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Identification of a novel P2 receptor associated with cyclooxygenase-2 upregulation and reactive astrogliosis

✍ Scribed by Roberta Brambilla; Paul Schiller; Gianluca D’Ippolito; Joseph T. Neary; Geoffrey Burnstock; Flaminio Cattabeni; Maria P. Abbracchio

Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
206 KB
Volume
53
Category
Article
ISSN
0272-4391

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Analysis of the human KCNH2(HERG) gene:
Analysis of the human KCNH2(HERG) gene: Identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion
✍ Aimée Paulussen; Ping Yang; Menelas Pangalos; Peter Verhasselt; Roger Marrannes; 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 30 KB 👁 2 views

Long QT (LQT) syndrome is a potentially life-threatening disorder, characterized by a distinct cardiac arrhythmia known as torsades de pointes. Mutations within a number of genes linked to the familial form, including that coding for a cardiac potassium channel called KCNH2 (HERG), have been describ