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Modulation of the endoplasmic reticulum–mitochondria interface in Alzheimer’s disease and related models

Proceedings of the National Academy of Sciences - PNAS, 2013-05, Vol.110 (19), p.7916-7921

2013

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Parkinson's disease: A genetic perspective

The FEBS journal, 2008-04, Vol.275 (7), p.1377-1383

2008

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Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden

Neurobiology of aging, 2016-09, Vol.45 (212.e5), p.212.e5-212.e11

2016

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Genetic Variations and mRNA Expression of NRF2 in Parkinson’s Disease

Parkinson's disease, 2017-01, Vol.2017, p.4020198-7

2017

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Adh1 and Adh1/ 4 knockout mice as possible rodent models for presymptomatic Parkinson's disease

Behavioural brain research, 2012-02, Vol.227 (1), p.252-257

2012

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Glucocerebrosidase variant T369M is not a risk factor for Parkinson’s disease in Sweden

Neuroscience letters, 2022-07, Vol.784, p.136767-136767, Article 136767

2022

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Effects of a full-body electrostimulation garment application in a cohort of subjects with cerebral palsy, multiple sclerosis, and stroke on upper motor neuron syndrome symptoms

Biomedizinische Technik, 2024-02, Vol.69 (1), p.49

2024

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High and complementary expression patterns of alcohol and aldehyde dehydrogenases in the gastrointestinal tract

The FEBS journal, 2007-03, Vol.274 (5), p.1212-1223

2007

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LRRK2 expression linked to dopamine-innervated areas

Annals of neurology, 2006-04, Vol.59 (4), p.714-719

2006

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Possible Involvement of a Mitochondrial Translation Initiation Factor 3 Variant Causing Decreased mRNA Levels in Parkinson's Disease

Parkinson's disease, 2010-01, Vol.2010, p.491751-5

2010

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Parkinson's disease: Exit toxins, enter genetics

Progress in neurobiology, 2010-02, Vol.90 (2), p.146-156

2010

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P2‐027: IDENTIFICATION OF A SORL1 MUTATION IN A FAMILY WITH ALZHEIMER DISEASE USING WHOLE EXOME SEQUENCING

Alzheimer's & dementia, 2014-07, Vol.10 (4S_Part_12), p.P480-P480

2014

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IDENTIFICATION OF A SORL1 MUTATION IN A FAMILY WITH ALZHEIMER DISEASE USING WHOLE EXOME SEQUENCING

Alzheimer's & dementia, 2014-07, Vol.10 (4), p.P480-P480

2014

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Expression of multi-drug resistance 1 mRNA in human and rodent tissues: reduced levels in Parkinson patients

Cell and tissue research, 2008-11, Vol.334 (2), p.179-185

2008

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Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease

Neuroscience letters, 2012-07, Vol.522 (1), p.30-35

2012

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Variations of the CAG trinucleotide repeat in DNA polymerase gamma ( POLG1) is associated with Parkinson's disease in Sweden

Neuroscience letters, 2010-11, Vol.485 (2), p.117-120

2010

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Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease

The FASEB journal, 2011-04, Vol.25 (4), p.1345-1352

2011

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Cerebellar α-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material

The FASEB journal, 2008-10, Vol.22 (10), p.3509-3514

2008

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Association of a polymorphism in the ABCB1 gene with Parkinson's disease

Parkinsonism & related disorders, 2009-07, Vol.15 (6), p.422-424

2009

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Tissue- and species-specific expression patterns of class I, III, and IV Adh and Aldh1 mRNAs in rodent embryos

Cell and tissue research, 2005-11, Vol.322 (2), p.227-236

2005

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Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration

European journal of human genetics : EJHG, 2013-11, Vol.21 (11), p.1260-1265

2013

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Genetic studies of the protein kinase AKT1 in Parkinson's disease

Neuroscience letters, 2011-08, Vol.501 (1), p.41-44

2011

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Modeling Parkinson's disease genetics: Altered function of the dopamine system in Adh4 knockout mice

Behavioural brain research, 2011-03, Vol.217 (2), p.439-445

2011

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Lrrk2 and α-synuclein are co-regulated in rodent striatum

Molecular and cellular neuroscience, 2008-11, Vol.39 (4), p.586-591

2008

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Modulation of the endoplasmic reticulum–mitochondria interface in Alzheimer’s disease and related models

Parkinson's disease: A genetic perspective

Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden

Genetic Variations and mRNA Expression of NRF2 in Parkinson’s Disease

Adh1 and Adh1/ 4 knockout mice as possible rodent models for presymptomatic Parkinson's disease

Dopaminergic neuronal loss, reduced neurite complexity and autophagic abnormalities in transgenic mice expressing G2019S mutant LRRK2

Glucocerebrosidase variant T369M is not a risk factor for Parkinson’s disease in Sweden

Effects of a full-body electrostimulation garment application in a cohort of subjects with cerebral palsy, multiple sclerosis, and stroke on upper motor neuron syndrome symptoms

High and complementary expression patterns of alcohol and aldehyde dehydrogenases in the gastrointestinal tract

LRRK2 expression linked to dopamine-innervated areas

Possible Involvement of a Mitochondrial Translation Initiation Factor 3 Variant Causing Decreased mRNA Levels in Parkinson's Disease

Parkinson's disease: Exit toxins, enter genetics

P2‐027: IDENTIFICATION OF A SORL1 MUTATION IN A FAMILY WITH ALZHEIMER DISEASE USING WHOLE EXOME SEQUENCING

IDENTIFICATION OF A SORL1 MUTATION IN A FAMILY WITH ALZHEIMER DISEASE USING WHOLE EXOME SEQUENCING

Expression of multi-drug resistance 1 mRNA in human and rodent tissues: reduced levels in Parkinson patients

Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease

Variations of the CAG trinucleotide repeat in DNA polymerase gamma ( POLG1) is associated with Parkinson's disease in Sweden

Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease

Cerebellar α-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material

Association of a polymorphism in the ABCB1 gene with Parkinson's disease

Tissue- and species-specific expression patterns of class I, III, and IV Adh and Aldh1 mRNAs in rodent embryos

Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration

Genetic studies of the protein kinase AKT1 in Parkinson's disease

Modeling Parkinson's disease genetics: Altered function of the dopamine system in Adh4 knockout mice

Lrrk2 and α-synuclein are co-regulated in rodent striatum

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