Acute regulated expression of pendrin in human urinary exosomes.

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Acute regulated expression of pendrin in human urinary exosomes.

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http://www.wikidata.org/entity/Q38627272

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

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2017年論文

@zh-hk

2017年論文

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2017年論文

@zh-tw

2017年论文

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2017年论文

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2017年论文

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Acute regulated expression of pendrin in human urinary exosomes.

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Acute regulated expression of pendrin in human urinary exosomes.

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Acute regulated expression of pendrin in human urinary exosomes.

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P1476

Acute regulated expression of pendrin in human urinary exosomes

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P2093

Carsten A Wagner

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Daniel G Fuster

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Ganesh Pathare

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Nilufar Mohebbi

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Thomas J Neuhaus

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P2860

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

The Pendred syndrome gene encodes a chloride-iodide transport protein

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

Identification and proteomic profiling of exosomes in human urine

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

Large-scale proteomics and phosphoproteomics of urinary exosomes

Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion

Bro1 is an endosome-associated protein that functions in the MVB pathway in Saccharomyces cerevisiae.

Renal tubular acidosis: the clinical entity

Regulation of the apical Cl-/HCO-3 exchanger pendrin in rat cortical collecting duct in metabolic acidosis

P2888

s00424-017-2049-0

P304

427-438

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P31

scholarly article

P356

10.1007/S00424-017-2049-0

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P433

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P478

470

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P50

Nasser Dhayat

Lydie Cheval

P577

2017-08-12T00:00:00Z

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P6179

1091160639

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P698

28803436

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