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, , , (2017) Lysine-Less Variants of Spinal Muscular Atrophy SMN and SMNΔ7 Proteins Are Degraded by the Proteasome Pathway. International Journal of Molecular Sciences, 18. 2667pp. doi:10.3390/ijms18122667

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Reference TypeJournal (article/letter/editorial)
TitleLysine-Less Variants of Spinal Muscular Atrophy SMN and SMNΔ7 Proteins Are Degraded by the Proteasome Pathway
JournalInternational Journal of Molecular Sciences
Authors, Author
, Author
Year2017 (December 8)Volume18
PublisherMDPI AG
DOIdoi:10.3390/ijms18122667Search in ResearchGate
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Mindat Ref. ID10064904Long-form Identifiermindat:1:5:10064904:2
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Full Reference, , , (2017) Lysine-Less Variants of Spinal Muscular Atrophy SMN and SMNΔ7 Proteins Are Degraded by the Proteasome Pathway. International Journal of Molecular Sciences, 18. 2667pp. doi:10.3390/ijms18122667
Plain Text, , , (2017) Lysine-Less Variants of Spinal Muscular Atrophy SMN and SMNΔ7 Proteins Are Degraded by the Proteasome Pathway. International Journal of Molecular Sciences, 18. 2667pp. doi:10.3390/ijms18122667
In(n.d.) International Journal of Molecular Sciences Vol. 18. MDPI AG

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Adami, Raffaella, Bottai, Daniele (2022) NSC Physiological Features in Spinal Muscular Atrophy: SMN Deficiency Effects on Neurogenesis. International Journal of Molecular Sciences, 23 (23) 15209 doi:10.3390/ijms232315209
Pellizzoni, L., Charroux, B., Dreyfuss, G. (1999) SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins. Proceedings of the National Academy of Sciences, 96 (20) 11167-11172 doi:10.1073/pnas.96.20.11167
Zilio, Eleonora, Piano, Valentina, Wirth, Brunhilde (2022) Mitochondrial Dysfunction in Spinal Muscular Atrophy. International Journal of Molecular Sciences, 23 (18) 10878 doi:10.3390/ijms231810878
Costa-Roger, Mar, Blasco-Pérez, Laura, Cuscó, Ivon, Tizzano, Eduardo F. (2021) The Importance of Digging into the Genetics of SMN Genes in the Therapeutic Scenario of Spinal Muscular Atrophy. International Journal of Molecular Sciences, 22 (16) 9029pp. doi:10.3390/ijms22169029
Salman, Badih, Bon, Emeline, Delers, Perrine, Cottin, Steve, Pasho, Elena, Ciura, Sorana, Sapaly, Delphine, Lefebvre, Suzie (2024) Understanding the Role of the SMN Complex Component GEMIN5 and Its Functional Relationship with Demethylase KDM6B in the Flunarizine-Mediated Neuroprotection of Motor Neuron Disease Spinal Muscular Atrophy. International Journal of Molecular Sciences, 25 (18). doi:10.3390/ijms251810039
Chudakova, Daria, Kuzenkova, Ludmila, Fisenko, Andrey, Savostyanov, Kirill (2024) In Search of Spinal Muscular Atrophy Disease Modifiers. International Journal of Molecular Sciences, 25 (20). doi:10.3390/ijms252011210
Tiziano, Francesco D., Neri, Giovanni, Brahe, Christina (2010) Biomarkers in Rare Disorders: The Experience with Spinal Muscular Atrophy. International Journal of Molecular Sciences, 12. 24-38 doi:10.3390/ijms12010024
Berciano, María T., Gatius, Alaó, Puente-Bedia, Alba, Rufino-Gómez, Alexis, Tarabal, Olga, Rodríguez-Rey, José C., Calderó, Jordi, Lafarga, Miguel, Tapia, Olga (2024) SMN Deficiency Induces an Early Non-Atrophic Myopathy with Alterations in the Contractile and Excitatory Coupling Machinery of Skeletal Myofibers in the SMN∆7 Mouse Model of Spinal Muscular Atrophy. International Journal of Molecular Sciences, 25 (22). doi:10.3390/ijms252212415
Ogino, Shuji, Wilson, Robert B. (2002) SMN Dosage Analysis and Risk Assessment for Spinal Muscular Atrophy. The American Journal of Human Genetics, 70 (6) 1596-1598 doi:10.1086/340789
Banno, Haruhiko, Katsuno, Masahisa, Suzuki, Keisuke, Tanaka, Fumiaki, Sobue, Gen (2009) Neuropathology and Therapeutic Intervention in Spinal and Bulbar Muscular Atrophy. International Journal of Molecular Sciences, 10. 1000-1012 doi:10.3390/ijms10031000
Caraballo-Miralles, Víctor, Cardona-Rossinyol, Andrea, Garcera, Ana, Torres-Benito, Laura, Soler, Rosa, Tabares, Lucía, Lladó, Jerònia, Olmos, Gabriel (2013) Notch Signaling Pathway Is Activated in Motoneurons of Spinal Muscular Atrophy. International Journal of Molecular Sciences, 14. 11424-11437 doi:10.3390/ijms140611424
 
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