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 *

137 related articles for article (PubMed ID: 25938595)

  • 61. Long-term enzymatic and phenotypic correction in the phenylketonuria mouse model by adeno-associated virus vector-mediated gene transfer.
    Oh HJ; Park ES; Kang S; Jo I; Jung SC
    Pediatr Res; 2004 Aug; 56(2):278-84. PubMed ID: 15181195
    [TBL] [Abstract][Full Text] [Related]  

  • 62. In hepatocytes the regulation of NOS-2 activity at physiological L-arginine levels suggests a close link to the urea cycle.
    Lerzynski G; Suschek CV; Kolb-Bachofen V
    Nitric Oxide; 2006 Jun; 14(4):300-8. PubMed ID: 16410053
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Overexpression of arginase I in enterocytes of transgenic mice elicits a selective arginine deficiency and affects skin, muscle, and lymphoid development.
    de Jonge WJ; Hallemeesch MM; Kwikkers KL; Ruijter JM; de Gier-de Vries C; van Roon MA; Meijer AJ; Marescau B; de Deyn PP; Deutz NE; Lamers WH
    Am J Clin Nutr; 2002 Jul; 76(1):128-40. PubMed ID: 12081826
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Arginase induction by sodium phenylbutyrate in mouse tissues and human cell lines.
    Kern RM; Yang Z; Kim PS; Grody WW; Iyer RK; Cederbaum SD
    Mol Genet Metab; 2007 Jan; 90(1):37-41. PubMed ID: 16935537
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Newborn screening for hyperargininemia due to arginase 1 deficiency.
    Therrell BL; Currier R; Lapidus D; Grimm M; Cederbaum SD
    Mol Genet Metab; 2017 Aug; 121(4):308-313. PubMed ID: 28659245
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Arginase expression in mouse embryonic development.
    Yu H; Iyer RK; Yoo PK; Kern RM; Grody WW; Cederbaum SD
    Mech Dev; 2002 Jul; 115(1-2):151-5. PubMed ID: 12049781
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Clinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiency.
    Scaglia F; Lee B
    Am J Med Genet C Semin Med Genet; 2006 May; 142C(2):113-20. PubMed ID: 16602094
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Recurrent hepatic failure and status epilepticus: an uncommon presentation of hyperargininemia.
    Yucel H; Kasapkara ÇS; Akcaboy M; Aksoy E; Sahin GE; Derinkuyu BE; Senel S; Ceylaner S
    Metab Brain Dis; 2018 Oct; 33(5):1775-1778. PubMed ID: 29961243
    [TBL] [Abstract][Full Text] [Related]  

  • 69. 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]  

  • 70. A new metabolic disorder in human cationic amino acid transporter-2 that mimics arginase 1 deficiency in newborn screening.
    Yahyaoui R; Blasco-Alonso J; Benito C; Rodríguez-García E; Andrade F; Aldámiz-Echevarría L; Muñoz-Hernández MC; Vega AI; Pérez-Cerdá C; García-Martín ML; Pérez B
    J Inherit Metab Dis; 2019 May; 42(3):407-413. PubMed ID: 30671984
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Phenotypic Pleiotropy in Arginase Deficiency: A Single Center Cohort.
    Bharathi NK; Thomas MM; Yoganathan S; Chandran M; Aaron R; Danda S
    Ann Indian Acad Neurol; 2022; 25(6):1104-1108. PubMed ID: 36911443
    [TBL] [Abstract][Full Text] [Related]  

  • 72. 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]  

  • 73. Hyperargininemia Due to Arginase 1 Deficiency: Variability in Clinical and Biochemical Presentations in Malaysian children.
    Habib A; Mohamed Shakrin N
    Clin Pathol; 2022; 15():2632010X221093274. PubMed ID: 35465134
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Adeno-Associated Virus Serotype 8-Mediated Genetic Labeling of Cholangiocytes in the Neonatal Murine Liver.
    Lee S; Zhou P; Whyte S; Shin S
    Pharmaceutics; 2020 Apr; 12(4):. PubMed ID: 32295003
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Arginase deficiency with new phenotype and a novel mutation: contemporary summary.
    Tsang JP; Poon WL; Luk HM; Fung CW; Ching CK; Mak CM; Lam CW; Siu TS; Tam S; Wong VC
    Pediatr Neurol; 2012 Oct; 47(4):263-9. PubMed ID: 22964440
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Neurological Deterioration in Three Siblings: Exploring the Spectrum of Argininemia.
    Garg D; Bijarnia-Mahay S; Elwadhi A; Ray S; Häberle J; Sharma S
    Indian J Pediatr; 2021 Mar; 88(3):266-268. PubMed ID: 32770317
    [TBL] [Abstract][Full Text] [Related]  

  • 77. A novel compound heterozygous mutation in the arginase-1 gene identified in a Chinese patient with argininemia: A case report.
    Cui D; Liu Y; Jin L; Hu L; Cao L
    Medicine (Baltimore); 2020 Aug; 99(32):e21634. PubMed ID: 32769929
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Anesthetic management of a pediatric patient with arginase-1 deficiency undergoing strabismus operation: a case report.
    Kato H; Kawaguchi K; Sawa T
    JA Clin Rep; 2019 Aug; 5(1):56. PubMed ID: 32025996
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiency.
    Keshavan N; Wood M; Alderson LM; Cortina-Borja M; Skeath R; McSweeney M; Dixon M; Cleary MA; Footitt E; Batzios S
    JIMD Rep; 2022 Mar; 63(2):123-130. PubMed ID: 35281666
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Impact of suitable control on a uniform interpretation of units for arginase assay.
    Suman M; Rajnikant M
    Biochem Biophys Rep; 2021 Mar; 25():100910. PubMed ID: 33506116
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.