In-depth Characterization of the Homodimerization Domain of the Transcription Factor THAP1 and Dystonia-Causing Mutations Therein

Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

(2016) Connie Marras et al.   MOVEMENT DISORDERS

Screening for rare sequence variants in theTHAP1gene in a primary dystonia cohort

(2013) Jeremy R.B. Newman et al.   MOVEMENT DISORDERS

Phenomenology and classification of dystonia: A consensus update

(2013) Alberto Albanese et al.   MOVEMENT DISORDERS

Genotype–phenotype correlations in THAP1 dystonia: Molecular foundations and description of new cases

(2012) Mark S. LeDoux et al.   PARKINSONISM & RELATED DISORDERS

Identification and functional analysis of novel THAP1 mutations

(2011) Katja Lohmann et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Performance of mutation pathogenicity prediction methods on missense variants

(2011) Janita Thusberg et al.   HUMAN MUTATION

Dimerization of the DYT6 dystonia protein, THAP1, requires residues within the coiled-coil domain

(2011) Cem Sengel et al.   JOURNAL OF NEUROCHEMISTRY

THAP1/DYT6 sequence variants in non-DYT1 early-onset primary dystonia in China and their effects on RNA expression

(2011) Fu Bo Cheng et al.   JOURNAL OF NEUROLOGY

Novel THAP1 gene mutations in patients with primary dystonia from Southwest China

(2011) Wei Song et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Truncating mutations in THAP1 define the nuclear localization signal

(2011) Alma Osmanovic et al.   MOVEMENT DISORDERS

Chemotrap-1: An Engineered Soluble Receptor That Blocks Chemokine-Induced Migration of Metastatic Cancer Cells In vivo

(2010) S. Lanati et al.   CANCER RESEARCH

Clinical and genetic evaluation of DYT1 and DYT6 primary dystonia in China

(2010) F. B. Cheng et al.   EUROPEAN JOURNAL OF NEUROLOGY

Prevalence of THAP1 sequence variants in German patients with primary dystonia

(2010) Anne S. Söhn et al.   MOVEMENT DISORDERS

Novel THAP1 sequence variants in primary dystonia

(2010) J. Xiao et al.   NEUROLOGY

THAP1 mutations (DYT6) are an additional cause of early-onset dystonia

(2010) H. Houlden et al.   NEUROLOGY

Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study

(2009) Susan B Bressman et al.   LANCET NEUROLOGY

GIGYF2 variants are not associated with Parkinson's disease in Italy

(2009) Monica Bonetti et al.   MOVEMENT DISORDERS

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

(2009) Tania Fuchs et al.   NATURE GENETICS

Ronin Is Essential for Embryogenesis and the Pluripotency of Mouse Embryonic Stem Cells

(2008) Marion Dejosez et al.   CELL