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Molecular genetics and electrophysiological studies of hypokalemic periodic paralysis (HypoPP)

Hang, ChaoUniversität Ulm

ulm-diss Repository record for Molecular genetics and electrophysiological studies of hypokalemic periodic paralysis (HypoPP) (opens in a new tab)

Understanding Potassium Homeostasis Using Human and Mouse Genetic Models

Cheng, Chih-Jen2013

… disorders, hypokalemic periodic paralysis (hypoPP) and pseudohypoaldosteronism type II (PHA2). Patients with hypoPP are characterized with ictal hypokalemia and muscle paralysis. HypoPP can be divided into familial and non-familial forms. Recent studies have revealed the pathogenesis of …

utswmed Repository record for Understanding Potassium Homeostasis Using Human and Mouse Genetic Models (opens in a new tab)

Voltage-Gated Sodium Channel Activity in Mouse Skeletal Muscle Fibers: Normal Gating and Defects Associated with Periodic Paralysis Mutants

Fu, Yu2010

… human R669H) in hypokalemic periodic paralysis (HypoPP) - were characterized with voltage-clamp recordings in fully differentiated fibers from knock-in mutant mice. The NaV1.4-M1592V mutation produced gain-of-function defects, with the major changes being a slightly increased persistent current …

utswmed Repository record for Voltage-Gated Sodium Channel Activity in Mouse Skeletal Muscle Fibers: Normal Gating and Defects Associated with Periodic Paralysis Mutants (opens in a new tab)

Wirkung von Carboanhydraseinhibitoren am Modell der Hypokaliämischen Periodischen Paralyse: In-vitro Untersuchungen zum Ruhemembranpotenzial des Skelettmuskels

Korzer, ChristineUniversität Ulm

ulm-diss Repository record for Wirkung von Carboanhydraseinhibitoren am Modell der Hypokaliämischen Periodischen Paralyse: In-vitro Untersuchungen zum Ruhemembranpotenzial des Skelettmuskels (opens in a new tab)