(Q33754793)

29 July 2017

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

1 reference

29 July 2017

1 reference

10

Serge Przedborski

1 reference

29 July 2017

Vernice Jackson-Lewis

6

object named as

Vernice Jackson-Lewis

1 reference

29 July 2017

11

M Flint Beal

1 reference

29 July 2017

Yanping Li

1

1 reference

29 July 2017

Wencheng Liu

2

1 reference

29 July 2017

Tinmarla F Oo

3

1 reference

29 July 2017

Lei Wang

4

1 reference

29 July 2017

Yi Tang

5

1 reference

29 July 2017

Chun Zhou

7

1 reference

29 July 2017

Kindiya Geghman

8

1 reference

29 July 2017

Mikhail Bogdanov

9

1 reference

29 July 2017

Robert E Burke

12

1 reference

29 July 2017

Chenjian Li

13

1 reference

29 July 2017

language of work or name

English

0 references

publication date

7 June 2009

1 reference

29 July 2017

1 reference

29 July 2017

12

1 reference

29 July 2017

826-828

1 reference

29 July 2017

7

1 reference

https://scigraph.springernature.com/pub.10.1038/nn.2349

29 July 2017

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

Tau-mediated neurodegeneration in Alzheimer's disease and related disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

In vivo imaging of axonal degeneration and regeneration in the injured spinal cord

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

A common LRRK2 mutation in idiopathic Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

Parkinson's disease: mechanisms and models

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

Cytochrome c release and caspase activation in traumatic axonal injury

21 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

21 June 2018

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

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

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

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNN.2349

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNN.2349

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845930

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

30 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNN.2349

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

21 January 2018

1 reference

PubMed

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

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NN.2349

1 reference

29 July 2017

1 reference

29 July 2017

1 reference