Open Access
| Numéro |
Med Sci (Paris)
Volume 38, Numéro 11, Novembre 2022
|
|
|---|---|---|
| Page(s) | 870 - 873 | |
| Section | Nouvelles | |
| DOI | https://doi.org/10.1051/medsci/2022134 | |
| Publié en ligne | 30 novembre 2022 | |
- Pappaccogli M, Di Monaco S, Warchol-Celinska E, et al. The European/international fibromuscular dysplasia registry and initiative (FEIRI)-clinical phenotypes and their predictors based on a cohort of 1 000 patients. Cardiovasc Res 2021; 117 : 950–9. [CrossRef] [PubMed] [Google Scholar]
- Kiando SR, Tucker NR, Castro-Vega LJet al. PHACTR1 is a genetic susceptibility locus for fibromuscular dysplasia supporting its complex genetic pattern of inheritance. PLoS Genet 2016 ; 12 : e1006367. [CrossRef] [PubMed] [Google Scholar]
- Gupta RM, Hadaya J, Trehan Aet al. A genetic variant associated with five vascular diseases is a distal regulator of endothelin-1 gene expression. Cell 2017 ; 170 : 522–33e15. [CrossRef] [PubMed] [Google Scholar]
- Georges A, Yang ML, Berrandou TE, et al. Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nat Commun 2021; 12 : 6031. [CrossRef] [PubMed] [Google Scholar]
- Bulik-Sullivan BK, Loh PR, Finucane HKet al. LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nat Genet 2015 ; 47 : 291–295. [CrossRef] [PubMed] [Google Scholar]
- Giambartolomei C, Vukcevic D, Schadt EEet al. Bayesian test for colocalisation between pairs of genetic association studies using summary statistics. PLoS Genet 2014 ; 10 : e1004383. [CrossRef] [PubMed] [Google Scholar]
- Wiezlak M, Diring J, Abella Jet al. G-actin regulates the shuttling and PP1 binding of the RPEL protein Phactr1 to control actomyosin assembly. J Cell Sci 2012 ; 125 : 5860–5872. [CrossRef] [PubMed] [Google Scholar]
- Au DT, Ying Z, Hernandez-Ochoa EOet al. LRP1 (low-density lipoprotein receptor-related protein 1) regulates smooth muscle contractility by modulating Ca2+ signaling and expression of cytoskeleton-related proteins. Arterioscler Thromb Vasc Biol 2018 ; 38 : 2651–2664. [CrossRef] [PubMed] [Google Scholar]
- Kobayashi Y, Hirawa N, Tabara Yet al. Mice lacking hypertension candidate gene ATP2B1 in vascular smooth muscle cells show significant blood pressure elevation. Hypertension 2012 ; 59 : 854–860. [CrossRef] [PubMed] [Google Scholar]
- Yang H, Ahn C, Shin EKet al. NCKX3 was compensated by calcium transporting genes and bone resorption in a NCKX3 KO mouse model. Mol Cell Endocrinol 2017 ; 454 : 93–102. [CrossRef] [PubMed] [Google Scholar]
Les statistiques affichées correspondent au cumul d'une part des vues des résumés de l'article et d'autre part des vues et téléchargements de l'article plein-texte (PDF, Full-HTML, ePub... selon les formats disponibles) sur la platefome Vision4Press.
Les statistiques sont disponibles avec un délai de 48 à 96 heures et sont mises à jour quotidiennement en semaine.
Le chargement des statistiques peut être long.