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 *

160 related articles for article (PubMed ID: 6404622)

  • 21. Arginase deficiency in two brothers.
    Candito M; Bebin B; Vianey-Saban C; Rabier D; Bekri S; Sebag F; Chambon P; Kamoun P
    J Inherit Metab Dis; 1993; 16(6):1054-6. PubMed ID: 8127062
    [No Abstract]   [Full Text] [Related]  

  • 22. Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginase.
    Ash DE; Scolnick LR; Kanyo ZF; Vockley JG; Cederbaum SD; Christianson DW
    Mol Genet Metab; 1998 Aug; 64(4):243-9. PubMed ID: 9758714
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hyperargininemia with arginase deficiency.
    Cederbaum SD; Shaw KN; Spector EB; Verity MA; Snodgrass PJ; Sugarman GI
    Pediatr Res; 1979 Jul; 13(7):827-33. PubMed ID: 481955
    [No Abstract]   [Full Text] [Related]  

  • 24. Arginase isoenzymes in human diploid fibroblasts.
    Van Elsen AF; Leroy JG
    Biochem Biophys Res Commun; 1975 Jan; 62(2):191-8. PubMed ID: 234223
    [No Abstract]   [Full Text] [Related]  

  • 25. Arginase deficiency presenting with convulsions.
    Patel JS; van't Hoff WV; Leonard JV
    J Inherit Metab Dis; 1994; 17(2):254. PubMed ID: 7967487
    [No Abstract]   [Full Text] [Related]  

  • 26. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies].
    Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP
    Z Kinderheilkd; 1970; 107(4):313-23. PubMed ID: 5438972
    [No Abstract]   [Full Text] [Related]  

  • 27. Purification and properties of liver arginase from teleostean fish Clarias batrachus (L.).
    Singh RA; Singh SN
    Arch Int Physiol Biochim; 1990 Dec; 98(6):411-9. PubMed ID: 1705780
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Unsuccessful trial of gene replacement in arginase deficiency.
    Terheggen HG; Lowenthal A; Lavinha F; Colombo JP; Rogers S
    Z Kinderheilkd; 1975; 119(1):1-3. PubMed ID: 164740
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Properties of fetal and adult red blood cell arginase: a possible prenatal diagnostic test for arginase deficiency.
    Spector EB; Kiernan M; Bernard B; Cederbaum SD
    Am J Hum Genet; 1980 Jan; 32(1):79-87. PubMed ID: 7361766
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Hyperargininemia.
    Cederbaum SD; Shaw KN; Valente M
    J Pediatr; 1977 Apr; 90(4):569-73. PubMed ID: 839368
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal diagnosis for arginase deficiency by second-trimester fetal erythrocyte arginase assay and first-trimester ARG1 mutation analysis.
    Korman SH; Gutman A; Stemmer E; Kay BS; Ben-Neriah Z; Zeigler M
    Prenat Diagn; 2004 Nov; 24(11):857-60. PubMed ID: 15565656
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Inducible arginase 1 deficiency in mice leads to hyperargininemia and altered amino acid metabolism.
    Sin YY; Ballantyne LL; Mukherjee K; St Amand T; Kyriakopoulou L; Schulze A; Funk CD
    PLoS One; 2013; 8(11):e80001. PubMed ID: 24224027
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissues.
    Endres W; Schaller R; Shin YS
    J Inherit Metab Dis; 1984; 7(1):8. PubMed ID: 6429443
    [No Abstract]   [Full Text] [Related]  

  • 38. Familial hyperargininemia.
    Terheggen HG; Lavinha F; Colombo JP; Van Sande M; Lowenthal A
    J Genet Hum; 1972 Mar; 20(1):69-84. PubMed ID: 4643877
    [No Abstract]   [Full Text] [Related]  

  • 39. Arginase and free amino acids in hyperargininemia: leukocyte arginine as a diagnostic parameter for heterozygotes.
    Marescau B; Pintens J; Lowenthal A; Terheggen HG; Adriaenssens K
    J Clin Chem Clin Biochem; 1979 Apr; 17(4):211-7. PubMed ID: 438730
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Periodic hyperammonemia, hyperlysinemia, and homocitrullinuria associated with decreased argininosuccinate synthetase and arginase activities.
    Sogawa H; Oyanagi K; Nakao T
    Pediatr Res; 1977 Sep; 11(9 Pt 1):949-53. PubMed ID: 904980
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.