Related references
Note: Only part of the references are listed.Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis
Elisa Teyssou et al.
NEUROBIOLOGY OF AGING (2021)
ANXA11 mutations in ALS cause dysregulation of calcium homeostasis and stress granule dynamics
Minyeop Nahm et al.
SCIENCE TRANSLATIONAL MEDICINE (2020)
RNA Granules Hitchhike on Lysosomes for Long-Distance Transport, Using Annexin A11 as a Molecular Tether
Ya-Cheng Liao et al.
CELL (2019)
ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia
Kang Zhang et al.
NEUROLOGY-GENETICS (2018)
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis
Bradley N. Smith et al.
SCIENCE TRANSLATIONAL MEDICINE (2017)
Annexin A11 in disease
Jiasheng Wang et al.
CLINICA CHIMICA ACTA (2014)
A harmonized classification system for FTLD-TDP pathology
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2011)
PrDOS: prediction of disordered protein regions from amino acid sequence
Takashi Ishida et al.
NUCLEIC ACIDS RESEARCH (2007)