المؤلفون: Boczek, N.J., Ye, D., Johnson, E.K., Wang, W., Crotti, L., Tester, D.J., Dagradi, F., Mizusawa, Y., Torchio, M., Alders, M., Giudicessi, J.R., Wilde, A.A.M., Schwartz, P.J., Nerbonne, J.M., Ackerman, M.J.

المصدر: Circ. Res. 115, 460-469 (2014)

مصطلحات موضوعية: Brugada Syndrome, Genetics, Ion Channels, Medical, Potassium Channels, Semaphorin-3a

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000340364700011; info:eu-repo/semantics/altIdentifier/isbn/0009-7330; info:eu-repo/semantics/altIdentifier/pissn/0009-7330; info:eu-repo/sema; https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=31909Test; urn:isbn:0009-7330; urn:issn:0009-7330; urn:issn:1524-4571

الإتاحة: https://doi.org/10.1161/CIRCRESAHA.115.303657Test
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=31909Test

المؤلفون: Adadi, N., Lahrouchi, N., Bouhouch, R., Fellat, I., Amri, R., Alders, M., Sefiani, A., Bezzina, C., Ratbi, I.

المصدر: Journal of Medical Case Reports; 4/2/2017, Vol. 11, p1-5, 5p

مصطلحات موضوعية: JERVELL-Lange Nielsen syndrome, ION channels, RARE diseases, TACHYARRHYTHMIAS, GENETIC mutation

المؤلفون: Van Langen, I. M., Birnie, E., Alders, M., Jongbloed, R. J., Le Marec, H., Wilde, A. A. M.

المصدر: Journal of Medical Genetics; Feb2003, Vol. 40 Issue 2, p141-145, 5p, 2 Charts

مصطلحات موضوعية: LONG QT syndrome, DIAGNOSIS, ION channels, MUSCLE cells, ADRENERGIC beta blockers, GENETIC mutation, GENETICS

المؤلفون: Wei Wang, Dan Ye, Jeanne M. Nerbonne, Peter J. Schwartz, Marielle Alders, David J. Tester, John R. Giudicessi, Lia Crotti, Michael J. Ackerman, Yuka Mizusawa, Federica Dagradi, Eric K. Johnson, Nicole J. Boczek, Margherita Torchio, Arthur A.M. Wilde

المساهمون: Boczek, N, Ye, D, Johnson, E, Wang, W, Crotti, L, Tester, D, Dagradi, F, Mizusawa, Y, Torchio, M, Alders, M, Giudicessi, J, Wilde, A, Schwartz, P, Nerbonne, J, Ackerman, M, Cardiology, ACS - Amsterdam Cardiovascular Sciences, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Other Research, Human Genetics

المصدر: Circ. Res. 115, 460-469 (2014)
Circulation research, 115(4), 460-469. Lippincott Williams and Wilkins

مصطلحات موضوعية: Adult, Male, Physiology, DNA Mutational Analysis, Mutation, Missense, BIO/18 - GENETICA, Biology, Transfection, Article, Membrane Potentials, Electrocardiography, Semaphorin, medicine, Potassium Channel Blockers, Humans, Immunoprecipitation, Hanatoxin, Genetic Predisposition to Disease, Myocytes, Cardiac, Brugada syndrome, Patch clamp, Ion channel, Genetics, Dose-Response Relationship, Drug, Brugada Syndrome, Ion Channels, Medical, Potassium Channels, Semaphorin-3a, HEK 293 cells, SEMA3A, semaphorin-3A, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, Middle Aged, medicine.disease, Molecular biology, Potassium channel, Kinetics, HEK293 Cells, Phenotype, Shal Potassium Channels, ion channel, cardiovascular system, genetics, medical, Female, Cardiology and Cardiovascular Medicine, Protein Binding, Signal Transduction, potassium channel

وصف الملف: application/pdf; STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63b4b4d8adbc8ee6d3be712d89a1ff01Test
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=31909Test

المؤلفون: Stray-Pedersen, A.¹, Cobben, J.², Prescott, T.¹, Lee, S.³, Cang, C.³, Aranda, K.³, Ahmed, S.⁴, Alders, M.², Gerstner, T.⁵, Aslaksen, K.⁶, Tétreault, M.⁷, Qin, W.⁸, Hartley, T.⁸, Jhangiani, S.⁹, Muzny, D.⁹, Tarailo-Graovac, M.¹⁰, van Karnebeek, C.¹⁰, Lupski, J.⁹, Ren, D.³, Yoon, G.⁴

المصدر: Neuromuscular Disorders. Oct2016 Supplement 2, Vol. 26, pS197-S198. 1p.

مصطلحات موضوعية: *MUSCLE diseases, *MUSCLE hypotonia, *MUSCLE weakness, *GENETIC mutation, *ALLELES, *MUSCLE growth, *INTELLECTUAL disabilities, *DWARFISM, *ION channels, *GENETICS