resources. National Library of Medicine. Hereditary haemorrhagic telangiectasia: aggravation by oral contraceptives?
HHT1 - old
HHT1 - deposit
Homology BLAST Basic Local Alignment Search Tool BLAST Stand-alone BLAST Link BLink Conserved Domain Database CDD Conserved Domain Search Service CD Search Genome ProtMap HomoloGene Protein Clusters All Homology Resources... Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. In vitro studies of mouse tissue showed that thalidomide stimulated the recruitment of mural cells to the vessel branches, resulting in a stabilization of blood vessels. Ideally this entry shall become one comprehensive and continuous article. Aminocoporic acid, an antifibrinolytic drug, can reduce epistaxis in HHT Saba et al.