Project Report from the year 2013 in the subject Biology - Diseases, Health, Nutrition, grade: 1.3, University of Göttingen (Max Plank Institute for Experimental Medicine), language: English, abstract: Kv10.1, the voltage-gated non-inactivating delayed rectifier potassium channel, is overexpressed in variety of cancer cells and is involved in oncogenesis and tumor progression. Its splice variants E65 and E70, which were discovered in melanoma cell lines, have no conducting abilities but may physically interact with Kv10.1 and thereby regulate its function. Here, we investigated possible influence of E65 and E70 on electrophysiological properties of Kv10.1. Analysis of current-voltage relationships revealed a dose-dependent reduction of Kv10.1 current mediated by both splice variants. The channel demonstrated characteristic feature of activation kinetics, a Cole-Moore shift, irrespective of the isoforms presence. Both E65 and E70 were able to increase the rise time after -60 mV conditioning when expressed at 1:10 ratio with full length channel. Co-expression of E65 or E70 with Kv1.4 did not resulted in considerable changes in channel activity; therefore interactions of splice variants with Kv10.1 are likely to be specific. Downregulation of Kv10.1 activity by E65 and E70 splice variants may modulate tumorigenesis and be associated with less aggressive forms of cancer.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
Project Report from the year 2013 in the subject Biology - Diseases, Health, Nutrition, grade: 1.3, University of Göttingen (Max Plank Institute for Experimental Medicine), language: English, abstract: Kv10.1, the voltage-gated non-inactivating delayed rectifier potassium channel, is overexpressed in variety of cancer cells and is involved in oncogenesis and tumor progression. Its splice variants E65 and E70, which were discovered in melanoma cell lines, have no conducting abilities but may physically interact with Kv10.1 and thereby regulate its function. Here, we investigated possible influence of E65 and E70 on electrophysiological properties of Kv10.1. Analysis of current-voltage relationships revealed a dose-dependent reduction of Kv10.1 current mediated by both splice variants. The channel demonstrated characteristic feature of activation kinetics, a Cole-Moore shift, irrespective of the isoforms presence. Both E65 and E70 were able to increase the rise time after -60 mV conditioning when expressed at 1:10 ratio with full length channel. Co-expression of E65 or E70 with Kv1.4 did not resulted in considerable changes in channel activity; therefore interactions of splice variants with Kv10.1 are likely to be specific. Downregulation of Kv10.1 activity by E65 and E70 splice variants may modulate tumorigenesis and be associated with less aggressive forms of cancer.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : Majestic Books, Hounslow, Royaume-Uni
Etat : New. Print on Demand pp. 24. N° de réf. du vendeur 131768253
Quantité disponible : 4 disponible(s)
Vendeur : California Books, Miami, FL, Etats-Unis
Etat : New. N° de réf. du vendeur I-9783656524229
Quantité disponible : Plus de 20 disponibles
Vendeur : Books Puddle, Woodside, NY, Etats-Unis
Etat : New. Print on Demand pp. 24. N° de réf. du vendeur 26128786530
Quantité disponible : 4 disponible(s)
Vendeur : Biblios, Frankfurt am main, HESSE, Allemagne
Etat : New. PRINT ON DEMAND pp. 24. N° de réf. du vendeur 18128786536
Quantité disponible : 4 disponible(s)
Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Project Report from the year 2013 in the subject Biology - Diseases, Health, Nutrition, grade: 1.3, University of Göttingen (Max Plank Institute for Experimental Medicine), language: English, abstract: Kv10.1, the voltage-gated non-inactivating delayed rectifier potassium channel, is overexpressed in variety of cancer cells and is involved in oncogenesis and tumor progression. Its splice variants E65 and E70, which were discovered in melanoma cell lines, have no conducting abilities but may physically interact with Kv10.1 and thereby regulate its function. Here, we investigated possible influence of E65 and E70 on electrophysiological properties of Kv10.1. Analysis of current-voltage relationships revealed a dose-dependent reduction of Kv10.1 current mediated by both splice variants. The channel demonstrated characteristic feature of activation kinetics, a Cole-Moore shift, irrespective of the isoforms presence. Both E65 and E70 were able to increase the rise time after -60 mV conditioning when expressed at 1:10 ratio with full length channel. Co-expression of E65 or E70 with Kv1.4 did not resulted in considerable changes in channel activity; therefore interactions of splice variants with Kv10.1 are likely to be specific. Downregulation of Kv10.1 activity by E65 and E70 splice variants may modulate tumorigenesis and be associated with less aggressive forms of cancer. 20 pp. Englisch. N° de réf. du vendeur 9783656524229
Quantité disponible : 2 disponible(s)
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Taschenbuch. Etat : Neu. Druck auf Anfrage Neuware - Printed after ordering - Project Report from the year 2013 in the subject Biology - Diseases, Health, Nutrition, grade: 1.3, University of Göttingen (Max Plank Institute for Experimental Medicine), language: English, abstract: Kv10.1, the voltage-gated non-inactivating delayed rectifier potassium channel, is overexpressed in variety of cancer cells and is involved in oncogenesis and tumor progression. Its splice variants E65 and E70, which were discovered in melanoma cell lines, have no conducting abilities but may physically interact with Kv10.1 and thereby regulate its function. Here, we investigated possible influence of E65 and E70 on electrophysiological properties of Kv10.1. Analysis of current-voltage relationships revealed a dose-dependent reduction of Kv10.1 current mediated by both splice variants. The channel demonstrated characteristic feature of activation kinetics, a Cole-Moore shift, irrespective of the isoforms presence. Both E65 and E70 were able to increase the rise time after -60 mV conditioning when expressed at 1:10 ratio with full length channel. Co-expression of E65 or E70 with Kv1.4 did not resulted in considerable changes in channel activity; therefore interactions of splice variants with Kv10.1 are likely to be specific. Downregulation of Kv10.1 activity by E65 and E70 splice variants may modulate tumorigenesis and be associated with less aggressive forms of cancer. N° de réf. du vendeur 9783656524229
Quantité disponible : 1 disponible(s)
Vendeur : buchversandmimpf2000, Emtmannsberg, BAYE, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Project Report from the year 2013 in the subject Biology - Diseases, Health, Nutrition, grade: 1.3, University of Göttingen (Max Plank Institute for Experimental Medicine), language: English, abstract: Kv10.1, the voltage-gated non-inactivating delayed rectifier potassium channel, is overexpressed in variety of cancer cells and is involved in oncogenesis and tumor progression. Its splice variants E65 and E70, which were discovered in melanoma cell lines, have no conducting abilities but may physically interact with Kv10.1 and thereby regulate its function. Here, we investigated possible influence of E65 and E70 on electrophysiological properties of Kv10.1. Analysis of current-voltage relationships revealed a dose-dependent reduction of Kv10.1 current mediated by both splice variants. The channel demonstrated characteristic feature of activation kinetics, a Cole-Moore shift, irrespective of the isoforms presence. Both E65 and E70 were able to increase the rise time after -60 mV conditioning when expressed at 1:10 ratio with full length channel. Co-expression of E65 or E70 with Kv1.4 did not resulted in considerable changes in channel activity; therefore interactions of splice variants with Kv10.1 are likely to be specific. Downregulation of Kv10.1 activity by E65 and E70 splice variants may modulate tumorigenesis and be associated with less aggressive forms of cancer.Books on Demand GmbH, Überseering 33, 22297 Hamburg 20 pp. Englisch. N° de réf. du vendeur 9783656524229
Quantité disponible : 1 disponible(s)
Vendeur : preigu, Osnabrück, Allemagne
Taschenbuch. Etat : Neu. Effect of E65 and E70 splice isoforms on electrophysiological properties of Kv10.1 | Vincenzo Romaniello (u. a.) | Taschenbuch | 20 S. | Englisch | 2013 | GRIN Verlag | EAN 9783656524229 | Verantwortliche Person für die EU: GRIN Publishing GmbH, Waltherstr. 23, 80337 München, info[at]grin[dot]com | Anbieter: preigu Print on Demand. N° de réf. du vendeur 105613301
Quantité disponible : 5 disponible(s)