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ASHIZAWA, TETSUO

One or more keywords matched the following items that are connected to ASHIZAWA, TETSUO

Item Type	Name
Academic Article	A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.
Academic Article	Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10.
Academic Article	Spinocerebellar ataxia type 10: disproportionate cerebellar symptoms among at-risk subjects induced by small amounts of alcohol.
Academic Article	Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity.
Academic Article	Ataxin 10 induces neuritogenesis via interaction with G-protein beta2 subunit.
Concept	MAP Kinase Signaling System
Concept	Phosphotransferases (Alcohol Group Acceptor)
Concept	Alcohol Dehydrogenase
Concept	Alcohol Drinking
Concept	Alcoholic Beverages
Concept	Extracellular Signal-Regulated MAP Kinases
Concept	Protein Kinase C-delta
Academic Article	Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3.
Academic Article	The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar ataxia type 3 pathogenesis.
Academic Article	Ataxia-telangiectasia - A historical review and a proposal for a new designation: ATM syndrome.
Academic Article	Genome Therapy of Myotonic Dystrophy Type 1 iPS Cells for Development of Autologous Stem Cell Therapy.
Academic Article	Body composition in Spinocerebellar ataxia type 3 and 10 patients: Comparative study with control group.
Academic Article	Therapeutic Genome Editing for Myotonic Dystrophy Type 1?Using CRISPR/Cas9.
Grant	Clinical Research Consortium for Spinocerebellar Ataxias
Grant	The 1st SCA Global Conference
Academic Article	Mutant huntingtin impairs PNKP and ATXN3, disrupting DNA repair and transcription.
Concept	Myotonin-Protein Kinase
Academic Article	Deficiency in classical nonhomologous end-joining-mediated repair of transcribed genes is linked to SCA3 pathogenesis.
Academic Article	Towards development of a statistical framework to evaluate myotonic dystrophy type 1 mRNA biomarkers in the context of a clinical trial.
Academic Article	Antisense oligonucleotide targeting DMPK in patients with myotonic dystrophy type 1: a multicentre, randomised, dose-escalation, placebo-controlled, phase 1/2a trial.
Academic Article	Correction: The Role of the Mammalian DNA End-processing Enzyme Polynucleotide Kinase 3'-Phosphatase in Spinocerebellar Ataxia Type 3 Pathogenesis.

Search Criteria

Phosphotransferases
Alcohol
Group
Acceptor