Hakutulokset - Angela M. Kaindl
- Näytetään 1 - 20 yhteensä 38 tuloksesta
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Missense mutations of ACTA1 cause dominant congenital myopathy with cores Tekijä Angela M. Kaindl
Julkaistu 2004Carta -
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Golgi-Cox Staining Step by Step Tekijä Sami Zaqout, Angela M. Kaindl
Julkaistu 2016Artigo -
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Autosomal Recessive Primary Microcephaly: Not Just a Small Brain Tekijä Sami Zaqout, Angela M. Kaindl
Julkaistu 2022Revisão -
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Molecular Mechanisms Involved in Injury to the Preterm Brain Tekijä Angela M. Kaindl, Géraldine Favrais, Pierre Gressèns
Julkaistu 2009Revisão -
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The Yin and Yang of Microglia Tekijä Melinda Czéh, Pierre Gressèns, Angela M. Kaindl
Julkaistu 2011Revisão -
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Immunofluorescence Staining of Paraffin Sections Step by Step Tekijä Sami Zaqout, Lena‐Luise Becker, Angela M. Kaindl
Julkaistu 2020Artigo -
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Antiepileptic drugs and the developing brain Tekijä Angela M. Kaindl, Stella Asimiadou, Daniela Manthey, Maja von der Hagen, L. Turski, Chrysanthy Ikonomidou
Julkaistu 2006Revisão -
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Brief Alteration of NMDA or GABAA Receptor-mediated Neurotransmission Has Long Term Effects on the Developing Cerebral Cortex Tekijä Angela M. Kaindl, Andrea Koppelstaetter, Grit Nebrich, Janine Stuwe, Marco Sifringer, Claus Zabel, Joachim Klose, Chrysanthy Ikonomidou
Julkaistu 2008Artigo -
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Synaptic NMDA receptor activity is coupled to the transcriptional control of the glutathione system Tekijä Paul Baxter, Karen Bell, Philip Hasel, Angela M. Kaindl, Michael Fricker, Derek Thomson, Sean P. Cregan, Thomas H. Gillingwater, Giles E. Hardingham
Julkaistu 2015Artigo -
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Diagnostic approach to microcephaly in childhood: a two‐center study and review of the literature Tekijä Maja von der Hagen, Mark Pivarcsi, Juliane Liebe, Horst von Bernuth, Nataliya Di Donato, Julia B. Hennermann, Christoph Bührer, Dagmar Wieczorek, Angela M. Kaindl
Julkaistu 2014Revisão -
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Somatic DNA Variants in Epilepsy Surgery Brain Samples from Patients with Lesional Epilepsy Tekijä Jana Marie Schwarz, Lena‐Luise Becker, Monika Wahle, Jessica Faßbender, Ulrich‐Wilhelm Thomale, Anna Tietze, Susanne Morales-Gonzalez, Ellen Knierim, Markus Schuelke, Angela M. Kaindl
Julkaistu 2025Artigo -
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Neutrophil oxidative burst activates ATM to regulate cytokine production and apoptosis Tekijä Christopher J. Harbort, Paulo V. Soeiro-Pereira, Horst von Bernuth, Angela M. Kaindl, Beatriz Tavares Costa‐Carvalho, Antônio Condino‐Neto, Janine Reichenbach, Joachim Roesler, Arturo Zychlinsky, Borko Amulic
Julkaistu 2015Artigo -
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Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease Tekijä Birgit Uhlenberg, Markus Schuelke, Franz Rüschendorf, Nico Ruf, Angela M. Kaindl, Marco Henneke, Hölger Thiele, Gisela Stoltenburg‐Didinger, Fuat Aksu, Haluk Topaloğlu, Peter Nürnberg, Christoph Hübner, Bernhard Weschke, Jutta Gärtner
Julkaistu 2004Artigo -
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Melatonin Promotes Oligodendroglial Maturation of Injured White Matter in Neonatal Rats Tekijä Paul Olivier, R Fontaine, Gauthier Loron, Juliette Van Steenwinckel, Valérie Biran, Véronique Massonneau, Angela M. Kaindl, Jérémie Dalous, Christiane Charriaut‐Marlangue, Marie‐Stéphane Aigrot, Julien Pansiot, Catherine Verney, Pierre Gressèns, Olivier Baud
Julkaistu 2009Artigo -
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NMDA antagonist inhibits the extracellular signal-regulated kinase pathway and suppresses cancer growth Tekijä Andrzej Stepulak, Marco Sifringer, Wojciech Rzeski, Stefanie Endesfelder, Alexander Gratopp, Elena E. Pohl, Petra Bittigau, Ursula Felderhoff‐Mueser, Angela M. Kaindl, Christoph Bührer, Henrik H. Hansen, Marta Stryjecka‐Zimmer, Lechosław Turski, Chrysanthy Ikonomidou
Julkaistu 2005Artigo -
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Epilepsy surgery in early infancy: A retrospective, multicenter study Tekijä Konstantin L. Makridis, Kerstin Alexandra Klotz, Georgia Ramantani, Lena‐Luise Becker, Victoria San Antonio‐Arce, Steffen Syrbe, Kathrin Wagner, Mukesch Shah, Ulrich‐Wilhelm Thomale, Anna Tietze, Christian E. Elger, Ingo Borggraefe, Angela M. Kaindl
Julkaistu 2023Artigo
Työkalut:
Liittyvät aiheet
Medicine
Biology
Neuroscience
Genetics
Internal medicine
Gene
Pathology
Epilepsy
Pediatrics
Psychology
Cell biology
Phenotype
Receptor
Biochemistry
Psychiatry
Chemistry
Disease
Missense mutation
Cognition
Exome sequencing
Immunology
Inflammation
Magnetic resonance imaging
Microcephaly
Mutation
NMDA receptor
Oxidative stress
Radiology
Retrospective cohort study
Atrophy