Search Results - "Filipova, Dilyana" :: K.UTB vyhledávací portál

Distinct transcriptomic changes in E14.5 mouse skeletal muscle lacking RYR1 or Cav1.1 converge at E18.5

by Filipova, Dilyana, Henry, Margit, Rotshteyn, Tamara, Brunn, Anna, Carstov, Mariana, Deckert, Martina, Hescheler, Jürgen, Sachinidis, Agapios, Pfitzer, Gabriele, Papadopoulos, Symeon
Published in PloS one (15.03.2018)

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Novel CB1-ligands maintain homeostasis of the endocannabinoid system in ω3- and ω6-long-chain-PUFA deficiency

by Hammels, Ina, Binczek, Erika, Schmidt-Soltau, Inga, Jenke, Britta, Thomas, Andreas, Vogel, Matthias, Thevis, Mario, Filipova, Dilyana, Papadopoulos, Symeon, Stoffel, Wilhelm
Published in Journal of lipid research (01.08.2019)

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Aging-related alterations in eNOS and nNOS responsiveness and smooth muscle reactivity of murine basilar arteries are modulated by apocynin and phosphorylation of myosin phosphatase targeting subunit-1

by Lubomirov, Lubomir T, Papadopoulos, Symeon, Pütz, Sandra, Welter, Johannes, Klöckener, Tim, Weckmüller, Kathrin, Ardestani, Mostafa A, Filipova, Dilyana, Metzler, Doris, Metzner, Harald, Staszewski, Jürgen, Zittrich, Stefan, Gagov, Hristo, Schroeter, Mechthild M, Pfitzer, Gabriele
Published in Journal of cerebral blood flow and metabolism (01.03.2017)

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Gene profiling of embryonic skeletal muscle lacking type I ryanodine receptor Ca2+ release channel

by Filipova, Dilyana, Walter, Anna M., Gaspar, John A., Brunn, Anna, Linde, Nina F., Ardestani, Mostafa A., Deckert, Martina, Hescheler, Jürgen, Pfitzer, Gabriele, Sachinidis, Agapios, Papadopoulos, Symeon
Published in Scientific reports (01.02.2016)

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A mutation in CaV2.1 linked to a severe neurodevelopmental disorder impairs channel gating

by Tyagi, Sidharth, Bendrick, Tyler R., Filipova, Dilyana, Papadopoulos, Symeon, Bannister, Roger A.
Published in The Journal of general physiology (03.06.2019)

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Distinct transcriptomic changes in E14.5 mouse skeletal muscle lacking RYR1 or Ca.sub.v1.1 converge at E18.5

by Filipova, Dilyana, Henry, Margit, Rotshteyn, Tamara, Brunn, Anna, Carstov, Mariana, Deckert, Martina, Hescheler, Jürgen, Sachinidis, Agapios, Pfitzer, Gabriele, Papadopoulos, Symeon
Published in PloS one (15.03.2018)

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Functional assessment of three Rem residues identified as critical for interactions with Ca2+ channel β subunits

by Beqollari, Donald, Romberg, Christin F., Filipova, Dilyana, Papadopoulos, Symeon, Bannister, Roger A.
Published in Pflügers Archiv (01.11.2015)

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Junctional trafficking and restoration of retrograde signaling by the cytoplasmic RyR1 domain

by Polster, Alexander, Perni, Stefano, Filipova, Dilyana, Moua, Ong, Ohrtman, Joshua D, Bichraoui, Hicham, Beam, Kurt G, Papadopoulos, Symeon
Published in The Journal of general physiology (05.02.2018)

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Rem uncouples excitation-contraction coupling in adult skeletal muscle fibers

by Beqollari, Donald, Romberg, Christin F, Filipova, Dilyana, Meza, Ulises, Papadopoulos, Symeon, Bannister, Roger A
Published in The Journal of general physiology (01.07.2015)

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Functional assessment of three Rem residues identified as critical for interactions with Ca^sup 2+^ channel [beta] subunits

by Beqollari, Donald, Romberg, Christin F, Filipova, Dilyana, Papadopoulos, Symeon, Bannister, Roger A
Published in Pflügers Archiv (01.11.2015)

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Functional assessment of three Rem residues identified as critical for interactions with Ca(2+) channel β subunits

by Beqollari, Donald, Romberg, Christin F, Filipova, Dilyana, Papadopoulos, Symeon, Bannister, Roger A
Published in Pflügers Archiv (01.11.2015)

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A mutation in Ca V 2.1 linked to a severe neurodevelopmental disorder impairs channel gating

by Tyagi, Sidharth, Bendrick, Tyler R, Filipova, Dilyana, Papadopoulos, Symeon, Bannister, Roger A
Published in The Journal of general physiology (03.06.2019)

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Correction: Corrigendum: Gene profiling of embryonic skeletal muscle lacking type I ryanodine receptor Ca2+ release channel

by Filipova, Dilyana, Walter, Anna M., Gaspar, John A., Brunn, Anna, Linde, Nina F., Ardestani, Mostafa A., Deckert, Martina, Hescheler, Jürgen, Pfitzer, Gabriele, Sachinidis, Agapios, Papadopoulos, Symeon
Published in Scientific reports (22.04.2016)

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Corrigendum: Gene profiling of embryonic skeletal muscle lacking type I ryanodine receptor Ca(2+) release channel

by Filipova, Dilyana, Walter, Anna M, Gaspar, John A, Brunn, Anna, Linde, Nina F, Ardestani, Mostafa A, Deckert, Martina, Hescheler, Jürgen, Pfitzer, Gabriele, Sachinidis, Agapios, Papadopoulos, Symeon
Published in Scientific reports (22.04.2016)

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Gene profiling of embryonic skeletal muscle lacking type I ryanodine receptor Ca(2+) release channel

by Filipova, Dilyana, Walter, Anna M, Gaspar, John A, Brunn, Anna, Linde, Nina F, Ardestani, Mostafa A, Deckert, Martina, Hescheler, Jürgen, Pfitzer, Gabriele, Sachinidis, Agapios, Papadopoulos, Symeon
Published in Scientific reports (01.02.2016)

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Corrigendum: Gene profiling of embryonic skeletal muscle lacking type I ryanodine receptor Ca2+ release channel

by Filipova, Dilyana, Walter, Anna M, Gaspar, John A, Brunn, Anna, Linde, Nina F, Ardestani, Mostafa A, Deckert, Martina, Hescheler, Jürgen, Pfitzer, Gabriele, Sachinidis, Agapios, Papadopoulos, Symeon
Published in Scientific reports (22.04.2016)

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