Human genetics (TRPM7)

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36095216 PDF 2022. A TRPM7 mutation linked to familial trigeminal neuralgia: Omega current and hyperexcitability of trigeminal ganglion neurons.Template:36095216
35561741 PDF 2023. Possible role for rare TRPM7 variants in patients with hypomagnesaemia with secondary hypocalcaemia.Template:35561741
31423533 PDF 2020. Genetic variants in TRPM7 associated with unexplained stillbirth modify ion channel function.Template:31423533
18227801 PDF 2008. Hereditary etiologies of hypomagnesemia.Template:18227801
19149903 PDF 2009. 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.Template:19149903
16051700 PDF 2005. A TRPM7 variant shows altered sensitivity to magnesium that may contribute to the pathogenesis of two Guamanian neurodegenerative disorders.Template:16051700
18448590 PDF 2008. Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel.Template:18448590
26273099 PDF 2015. Hypomagnesemia and functional hypoparathyroidism due to novel mutations in the Mg-channel TRPM6.Template:26273099
25313976 PDF 2014. X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia disease: a combined immune deficiency with magnesium defect.Template:25313976
31207912 PDF 2019. Magnesium Supplement and the 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome: A Potential Treatment?Template:31207912
34784661 PDF 2021. Hereditary kidney diseases associated with hypomagnesemia.Template:34784661
29344503 PDF 2017. Genetics of Magnesium Disorders.Template:29344503
25733456 PDF 2015. Genetic variations in magnesium-related ion channels may affect diabetes risk among African American and Hispanic American women.Template:25733456
24322525 PDF 2013. Dietary magnesium and genetic interactions in diabetes and related risk factors: a brief overview of current knowledge.Template:24322525
20700443 PDF 2010. Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.Template:20700443
34578838 PDF 2021. The Dietary Approach to the Treatment of the Rare Genetic Tubulopathies Gitelman's and Bartter's Syndromes.Template:34578838
33159963 PDF 2021. Targeting fibroblast growth factor 23-responsive pathways uncovers controlling genes in kidney mineral metabolism.Template:33159963
32302086 PDF 2021. Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation.Template:32302086
31993563 PDF 2019. Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid.Template:31993563
27234911 PDF 2017. Genetic causes of hypomagnesemia, a clinical overview.Template:27234911
26759217 PDF 2016. A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report.Template:26759217
18818955 PDF 2009. Inherited forms of renal hypomagnesemia: an update.Template:18818955

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