Ion channel phosphorylopathy: a link between genomic variation and human disease.

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Identification of drug targets related to the induction of ventricular tachyarrhythmia through a systems chemical biology approach.Isoform-specific dynamic translocation of PKC by α1-adrenoceptor stimulation in live cells.Roles of PKC Isoforms in PMA-Induced Modulation of the hERG Channel (Kv11.1).

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Ion channel phosphorylopathy: a link between genomic variation and human disease.

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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Ion channel phosphorylopathy: a link between genomic variation and human disease.

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Ion channel phosphorylopathy: a link between genomic variation and human disease.

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Ion channel phosphorylopathy: a link between genomic variation and human disease.

@en

Ion channel phosphorylopathy: a link between genomic variation and human disease.

@nl

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Ion channel phosphorylopathy: a link between genomic variation and human disease.

@en

Ion channel phosphorylopathy: a link between genomic variation and human disease.

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P1476

Ion channel phosphorylopathy: a link between genomic variation and human disease.

@en

P2093

Saverio Gentile

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

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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

The protein kinase complement of the human genome

Rac GTPase signaling through the PP5 protein phosphatase

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

Rapid signaling at the plasma membrane by a nuclear receptor for thyroid hormone

Modulation of rat erg1, erg2, erg3 and HERG K+ currents by thyrotropin-releasing hormone in anterior pituitary cells via the native signal cascade

Peptide and protein library screening defines optimal substrate motifs for AKT/PKB.

Structural basis of protein kinase C isoform function

Ion channel voltage sensors: structure, function, and pathophysiology.

Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2.

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1757-1761

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scholarly article

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10.1002/CMDC.201200236

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2012-08-24T00:00:00Z

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P5875

230748761

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P698

22927196

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Ion channel phosphorylopathy: a link between genomic variation and human disease.

about

P2860

P2860

Ion channel phosphorylopathy: a link between genomic variation and human disease.

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698