Bicistronic CACNA1A Gene Expression in Neurons Derived from Spinocerebellar Ataxia Type 6 Patient-Induced Pluripotent Stem Cells.

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Self-Organized Cerebellar Tissue from Human Pluripotent Stem Cells and Disease Modeling with Patient-Derived iPSCs.

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Bicistronic CACNA1A Gene Expression in Neurons Derived from Spinocerebellar Ataxia Type 6 Patient-Induced Pluripotent Stem Cells.

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2017年の論文

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2017年学术文章

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2017年学术文章

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Bicistronic CACNA1A Gene Expre ...... nduced Pluripotent Stem Cells.

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Bicistronic CACNA1A Gene Expre ...... nduced Pluripotent Stem Cells.

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Bicistronic CACNA1A Gene Expre ...... nduced Pluripotent Stem Cells.

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Bicistronic CACNA1A Gene Expre ...... nduced Pluripotent Stem Cells.

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Bicistronic CACNA1A Gene Expre ...... nduced Pluripotent Stem Cells.

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Bicistronic CACNA1A Gene Expre ...... nduced Pluripotent Stem Cells.

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P1476

Bicistronic CACNA1A Gene Expre ...... Induced Pluripotent Stem Cells

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P2093

Andreas Eigentler

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Carlo Bavassano

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Georg Dechant

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Gerald J Obermair

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Ruslan Stanika

http://www.w3.org/2001/XMLSchema#string

Sylvia Boesch

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P2860

Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function

C-termini of P/Q-type Ca2+ channel alpha1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.

Chronic Glutamate Toxicity in Neurodegenerative Diseases-What is the Evidence?

Capture of neuroepithelial-like stem cells from pluripotent stem cells provides a versatile system for in vitro production of human neurons

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling

The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes.

Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6

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1612-1625

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scholarly article

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10.1089/SCD.2017.0085

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Bicistronic CACNA1A Gene Expression in Neurons Derived from Spinocerebellar Ataxia Type 6 Patient-Induced Pluripotent Stem Cells.

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P2860

P2860

Bicistronic CACNA1A Gene Expression in Neurons Derived from Spinocerebellar Ataxia Type 6 Patient-Induced Pluripotent Stem Cells.

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