Alzheimer’s Disease-Associated SNP rs708727 in SLC41A1 May Increase Risk for Parkinson’s Disease: Report from Enlarged Slovak Study

Mutation Analysis of Seven SLC Family Transporters for Early-onset Parkinson's Disease in Chinese Population

(2021) ChunYu Li et al.   NEUROBIOLOGY OF AGING

Kir6.2 is essential to maintain neurite features by modulating PM20D1-reduced mitochondrial ATP generation

(2021) Nanshan Song et al.   Redox Biology

NIPA2 regulates osteoblast function by modulating mitophagy in type 2 diabetes osteoporosis

(2020) Wei Zhao et al.   Scientific Reports

Neurodegenerative Diseases – Is Metabolic Deficiency the Root Cause?

(2020) Vignayanandam Ravindernath Muddapu et al.   Frontiers in Neuroscience

Longitudinal data in peripheral blood confirm that PM20D1 is a quantitative trait locus (QTL) for Alzheimer’s disease and implicate its dynamic role in disease progression

(2020) Qi Wang et al.   Clinical Epigenetics

Differentially methylated DNA regions in early childhood wheezing: An epigenome-wide study using saliva

(2019) Maja Popovic et al.   PEDIATRIC ALLERGY AND IMMUNOLOGY

SNPs rs11240569, rs708727, and rs823156 in SLC41A1 Do Not Discriminate Between Slovak Patients with Idiopathic Parkinson’s Disease and Healthy Controls: Statistics and Machine-Learning Evidence

(2019) Michal Cibulka et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Magnesium-Induced Cell Survival Is Dependent on TRPM7 Expression and Function

(2019) Yuyang Sun et al.   MOLECULAR NEUROBIOLOGY

Investigating the energy crisis in Alzheimer disease using transcriptome study

(2019) S. Akila Parvathy Dharshini et al.   Scientific Reports

PM20D1 is a quantitative trait locus associated with Alzheimer’s disease

(2018) Jose V. Sanchez-Mut et al.   NATURE MEDICINE

Effects of MgSO 4 and magnesium transporters on 6-hydroxydopamine-induced SH-SY5Y cells

(2017) Ling Lin et al.   LIFE SCIENCES

5-LOX in Alzheimer’s Disease: Potential Serum Marker and In Vitro Evidences for Rescue of Neurotoxicity by Its Inhibitor YWCS

(2017) Shashank Shekhar et al.   MOLECULAR NEUROBIOLOGY

Associations of rs823128, rs1572931, and rs823156 polymorphisms with reduced Parkinson’s disease risks

(2017) Ye Bai et al.   NEUROREPORT

Overexpression of Na+/Mg2+ exchanger SLC41A1 attenuates pro-survival signaling

(2017) Gerhard Sponder et al.   Oncotarget

Differential methylation at MHC in CD4+ T cells is associated with multiple sclerosis independently of HLA-DRB1

(2017) Vicki E. Maltby et al.   Clinical Epigenetics

How Native and Alien Metal Cations Bind ATP: Implications for Lithium as a Therapeutic Agent

(2017) Todor Dudev et al.   Scientific Reports

PARK16is associated with PD in the Malaysian population

(2016) Aroma Agape Gopalai et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

The Secreted Enzyme PM20D1 Regulates Lipidated Amino Acid Uncouplers of Mitochondria

(2016) Jonathan Z. Long et al.   CELL

Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population

(2016) Faranak Madadi et al.   Genetic Testing and Molecular Biomarkers

PARK16 polymorphisms, interaction with smoking, and sporadic Parkinson's disease in Japan

(2016) Yoshihiro Miyake et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Uncoupling Mitochondrial Respiration for Diabesity

(2016) James W. Larrick et al.   REJUVENATION RESEARCH

Mitochondrial Mg2+ homeostasis decides cellular energy metabolism and vulnerability to stress

(2016) Ryu Yamanaka et al.   Scientific Reports

Genetic analysis ofSLC41A1in Chinese Parkinson's disease patients

(2015) Ling Wang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Machine Learning in Medicine

(2015) R. C. Deo   CIRCULATION

Fine mapping and resequencing of the PARK16 locus in Parkinson’s disease

(2015) Lasse Pihlstrøm et al.   JOURNAL OF HUMAN GENETICS

Insulin Modulates the Na+/Mg2+ Exchanger SLC41A1 and Influences Mg2+ Efflux from Intracellular Stores in Transgenic HEK293 Cells

(2015) Lucia Mastrototaro et al.   JOURNAL OF NUTRITION

Variant R244H in Na+/Mg2+ exchanger SLC41A1 in Taiwanese Parkinson's disease is associated with loss of Mg2+ efflux function

(2014) Chih-Hsin Lin et al.   PARKINSONISM & RELATED DISORDERS

Energy Failure

(2013) Divya Pathak et al.   ANNALS OF NEUROLOGY

Alzheimer's disease and Parkinson's disease genome-wide association study top hits and risk of Parkinson's disease in Korean population

(2013) Sun Ju Chung et al.   NEUROBIOLOGY OF AGING

Protection of dopaminergic neurons by 5-lipoxygenase inhibitor

(2013) Kai-Hsiang Kang et al.   NEUROPHARMACOLOGY

Substitution p.A350V in Na+/Mg2+ Exchanger SLC41A1, Potentially Associated with Parkinson's Disease, Is a Gain-of-Function Mutation

(2013) Martin Kolisek et al.   PLoS One

Cognitive Impairment and Dementia in Parkinson’s Disease: Clinical Features, Diagnosis, and Management

(2012) Joana Meireles et al.   Frontiers in Neurology

Association of GWAS loci with PD in China

(2011) Xue-Li Chang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Human gene SLC41A1 encodes for the Na+/Mg2+ exchanger

(2011) Martin Kolisek et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

Lewy- and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important?

(2011) Y. Compta et al.   BRAIN

Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease

(2011) Ignacio F. Mata et al.   MOVEMENT DISORDERS

An association between the PARK16 locus and Parkinson’s disease in a cohort from eastern China

(2011) Ya-Ping Yan et al.   PARKINSONISM & RELATED DISORDERS

The Interplay Between Mitochondrial Dynamics and Mitophagy

(2010) Gilad Twig et al.   ANTIOXIDANTS & REDOX SIGNALING

N-Acyl amino acids and N-acyl neurotransmitter conjugates: neuromodulators and probes for new drug targets

(2010) Mark Connor et al.   BRITISH JOURNAL OF PHARMACOLOGY

Genetic variability at the PARK16 locus

(2010) Arianna Tucci et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genome-wide association study reveals genetic risk underlying Parkinson's disease

(2009) Javier Simón-Sánchez et al.   NATURE GENETICS

Interpretation of Genetic Association Studies: Markers with Replicated Highly Significant Odds Ratios May Be Poor Classifiers

(2009) Johanna Jakobsdottir et al.   PLoS Genetics

SLC41A1 Is a Novel Mammalian Mg2+Carrier

(2008) Martin Kolisek et al.   JOURNAL OF BIOLOGICAL CHEMISTRY