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apl. Prof. Dr. Said Hashemolhosseini
Scopus Author ID:
6602735177
Orcid ID:
0000-0002-6564-5649
List of publications:
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Medizinische Fakultät
Lehrstuhl für Biochemie und Pathobiochemie
Publications
(28)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Authored book
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Translation
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Thesis
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Conference contribution
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In Adult Skeletal Muscles, the Co-Receptors of Canonical Wnt Signaling, Lrp5 and Lrp6, Determine the Distribution and Size of Fiber Types, and Structure and Function of Neuromuscular Junctions (2022)
Geßler L, Kurtek C, Merholz M, Jian Y, Hashemolhosseini S
Journal article
In Skeletal Muscle Fibers, Protein Kinase Subunit CSNK2A1/CK2 alpha Is Required for Proper Muscle Homeostasis and Structure and Function of Neuromuscular Junctions (2022)
Merholz M, Jian Y, Wimberg J, Geßler L, Hashemolhosseini S
Journal article
The desmin mutation R349P increases contractility and fragility of stem cell-generated muscle micro-tissues (2021)
Spörrer M, Kah DTE, Gerum R, Reischl B, Huraskin D, Dessalles CA, Schneider W, et al.
Journal article, Original article
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP sydrome) caused by a novel mutation in ADPRHL2 (AHR3) (2021)
Durmus H, Mertoğlu E, Sticht H, Ceylaner S, Kulaksızoğlu IB, Hashemolhosseini S, Uçar EÖ, Parman Y
Journal article
Lack of Desmin in Mice Causes Structural and Functional Disorders of Neuromuscular Junctions (2020)
Eiber N, Fröb F, Schowalter M, Thiel C, Clemen CS, Schröder R, Hashemolhosseini S
Journal article
The role of protein kinase CK2 in skeletal muscle: Myogenesis, neuromuscular junctions, and rhabdomyosarcoma (2020)
Hashemolhosseini S
Journal article, Review article
EPISODIC PSYCHOSIS, ATAXIA, MOTOR NEUROPATHY CAUSED BY A NOVEL MUTATION IN ADPRHL2 (2020)
Durmus H, Sticht H, Ceylaner S, Hashemolhosseini S, Parmn Y
Conference contribution
Methocarbamol blocks muscular Nav1.4 channels and decreases isometric force of mouse muscles (2020)
Zhang Y, Otto P, Qin L, Eiber N, Hashemolhosseini S, Kröger S, Brinkmeier H
Journal article
Rare slow channel congenital myasthenic syndromes without repetitive compound muscle action potential and dramatic response to low dose fluoxetine (2020)
Durmus H, Sticht H, Ceylaner S, Hashemolhosseini S, Deymeer F
Journal article
Loss of Protein Kinase Csnk2b/CK2 beta at Neuromuscular Junctions Affects Morphology and Dynamics of Aggregated Nicotinic Acetylcholine Receptors, Neuromuscular Transmission, and Synaptic Gene Expression (2019)
Eiber N, Rehman M, Kravic B, Rudolf R, Sandri M, Hashemolhosseini S
Journal article
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