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.
339 related articles for article (PubMed ID: 31501335)
21. Human hepatocyte transplantation corrects the inherited metabolic liver disorder arginase deficiency in mice. Angarita SAK; Truong B; Khoja S; Nitzahn M; Rajbhandari AK; Zhuravka I; Duarte S; Lin MG; Lam AK; Cederbaum SD; Lipshutz GS Mol Genet Metab; 2018 Jun; 124(2):114-123. PubMed ID: 29724658 [TBL] [Abstract][Full Text] [Related]
22. Arginase-1 deficiency in neural cells does not contribute to neurodevelopment or functional outcomes after sciatic nerve injury. Richmond CR; Ballantyne LL; de Guzman AE; Nieman BJ; Funk CD; Ghasemlou N Neurochem Int; 2021 May; 145():104984. PubMed ID: 33561495 [TBL] [Abstract][Full Text] [Related]
23. 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]
24. Hepatic glutamine synthetase augmentation enhances ammonia detoxification. Soria LR; Nitzahn M; De Angelis A; Khoja S; Attanasio S; Annunziata P; Palmer DJ; Ng P; Lipshutz GS; Brunetti-Pierri N J Inherit Metab Dis; 2019 Nov; 42(6):1128-1135. PubMed ID: 30724386 [TBL] [Abstract][Full Text] [Related]
25. Farnesoid X receptor agonist tropifexor detoxifies ammonia by regulating the glutamine metabolism and urea cycles in cholestatic livers. Xiao Y; Wang W; Peng S; Lu Y; Du J; Cai W Eur J Pharmacol; 2024 Mar; 966():176334. PubMed ID: 38286357 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. Case series of arginase 1 deficiency: Expanding the spectrum in hyperargininemia. Dorum S; Havalı C Pediatr Int; 2022 Jan; 64(1):e14945. PubMed ID: 34343381 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. Rescue of the Functional Alterations of Motor Cortical Circuits in Arginase Deficiency by Neonatal Gene Therapy. Cantero G; Liu XB; Mervis RF; Lazaro MT; Cederbaum SD; Golshani P; Lipshutz GS J Neurosci; 2016 Jun; 36(25):6680-90. PubMed ID: 27335400 [TBL] [Abstract][Full Text] [Related]
31. Enhancement of hepatic autophagy increases ureagenesis and protects against hyperammonemia. Soria LR; Allegri G; Melck D; Pastore N; Annunziata P; Paris D; Polishchuk E; Nusco E; Thöny B; Motta A; Häberle J; Ballabio A; Brunetti-Pierri N Proc Natl Acad Sci U S A; 2018 Jan; 115(2):391-396. PubMed ID: 29279371 [TBL] [Abstract][Full Text] [Related]
32. 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]
37. Argininosuccinate lyase deficiency-argininosuccinic aciduria and beyond. Erez A; Nagamani SC; Lee B Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):45-53. PubMed ID: 21312326 [TBL] [Abstract][Full Text] [Related]
38. 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]
39. Arginase 2 deficiency results in spontaneous steatohepatitis: a novel link between innate immune activation and hepatic de novo lipogenesis. Navarro LA; Wree A; Povero D; Berk MP; Eguchi A; Ghosh S; Papouchado BG; Erzurum SC; Feldstein AE J Hepatol; 2015 Feb; 62(2):412-20. PubMed ID: 25234945 [TBL] [Abstract][Full Text] [Related]