نتائج البحث

المساهمون: Wren, L, Jiménez-Jáimez, J, Al-Ghamdi, S, Al-Aama, J, Bdeir, A, Al-Hassnan, Z, Kuan, J, Foo, R, Potet, F, Johnson, C, Aziz, M, Carvill, G, Kaski, J, Crotti, L, Perin, F, Monserrat, L, Burridge, P, Schwartz, P, Chazin, W, Bhuiyan, Z, George AL, J

مصطلحات موضوعية: arrhythmia, calmodulin, genotype, long QT syndrome, mosaicism, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, BIO/18 - GENETICA

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31454269; info:eu-repo/semantics/altIdentifier/wos/WOS:000490939600001; volume:12; issue:9; firstpage:375; lastpage:385; numberofpages:11; journal:CIRCULATION; http://hdl.handle.net/10281/281507Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85072369078

الإتاحة: https://doi.org/10.1161/CIRCGEN.119.002581Test
http://hdl.handle.net/10281/281507Test

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4

دورية أكاديمية

Genetic Mosaicism in Calmodulinopathy

المؤلفون: Wren, LM, Jiménez-Jáimez, J, Al-Ghamdi, S, Al-Aama, JY, Bdeir, A, Al-Hassnan, ZN, Kuan, JL, Foo, RY, Potet, F, Johnson, CN, Aziz, MC, Carvill, GL, Kaski, J-P, Crotti, L, Perin, F, Monserrat, L, Burridge, PW, Schwartz, PJ, Chazin, WJ, Bhuiyan, ZA, George, AL

المصدر: Circulation: Genomic and Precision Medicine , 12 (9) pp. 375-385. (2019)

مصطلحات موضوعية: arrhythmia, calmodulin, mosaicism, L-type Ca2+channel

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10081668/1/CIRCCVG2019002581%20Revised%20June%202019%20TRACKED-1.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10081668/7/CIRCCVG2019002581%20Supplemental%20Information%20Revised%20June%202019-1.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10081668Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10081668/1/CIRCCVG2019002581%20Revised%20June%202019%20TRACKED-1.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10081668/7/CIRCCVG2019002581%20Supplemental%20Information%20Revised%20June%202019-1.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10081668Test/

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5

دورية أكاديمية

Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility (Nature Genetics, (2022), 54, 3, (232-239), 10.1038/s41588-021-01007-6)

المؤلفون: Barc J., Tadros R., Glinge C., Chiang D. Y., Jouni M., Simonet F., Jurgens S. J., Baudic M., Nicastro M., Potet F., Offerhaus J. A., Walsh R., Choi S. H., Verkerk A. O., Mizusawa Y., Anys S., Minois D., Arnaud M., Duchateau J., Wijeyeratne Y. D., Muir A., Papadakis M., Castelletti S., Torchio M., Ortuno C. G., Lacunza J., Giachino D. F., Cerrato N., Martins R. P., Campuzano O., Van Dooren S., Thollet A., Kyndt F., Mazzanti A., Clementy N., Bisson A., Corveleyn A., Stallmeyer B., Dittmann S., Saenen J., Noel A., Honarbakhsh S., Rudic B., Marzak H., Rowe M. K., Federspiel C., Le Page S., Placide L., Milhem A., Barajas-Martinez H., Beckmann B. -M., Krapels I. P., Steinfurt J., Winkel B. G., Jabbari R., Shoemaker M. B., Boukens B. J., Skoric-Milosavljevic D., Bikker H., Manevy F., Lichtner P., Ribases M., Meitinger T., Muller-Nurasyid M., Strauch K., Peters A., Schulz H., Schwettmann L., Leidl R., Heier M., Veldink J. H., van den Berg L. H., Van Damme P., Cusi D., Lanzani C., Rigade S., Charpentier E., Baron E., Bonnaud S., Lecointe S., Donnart A., Le Marec H., Chatel S., Karakachoff M., Bezieau S., London B., Tfelt-Hansen J., Roden D., Odening K. E., Cerrone M., Chinitz L. A., Volders P. G., van de Berg M. P., Laurent G., Faivre L., Antzelevitch C., Kaab S., Arnaout A. A., Dupuis J. -M., Pasquie J. -L., Billon O., Roberts J. D., Jesel L., Borggrefe M., Lambiase P. D., Mansourati J., Loeys B., Leenhardt A., Guicheney P., Maury P., Schulze-Bahr E., Robyns T., Breckpot J., Babuty D., Priori S. G., Napolitano C., Defaye P., Anselme F., Darmon J. P., Wiart F., de Asmundis C., Brugada P., Brugada R., Arbelo E., Brugada J., Mabo P., Behar N., Giustetto C., Molina M. S., Gimeno J. R., Hasdemir C., Schwartz P. J., Crotti L., McKeown P. P., Sharma S., Behr E. R., Haissaguerre M., Sacher F., Rooryck C., Tan H. L., Remme C. A., Postema P. G., Delmar M., Ellinor P. T., Lubitz S. A., Gourraud J. -B., Tanck M. W., George A. L., MacRae C. A., Burridge P. W., Dina C., Probst V., Wilde A. A., Schott J. -J., Redon R., Bezzina C. R.

المساهمون: Barc, J., Tadros, R., Glinge, C., Chiang, D. Y., Jouni, M., Simonet, F., Jurgens, S. J., Baudic, M., Nicastro, M., Potet, F., Offerhaus, J. A., Walsh, R., Choi, S. H., Verkerk, A. O., Mizusawa, Y., Anys, S., Minois, D., Arnaud, M., Duchateau, J., Wijeyeratne, Y. D., Muir, A., Papadakis, M., Castelletti, S., Torchio, M., Ortuno, C. G., Lacunza, J., Giachino, D. F., Cerrato, N., Martins, R. P., Campuzano, O., Van Dooren, S., Thollet, A., Kyndt, F., Mazzanti, A., Clementy, N., Bisson, A., Corveleyn, A., Stallmeyer, B., Dittmann, S., Saenen, J., Noel, A., Honarbakhsh, S., Rudic, B., Marzak, H., Rowe, M. K., Federspiel, C., Le Page, S., Placide, L., Milhem, A., Barajas-Martinez, H., Beckmann, B. -M., Krapels, I. P., Steinfurt, J., Winkel, B. G., Jabbari, R., Shoemaker, M. B., Boukens, B. J., Skoric-Milosavljevic, D., Bikker, H., Manevy, F., Lichtner, P., Ribases, M., Meitinger, T., Muller-Nurasyid, M., Strauch, K., Peters, A., Schulz, H., Schwettmann, L., Leidl, R., Heier, M., Veldink, J. H., van den Berg, L. H., Van Damme, P., Cusi, D., Lanzani, C., Rigade, S., Charpentier, E., Baron, E., Bonnaud, S., Lecointe, S., Donnart, A., Le Marec, H., Chatel, S., Karakachoff, M., Bezieau, S., London, B., Tfelt-Hansen, J., Roden, D., Odening, K. E., Cerrone, M., Chinitz, L. A., Volders, P. G., van de Berg, M. P., Laurent, G., Faivre, L., Antzelevitch, C., Kaab, S., Arnaout, A. A., Dupuis, J. -M., Pasquie, J. -L.

وصف الملف: STAMPA

العلاقة: volume:54; issue:5; firstpage:735; lastpage:735; numberofpages:1; journal:NATURE GENETICS; https://hdl.handle.net/11571/1472849Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85130214950

الإتاحة: https://doi.org/10.1038/s41588-022-01079-yTest
https://hdl.handle.net/11571/1472849Test

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