Associated Papers
Reviewing critical TRPM2 variants through a structure-function lens.
Tóth ÁV et al.
Journal of Biotechnology, 2024
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
Calender A et al.
Bmc Medical Genomics, 2018
29510755 (PubMed )
Supplement: 12920_2018_338_MOESM6_ESM.xlsx › T1
Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.
Molnár J et al.
Plos One, 2016
26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › polymorphism
TRPM2, a Susceptibility Gene for Bipolar Disorder, Regulates Glycogen Synthase Kinase-3 Activity in the Brain.
Jang Y et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2015
Role of an N-terminal splice segment in the activation of the cation channel TRPM2 by ADP-ribose and hydrogen peroxide.
Kühn FJ et al.
Neurochemical Research, 2009
TRPM2 variants and bipolar disorder risk: confirmation in a family-based association study.
Xu C et al.
Bipolar Disorders, 2009
Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22.3.
McQuillin A et al.
Molecular Psychiatry, 2006
Extended haplotype association study in Crohn's disease identifies a novel, Ashkenazi Jewish-specific missense mutation in the NF-κB pathway gene, HEATR3.
Zhang W et al.
Genes and Immunity, 0
23615072 (PubMed )
Supplement: NIHMS458938-supplement-1.xls › Supplemental_table_3
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