BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 14107447)

  • 21. Cystinuria and mental deficiency.
    Gold RJ; Dobrinski MJ; Gold DP
    Clin Genet; 1977 Dec; 12(6):329-32. PubMed ID: 589855
    [TBL] [Abstract][Full Text] [Related]  

  • 22. HOMOCYSTINURIA. BIOCHEMICAL STUDIES OF TISSUES INCLUDING A COMPARISON WITH CYSTATHIONINURIA.
    BRENTON DP; CUSWORTH DC; GAULL GE
    Pediatrics; 1965 Jan; 35():50-6. PubMed ID: 14223225
    [No Abstract]   [Full Text] [Related]  

  • 23. Homocystinuria. A recently discovered cause of mental defect and cerebrovascular thrombosis.
    Dunn HG; Perry TL; Dolman CL
    Neurology; 1966 Apr; 16(4):407-20. PubMed ID: 5948649
    [No Abstract]   [Full Text] [Related]  

  • 24. PARTIAL PURIFICATION AND PROPERTIES OF PROLYL-RNA SYNTHETASE OF RAT LIVER.
    FRASER MJ; KLASS DB
    Can J Biochem Physiol; 1963 Oct; 41():2123-40. PubMed ID: 14083977
    [No Abstract]   [Full Text] [Related]  

  • 25. Isotachophoretic analyses of cystine, homocystine and cystathionine in urines from patients with inborn errors of metabolism.
    Mizobuchi N; Ageta T; Sasaki K; Kodama H
    J Chromatogr; 1986 Oct; 382():321-5. PubMed ID: 3782401
    [No Abstract]   [Full Text] [Related]  

  • 26. Treatment of homocystinuria with a low-methionine diet, supplemental cystine, and a methyl donor.
    Perry TL; Hansen S; Love DL; Crawford LE; Tischler B
    Lancet; 1968 Aug; 2(7566):474-8. PubMed ID: 4175242
    [No Abstract]   [Full Text] [Related]  

  • 27. [SPECIFICITY OF ACTIVATION ENZYMES WITH RESPECT TO RIBONUCLEIC ACIDS ESTERIFIED BY AMINO ACIDS].
    HERVE G; CHAPEVILLE F
    Biochim Biophys Acta; 1963 Dec; 76():493-500. PubMed ID: 14099611
    [No Abstract]   [Full Text] [Related]  

  • 28. [Ocular and systemic complications of homocystinuria: a report of five cases].
    Rais L; Wafi M; Lahbil D; Iraki M; Fekkak J; Hamdani M; Benchekroun W; Rachid R; Belhadji M; Laouissi N; Zaghloul K; Amraoui A
    J Fr Ophtalmol; 2003 Dec; 26(10):1045-50. PubMed ID: 14691398
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two siblings with vitamin B6-nonresponsive cystathionine beta-synthase deficiency and differing blood methionine levels during the neonatal period.
    Watanabe T; Ito M; Naito E; Yokota I; Matsuda J; Kuroda Y
    J Med Invest; 1997 Aug; 44(1-2):95-7. PubMed ID: 9395725
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Folate metabolism in homocystinuria.
    Carey M; Fennelly JJ; FitzGerald O
    Ir J Med Sci; 1966 Nov; 6(491):488-92. PubMed ID: 5981556
    [No Abstract]   [Full Text] [Related]  

  • 31. Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine.
    Laster L; Mudd SH; Finkelstein JD; Irreverre F
    J Clin Invest; 1965 Oct; 44(10):1708-19. PubMed ID: 5840537
    [No Abstract]   [Full Text] [Related]  

  • 32. [Biochemical aspects of some congenital anomalies of the metabolism of sulfur amino acids].
    Chatagner F
    Expos Annu Biochim Med; 1967; 28():53-76. PubMed ID: 4883168
    [No Abstract]   [Full Text] [Related]  

  • 33. Homocystinuria and schizophrenia. Literature review and case report.
    Bracken P; Coll P
    J Nerv Ment Dis; 1985 Jan; 173(1):51-5. PubMed ID: 3965612
    [TBL] [Abstract][Full Text] [Related]  

  • 34. CONTROL MECHANISM IN THE RAT LIVER ENZYME SYSTEM CONVERTING L-METHIONINE TO L-CYSTINE. I. ENZYMATIC BASIS FOR THE METHIONINE-SPARING ACTION OF L-CYSTINE.
    KATO A; MATSUZAWA T; SUDA M; NAKAGAWA H; ISHIZUKA J
    J Biochem; 1964 Apr; 55():401-9. PubMed ID: 14170092
    [No Abstract]   [Full Text] [Related]  

  • 35. Enzyme replacement with PEGylated cystathionine β-synthase ameliorates homocystinuria in murine model.
    Bublil EM; Majtan T; Park I; Carrillo RS; Hůlková H; Krijt J; Kožich V; Kraus JP
    J Clin Invest; 2016 Jun; 126(6):2372-84. PubMed ID: 27183385
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [STUDIES ON INFUSIONS. I. AMINO ACID INFUSION AND ITS METABOLISM].
    UEDA A
    Sapporo Igaku Zasshi; 1963; 23():303-12. PubMed ID: 14073881
    [No Abstract]   [Full Text] [Related]  

  • 37. HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.
    CARSON NA; CUSWORTH DC; DENT CE; FIELD CM; NEILL DW; WESTALL RG
    Arch Dis Child; 1963 Oct; 38(201):425-36. PubMed ID: 14065982
    [No Abstract]   [Full Text] [Related]  

  • 38. DETERMINATION OF ACYL-COA SYNTHETASE ACTIVITY FOR VOLATILE FATTY ACIDS.
    STACEY RE; LATIMER SB; TOVE SB
    Biochim Biophys Acta; 1964 Apr; 84():192-5. PubMed ID: 14181297
    [No Abstract]   [Full Text] [Related]  

  • 39. [Hereditary metabolic disorders with significance for adult age. Homocystinuria, histidinemia, cystinuria, vitamin-D-resistant rickets, alpha1-antitrypsin deficiency].
    Przyrembel H; Bremer HJ
    Internist (Berl); 1976 Jul; 17(7):348-53. PubMed ID: 181342
    [No Abstract]   [Full Text] [Related]  

  • 40. Reduction of false negative results in screening of newborns for homocystinuria.
    Peterschmitt MJ; Simmons JR; Levy HL
    N Engl J Med; 1999 Nov; 341(21):1572-6. PubMed ID: 10564686
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.