Drosophila models to study causative genes for human rare intractable neurological diseases

This publication has 201 references indexed in Scilit:

• ALKBH4-dependent demethylation of actin regulates actomyosin dynamics
  Nature Communications, 2013
• Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase
  The American Journal of Human Genetics, 2013
• Generation of the Sotos syndrome deletion in mice
  Mammalian Genome, 2012
• Pattern of ubiquilin pathology in ALS and FTLD indicates presence of C9ORF72 hexanucleotide expansion
  Acta Neuropathologica, 2012
• Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly
  Molecular Syndromology, 2012
• Expression of human FUS protein in Drosophila leads to progressive neurodegeneration
  Protein & Cell, 2011
• Charcot‐marie‐tooth disease subtypes and genetic testing strategies
  Annals of Neurology, 2011
• Sensory Functions for Degenerin/Epithelial Sodium Channels (DEG/ENaC)
  2011
• Deleterious Variants of FIG4, a Phosphoinositide Phosphatase, in Patients with ALS
  The American Journal of Human Genetics, 2009
• TDP‐43 A315T mutation in familial motor neuron disease
  Annals of Neurology, 2008