AKT Signaling Modifies the Balance between Cell Proliferation and Migration in Neural Crest Cells from Patients Affected with Bosma Arhinia and Microphthalmia Syndrome

Lignende værker

• FSHD type 2 and Bosma arhinia microphthalmia syndrome: Two faces of the same mutation
  af: Mul, Karlien, et al.
  Udgivet: (2018)
• SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome
  af: Shaw, Natalie D, et al.
  Udgivet: (2017)
• SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain
  af: Lemmers, Richard J L F, et al.
  Udgivet: (2019)
• Analysis of the 4q35 chromatin organization reveals distinct long-range interactions in patients affected with Facio-Scapulo-Humeral Dystrophy
  af: Gaillard, Marie-Cécile, et al.
  Udgivet: (2019)
• Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells
  af: Mazaleyrat, Kilian, et al.
  Udgivet: (2020)