Associated Papers
Magnesium treatment increases gut microbiome synthesizing vitamin D and inhibiting colorectal cancer: results from a double-blind precision-based randomized placebo-controlled trial.
Sun E et al.
The American Journal of Clinical Nutrition, 2025
Whole-Genome Sequencing Reveals a Novel GATA2 Mutation in Lower-Grade Glioma: Bioinformatics Analysis of Functional and Therapeutic Implications.
Handoko et al.
Cancers, 2025
Ion channel mutations and cancer.
Cao X et al.
Biochemistry and Biophysics Reports, 2025
Zebrafish trpm7 mutants show reduced motility in free movement.
Watai K et al.
Development, Growth & Differentiation, 2024
Genetic forms of tauopathies: inherited causes and implications of Alzheimer's disease-like TAU pathology in primary and secondary tauopathies.
Langerscheidt F et al.
Journal of Neurology, 2024
Whole-exome sequencing identifies cancer-associated variants of the endo-lysosomal ion transport channels in the Saudi population.
Binobaid L et al.
Saudi Pharmaceutical Journal : Spj : the Official Publication of the Saudi Pharmaceutical Society, 2024
Roles of Intramolecular Interactions in the Regulation of TRP Channels.
Cai R et al.
Reviews of Physiology, Biochemistry and Pharmacology, 2023
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database.
Tunca C et al.
Human Mutation, 2020
Genetic variants in TRPM7 associated with unexplained stillbirth modify ion channel function.
Cartwright JH et al.
Human Molecular Genetics, 2020
FUS P525L mutation causing amyotrophic lateral sclerosis and movement disorders.
Zhou B et al.
Brain and Behavior, 2020
Postmortem Genetic Testing for Cardiac Ion Channelopathies in Stillbirths.
Munroe PB et al.
Circulation. Genomic and Precision Medicine, 2018
Exploring Missense Mutations in Tyrosine Kinases Implicated with Neurodegeneration.
Sami N et al.
Molecular Neurobiology, 2017
Function and regulation of TRPM7, as well as intracellular magnesium content, are altered in cells expressing ΔF508-CFTR and G551D-CFTR.
Huguet F et al.
Cellular and Molecular Life Sciences : Cmls, 2016
SLC41A1 and TRPM7 in magnesium homeostasis and genetic risk for Parkinson's disease.
Sturgeon M et al.
Journal of Neurology & Neuromedicine, 2016
The distinct genetic pattern of ALS in Turkey and novel mutations.
Özoğuz A et al.
Neurobiology of Aging, 2015
Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.
Holehouse AS et al.
Plos One, 2015
TRPM channels and magnesium in early embryonic development.
Komiya Y et al.
The International Journal of Developmental Biology, 2015
The association between single-nucleotide polymorphisms of TRPM7 gene and breast cancer in Han Population of Northeast China.
Shen B et al.
Medical Oncology (northwood, London, England), 2014
TRPM6 and TRPM7: A Mul-TRP-PLIK-cation of channel functions.
Runnels LW
Current Pharmaceutical Biotechnology, 2011
TRPM7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the Kii peninsula of Japan.
Hara K et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2010
Common genetic variants of the ion channel transient receptor potential membrane melastatin 6 and 7 (TRPM6 and TRPM7), magnesium intake, and risk of type 2 diabetes in women.
Song Y et al.
Bmc Medical Genetics, 2009
Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, Japan.
Tomiyama H et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2008
The contribution of mitochondrial dysfunction to a gene-environment model of Guamanian ALS and PD.
Lynch D et al.
Mitochondrion, 2008
The relation of magnesium and calcium intakes and a genetic polymorphism in the magnesium transporter to colorectal neoplasia risk.
Dai Q et al.
The American Journal of Clinical Nutrition, 2007
TRPM7 and TRPM2-Candidate susceptibility genes for Western Pacific ALS and PD?
Hermosura MC et al.
Biochimica Et Biophysica Acta, 2007
TRPM6 and TRPM7--Gatekeepers of human magnesium metabolism.
Schlingmann KP et al.
Biochimica Et Biophysica Acta, 2007
A TRPM7 variant shows altered sensitivity to magnesium that may contribute to the pathogenesis of two Guamanian neurodegenerative disorders.
Hermosura MC et al.
Proceedings of the National Academy of Sciences of the United States of America, 2005