Zobrazeno 1 - 10
of 44
pro vyhledávání: '"burst-like"'
Autor:
Valentin Burkart, Kathrin Kowalski, David Aldag-Niebling, Julia Beck, Dirk Alexander Frick, Tim Holler, Ante Radocaj, Birgit Piep, Andre Zeug, Denise Hilfiker-Kleiner, Cristobal G. dos Remedios, Jolanda van der Velden, Judith Montag, Theresia Kraft
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Transcriptional bursting is a common expression mode for most genes where independent transcription of alleles leads to different ratios of allelic mRNA from cell to cell. Here we investigated burst-like transcription and its consequences in cardiac
Externí odkaz:
https://doaj.org/article/b474c750ea6f47e1a619c482725c63c5
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
Publikováno v:
Materials; Volume 15; Issue 24; Pages: 9010
In some shape-memory single crystals the stress–strain (σ~ε) curves, belonging to stress induced martensitic transformations from austenite to martensite at fixed temperature, instead of being the usual slightly increasing function or horizontal,
Autor:
Theresia Kraft, Judith Montag
Publikováno v:
Biophysical Reviews
Hypertrophic cardiomyopathy (HCM), the most common inherited cardiac disease, is caused by several mostly heterozygous mutations in sarcomeric genes. Hallmarks of HCM are cardiomyocyte and myofibrillar disarray and hypertrophy and fibrosis of the sep
Publikováno v:
J Neurophysiol
Journal of neurophysiology, Vol. 123, no.1, p. 323-328 (2020)
Journal of neurophysiology, Vol. 123, no.1, p. 323-328 (2020)
The aim of the present study was to compare the efficacy of burst-like conditioning electrical stimulation vs. continuous stimulation of cutaneous nociceptors for inducing increased pinprick sensitivity in the surrounding unstimulated skin (a phenome
Akademický článek
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Akademický článek
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Autor:
Theresia Kraft, Judith Montag
Publikováno v:
Pflugers Archiv
Hypertrophic cardiomyopathy (HCM) is mainly caused by mutations in sarcomeric proteins. Thirty to forty percent of identified mutations are found in the ventricular myosin heavy chain (β-MyHC). A common mechanism explaining how numerous mutations in
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