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 *

214 related articles for article (PubMed ID: 858206)

  • 1. Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria.
    Weyler W; Sweetman L; Maggio DC; Nyhan WL
    Clin Chim Acta; 1977 May; 76(3):321-8. PubMed ID: 858206
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.
    Burri BJ; Sweetman L; Nyhan WL
    J Clin Invest; 1981 Dec; 68(6):1491-5. PubMed ID: 6798072
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
    Bartlett K; Ng H; Leonard JV
    Clin Chim Acta; 1980 Jan; 100(2):183-6. PubMed ID: 6766095
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biotin-response organicaciduria. Multiple carboxylase defects and complementation studies with propionicacidemia in cultured fibroblasts.
    Saunders M; Sweetman L; Robinson B; Roth K; Cohn R; Gravel RA
    J Clin Invest; 1979 Dec; 64(6):1695-702. PubMed ID: 115903
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biochemical characterization of biotin-responsive multiple carboxylase deficiency: heterogeneity within the bio genetic complementation group.
    Feldman GL; Hsia YE; Wolf B
    Am J Hum Genet; 1981 Sep; 33(5):692-701. PubMed ID: 6794361
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deficient acetyl CoA carboxylase activity in multiple carboxylase deficiency.
    Feldman GL; Wolf B
    Clin Chim Acta; 1981 Apr; 111(2-3):147-51. PubMed ID: 6112081
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Acetyl CoA carboxylase in cultured fibroblasts: differential biotin dependence in the two types of biotin-responsive multiple carboxylase deficiency.
    Packman S; Caswell N; Gonzalez-Rios MC; Kadlecek T; Cann H; Rassin D; McKay C
    Am J Hum Genet; 1984 Jan; 36(1):80-92. PubMed ID: 6141728
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuria.
    Sweetman L; Bates SP; Hull D; Nyhan WL
    Pediatr Res; 1977 Nov; 11(11):1144-7. PubMed ID: 917614
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lactic acidosis in biotin-responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onset.
    Sherwood WG; Saunders M; Robinson BH; Brewster T; Gravel RA
    J Pediatr; 1982 Oct; 101(4):546-50. PubMed ID: 6811711
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evidence for a defect of holocarboxylase synthetase activity in cultured lymphoblasts from a patient with biotin-responsive multiple carboxylase deficiency.
    Saunders ME; Sherwood WG; Duthie M; Surh L; Gravel RA
    Am J Hum Genet; 1982 Jul; 34(4):590-601. PubMed ID: 7102675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stimulation of propionyl CoA and beta-methylcrotonyl CoA carboxylase activities in human leukocytes and cultured fibroblasts by biotin.
    Wolf B; Rosenberg LE
    Pediatr Res; 1979 Nov; 13(11):1275-9. PubMed ID: 514693
    [No Abstract]   [Full Text] [Related]  

  • 12. Multiple carboxylase deficiency.
    Nyhan WL
    Int J Biochem; 1988; 20(4):363-70. PubMed ID: 3284772
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of biotin responsiveness in cultured fibroblasts from patients with propionic acidemia: absence of response by structurally altered carboxylases.
    Wolf B
    Biochem Genet; 1979 Aug; 17(7-8):709-13. PubMed ID: 540014
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biotin activation of carboxylase activity in cultured fibroblasts from a child with a combined carboxylase defect.
    Bartlett K; Gompertz D
    Clin Chim Acta; 1978 Mar; 84(3):399-401. PubMed ID: 639329
    [No Abstract]   [Full Text] [Related]  

  • 15. Essential arginine residues in the active sites of propionyl CoA carboxylase and beta-methylcrotonyl CoA carboxylase.
    Wolf B; Kalousek F; Rosenberg LE
    Enzyme; 1979; 24(5):302-6. PubMed ID: 510274
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Kinetic characterization of mutations found in propionic acidemia and methylcrotonylglycinuria: evidence for cooperativity in biotin carboxylase.
    Sloane V; Waldrop GL
    J Biol Chem; 2004 Apr; 279(16):15772-8. PubMed ID: 14960587
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rapid differential diagnosis of carboxylase deficiencies and evaluation for biotin-responsiveness in a single blood sample.
    Suormala T; Wick H; Bonjour JP; Baumgartner ER
    Clin Chim Acta; 1985 Jan; 145(2):151-62. PubMed ID: 3918814
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Five patients with a biotin-responsive defect in holocarboxylase formation: evaluation of responsiveness to biotin therapy in vivo and comparative biochemical studies in vitro.
    Suormala T; Fowler B; Duran M; Burtscher A; Fuchshuber A; Tratzmüller R; Lenze MJ; Raab K; Baur B; Wick H; Baumgartner R
    Pediatr Res; 1997 May; 41(5):666-73. PubMed ID: 9128289
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Biotin-responsive alopecia and developmental regression.
    Charles BM; Hosking G; Green A; Pollitt R; Bartlett K; Taitz LS
    Lancet; 1979 Jul; 2(8134):118-20. PubMed ID: 88555
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Immunological studies of propionyl CoA carboxylase in livers and fibroblasts of patients with propionic acidemia.
    McKeon C; Eanes RZ; Fall RR; Tasset DM; Wolf B
    Clin Chim Acta; 1980 Feb; 101(2-3):217-33. PubMed ID: 6766827
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.