Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Pia Ernstberger"'
Autor:
Judith Montag, Kathrin Kowalski, Mirza Makul, Pia Ernstberger, Ante Radocaj, Julia Beck, Edgar Becker, Snigdha Tripathi, Britta Keyser, Christian Mühlfeld, Kirsten Wissel, Andreas Pich, Jolanda van der Velden, Cristobal G. dos Remedios, Andreas Perrot, Antonio Francino, Francesco Navarro-López, Bernhard Brenner, Theresia Kraft
Publikováno v:
Frontiers in Physiology, Vol 9 (2018)
Hypertrophic Cardiomyopathy (HCM) has been related to many different mutations in more than 20 different, mostly sarcomeric proteins. While development of the HCM-phenotype is thought to be triggered by the different mutations, a common mechanism rem
Externí odkaz:
https://doaj.org/article/f13e55711d92489faeb3bc79c751aa43
Autor:
Anna Lena Weber, Anne Kathrin Mayer, Bernhard Brenner, Carolyn Y. Ho, Theresia Kraft, Andreas Perrot, Judith Montag, Antonio Francino, Francesco Navarro-Lopez, Pia Ernstberger, Julia Rose, Britta Keyser, Jolanda van der Velden, Cristobal G. dos Remedios, Edgar Becker, Mandy Syring
Publikováno v:
Journal of Muscle Research and Cell Motility
Journal of Muscle Research and Cell Motility, 1-12. Springer Netherlands
STARTPAGE=1;ENDPAGE=12;ISSN=0142-4319;TITLE=Journal of Muscle Research and Cell Motility
Montag, J, Syring, M, Rose, J, Weber, A L, Ernstberger, P, Mayer, A K, Becker, E, Keyser, B, Dos Remedios, C, Perrot, A, van der Velden, J, Francino, A, Navarro-Lopez, F, Ho, C Y, Brenner, B & Kraft, T 2017, ' Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy ', Journal of Muscle Research and Cell Motility, pp. 1-12 . https://doi.org/10.1007/s10974-017-9486-4
Journal of Muscle Research and Cell Motility, 1-12. Springer Netherlands
STARTPAGE=1;ENDPAGE=12;ISSN=0142-4319;TITLE=Journal of Muscle Research and Cell Motility
Montag, J, Syring, M, Rose, J, Weber, A L, Ernstberger, P, Mayer, A K, Becker, E, Keyser, B, Dos Remedios, C, Perrot, A, van der Velden, J, Francino, A, Navarro-Lopez, F, Ho, C Y, Brenner, B & Kraft, T 2017, ' Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy ', Journal of Muscle Research and Cell Motility, pp. 1-12 . https://doi.org/10.1007/s10974-017-9486-4
HCM, the most common inherited cardiac disease, is mainly caused by mutations in sarcomeric genes. More than a third of the patients are heterozygous for mutations in the MYH7 gene encoding for the β-myosin heavy chain. In HCM-patients, expression o
Autor:
Edgar Becker, Judith Montag, Ante Radocaj, Mirza Makul, Bernhard Brenner, Pia Ernstberger, Julia Beck, Andreas Perrot, Cristobal G. dos Remedios, Kathrin Kowalski, Snigdha Tripathi, Francesco Navarro-Lopez, Jolanda van der Velden, Andreas Pich, Antonio Francino, Theresia Kraft, Christian Mühlfeld, Kirsten Wissel, Britta Keyser
Publikováno v:
Frontiers in Physiology, 9(APR):359. Frontiers Research Topics
Frontiers in Physiology, Vol 9 (2018)
Frontiers in Physiology
Montag, J, Kowalski, K, Makul, M, Ernstberger, P, Radocaj, A, Beck, J, Becker, E, Tripathi, S, Keyser, B, Mühlfeld, C, Wissel, K, Pich, A, van der Velden, J, dos Remedios, C G, Perrot, A, Francino, A, Navarro-López, F, Brenner, B & Kraft, T 2018, ' Burst-like transcription of mutant and wildtype MYH7-alleles as possible origin of cell-to-cell contractile imbalance in Hypertrophic Cardiomyopathy ', Frontiers in Physiology, vol. 9, no. APR, 359 . https://doi.org/10.3389/fphys.2018.00359
Frontiers in Physiology, Vol 9 (2018)
Frontiers in Physiology
Montag, J, Kowalski, K, Makul, M, Ernstberger, P, Radocaj, A, Beck, J, Becker, E, Tripathi, S, Keyser, B, Mühlfeld, C, Wissel, K, Pich, A, van der Velden, J, dos Remedios, C G, Perrot, A, Francino, A, Navarro-López, F, Brenner, B & Kraft, T 2018, ' Burst-like transcription of mutant and wildtype MYH7-alleles as possible origin of cell-to-cell contractile imbalance in Hypertrophic Cardiomyopathy ', Frontiers in Physiology, vol. 9, no. APR, 359 . https://doi.org/10.3389/fphys.2018.00359
Hypertrophic Cardiomyopathy (HCM) has been related to many different mutations in more than 20 different, mostly sarcomeric proteins. While development of the HCM-phenotype is thought to be triggered by the different mutations, a common mechanism rem
Autor:
Judith Montag, Bernhard Brenner, Theresia Kraft, Ante Radocaj, Kathrin Kowalski, Britta Keyser, Pia Ernstberger, Cris dos Remedios, Andreas Perrot, Mirza Makul
Publikováno v:
Biophysical Journal. 116:262a