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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders Volume 4, 2003 - Issue 3
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Review article

Molecular and cellular basis of spinal muscular atrophy

Sibylle Jablonka Institute for Clinical Neurobiology, University of Wuerzburg, Wuerzburg, GermanyCorrespondence[email protected]‐wuerzburg.de
&
Michael Sendtner Institute for Clinical Neurobiology, University of Wuerzburg, Wuerzburg, Germany
Pages 144-149 | Published online: 10 Jul 2009

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Sylvia Balabanian, Nathalie H. Gendron & Alex E. MacKenzie. (2007) Histologic and transcriptional assessment of a mild SMA model. Neurological Research 29:5, pages 413-424.
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Articles from other publishers (13)

K.R. Sabitha, Ashok K. Shetty & Dinesh Upadhya. (2021) Patient-derived iPSC modeling of rare neurodevelopmental disorders: Molecular pathophysiology and prospective therapies. Neuroscience & Biobehavioral Reviews 121, pages 201-219.
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Michael Schoen, Jochen M. Reichel, Maria Demestre, Stefan Putz, Dhruva Deshpande, Christian Proepper, Stefan Liebau, Michael J. Schmeisser, Albert C. Ludolph, Jens Michaelis & Tobias M. Boeckers. (2016) Super-Resolution Microscopy Reveals Presynaptic Localization of the ALS/FTD Related Protein FUS in Hippocampal Neurons. Frontiers in Cellular Neuroscience 9.
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Eileen Workman, Caitlin Kalda, Aalapi Patel & Daniel J. Battle. (2015) Gemin5 Binds to the Survival Motor Neuron mRNA to Regulate SMN Expression. Journal of Biological Chemistry 290:25, pages 15662-15669.
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Sibylle Jablonka, Benjamin Dombert, Esther Asan & Michael Sendtner. (2014) Mechanisms for axon maintenance and plasticity in motoneurons: alterations in motoneuron disease. Journal of Anatomy 224:1, pages 3-14.
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Jonathan J. Cherry, Erkan Y. Osman, Matthew C. Evans, Sungwoon Choi, Xuechao Xing, Gregory D. Cuny, Marcie A. Glicksman, Christian L. Lorson & Elliot J. Androphy. (2013) Enhancement of SMN protein levels in a mouse model of spinal muscular atrophy using novel drug‐like compounds . EMBO Molecular Medicine 5:7, pages 1103-1118.
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Jonathan J. Cherry, Matthew C. Evans, Jake Ni, Gregory D. Cuny, Marcie A. Glicksman & Elliot J. Androphy. (2012) Identification of Novel Compounds That Increase SMN Protein Levels Using an Improved SMN2 Reporter Cell Assay. SLAS Discovery 17:4, pages 481-495.
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Alexander-Francisco Bruns, Jeroen van Bergeijk, Christina Lorbeer, Anna Nölle, Julia Jungnickel, Claudia Grothe & Peter Claus. (2009) Fibroblast growth factor–2 regulates the stability of nuclear bodies. Proceedings of the National Academy of Sciences 106:31, pages 12747-12752.
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Micheal Sendtner, Daniel Bachteler, Rainer Spanagel, Ulrich Schmitt, Barbava Vollmayr, Fritz A. Henn, Alexandra Wigger & Rainer Landgraf. 2008. Handbuch der Psychopharmakotherapie. Handbuch der Psychopharmakotherapie 201 231 .
Ming S. Tsai, Yung T. Chiu, Sue H. Wang, Hsiu M. Hsieh-Li, Wei C. Lian & Hung Li. (2006) Abolishing Bax-Dependent Apoptosis Shows Beneficial Effects on Spinal Muscular Atrophy Model Mice. Molecular Therapy 13:6, pages 1149-1155.
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Ming Shiun Tsai, Yung Tsung Chiu, Sue Hong Wang, Hsiu Mei Hsieh-Li & Hung Li. (2006) Abolishing Trp53-dependent apoptosis does not benefit spinal muscular atrophy model mice. European Journal of Human Genetics 14:3, pages 372-375.
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Thais Federici & Nicholas M. Boulis. (2006) Gene-based treatment of motor neuron diseases. Muscle & Nerve 33:3, pages 302-323.
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Qingshan Teng, Thais Federici & Nicholas M. Boulis. 2006. Gene Therapy of the Central Nervous System. Gene Therapy of the Central Nervous System 253 271 .
J. H. VeldinkS. KalmijnA. H. Van der HoutH. H. LemminkG. J. GroeneveldC. LummenH. SchefferJ.H.J. WokkeL. H. Van den Berg. (2005) SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS . Neurology 65:6, pages 820-825.
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