Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Jan Claudius, Schwitalla"'
Autor:
Raziye Karapinar, Jan Claudius Schwitalla, Dennis Eickelbeck, Johanna Pakusch, Brix Mücher, Michelle Grömmke, Tatjana Surdin, Thomas Knöpfel, Melanie D. Mark, Ida Siveke, Stefan Herlitze
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
Microbial rhodopsins can be used to control action potentials, while animal opsins can be used to control intracellular signaling pathways. The authors identify Opn7b as constitutively active Gi/o coupled receptor that can be deactivated by light and
Externí odkaz:
https://doaj.org/article/cd6b728c8c2a41f6902c7cf1ab408a53
Autor:
Daniel Strunk, Jana Becker, Roland Veltkamp, Sven G. Meuth, Peter Bauer, Tobias Böttcher, Arndt Rolfs, Jan Claudius Schwitalla, Markus Kraemer
Publikováno v:
Neurological Sciences. 44:1375-1381
Fabry disease is an inherited metabolic disorder with various symptoms. Neurological manifestations are small fiber neuropathy, cerebral white matter lesions (WML), megadolicho basilar artery, and stroke. The relevance of the D313Y variant in the gal
Autor:
Claudia Santoro, Teresa Giugliano, Markus Kraemer, Annalaura Torella, Jan Claudius Schwitalla, Mario Cirillo, Daniela Melis, Peter Berlit, Vincenzo Nigro, Silverio Perrotta, Giulio Piluso
Publikováno v:
PLoS ONE, Vol 13, Iss 7, p e0200446 (2018)
BACKGROUND AND PURPOSE:Moyamoya angiopathy is a progressive cerebral vasculopathy. The p.R4810K substitution in RNF213 has previously been linked to moyamoya disease in Asian populations. When associated with other medical conditions, such as neurofi
Externí odkaz:
https://doaj.org/article/7c3f956a78814552949a051d68ca17aa
Publikováno v:
Voltage-Gated Calcium Channels ISBN: 9783031088803
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9612739323ec820eb0b94fc2407bb164
https://doi.org/10.1007/978-3-031-08881-0_7
https://doi.org/10.1007/978-3-031-08881-0_7
Autor:
Melanie D. Mark, Maurice Meseke, Solieman Daoud, Abdalrahim Jbara, Mohammad I. K. Hamad, Jan Claudius Schwitalla, Elisabeth Petrasch-Parwez, David Lutz, Eckart Förster, Gebhard Reiss, Joachim Herz, Petya Petrova, Stefan Herlitze, Obada Rabaya, Nesrine Melliti
Publikováno v:
Journal of Neurochemistry. 156:589-603
Reelin is a protein that is best known for its role in controlling neuronal layer formation in the developing cortex. Here, we studied its role for post-natal cortical network function, which is poorly explored. To preclude early cortical migration d
Autor:
Till Rudack, Tatjana Surdin, Stefan Alexander Tennigkeit, Maiia Shulman, Jan‐Claudius Schwitalla, Dennis Eickelbeck, Klaus Gerwert, Philipp Althoff, Brix Mücher, Stefan Herlitze, Raziye Karapinar, Marvin Scherlo, Melanie D. Mark
Publikováno v:
Chembiochem
Optogenetics uses light‐sensitive proteins, so‐called optogenetic tools, for highly precise spatiotemporal control of cellular states and signals. The major limitations of such tools include the overlap of excitation spectra, phototoxicity, and l
Autor:
Jan Claudius, Schwitalla, Johanna, Pakusch, Brix, Mücher, Alexander, Brückner, Dominic Alexej, Depke, Thomas, Fenzl, Chris I, De Zeeuw, Lieke, Kros, Freek E, Hoebeek, Melanie D, Mark
Publikováno v:
Cellular and molecular life sciences : CMLS. 79(4)
Absence seizures (ASs) are characterized by pathological electrographic oscillations in the cerebral cortex and thalamus, which are called spike-and-wave discharges (SWDs). Subcortical structures, such as the cerebellum, may well contribute to the em
Autor:
Lou Grangeon, Jeffrie Hadisurya, Stéphanie Guey, Markus Kraemer, Michaelle Corpechot, Dagmar Wieczorek, Jan Claudius Schwitalla
Publikováno v:
Child's Nervous System. 35:1231-1237
Moyamoya angiopathy is a rare vasculopathy with stenosis and/or occlusion of bilateral intracranial parts of internal carotid arteries and/or proximal parts of middle and anterior cerebral arteries. PHACE syndrome is characterized by large segmental
Autor:
Dominique Vidaud, Florence Riant, Lou Grangeon, Chaker Aloui, Françoise Bergametti, Jan Claudius Schwitalla, Markus Kraemer, Jessica Hadjadj, Stéphanie Guey, Severine Drunat, Minh Arnould, Michaelle Corpechot, Elisabeth Tournier-Lasserve
Publikováno v:
Stroke. 50:789-796
Background and Purpose Moyamoya angiopathy (MMA) is a rare cerebral vasculopathy outside of Asia. In Japanese patients, a vast majority of patients carry the founder p.R4810K variant in the RNF213 gene, and familial cases are around 10%. In European
Autor:
Markus Kraemer, Jonas Graf, Peter Berlit, Roland Veltkamp, Orhan Aktas, Jan Claudius Schwitalla, Hans-Peter Hartung, Philipp Albrecht
Publikováno v:
Journal of Neurology. 266:1153-1159
The lacking awareness of healthcare providers bears the risk of delayed or false diagnoses in rare diseases. No systematic data about misdiagnoses of Moyamoya angiopathy (MMA) are available. To evaluate the rate and pattern of missed diagnoses in MMA