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New Strategies for the Treatment of Phenylketonuria (PKU)Phenylketonuria: translating research into novel therapiesTreating inborn errors of liver metabolism with stem cells: current clinical developmentPhenylalanine hydroxylase deficiency.Up to date knowledge on different treatment strategies for phenylketonuria.Hepatocytes from wild-type or heterozygous donors are equally effective in achieving successful therapeutic liver repopulation in murine phenylketonuria (PKU).In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria.
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description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
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scientific article published on 22 May 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Therapeutic liver repopulation for phenylketonuria.
@en
Therapeutic liver repopulation for phenylketonuria.
@nl
type
label
Therapeutic liver repopulation for phenylketonuria.
@en
Therapeutic liver repopulation for phenylketonuria.
@nl
prefLabel
Therapeutic liver repopulation for phenylketonuria.
@en
Therapeutic liver repopulation for phenylketonuria.
@nl
P2860
P1476
Therapeutic liver repopulation for phenylketonuria.
@en
P2093
Cary O Harding
K M Gibson
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P2888
P304
P356
10.1007/S10545-010-9099-1
P577
2010-05-22T00:00:00Z