(Q37039473)

17 August 2017

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title

Mutations in LRRK2 as a cause of Parkinson's disease (English)

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17 August 2017

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Benoit I Giasson

1

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17 August 2017

Vivianna M Van Deerlin

series ordinal

2

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17 August 2017

publication date

5 December 2007

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17 August 2017

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17 August 2017

volume

16

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17 August 2017

issue

1

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17 August 2017

page(s)

99-105

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Diagnostic criteria for Parkinson disease

17 August 2017

cites work

1 reference

The substantia nigra of the human brain. II. Patterns of loss of dopamine-containing neurons in Parkinson's disease

21 January 2018

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Nosology of Parkinson's disease: looking for the way out of a quagmire

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Staging of brain pathology related to sporadic Parkinson's disease

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Alpha-synuclein and neurodegenerative diseases

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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

21 January 2018

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Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity

21 January 2018

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The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity

21 January 2018

1 reference

Biochemical and pathological characterization of Lrrk2.

21 January 2018

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Localization of LRRK2 to membranous and vesicular structures in mammalian brain

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Direct binding of alpha-actinin enhances TRPP3 channel activity

21 January 2018

1 reference

Localization of Parkinson's disease-associated LRRK2 in normal and pathological human brain.

21 January 2018

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Expression and localization of Parkinson's disease-associated leucine-rich repeat kinase 2 in the mouse brain.

21 January 2018

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Anatomical localization of leucine-rich repeat kinase 2 in mouse brain

21 January 2018

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

21 January 2018

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Distribution of PINK1 and LRRK2 in rat and mouse brain

21 January 2018

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LRRK2 expression linked to dopamine-innervated areas

21 January 2018

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LRRK2 is expressed in areas affected by Parkinson's disease in the adult mouse brain.

21 January 2018

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Kinase activity of mutant LRRK2 mediates neuronal toxicity

21 January 2018

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Parkinson's disease-associated mutations in LRRK2 link enhanced GTP-binding and kinase activities to neuronal toxicity

21 January 2018

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LRRK2 phosphorylates moesin at threonine-558: characterization of how Parkinson's disease mutants affect kinase activity

21 January 2018

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The R1441C mutation of LRRK2 disrupts GTP hydrolysis

21 January 2018

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GTP binding is essential to the protein kinase activity of LRRK2, a causative gene product for familial Parkinson's disease

21 January 2018

1 reference

The familial Parkinsonism gene LRRK2 regulates neurite process morphology

21 January 2018

1 reference

LRRK2 in Parkinson's disease: protein domains and functional insights

21 January 2018

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LRRK2: a common pathway for parkinsonism, pathogenesis and prevention?

21 January 2018

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Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

21 January 2018

1 reference

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

21 January 2018

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LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

21 January 2018

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The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

21 January 2018

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Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

21 January 2018

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Clinical features of LRRK2-associated Parkinson's disease in central Norway

21 January 2018

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Neuropathology of Parkinson's disease associated with the LRRK2 Ile1371Val mutation.

21 January 2018

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LRRK2 mutations are not common in Alzheimer's disease.

21 January 2018

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Analysis of the LRRK2 G2019S mutation in Alzheimer Disease

21 January 2018

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G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy.

21 January 2018

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Lrrk2 and Lewy body disease

21 January 2018

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G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies

21 January 2018

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Parkinsonism, Lrrk2 G2019S, and tau neuropathology

21 January 2018

1 reference

An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.

21 January 2018

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Autosomal dominant parkinsonism associated with variable synuclein and tau pathology

21 January 2018

1 reference

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

21 January 2018

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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

21 January 2018

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Leucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degeneration

21 January 2018

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Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

21 January 2018

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LRRK2 gene in Parkinson disease: Mutation analysis and case control association study

21 January 2018

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Lrrk2 R1441 substitution and progressive supranuclear palsy

21 January 2018

1 reference

LRRK2 mutations in Parkinson disease

21 January 2018

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Clinical Heterogeneity of the LRRK2 G2019S Mutation

21 January 2018

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LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

21 January 2018

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

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000109764

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17 August 2017

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