Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's disease (Q33754793)

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• Mutant LRRK2R1441G BAC transgenic mice recapitulate cardinal features of Parkinson's disease

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English	Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's disease	scientific article	Mutant LRRK2R1441G BAC transgenic mice recapitulate cardinal features of Parkinson's disease

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PubMed publication ID

19503083

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29 July 2017

title

Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's disease (English)

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19503083

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29 July 2017

main subject

Parkinson's disease

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inferred from title

author

Serge Przedborski

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10

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Serge Przedborski

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Europe PubMed Central

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19503083

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29 July 2017

Vernice Jackson-Lewis

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6

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Vernice Jackson-Lewis

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Europe PubMed Central

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19503083

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29 July 2017

M. Flint Beal

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11

object named as

M Flint Beal

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Europe PubMed Central

PubMed publication ID

19503083

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29 July 2017

author name string

Yanping Li

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1

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19503083

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29 July 2017

Wencheng Liu

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2

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19503083

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29 July 2017

Tinmarla F Oo

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3

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19503083

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29 July 2017

Lei Wang

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4

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19503083

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29 July 2017

Yi Tang

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5

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19503083

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29 July 2017

Chun Zhou

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7

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19503083

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29 July 2017

Kindiya Geghman

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8

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Europe PubMed Central

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19503083

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29 July 2017

Mikhail Bogdanov

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9

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19503083

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29 July 2017

Robert E Burke

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12

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19503083

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29 July 2017

Chenjian Li

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13

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PubMed publication ID

19503083

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29 July 2017

language of work or name

English

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publication date

7 June 2009

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19503083

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29 July 2017

published in

Nature Neuroscience

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19503083

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29 July 2017

volume

12

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Europe PubMed Central

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19503083

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29 July 2017

issue

7

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19503083

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29 July 2017

page(s)

826-828

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19503083

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29 July 2017

cites work

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

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A comparative analysis of leucine-rich repeat kinase 2 (Lrrk2) expression in mouse brain and Lewy body disease

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A common LRRK2 mutation in idiopathic Parkinson's disease

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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

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Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

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The switch of tau protein to an Alzheimer-like state includes the phosphorylation of two serine-proline motifs upstream of the microtubule binding region

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Medial forebrain bundle axotomy during development induces apoptosis in dopamine neurons of the substantia nigra and activation of caspases in their degenerating axons

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Novel antibodies to synuclein show abundant striatal pathology in Lewy body diseases

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A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.

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A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

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Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementia

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19503083

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12 December 2020

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Identifiers

DOI

10.1038/NN.2349

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stated in

Europe PubMed Central

PubMed publication ID

19503083

retrieved

29 July 2017

PMC publication ID

2845930

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19503083

retrieved

29 July 2017

PubMed publication ID

19503083

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19503083

retrieved

29 July 2017

ResearchGate publication ID

26273001

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