BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 7070876)

  • 1. Glycine cleavage system in ketotic hyperglycinemia: a reduction of H-protein activity.
    Hayasaka K; Narisawa K; Satoh T; Tateda H; Metoki K; Tada K; Hiraga K; Aoki T; Kawakami T; Akamatsu H; Matsuo N
    Pediatr Res; 1982 Jan; 16(1):5-7. PubMed ID: 7070876
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Defective glycine cleavage system in nonketotic hyperglycinemia. Occurrence of a less active glycine decarboxylase and an abnormal aminomethyl carrier protein.
    Hiraga K; Kochi H; Hayasaka K; Kikuchi G; Nyhan WL
    J Clin Invest; 1981 Aug; 68(2):525-34. PubMed ID: 6790577
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Non-ketotic hyperglycinemia: an aim of the second generation of studies on pathogenesis.
    Hiraga K; Koyata H; Sakakibara T; Ishiguro Y; Matsui C
    Mol Biol Med; 1991 Feb; 8(1):65-79. PubMed ID: 1943691
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Nonketotic hyperglycinemia: two patients with primary defects of P-protein and T-protein, respectively, in the glycine cleavage system.
    Hayasaka K; Tada K; Kikuchi G; Winter S; Nyhan WL
    Pediatr Res; 1983 Dec; 17(12):967-70. PubMed ID: 6336599
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The impaired expression of glycine decarboxylase in patients with hyperglycinemias.
    Kume A; Kure S; Tada K; Hiraga K
    Biochem Biophys Res Commun; 1988 Jul; 154(1):292-7. PubMed ID: 3395333
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Non-ketotic hyperglycinemia: a life-threatening disorder in the neonate.
    Tada K; Kure S; Takayanagi M; Kume A; Narisawa K
    Early Hum Dev; 1992; 29(1-3):75-81. PubMed ID: 1396281
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The oxidation of glycine and propionic acid in propionic acidemia with ketotic hyperglycinemia.
    Ando T; Nyhan WL; Connor JD; Rasmussen K; Donnell G; Barnes N; Cottom D; Hull D
    Pediatr Res; 1972 Jun; 6(6):576-83. PubMed ID: 5046977
    [No Abstract]   [Full Text] [Related]  

  • 8. [Hyperglycinemia in clinical-laboratory practice].
    Ciani F; Pasquini E; Ciardetti A; Donati MA; Zammarchi E
    Pediatr Med Chir; 1997; 19(2):109-12. PubMed ID: 9312744
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Reduced level of glycine cleavage system in the liver of hyperglycinemia patients.
    Motokawa Y; Kikuchi G; Narisawa K; Arakawa T
    Clin Chim Acta; 1977 Aug; 79(1):173-81. PubMed ID: 890950
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Effect of valine on propionate metabolism in control and hyperglycinemic fibroblasts and in rat liver.
    Revsin B; Lebowitz J; Morrow G
    Pediatr Res; 1977 Jun; 11(6):749-53. PubMed ID: 17092
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Inhibition of glycine synthase by branched-chain alpha-keto acids. A possible mechanism for abnormal glycine metabolism in ketotic hyperglycinemia.
    O'Brien WE
    Arch Biochem Biophys; 1978 Aug; 189(2):291-7. PubMed ID: 708054
    [No Abstract]   [Full Text] [Related]  

  • 12. Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N145I): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH).
    Toone JR; Applegarth DA; Coulter-Mackie MB; James ER
    Mol Genet Metab; 2001 Apr; 72(4):322-5. PubMed ID: 11286506
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structure and expression of the glycine cleavage system in rat central nervous system.
    Sakata Y; Owada Y; Sato K; Kojima K; Hisanaga K; Shinka T; Suzuki Y; Aoki Y; Satoh J; Kondo H; Matsubara Y; Kure S
    Brain Res Mol Brain Res; 2001 Oct; 94(1-2):119-30. PubMed ID: 11597772
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Propionic acidemia in patients with ketotic hyperglycinemia.
    Ando T; Rasmussen K; Nyhan WL; Donnell GN; Barnes ND
    J Pediatr; 1971 May; 78(5):827-32. PubMed ID: 5581587
    [No Abstract]   [Full Text] [Related]  

  • 15. Nonketotic hyperglycinemia: report of a case and review of the clinical, chemical, and pathological changes.
    Slager UT; Berggren RL; Marubayashi S
    Ann Neurol; 1977 Apr; 1(4):399-402. PubMed ID: 617256
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Non-ketotic hyperglycinaemia: clinical and biochemical aspects.
    Tada K; Hayasaka K
    Eur J Pediatr; 1987 May; 146(3):221-7. PubMed ID: 3297708
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Concurrent non-ketotic hyperglycinemia and propionic acidemia in an eight year old boy.
    Kruszka PS; Kirmse B; Zand DJ; Cusmano-Ozog K; Spector E; Van Hove JL; Chapman KA
    Mol Genet Metab Rep; 2014; 1():237-240. PubMed ID: 27896094
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The vitamin B12-deficient rat as a possible model of ketotic hyperglycinemia.
    Rowley BO; Brothers V; Gerritsen T
    Pediatr Res; 1975 Oct; 9(10):782-6. PubMed ID: 1187241
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The glycine cleavage system: structure of a cDNA encoding human H-protein, and partial characterization of its gene in patients with hyperglycinemias.
    Koyata H; Hiraga K
    Am J Hum Genet; 1991 Feb; 48(2):351-61. PubMed ID: 1671321
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel mutations in the P-protein (glycine decarboxylase) gene in patients with glycine encephalopathy (non-ketotic hyperglycinemia).
    Toone JR; Applegarth DA; Kure S; Coulter-Mackie MB; Sazegar P; Kojima K; Ichinohe A
    Mol Genet Metab; 2002 Jul; 76(3):243-9. PubMed ID: 12126939
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.