Role of Gα(olf) in familial and sporadic adult-onset primary dystonia

Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis

(2012) Gavin Charlesworth et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in CIZ1 cause adult onset primary cervical dystonia

(2012) Jianfeng Xiao et al.   ANNALS OF NEUROLOGY

Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia

(2012) Joshua Hersheson et al.   ANNALS OF NEUROLOGY

Phenotypic overlap in familial and sporadic primary adult-onset extracranial dystonia

(2012) Giovanni Defazio et al.   JOURNAL OF NEUROLOGY

G olf Mutation Allows Parsing the Role of cAMP-Dependent and Extracellular Signal-Regulated Kinase-Dependent Signaling in L-3,4-Dihydroxyphenylalanine-Induced Dyskinesia

(2012) C. Alcacer et al.   JOURNAL OF NEUROSCIENCE

DYT7gene locus for cervical dystonia on chromosome 18p is questionable

(2012) Pia Winter et al.   MOVEMENT DISORDERS

Mutations in GNAL cause primary torsion dystonia

(2012) Tania Fuchs et al.   NATURE GENETICS

Phosphorylation of histone H3 Ser10 establishes a hierarchy for subsequent intramolecular modification events

(2012) Stamatios Liokatis et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions

(2011) Xiaoming Liu et al.   HUMAN MUTATION

A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3

(2011) Nina Norgren et al.   NEUROGENETICS

An African–American family with dystonia

(2011) Andreas Puschmann et al.   PARKINSONISM & RELATED DISORDERS

Dystonia: phenomenology

(2011) Mark S. LeDoux   PARKINSONISM & RELATED DISORDERS

Myoclonus-dystonia in 18p deletion syndrome

(2010) Markus C. Kowarik et al.   MOVEMENT DISORDERS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

MutationTaster evaluates disease-causing potential of sequence alterations

(2010) Jana Marie Schwarz et al.   NATURE METHODS

Animal models of dystonia: Lessons from a mutant rat

(2010) Mark S. LeDoux   NEUROBIOLOGY OF DISEASE

Novel THAP1 sequence variants in primary dystonia

(2010) J. Xiao et al.   NEUROLOGY

Dystonia, autoimmune disease and cerebral white matter abnormalities in a patient with 18p deletion

(2009) Carla Graziadio et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

Characteristics of dystonia in the 18p deletion syndrome, including a new case

(2009) Anna G. Postma et al.   CLINICAL NEUROLOGY AND NEUROSURGERY

Cerebellothalamocortical Connectivity Regulates Penetrance in Dystonia

(2009) M. Argyelan et al.   JOURNAL OF NEUROSCIENCE

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia

(2009) Tania Fuchs et al.   NATURE GENETICS

Histone H3 Phosphorylation is Under the Opposite Tonic Control of Dopamine D2 and Adenosine A2A Receptors in Striatopallidal Neurons

(2009) Jesus Bertran-Gonzalez et al.   NEUROPSYCHOPHARMACOLOGY

The basal ganglia and cerebellum interact in the expression of dystonic movement

(2008) V. K. Neychev et al.   BRAIN

cAMP signaling induces rapid loss of histone H3 phosphorylation in mammary adenocarcinoma-derived cell lines

(2007) Pedro Rodriguez-Collazo et al.   EXPERIMENTAL CELL RESEARCH