Quantification of ATP7B Protein in Dried Blood Spots by Peptide Immuno-SRM as a Potential Screen for Wilson's Disease.

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Quantification of ATP7B Protein in Dried Blood Spots by Peptide Immuno-SRM as a Potential Screen for Wilson's Disease.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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Quantification of ATP7B Protei ...... l Screen for Wilson's Disease.

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Quantification of ATP7B Protei ...... l Screen for Wilson's Disease.

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Quantification of ATP7B Protei ...... l Screen for Wilson's Disease.

@en

Quantification of ATP7B Protei ...... l Screen for Wilson's Disease.

@nl

prefLabel

Quantification of ATP7B Protei ...... l Screen for Wilson's Disease.

@en

Quantification of ATP7B Protei ...... l Screen for Wilson's Disease.

@nl

P1476

Quantification of ATP7B Protei ...... al Screen for Wilson's Disease

@en

P2093

Amanda G Paulovich

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Han-Wook Yoo

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Jeffrey R Whiteaker

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Lei Zhao

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Sunhee Jung

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P2860

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

The nonsense-mediated decay RNA surveillance pathway

Developing multiplexed assays for troponin I and interleukin-33 in plasma by peptide immunoaffinity enrichment and targeted mass spectrometry

Skyline: an open source document editor for creating and analyzing targeted proteomics experiments

Quantification of thyroglobulin, a low-abundance serum protein, by immunoaffinity peptide enrichment and tandem mass spectrometry

Truncating mutations in the Wilson disease gene ATP7B are associated with very low serum ceruloplasmin oxidase activity and an early onset of Wilson disease.

Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation.

An automated and multiplexed method for high throughput peptide immunoaffinity enrichment and multiple reaction monitoring mass spectrometry-based quantification of protein biomarkers.

Human copper-transporting ATPase ATP7B (the Wilson's disease protein): biochemical properties and regulation.

Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).

P304

862-871

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P31

scholarly article

P356

10.1021/ACS.JPROTEOME.6B00828

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P433

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P478

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P50

Si Houn Hahn

P577

2016-12-09T00:00:00Z

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P698

27935710

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P932

5574172

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