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Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation.

作者信息

Terlizzi Rossana, Valentino Maria Lucia, Bartoletti-Stella Anna, Columbaro Marta, Piras Silvia, Stanzani-Maserati Michelangelo, Quadri Marialuisa, Breedveld Guido J, Bonifati Vincenzo, Martinelli Paolo, Parchi Piero, Capellari Sabina

机构信息

IRCCS Institute of Neurological Sciences of Bologna, Bologna, Italy.

Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.

出版信息

Mov Disord. 2017 Aug;32(8):1259-1260. doi: 10.1002/mds.27049. Epub 2017 May 22.

DOI:10.1002/mds.27049
PMID:28543767
Abstract
摘要

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引用本文的文献

1
Early lysosomal maturation deficits in microglia triggers enhanced lysosomal activity in other brain cells of progranulin knockout mice.早发性溶酶体成熟缺陷触发颗粒蛋白前体基因敲除小鼠其他脑细胞溶酶体活性增强。
Mol Neurodegener. 2018 Sep 4;13(1):48. doi: 10.1186/s13024-018-0281-5.
2
Selective depletion of microglial progranulin in mice is not sufficient to cause neuronal ceroid lipofuscinosis or neuroinflammation.在小鼠中选择性耗竭小胶质细胞颗粒蛋白前体不足以引起神经元蜡样脂褐质沉积病或神经炎症。
J Neuroinflammation. 2017 Nov 17;14(1):225. doi: 10.1186/s12974-017-1000-9.