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New overlapping and disease-specific genetic risk factors for rheumatoid arthritis & ankylosing spondylitis, 2026, Cabrera-Serrano et al
Identification of new overlapping and disease-specific genetic risk factors for rheumatoid arthritis and radiographic axial spondyloarthritis: a meta-analysis of three large European populations and functional characterization Abstract This study conducted a meta-analysis across three large...- hotblack
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- ankylosing spondylitis btn2a1 hmgn4 htt rheumatoid arthritis trim38 znf322
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- Forum: Other health news and research
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Dysfunction of Primary Cilium in Huntington’s Disease: How Mutant Huntingtin Disrupts This Cellular Signaling Hub, 2026, Churkina et al.
Dysfunction of Primary Cilium in Huntington’s Disease: How Mutant Huntingtin Disrupts This Cellular Signaling Hub Churkina, Aleksandra S; Shakhov, Anton S; Alieva, Irina B Primary cilia are solitary, antenna-like organelles that project from the surface of most vertebrate cells. They consist of...- SNT Gatchaman
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- extracellular matrix htt tgf-beta
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Genetics: Chromosome 4, HTT
From a discussion on the Eccentric Medium Spiny Neurons thread: DecodeME identified HTT as of interest.- Hutan
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- decodemehit genetics htt
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- Forum: Possible causes and predisposing factor discussion
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Genetics: Chromosome 1 RABGAP1L, GPR52, SERPINC1
From DecodeME Candidate Genes: RABGAP1L (Tier 1) • Protein: RAB GTPase-activating protein 1-like, also known as TBC1D18. UniProt. GeneCards. The allele that increases the risk of ME/CFS is associated with decreasing RABGAP1L gene expression. • Molecular function: GTP-hydrolysis activating...- Hutan
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- decodeme decodemehit genetics gpr52 htt rabgap1l serpinc1
- Replies: 43
- Forum: Possible causes and predisposing factor discussion