Resultados da pesquisa - Holger Lerche
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Eryptosis, a Window to Systemic Disease Por Florian Läng, Erich Gulbins, Holger Lerche, Stephan M. Huber, Daniela S. Kempe, Michael Föller
Publicado em 2008Revisão -
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Ion channels in genetic and acquired forms of epilepsy Por Holger Lerche, Mala M. Shah, Heinz Beck, Jeffrey L. Noebels, Dan Johnston, Angela Vincent
Publicado em 2012Revisão -
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Early-onset familial hemiplegic migraine due to a novel <i>SCN1A</i> mutation Por Chunxiang Fan, Stefan Wolking, Frank Lehmann‐Horn, Ulrike B. S. Hedrich, Tobias Freilinger, Holger Lerche, Guntram Borck, Christian Kubisch, Karin Jurkat‐Rott
Publicado em 2016Artigo -
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SRF modulates seizure occurrence, activity induced gene transcription and hippocampal circuit reorganization in the mouse pilocarpine epilepsy model Por Pascal Lösing, Cristina Elena Niturad, Merle Harrer, Christopher Meyer zu Reckendorf, Theresa Schatz, Daniela Sinske, Holger Lerche, Snezana Maljevic, Bernd Knöll
Publicado em 2017Artigo -
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K(+)‐aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation. Por N Mitrovié, Alfred L. George, R Heine, Susanne Wagner, Ursula Pika, U Hartlaub, Min Zhou, Holger Lerche, Christoph Fahlke, F. Lehmann‐Horn
Publicado em 1994Artigo -
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Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III‐IV linker. Por Holger Lerche, R Heine, Ursula Pika, Alfred L. George, Nenad Mitrović, M Browatzki, Tomer Weiss, M. Rivet-Bastide, Ch. Franke, Mauro LoMonaco
Publicado em 1993Artigo -
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Efficient generation of neural stem cell-like cells from adult human bone marrow stromal cells Por Andreas Hermann, Regina Gastl, Stefan Liebau, M. Oana Popa, Jörg Fiedler, Bernhard O. Boehm, Martina Maisel, Holger Lerche, Johannes Schwarz, Rolf E. Brenner, Alexander Storch
Publicado em 2004Artigo -
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Human Cerebrospinal fluid promotes long-term neuronal viability and network function in human neocortical organotypic brain slice cultures Por Niklas Schwarz, Ulrike B. S. Hedrich, Hannah Schwarz, Harshad Pannikkaveettil Ashraf, Nele Dammeier, Eva Auffenberg, Francesco Bedogni, Jürgen Honegger, Holger Lerche, Thomas V. Wuttke, Henner Koch
Publicado em 2017Artigo -
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<i>KCNA1</i> gain‐of‐function epileptic encephalopathy treated with 4‐aminopyridine Por Peter Müller, Danielle Takacs, Ulrike B. S. Hedrich, Rohini Coorg, Laura Masters, Kevin E. Glinton, Hongzheng Dai, Jon Cokley, James J. Riviello, Holger Lerche, Edward C. Cooper
Publicado em 2023Artigo -
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Impaired Action Potential Initiation in GABAergic Interneurons Causes Hyperexcitable Networks in an Epileptic Mouse Model Carrying a Human Na<sub>V</sub>1.1 Mutation Por Ulrike B. S. Hedrich, Camille Liautard, Daniel S. Kirschenbaum, Martin Pofahl, Jennifer Lavigne, Yuanyuan Liu, Stephan Theiss, Johannes Slotta, Andrew Escayg, Marcel Dihné, Heinz Beck, Massimo Mantegazza, Holger Lerche
Publicado em 2014Artigo
Ferramentas de pesquisa:
Assuntos relacionados
Biology
Medicine
Epilepsy
Genetics
Gene
Neuroscience
Psychiatry
Internal medicine
Phenotype
Mutation
Psychology
Chemistry
Pathology
Pediatrics
Genome
Organic chemistry
Biochemistry
Bioinformatics
Sodium
Sodium channel
Endocrinology
Copy-number variation
Encephalopathy
Genotype
Disease
Missense mutation
Ataxia
Computational biology
Epilepsy syndromes
Idiopathic generalized epilepsy