Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis

Genetic studies of amyotrophic lateral sclerosis: Controversies and perspectives

(2009) Ana Beleza-Meireles et al.   Amyotrophic Lateral Sclerosis

Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

(2009) C. Vance et al.   SCIENCE

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

(2009) T. J. Kwiatkowski et al.   SCIENCE

Influence of the M3-M4 intracellular domain upon nicotinic acetylcholine receptor assembly, targeting and function

(2008) S Kracun et al.   BRITISH JOURNAL OF PHARMACOLOGY

Common and rare variants in multifactorial susceptibility to common diseases

(2008) Walter Bodmer et al.   NATURE GENETICS

Natural history of young-adult amyotrophic lateral sclerosis

(2008) M. Sabatelli et al.   NEUROLOGY

Nonsynaptic Chemical Transmission Through Nicotinic Acetylcholine Receptors

(2008) Balázs Lendvai et al.   PHYSIOLOGICAL REVIEWS

TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

(2008) J. Sreedharan et al.   SCIENCE

Neuroprotection via nAChRs: the role of nAChRs in neurodegenerative disorders such as Alzheimer's and Parkinson's disease

(2007) Marina et al.   Frontiers in Bioscience-Landmark