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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]  

  • 28. Mouse model for human arginase deficiency.
    Iyer RK; Yoo PK; Kern RM; Rozengurt N; Tsoa R; O'Brien WE; Yu H; Grody WW; Cederbaum SD
    Mol Cell Biol; 2002 Jul; 22(13):4491-8. PubMed ID: 12052859
    [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]  

  • 33. Characterization and mRNA expression analysis of a novel ARG1 splicing mutation causing hyperargininemia.
    Villegas-Ruiz V; Campos-Garcia FJ; Contreras-Capetillo S; Moreno-Graciano CM; Maldonado-Solis FA; Maldonado-Solis MA; Zenteno JC
    Clin Biochem; 2015 Dec; 48(18):1273-6. PubMed ID: 26169240
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Epidemiology, methods of diagnosis, and clinical management of patients with arginase 1 deficiency (ARG1-D): A systematic review.
    Bin Sawad A; Jackimiec J; Bechter M; Trucillo A; Lindsley K; Bhagat A; Uyei J; Diaz GA
    Mol Genet Metab; 2022; 137(1-2):153-163. PubMed ID: 36049366
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Arginase impedes the resolution of colitis by altering the microbiome and metabolome.
    Baier J; Gänsbauer M; Giessler C; Arnold H; Muske M; Schleicher U; Lukassen S; Ekici A; Rauh M; Daniel C; Hartmann A; Schmid B; Tripal P; Dettmer K; Oefner PJ; Atreya R; Wirtz S; Bogdan C; Mattner J
    J Clin Invest; 2020 Nov; 130(11):5703-5720. PubMed ID: 32721946
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Comprehensive characterization of ureagenesis in the spf
    Allegri G; Deplazes S; Rimann N; Causton B; Scherer T; Leff JW; Diez-Fernandez C; Klimovskaia A; Fingerhut R; Krijt J; Kožich V; Nuoffer JM; Grisch-Chan HM; Thöny B; Häberle J
    J Inherit Metab Dis; 2019 Nov; 42(6):1064-1076. PubMed ID: 30714172
    [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]  

  • 40. Arginase 1 Deficiency in Patients Initially Diagnosed with Hereditary Spastic Paraplegia.
    McNutt MC; Foreman N; Gotway G
    Mov Disord Clin Pract; 2023 Jan; 10(1):109-114. PubMed ID: 36698992
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.