Muscle channelopathies and critical points in functional and genetic studies

Por Jurkat-Rott, Karin, Lehmann-Horn, Frank
Publicado em 2005

The impact of splice isoforms on voltage-gated calcium channel α(1) subunits

Por Jurkat-Rott, Karin, Lehmann-Horn, Frank
Publicado em 2004

Do Hyperpolarization-induced Proton Currents Contribute to the Pathogenesis of Hypokalemic Periodic Paralysis, a Voltage Sensor Channelopathy?

Por Jurkat-Rott, Karin, Lehmann-Horn, Frank
Publicado em 2007

Pathophysiological Role of Omega Pore Current in Channelopathies

Por Jurkat-Rott, Karin, Groome, James, Lehmann-Horn, Frank
Publicado em 2012

Rare KCNJ18 variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients

Por Kuhn, Marius, Jurkat-Rott, Karin, Lehmann-Horn, Frank
Publicado no J Neurol Neurosurg Psychiatry (2016)

Eplerenone repolarizes muscle membrane through Na,K-ATPase activation by Tyr10 dephosphorylation

Por Breitenbach, Simon, Lehmann-Horn, Frank, Jurkat-Rott, Karin
Publicado no Acta Myol (2016)

Letter to the Editor concerning “A hypothesis of chronic back pain: ligament subfailure injuries lead to muscle control dysfunction” (M. Panjabi)

Por Schleip, Robert, Vleeming, Andry, Lehmann-Horn, Frank, Klingler, Werner
Publicado em 2007

Open- and closed-state fast inactivation in sodium channels: Differential effects of a site-3 anemone toxin

Por Groome, James R, Lehmann-Horn, Frank, Holzherr, Boris D
Publicado em 2011

The impact of permanent muscle weakness on quality of life in periodic paralysis: a survey of 66 patients

Por CAVEL-GREANT, DEBORAH, LEHMANN-HORN, FRANK, JURKAT-ROTT, KARIN
Publicado em 2012

Domain III S4 in closed-state fast inactivation: Insights from a periodic paralysis mutation

Por Groome, James R, Jurkat-Rott, Karin, Lehmann-Horn, Frank
Publicado no Channels (Austin) (2014)

Sodium channelopathies of skeletal muscle result from gain or loss of function

Por Jurkat-Rott, Karin, Holzherr, Boris, Fauler, Michael, Lehmann-Horn, Frank
Publicado em 2010

The role of fibrosis in Duchenne muscular dystrophy

Por KLINGLER, WERNER, JURKAT-ROTT, KARIN, LEHMANN-HORN, FRANK, SCHLEIP, ROBERT
Publicado em 2012

Successful treatment of periodic paralysis with coenzyme Q10: two case reports

Por Da, Yuwei, Lei, Lin, Jurkat-Rott, Karin, Lehmann-Horn, Frank
Publicado no Acta Myol (2016)

Mechanisms of cold sensitivity of paramyotonia congenita mutation R1448H and overlap syndrome mutation M1360V

Por Mohammadi, Bahram, Mitrovic, Nenad, Lehmann-Horn, Frank, Dengler, Reinhard, Bufler, Johannes
Publicado em 2003

A gating model for wildtype and R1448H Nav1.4 channels in paramyotonia

Por HOLZHERR, BORIS, LEHMANN-HORN, FRANK, KUZMENKINA, ELZA, FAN, CHUNXIANG, JURKAT-ROTT, KARIN
Publicado em 2014

Cooperative effect of S4–S5 loops in domains D3 and D4 on fast inactivation of the Na(+) channel

Por Oana Popa, M, Alekov, Alexi K, Bail, Sigrid, Lehmann-Horn, Frank, Lerche, Holger
Publicado em 2004

A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro

Por Alekov, Alexi K, Rahman, Md Masmudur, Mitrovic, Nenad, Lehmann-Horn, Frank, Lerche, Holger
Publicado em 2000

Neutralization of a negative charge in the S1–S2 region of the K(V)7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsy

Por Wuttke, Thomas V, Penzien, Johann, Fauler, Michael, Seebohm, Guiscard, Lehmann-Horn, Frank, Lerche, Holger, Jurkat-Rott, Karin
Publicado em 2008

Na(V)1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery

Por Groome, James R., Lehmann-Horn, Frank, Fan, Chunxiang, Wolf, Markus, Winston, Vern, Merlini, Luciano, Jurkat-Rott, Karin
Publicado em 2014

Hypermetabolism in B–lymphocytes from malignant hyperthermia susceptible individuals

Por Hoppe, Kerstin, Hack, Guido, Lehmann–Horn, Frank, Jurkat–Rott, Karin, Wearing, Scott, Zullo, Alberto, Carsana, Antonella, Klingler, Werner
Publicado no Sci Rep (2016)