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780 citation(s) found for "Dickson, Dennis W".

Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis
Cannon, Ashley , Fujioka, Shinsuke , Rutherford, Nicola J., Ferman, Tanis J. , Broderick, Daniel F. , Graff‐Radford, Neill R. , Uitti, Ryan J. , Rademakers, Rosa , Dickson, Dennis W. , Boylan, Khrista , Wszołek, Zbigniew K. , Dickson, Dennis W , Ferman, Tanis J

Mayo Clinic

Neurology | April 18, 2013 | Volume: 80 | Issue: 19 | Pages: 1771-1777

10.1212/wnl.0b013e3182919059 | PMID 23596077 Get It

Misregulation of human sortilin splicing leads to the generation of a nonfunctional progranulin receptor
Prudencio, Mercedes , Jansen‐West, Karen , Lee, Chris W. , Zhang, Yong‐Jie , Xu, Ya-Fei, Gass, Jennifer , Stuani, Cristiana , Stetler, Caroline, Rademakers, Rosa , Dickson, Dennis W. , Buratti, Emanuele , Petrucelli, Leonard , Gendron, Tania F. , Zhang, Yong-Jie , Prudencio, Mercedes , Dickson, Dennis W

Mayo Clinic

Proceedings of the National Academy of Sciences | December 11, 2012 | Volume: 109 | Issue: 52 | Pages: 21510-21515

10.1073/pnas.1211577110 | PMID 23236149 Get It

Sortilin 1 regulates the levels of brain progranulin (PGRN), a neurotrophic growth factor that, when deficient, is linked to cases of frontotemporal lobar degeneration with TAR DNA-binding protein-43 (TDP-43)–positive inclusions (FTLD-TDP). We identified a specific splicing enhancer element that regulates the inclusion of a sortilin exon cassette (termed Ex17b) not normally present in the mature sortilin mRNA. This enhancer element is consistently present in sortilin RNA of mice and other species but absent in primates, which carry a premature stop codon within the Ex17b sequence. In the absence of TDP-43, which acts as a regulatory inhibitor, Ex17b is included in the sortilin mRNA. In humans, in contrast to mice, the inclusion of Ex17b in sortilin mRNA generates a truncated, nonfunctional, extracellularly released protein that binds to but does not internalize PGRN, essentially acting as a decoy receptor. Based on these results, we propose a potential mechanism linking misregulation of sortilin splicing with altered PGRN metabolism.
IC‐O2‐02: In dementia with Lewy bodies RBD is associated with reduced Alzheimer's disease pathology and hippocampal atrophy
Murray, Melissa E. , Petersen, Ronald C. , Parisi, Joseph E., Vemuri, Prashanthi , Ferman, Tanis J. , Dugger, Brittany N. , Jack, Clifford R. , Boeve, Bradley F. , Knopman, David S. , Dickson, Dennis W. , Kantarci, Kejal , Murray, Melissa E

Mayo Clinic

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_1 | Pages: No page available

10.1016/j.jalz.2012.05.024 Get It

P1‐195: LRRK2 modulation of neuropathology in a mouse model of tauopathy
Bailey, Rachel M. , Melrose, Heather L. , Lewis, Jada , Cannon, Ashley , Farrer, Matthew J. , Dickson, Dennis W.

Mayo Clinic

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_5 | Pages: No page available

10.1016/j.jalz.2012.05.473 Get It

O4‐04‐01: Differentiating clinicopathologic and genetic aspects of hippocampal sclerosis in Alzheimer's disease from limbic predominant Alzheimer's disease and “pure” hippocampal sclerosis
Graff‐Radford, Neill R. , Murray, Melissa E. , Duara, Ranjan , Rademakers, Rosa , Whitwell, Jennifer , Ross, Owen A. , Duara, Ranjan , Dickson, Dennis W. , Murray, Melissa E

Mayo Clinic

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_17 | Pages: No page available

10.1016/j.jalz.2012.05.1652 Get It