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Catecholaminergic dysfunction drives postural and locomotor deficits in a mouse model of spinal muscular atrophy.
Cell Rep. 2025 Jan 2;44(1):115147. doi: 10.1016/j.celrep.2024.115147. Online ahead of print.
Cell Rep. 2025.
PMID: 39752251
Free article.
Dysfunction of proprioceptive sensory synapses is a pathogenic event and therapeutic target in mice and humans with spinal muscular atrophy.
Simon CM, Delestree N, Montes J, Gerstner F, Carranza E, Sowoidnich L, Buettner JM, Pagiazitis JG, Prat-Ortega G, Ensel S, Donadio S, Garcia JL, Kratimenos P, Chung WK, Sumner CJ, Weimer LH, Pirondini E, Capogrosso M, Pellizzoni L, De Vivo DC, Mentis GZ.
Simon CM, et al. Among authors: sowoidnich l.
medRxiv [Preprint]. 2024 Jun 4:2024.06.03.24308132. doi: 10.1101/2024.06.03.24308132.
medRxiv. 2024.
PMID: 38883729
Free PMC article.
Preprint.
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p53-dependent c-Fos expression is a marker but not executor for motor neuron death in spinal muscular atrophy mouse models.
Buettner JM, Sowoidnich L, Gerstner F, Blanco-Redondo B, Hallermann S, Simon CM.
Buettner JM, et al. Among authors: sowoidnich l.
Front Cell Neurosci. 2022 Nov 7;16:1038276. doi: 10.3389/fncel.2022.1038276. eCollection 2022.
Front Cell Neurosci. 2022.
PMID: 36419936
Free PMC article.
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Central synaptopathy is the most conserved feature of motor circuit pathology across spinal muscular atrophy mouse models.
Buettner JM, Sime Longang JK, Gerstner F, Apel KS, Blanco-Redondo B, Sowoidnich L, Janzen E, Langenhan T, Wirth B, Simon CM.
Buettner JM, et al. Among authors: sowoidnich l.
iScience. 2021 Oct 30;24(11):103376. doi: 10.1016/j.isci.2021.103376. eCollection 2021 Nov 19.
iScience. 2021.
PMID: 34825141
Free PMC article.
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