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Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions. [electronic resource] by
- Dächsel, Justus C
- Ross, Owen A
- Mata, Ignacio F
- Kachergus, Jennifer
- Toft, Mathias
- Cannon, Ashley
- Baker, Matt
- Adamson, Jennifer
- Hutton, Mike
- Dickson, Dennis W
- Farrer, Matthew J
Producer: 20070831
In:
Acta neuropathologica vol. 113
Availability: No items available.
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11.
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Digenic parkinsonism: investigation of the synergistic effects of PRKN and LRRK2. [electronic resource] by
- Dächsel, Justus C
- Mata, Ignacio F
- Ross, Owen A
- Taylor, Julie P
- Lincoln, Sarah J
- Hinkle, Kelly M
- Huerta, Cecilia
- Ribacoba, Renee
- Blazquez, Marta
- Alvarez, Victoria
- Farrer, Matthew J
Producer: 20070123
In:
Neuroscience letters vol. 410
Availability: No items available.
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12.
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Identification of potential protein interactors of Lrrk2. [electronic resource] by
- Dächsel, Justus C
- Taylor, Julie P
- Mok, Su San
- Ross, Owen A
- Hinkle, Kelly M
- Bailey, Rachel M
- Hines, Jacob H
- Szutu, Jennifer
- Madden, Benjamin
- Petrucelli, Leonard
- Farrer, Matthew J
Producer: 20080109
In:
Parkinsonism & related disorders vol. 13
Availability: No items available.
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13.
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GCH1 expression in human cerebellum from healthy individuals is not gender dependent. [electronic resource] by
- Wider, Christian
- Lincoln, Sarah
- Dachsel, Justus C
- Kapatos, Gregory
- Heckman, Michael G
- Diehl, Nancy N
- Papapetropoulos, Spiridon
- Mash, Deborah
- Rajput, Alex
- Rajput, Ali H
- Dickson, Dennis W
- Wszolek, Zbigniew K
- Farrer, Matthew J
Producer: 20091007
In:
Neuroscience letters vol. 462
Availability: No items available.
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14.
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Heterodimerization of Lrrk1-Lrrk2: Implications for LRRK2-associated Parkinson disease. [electronic resource] by
- Dachsel, Justus C
- Nishioka, Kenya
- Vilariño-Güell, Carles
- Lincoln, Sarah J
- Soto-Ortolaza, Alexandra I
- Kachergus, Jennifer
- Hinkle, Kelly M
- Heckman, Michael G
- Jasinska-Myga, Barbara
- Taylor, Julie P
- Dickson, Dennis W
- Gibson, Rachel A
- Hentati, Faycal
- Ross, Owen A
- Farrer, Matthew J
Producer: 20100629
In:
Mechanisms of ageing and development vol. 131
Availability: No items available.
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15.
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LRRK2 knockout mice have an intact dopaminergic system but display alterations in exploratory and motor co-ordination behaviors. [electronic resource] by
- Hinkle, Kelly M
- Yue, Mei
- Behrouz, Bahareh
- Dächsel, Justus C
- Lincoln, Sarah J
- Bowles, Erin E
- Beevers, Joel E
- Dugger, Brittany
- Winner, Beate
- Prots, Iryna
- Kent, Caroline B
- Nishioka, Kenya
- Lin, Wen-Lang
- Dickson, Dennis W
- Janus, Christopher J
- Farrer, Matthew J
- Melrose, Heather L
Producer: 20130409
In:
Molecular neurodegeneration vol. 7
Availability: No items available.
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16.
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LINGO1 rs9652490 is associated with essential tremor and Parkinson disease. [electronic resource] by
- Vilariño-Güell, Carles
- Ross, Owen A
- Wider, Christian
- Jasinska-Myga, Barbara
- Cobb, Stephanie A
- Soto-Ortolaza, Alexandra I
- Kachergus, Jennifer M
- Keeling, Brett H
- Dachsel, Justus C
- Melrose, Heather L
- Behrouz, Bahareh
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Aasly, Jan O
- Rajput, Alex
- Farrer, Matthew J
Producer: 20100504
In:
Parkinsonism & related disorders vol. 16
Availability: No items available.
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17.
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Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease. [electronic resource] by
- Aasly, Jan O
- Vilariño-Güell, Carles
- Dachsel, Justus C
- Webber, Philip J
- West, Andrew B
- Haugarvoll, Kristoffer
- Johansen, Krisztina K
- Toft, Mathias
- Nutt, John G
- Payami, Haydeh
- Kachergus, Jennifer M
- Lincoln, Sarah J
- Felic, Amela
- Wider, Christian
- Soto-Ortolaza, Alexandra I
- Cobb, Stephanie A
- White, Linda R
- Ross, Owen A
- Farrer, Matthew J
Producer: 20110126
In:
Movement disorders : official journal of the Movement Disorder Society vol. 25
Availability: No items available.
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18.
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FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression. [electronic resource] by
- Wider, Christian
- Dachsel, Justus C
- Soto, Alexandra I
- Heckman, Michael G
- Diehl, Nancy N
- Yue, Mei
- Lincoln, Sarah
- Aasly, Jan O
- Haugarvoll, Kristoffer
- Trojanowski, John Q
- Papapetropoulos, Spiridon
- Mash, Deborah
- Rajput, Alex
- Rajput, Ali H
- Gibson, J Mark
- Lynch, Timothy
- Dickson, Dennis W
- Uitti, Ryan J
- Wszolek, Zbigniew K
- Farrer, Matthew J
- Ross, Owen A
Producer: 20090727
In:
Movement disorders : official journal of the Movement Disorder Society vol. 24
Availability: No items available.
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19.
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DCTN1 mutations in Perry syndrome. [electronic resource] by
- Farrer, Matthew J
- Hulihan, Mary M
- Kachergus, Jennifer M
- Dächsel, Justus C
- Stoessl, A Jon
- Grantier, Linda L
- Calne, Susan
- Calne, Donald B
- Lechevalier, Bernard
- Chapon, Francoise
- Tsuboi, Yoshio
- Yamada, Tatsuo
- Gutmann, Ludwig
- Elibol, Bülent
- Bhatia, Kailash P
- Wider, Christian
- Vilariño-Güell, Carles
- Ross, Owen A
- Brown, Laura A
- Castanedes-Casey, Monica
- Dickson, Dennis W
- Wszolek, Zbigniew K
Producer: 20090213
In:
Nature genetics vol. 41
Availability: No items available.
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20.
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VPS35 mutations in Parkinson disease. [electronic resource] by
- Vilariño-Güell, Carles
- Wider, Christian
- Ross, Owen A
- Dachsel, Justus C
- Kachergus, Jennifer M
- Lincoln, Sarah J
- Soto-Ortolaza, Alexandra I
- Cobb, Stephanie A
- Wilhoite, Greggory J
- Bacon, Justin A
- Behrouz, Bahareh
- Melrose, Heather L
- Hentati, Emna
- Puschmann, Andreas
- Evans, Daniel M
- Conibear, Elizabeth
- Wasserman, Wyeth W
- Aasly, Jan O
- Burkhard, Pierre R
- Djaldetti, Ruth
- Ghika, Joseph
- Hentati, Faycal
- Krygowska-Wajs, Anna
- Lynch, Tim
- Melamed, Eldad
- Rajput, Alex
- Rajput, Ali H
- Solida, Alessandra
- Wu, Ruey-Meei
- Uitti, Ryan J
- Wszolek, Zbigniew K
- Vingerhoets, François
- Farrer, Matthew J
Producer: 20110919
In:
American journal of human genetics vol. 89
Availability: No items available.
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