bioRxivBioinformaticsPreprint
New insights in Tibial muscular dystrophy revealed by protein-protein interaction networks
Abstract
1. Introduction 1. Introduction 2. Materials and Methods 3. Results and discussion 4. Conclusion Conflict of interest Reference Tibial muscular dystrophy (TMD; OMIM: #600334) or Udd myopathy is an autosomal dominant distal myopathy that shows a high prevalence in the Finnish population (Udd et al., 1991; Udd et al., 1993; Udd et al., 2005; Pollazzon et al., 2010), however, other cases in European countries have been reported as in France (de Seze et al., 1998), Belgium (Van den Bergh et al., 2003), Italy (Pollazzon et al., 2010), and Spain (Hackman et al., 2008).\n\nTMD is caused by mutations (11-bp insertion-deletion) in the final exon, exon 364, in the TTN ...
- organism: human
- assay: protein structure
- research focus: gene regulatory network inference
- approach: statistical model
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Human and zebrafish data corroborate gene x gene interactions in ameliorating Duchenne muscular dystrophy disease progression
Veronica J Vieland, Geremy T Lerma, … Robert Weiss·medRxiv·Nov 2, 2026
- Myofibrillar malformations that arise in mdx muscle fibers are driven by detyrosinated microtubules
A. Harriot, T. Altair-Morris, … C. Ward·bioRxiv·Mar 27, 2023
- System-level analysis of genes mutated in muscular dystrophies reveals a functional pattern associated with muscle weakness distribution
Ozan Özışık, Svetlana Gorokhova, … Anaı̈s Baudot·Scientific ReportsPeer-reviewed·May 16, 2024
- Dystrophin is a mechanical tension modulator
A. D. Hofemeier, M. Ristau, … T. Betz·bioRxiv·Dec 23, 2022
- Novel model of distal myopathy caused by the myosin rod mutation R1500P disrupts acto-myosin binding
Genevieve C. K. Wilson, Ada E. Buvoli, … Leslie Anne Leinwand·bioRxiv·Sep 8, 2019
- EMILIN1 emerges as a TGFβ/SETDB1-regulated secreted biomarker in Duchenne Muscular Dystrophy
Maeva Zamperoni, Laura Muraine, … Slimane Ait‐Si‐Ali·Cell Death and DiseasePeer-reviewed·May 9, 2026