207 related articles for article (PubMed ID: 22760543)
21. 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]
22. Split AAV-Mediated Gene Therapy Restores Ureagenesis in a Murine Model of Carbamoyl Phosphate Synthetase 1 Deficiency.
Nitzahn M; Allegri G; Khoja S; Truong B; Makris G; Häberle J; Lipshutz GS
Mol Ther; 2020 Jul; 28(7):1717-1730. PubMed ID: 32359471
[TBL] [Abstract][Full Text] [Related]
23. Generation of a mouse model for arginase II deficiency by targeted disruption of the arginase II gene.
Shi O; Morris SM; Zoghbi H; Porter CW; O'Brien WE
Mol Cell Biol; 2001 Feb; 21(3):811-3. PubMed ID: 11154268
[TBL] [Abstract][Full Text] [Related]
24. Arginase I deficiency: severe infantile presentation with hyperammonemia: more common than reported?
Jain-Ghai S; Nagamani SC; Blaser S; Siriwardena K; Feigenbaum A
Mol Genet Metab; 2011; 104(1-2):107-11. PubMed ID: 21802329
[TBL] [Abstract][Full Text] [Related]
25. Neonatal cholestasis: an uncommon presentation of hyperargininemia.
Gomes Martins E; Santos Silva E; Vilarinho S; Saudubray JM; Vilarinho L
J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S503-6. PubMed ID: 21229317
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Delivery of cytosolic liver arginase into the mitochondrial matrix space: a possible novel site for gene replacement therapy.
Wissmann PB; Goodman BK; Vockley JG; Kern RM; Cederbaum SD; Grody WW
Somat Cell Mol Genet; 1996 Nov; 22(6):489-98. PubMed ID: 9131018
[TBL] [Abstract][Full Text] [Related]
28. A novel mutation in ARG1 gene is responsible for arginase deficiency in an Asian family.
Hertecant JL; Al-Gazali LI; Karuvantevida NS; Ali BR
Saudi Med J; 2009 Dec; 30(12):1601-3. PubMed ID: 19936428
[TBL] [Abstract][Full Text] [Related]
29. Adeno-associated virus serotype 8 gene transfer rescues a neonatal lethal murine model of propionic acidemia.
Chandler RJ; Chandrasekaran S; Carrillo-Carrasco N; Senac JS; Hofherr SE; Barry MA; Venditti CP
Hum Gene Ther; 2011 Apr; 22(4):477-81. PubMed ID: 20950151
[TBL] [Abstract][Full Text] [Related]
30. Arginase deficiency in multiple tissues in argininemia.
Michels VV; Beaudet AL
Clin Genet; 1978 Jan; 13(1):61-7. PubMed ID: 624188
[TBL] [Abstract][Full Text] [Related]
31. Adeno-associated virus-mediated rescue of neonatal lethality in argininosuccinate synthetase-deficient mice.
Kok CY; Cunningham SC; Carpenter KH; Dane AP; Siew SM; Logan GJ; Kuchel PW; Alexander IE
Mol Ther; 2013 Oct; 21(10):1823-31. PubMed ID: 23817206
[TBL] [Abstract][Full Text] [Related]
32. Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiency.
Diaz GA; Schulze A; McNutt MC; Leão-Teles E; Merritt JL; Enns GM; Batzios S; Bannick A; Zori RT; Sloan LS; Potts SL; Bubb G; Quinn AG
J Inherit Metab Dis; 2021 Jul; 44(4):847-856. PubMed ID: 33325055
[TBL] [Abstract][Full Text] [Related]
33. Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemia.
Huang Y; Sharma R; Feigenbaum A; Lee C; Sahai I; Sanchez Russo R; Neira J; Brooks SS; Jackson KE; Wong D; Cederbaum S; Lacbawan FL; Rowland CM; Tanpaiboon P; Salazar D
Mol Genet Metab Rep; 2021 Jun; 27():100735. PubMed ID: 33732618
[TBL] [Abstract][Full Text] [Related]
34. Two Japanese siblings with arginase-1 deficiency identified using a novel frameshift mutation of
Nakajima H; Fukuhara S
J Pediatr Endocrinol Metab; 2022 Jan; 35(1):125-129. PubMed ID: 34653322
[TBL] [Abstract][Full Text] [Related]
35. Parvovirus-mediated gene transfer for the haemophilias.
Walsh CE; Chao H
Haemophilia; 2002 Mar; 8 Suppl 2():60-7. PubMed ID: 11966856
[TBL] [Abstract][Full Text] [Related]
36. Hyperargininemia due to arginase I deficiency: the original patients and their natural history, and a review of the literature.
Schlune A; Vom Dahl S; Häussinger D; Ensenauer R; Mayatepek E
Amino Acids; 2015 Sep; 47(9):1751-62. PubMed ID: 26123990
[TBL] [Abstract][Full Text] [Related]
37. Liver-specific knockout of arginase-1 leads to a profound phenotype similar to inducible whole body arginase-1 deficiency.
Ballantyne LL; Sin YY; Al-Dirbashi OY; Li X; Hurlbut DJ; Funk CD
Mol Genet Metab Rep; 2016 Dec; 9():54-60. PubMed ID: 27761413
[TBL] [Abstract][Full Text] [Related]
38. Repeated AAV-mediated gene transfer by serotype switching enables long-lasting therapeutic levels of hUgt1a1 enzyme in a mouse model of Crigler-Najjar Syndrome Type I.
Bočkor L; Bortolussi G; Iaconcig A; Chiaruttini G; Tiribelli C; Giacca M; Benvenuti F; Zentilin L; Muro AF
Gene Ther; 2017 Oct; 24(10):649-660. PubMed ID: 28805798
[TBL] [Abstract][Full Text] [Related]
39. Sodium phenylbutyrate improved the clinical state in an adult patient with arginase 1 deficiency.
Matsufuji M; Takeshita E; Nakashima M; Watanabe Y; Fukui K; Hanai T; Ishibashi H; Takashima S
Brain Dev; 2020 Feb; 42(2):231-235. PubMed ID: 31604595
[TBL] [Abstract][Full Text] [Related]
40. The human arginases and arginase deficiency.
Iyer R; Jenkinson CP; Vockley JG; Kern RM; Grody WW; Cederbaum S
J Inherit Metab Dis; 1998; 21 Suppl 1():86-100. PubMed ID: 9686347
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
