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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
Autophagy. 2021 Jan;17(1):1-382. doi: 10.1080/15548627.2020.1797280. Epub 2021 Feb 8.
Autophagy. 2021.
PMID: 33634751
Free PMC article.
Glial Dysfunction and Its Contribution to the Pathogenesis of the Neuronal Ceroid Lipofuscinoses.
Takahashi K, Nelvagal HR, Lange J, Cooper JD.
Takahashi K, et al.
Front Neurol. 2022 Apr 4;13:886567. doi: 10.3389/fneur.2022.886567. eCollection 2022.
Front Neurol. 2022.
PMID: 35444603
Free PMC article.
Review.
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Defective synaptic transmission causes disease signs in a mouse model of juvenile neuronal ceroid lipofuscinosis.
Grünewald B, Lange MD, Werner C, O'Leary A, Weishaupt A, Popp S, Pearce DA, Wiendl H, Reif A, Pape HC, Toyka KV, Sommer C, Geis C.
Grünewald B, et al.
Elife. 2017 Nov 14;6:e28685. doi: 10.7554/eLife.28685.
Elife. 2017.
PMID: 29135436
Free PMC article.
Juvenile neuronal ceroid lipofuscinosis (JNCL or Batten disease) caused by mutations in the CLN3 gene is the most prevalent inherited neurodegenerative disease in childhood resulting in widespread central nervous system dysfunction and premature death. ...
Juvenile neuronal ceroid lipofuscinosis (JNCL or Batten disease) caused by mutations in the CLN3 gene is the most prevalent inherited …
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Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis.
Lange J, Haslett LJ, Lloyd-Evans E, Pocock JM, Sands MS, Williams BP, Cooper JD.
Lange J, et al.
Acta Neuropathol Commun. 2018 Aug 8;6(1):74. doi: 10.1186/s40478-018-0575-4.
Acta Neuropathol Commun. 2018.
PMID: 30089511
Free PMC article.
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