These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
233 related articles for article (PubMed ID: 11154268)
21. Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia. Vockley JG; Tabor DE; Kern RM; Goodman BK; Wissmann PB; Kang DS; Grody WW; Cederbaum SD Hum Mutat; 1994; 4(2):150-4. PubMed ID: 7981719 [No Abstract] [Full Text] [Related]
22. Lipid nanoparticle-targeted mRNA therapy as a treatment for the inherited metabolic liver disorder arginase deficiency. Truong B; Allegri G; Liu XB; Burke KE; Zhu X; Cederbaum SD; Häberle J; Martini PGV; Lipshutz GS Proc Natl Acad Sci U S A; 2019 Oct; 116(42):21150-21159. PubMed ID: 31501335 [TBL] [Abstract][Full Text] [Related]
23. Molecular basis of phenotypic variation in patients with argininemia. Uchino T; Snyderman SE; Lambert M; Qureshi IA; Shapira SK; Sansaricq C; Smit LM; Jakobs C; Matsuda I Hum Genet; 1995 Sep; 96(3):255-60. PubMed ID: 7649538 [TBL] [Abstract][Full Text] [Related]
24. Ornithine transcarbamylase and arginase I deficiency are responsible for diminished urea cycle function in the human hepatoblastoma cell line HepG2. Mavri-Damelin D; Eaton S; Damelin LH; Rees M; Hodgson HJ; Selden C Int J Biochem Cell Biol; 2007; 39(3):555-64. PubMed ID: 17098461 [TBL] [Abstract][Full Text] [Related]
25. A role for PPARα in the regulation of arginine metabolism and nitric oxide synthesis. Guelzim N; Mariotti F; Martin PG; Lasserre F; Pineau T; Hermier D Amino Acids; 2011 Oct; 41(4):969-79. PubMed ID: 21063737 [TBL] [Abstract][Full Text] [Related]
26. Short-term correction of arginase deficiency in a neonatal murine model with a helper-dependent adenoviral vector. Gau CL; Rosenblatt RA; Cerullo V; Lay FD; Dow AC; Livesay J; Brunetti-Pierri N; Lee B; Cederbaum SD; Grody WW; Lipshutz GS Mol Ther; 2009 Jul; 17(7):1155-63. PubMed ID: 19367256 [TBL] [Abstract][Full Text] [Related]
27. Proof-of-Concept Gene Editing for the Murine Model of Inducible Arginase-1 Deficiency. Sin YY; Price PR; Ballantyne LL; Funk CD Sci Rep; 2017 May; 7(1):2585. PubMed ID: 28566761 [TBL] [Abstract][Full Text] [Related]
28. The role and control of arginine levels in arginase 1 deficiency. Diaz GA; Bechter M; Cederbaum SD J Inherit Metab Dis; 2023 Jan; 46(1):3-14. PubMed ID: 36175366 [TBL] [Abstract][Full Text] [Related]
29. Use of enzyme-loaded erythrocytes in in-vitro correction of arginase-deficient erythrocytes in familial hyperargininemia. Adriaenssens K; Karcher D; Lowenthal A; Terheggen HG Clin Chem; 1976 Mar; 22(3):323-6. PubMed ID: 1253407 [TBL] [Abstract][Full Text] [Related]
30. Analysis of novel ARG1 mutations causing hyperargininemia and correlation with arginase I activity in erythrocytes. Carvalho DR; Brand GD; Brum JM; Takata RI; Speck-Martins CE; Pratesi R Gene; 2012 Nov; 509(1):124-30. PubMed ID: 22959135 [TBL] [Abstract][Full Text] [Related]
31. Argocytes containing enzyme nanoparticles reduce toxic concentrations of arginine in the blood. Kaminsky YG; Kosenko EA Bull Exp Biol Med; 2012 Jul; 153(3):406-8. PubMed ID: 22866323 [TBL] [Abstract][Full Text] [Related]