about
Functional Human and Murine Tissue-Engineered Liver Is Generated from Adult Stem/Progenitor Cells.Proof-of-Concept Gene Editing for the Murine Model of Inducible Arginase-1 DeficiencyLiver-specific knockout of arginase-1 leads to a profound phenotype similar to inducible whole body arginase-1 deficiency.An update on the use of benzoate, phenylacetate and phenylbutyrate ammonia scavengers for interrogating and modifying liver nitrogen metabolism and its implications in urea cycle disorders and liver disease.Profile of sodium phenylbutyrate granules for the treatment of urea-cycle disorders: patient perspectives.Transplantation of Gene-Edited Hepatocyte-like Cells Modestly Improves Survival of Arginase-1-Deficient Mice.
P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Arginase-1 deficiency.
@en
type
label
Arginase-1 deficiency.
@en
prefLabel
Arginase-1 deficiency.
@en
P2093
P2860
P1476
Arginase-1 deficiency.
@en
P2093
Andreas Schulze
Colin D Funk
Garrett Baron
P2860
P2888
P304
P356
10.1007/S00109-015-1354-3
P50
P577
2015-10-14T00:00:00Z
P5875
P6179
1001836943