| M |
| Making waves: Optogenetic probing of slow-wave-associated calcium network spikes in vivo |
| *Stroh A., Adelsberger H., Fischer S., Ruhlmann C., Schierloh A., Deisseroth K., Konnerth A. |
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| Mast cell tryptase stimulates production of decorin by human testicular peritubular cells: Possible role in male infertility by interfering with growth factor signaling |
| *Adam M., Schwarzer J.U., Kohn F.M., Strauss L., Poutanen M., Mayerhofer A. |
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| Mechanical impacts induce phosphorylation of the ryanodine receptor in skeletal muscles of rats |
| *Suhr F., Braun K., Bloch W. |
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| Mechanical stretch and angiotensin-II up-regulate connexin 43 expression in rat heart via type 1 angiotensin-receptors |
| *Salameh A., Gonzalez J., Apel D., Dhein S., Dahnert I. |
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| Members of TRPC channel family affect firing properties of neurons in cultured lateral septum of mouse |
| *Kravchenko M., Flockerzi V., Freichel M., Cavalie A. |
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| Membrane expression of F508del mutant increases epithelial HCO3- secretion via functional Cl-/HCO3-exchanger(s) |
| *Xiao F., Li J., Sultan A., Wang J., Riederer B., Engelhardt R., Rausch B., Lamprecht G., De Jonge H.R., Scholte B.J., Seidler U. |
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| Merkel cell carcinoma cells form functional tight junctions |
| *Brandner J.M., Fuchs F., Krug S.M., Houdek P., Piontek J., Fischer N., Peitsch W., Moll I., Fromm M. |
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| Mitochondria in cardioprotection |
| *Boengler K., Heusch G., Schulz R. |
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| Mode shift of the voltage sensors in Shaker K+ channels is caused by energetic coupling to the pore domain. |
| *Haddad G.A., Blunck R. |
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| Modelling of long QT syndrome in patient-specific induced pluripotent stem cell-derived cardiomyocytes |
| *Welling A., Bellin M., Jung C.B., Lam J.T., Laugwitz K.-L., Moretti A. |
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| Moderate hypertrophic cardiac growth in renovascular hypertensive mice |
| *Hill C., Wrfel A., Heger J., Meyering B., Euler G. |
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| Modulation of cardiac ion channels by Coxsackievirus B3 |
| *Steinke K., Klingel K., Lang F., Strutz-Seebomh N., Seebohm G. |
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| Modulation of Immune Response by CD73-derived Adenosine during Myocardial Remodeling after Ischemia/Reperfusion |
| *Bnner F., Borg N., Christoph J., Bongardt S., Flogel U., Schrader J. |
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| Modulation of ion channels in RPE cells by sublytic complement activation |
| *Genewsky A., Rohrer B., Strauss O. |
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| Modulation of somatodendritic A-type channels and spread of dendritic excitation by the Kv4 channel gating modifier NS5806 |
| Minge D., *Witzel K., Bahring R. |
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| Molecular basis of epithelial cell response to streptococcal exotoxin: Role of STIM1 and Orai1 proteins |
| *Usmani S.M., Von Einem J., Dietl P., Wittekindt O.H. |
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| Molecular Determinants of IKs channel sensitivity to JNJ-303 |
| *Wrobel E., Linders J.T.M., Strutz-Seebohm N., Towart R., Seebohm G. |
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| Molecular regulation of titin-based myocardial stiffness |
| *Krger M. |
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| Muscarinic modulation of CA3 synapses |
| *Alzheimer C., Zheng F. |
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| Mutagenesis studies investigating slow inactivation of sodium channel Nav1.6 |
| *Eberhardt E., O'Reilly A.O., Lampert A. |
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| Mutations C277Y and C277R cause dysfunction of human ClC-1 chloride channels resulting in myotonia congenita |
| *Weinberger S., Sternberg D., Lehmann-Horn F., Fahlke C., Fischer M. |
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| Mutations of hClC-1 channels without functional deficits cause myotonia congenita by impaired surface membrane insertion: a new approach combining electrophysiology with single cell fluorescence measurements |
| *Peter K., Sternberg D., Fischer M., Fahlke C. |
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| Myeloperoxidase acts as a mediator of angiotensin II-dependent increase in vascular tone |
| *Seniuk A., Schwoerer A., Klinke A., Baldus S., Ehmke H. |
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| Myocardial Function Cytokine-associated paracrine effects of cardiac progenitor cells |
| *Wenzel S., Mufti S., Scheufen S., Maxeiner H., Schluter K.-D. |
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