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Medical Hypotheses|May 16, 2006
A common structural mechanism underlying GCMB mutations that cause hypoparathyroidismHeinrich Sticht, Said Hashemolhosseini
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 2, 2021
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP syndrome) caused by a novel mutation in ADPRHL2 (AHR3)Hacer Durmus, Elif Mertoğlu, Heinrich Sticht, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|July 29, 2014
Lambert-Eaton myasthenic syndrome - diagnosis, pathogenesis and therapyRobert Hülsbrink, Said Hashemolhosseini
The Journal of Cell Biology|September 9, 2004
Impacts of a new transcription factor family: mammalian GCM proteins in health and diseaseSaid Hashemolhosseini, Michael Wegner
Neural Regeneration Research|September 9, 2024
Crosstalk among canonical Wnt and Hippo pathway members in skeletal muscle and at the neuromuscular junctionSaid Hashemolhosseini, Lea Gessler
Genes & Development|July 5, 2006
Casein kinase 2-dependent serine phosphorylation of MuSK regulates acetylcholine receptor aggregation at the neuromuscular junctionTatiana Cheusova, Muhammad Amir Khan, Steffen Wolfgang Schubert, et al.
Pharmaceuticals (Basel, Switzerland)|January 21, 2017
Ablation of Protein Kinase CK2β in Skeletal Muscle Fibers Interferes with Their Oxidative CapacityNane Eiber, Luca Simeone, Said Hashemolhosseini
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