Accumulation of multiple neurodegenerative disease-related proteins in familial frontotemporal lobar degeneration associated with granulin mutation
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Accumulation of multiple neurodegenerative disease-related proteins in familial frontotemporal lobar degeneration associated with granulin mutation
Authors
Keywords
-
Journal
Scientific Reports
Volume 7, Issue 1, Pages -
Publisher
Springer Nature
Online
2017-04-28
DOI
10.1038/s41598-017-01587-6
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Evolutional Aspects of Alzheimer's Disease Pathogenesis
- (2018) Heiko Braak et al. JOURNAL OF ALZHEIMERS DISEASE
- Progranulin regulates lysosomal function and biogenesis through acidification of lysosomes
- (2017) Yoshinori Tanaka et al. HUMAN MOLECULAR GENETICS
- Rs5848 Variant Influences GRN mRNA Levels in Brain and Peripheral Mononuclear Cells in Patients with Alzheimer's Disease
- (2017) Chiara Fenoglio et al. JOURNAL OF ALZHEIMERS DISEASE
- Progranulin Reduction Is Associated With Increased Tau Phosphorylation in P301L Tau Transgenic Mice
- (2015) Masato Hosokawa et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- Arizona Study of Aging and Neurodegenerative Disorders and Brain and Body Donation Program
- (2015) Thomas G. Beach et al. NEUROPATHOLOGY
- Possible involvement of lysosomal dysfunction in pathological changes of the brain in aged progranulin-deficient mice
- (2014) Yoshinori Tanaka et al. Acta Neuropathologica Communications
- Progranulin Mutations as Risk Factors for Alzheimer Disease
- (2013) David C. Perry et al. JAMA Neurology
- A harmonized classification system for FTLD-TDP pathology
- (2011) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Progranulin Is a Chemoattractant for Microglia and Stimulates Their Endocytic Activity
- (2011) Fiona Pickford et al. AMERICAN JOURNAL OF PATHOLOGY
- rs5848 Variant of Progranulin Gene Is a Risk of Alzheimer’s Disease in the Taiwanese Population
- (2011) Ming-Jen Lee et al. Neurodegenerative Diseases
- Alzheimer Disease–like Phenotype Associated With the c.154delA Mutation in Progranulin
- (2010) Brendan J. Kelley et al. ARCHIVES OF NEUROLOGY
- Postmortem interval effect on RNA and gene expression in human brain tissue
- (2010) Alex C. Birdsill et al. CELL AND TISSUE BANKING
- Serum biomarker for progranulin-associated frontotemporal lobar degeneration
- (2009) Kristel Sleegers et al. ANNALS OF NEUROLOGY
- Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
- (2009) N. Finch et al. BRAIN
- Exaggerated inflammation, impaired host defense, and neuropathology in progranulin-deficient mice
- (2009) Fangfang Yin et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease
- (2009) Miryam Carecchio et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study
- (2008) Isabelle Le Ber et al. BRAIN
- Novel exon 1 progranulin gene variant in Alzheimer’s disease
- (2008) F. Cortini et al. EUROPEAN JOURNAL OF NEUROLOGY
- Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival
- (2008) Philip Van Damme et al. JOURNAL OF CELL BIOLOGY
- Prominent phenotypic variability associated with mutations in Progranulin
- (2007) Brendan J. Kelley et al. NEUROBIOLOGY OF AGING
- A novel deletion in progranulin gene is associated with FTDP-17 and CBS
- (2006) Luisa Benussi et al. NEUROBIOLOGY OF AGING
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationPublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More