G418-mediated ribosomal read-through of a nonsense mutation causing autosomal recessive proximal renal tubular acidosis.
about
NBCe1 as a model carrier for understanding the structure-function properties of Na⁺ -coupled SLC4 transporters in health and disease.Aminoglycoside-Induced Premature Stop Codon Read-Through of Mucopolysaccharidosis Type I Patient Q70X and W402X Mutations in Cultured Cells.Translational read-through of a nonsense mutation causing Bartter syndrome.Proximal renal tubular acidosis mediated by mutations in NBCe1-A: unraveling the transporter's structure-functional properties.
P2860
G418-mediated ribosomal read-through of a nonsense mutation causing autosomal recessive proximal renal tubular acidosis.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 09 July 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
G418-mediated ribosomal read-t ...... oximal renal tubular acidosis.
@en
G418-mediated ribosomal read-t ...... oximal renal tubular acidosis.
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type
label
G418-mediated ribosomal read-t ...... oximal renal tubular acidosis.
@en
G418-mediated ribosomal read-t ...... oximal renal tubular acidosis.
@nl
prefLabel
G418-mediated ribosomal read-t ...... oximal renal tubular acidosis.
@en
G418-mediated ribosomal read-t ...... oximal renal tubular acidosis.
@nl
P2093
P2860
P1476
G418-mediated ribosomal read-t ...... roximal renal tubular acidosis
@en
P2093
Alexander Pushkin
Debra Newman
Natalia Abuladze
Nicholas Orozco
Pakan Sassani
Rustam Azimov
Weixin Liu
P2860
P304
P356
10.1152/AJPRENAL.00015.2008
P577
2008-07-09T00:00:00Z