The granulin gene family: from cancer to dementia
A Bateman, HPJ Bennett - Bioessays, 2009 - Wiley Online Library
The growth factor progranulin (PGRN) regulates cell division, survival, and migration. PGRN
is an extracellular glycoprotein bearing multiple copies of the cysteine‐rich granulin motif …
is an extracellular glycoprotein bearing multiple copies of the cysteine‐rich granulin motif …
Progranulin as a biomarker and potential therapeutic agent
Highlights•PGRN is a growth factor with pleiotropic actions.•PGRN shows potential as a
biomarker in different diseases.•Attstrin (a PGRN-derived peptide) is a potential therapeutic …
biomarker in different diseases.•Attstrin (a PGRN-derived peptide) is a potential therapeutic …
Dissociation of frontotemporal dementia–related deficits and neuroinflammation in progranulin haploinsufficient mice
AJ Filiano, LH Martens, AH Young… - Journal of …, 2013 - Soc Neuroscience
Frontotemporal dementia (FTD) is a neurodegenerative disease with hallmark deficits in
social and emotional function. Heterozygous loss-of-function mutations in GRN, the …
social and emotional function. Heterozygous loss-of-function mutations in GRN, the …
Microglial upregulation of progranulin as a marker of motor neuron degeneration
T Philips, L De Muynck… - … of Neuropathology & …, 2010 - academic.oup.com
Frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS) are
overlapping neurodegenerative disorders. Mutations in the growth factor progranulin …
overlapping neurodegenerative disorders. Mutations in the growth factor progranulin …
Pathogenic cysteine mutations affect progranulin function and production of mature granulins
J Wang, P Van Damme, C Cruchaga… - Journal of …, 2010 - Wiley Online Library
J. Neurochem.(2010) 112, 1305–1315. Abstract Frontotemporal dementia with ubiquitin‐
positive inclusions (FTLD‐U) can be caused by mutations in the progranulin gene (GRN) …
positive inclusions (FTLD‐U) can be caused by mutations in the progranulin gene (GRN) …
Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia
O Mukherjee, J Wang, M Gitcho, S Chakraverty… - Human …, 2008 - Wiley Online Library
Frontotemporal dementia (FTD) is a clinical term encompassing dementia characterized by
the presence of two major phenotypes: 1) behavioral and personality disorder, and 2) …
the presence of two major phenotypes: 1) behavioral and personality disorder, and 2) …
Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration
AS Chen-Plotkin, F Geser, JB Plotkin… - Human molecular …, 2008 - academic.oup.com
Frontotemporal lobar degeneration is a fatal neurodegenerative disease that results in
progressive decline in behavior, executive function and sometimes language. Disease …
progressive decline in behavior, executive function and sometimes language. Disease …
Progranulin regulates lysosomal function and biogenesis through acidification of lysosomes
Y Tanaka, G Suzuki, T Matsuwaki… - Human molecular …, 2017 - academic.oup.com
Progranulin (PGRN) haploinsufficiency resulting from loss-of-function mutations in the
PGRN gene causes frontotemporal lobar degeneration accompanied by TDP-43 …
PGRN gene causes frontotemporal lobar degeneration accompanied by TDP-43 …
[HTML][HTML] Progranulin regulates neuronal outgrowth independent of sortilin
J Gass, WC Lee, C Cook, N Finch, C Stetler… - Molecular …, 2012 - Springer
Background Progranulin (PGRN), a widely secreted growth factor, is involved in multiple
biological functions, and mutations located within the PGRN gene (GRN) are a major cause …
biological functions, and mutations located within the PGRN gene (GRN) are a major cause …
A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells
AW Kao, RJ Eisenhut, LH Martens… - Proceedings of the …, 2011 - National Acad Sciences
Frontotemporal lobar degeneration is a progressive neurodegenerative syndrome that is the
second most common cause of early-onset dementia. Mutations in the progranulin gene are …
second most common cause of early-onset dementia. Mutations in the progranulin gene are …