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Journal Abstract Search

64 related items for PubMed ID: 917612

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Effect of methionine-loading on methyl group synthesis and activation in rat brain and liver.
    Carl GF, Benesh FC, Hudson JL.
    Biol Psychiatry; 1978 Dec; 13(6):661-9. PubMed ID: 737254
    [Abstract] [Full Text] [Related]

  • 23. Type II hyperprolinemia. Delta1-pyrroline-5-carboxylic acid dehydrogenase deficiency in cultured skin fibroblasts and circulating lymphocytes.
    Valle D, Goodman SI, Applegarth DA, Shih VE, Phang JM.
    J Clin Invest; 1976 Sep; 58(3):598-603. PubMed ID: 956388
    [Abstract] [Full Text] [Related]

  • 24. [Amniotic fluid cell culture for the prenatal diagnosis of the fetal karyotype].
    Zolotukhina TV.
    Tsitol Genet; 1980 Sep; 14(2):57-63. PubMed ID: 7003859
    [Abstract] [Full Text] [Related]

  • 25. [Culture of amniotic fluid cells in a semisynthetic medium (Chang medium)].
    Giardino D, Morandi E, Buscaglia M, Simoni G.
    Pathologica; 1983 Sep; 75 Suppl():184-7. PubMed ID: 6680424
    [No Abstract] [Full Text] [Related]

  • 26. Inhibition of pig liver methylenetetrahydrofolate reductase by dihydrofolate: some mechanistic and regulatory implications.
    Matthews RG, Haywood BJ.
    Biochemistry; 1979 Oct 30; 18(22):4845-51. PubMed ID: 508720
    [No Abstract] [Full Text] [Related]

  • 27. Maternal serum for the culture of amniotic fluid cells.
    Ogita S, Matsumoto M, Sugawa T.
    Acta Obstet Gynaecol Jpn; 1972 Oct 30; 19(4):266-7. PubMed ID: 4679533
    [No Abstract] [Full Text] [Related]

  • 28. Folate-responsive homocystinuria and "schizophrenia'.
    Nutr Rev; 1982 Aug 30; 40(8):242-5. PubMed ID: 6982438
    [No Abstract] [Full Text] [Related]

  • 29. [Cultivation of amniotic fluid cells from weeks 11 and 12 of pregnancy (author's transl)].
    Novotná J, Bráza J, Cinátl J.
    Sb Lek; 1978 Apr 30; 80(4):124-8. PubMed ID: 653298
    [No Abstract] [Full Text] [Related]

  • 30. [Histochemical studies of explant cultures from cerebral cortex of newborn rats].
    Goworek K, Meyer U, Lindner G.
    Z Mikrosk Anat Forsch; 1973 Apr 30; 87(3):423-43. PubMed ID: 4149995
    [No Abstract] [Full Text] [Related]

  • 31. Metabolic role of cytoplasmic isozymes of 5,10-methylenetetrahydrofolate dehydrogenase in Saccharomyces cerevisiae.
    West MG, Horne DW, Appling DR.
    Biochemistry; 1996 Mar 05; 35(9):3122-32. PubMed ID: 8608153
    [Abstract] [Full Text] [Related]

  • 32. Succinate dehydrogenase activity in cultured human skin fibroblasts and amniotic fluid cells. A methodological study.
    Hansen TL, Andersen H.
    Histochemistry; 1983 Mar 05; 78(2):211-25. PubMed ID: 6874423
    [Abstract] [Full Text] [Related]

  • 33. NAD-dependent methylenetetrahydrofolate dehydrogenase is expressed by immortal cells.
    Mejia NR, MacKenzie RE.
    J Biol Chem; 1985 Nov 25; 260(27):14616-20. PubMed ID: 3877056
    [Abstract] [Full Text] [Related]

  • 34. Morphologic studies in a patient with homocystinuria due to 5, 10-methylenetetrahydrofolate reductase deficiency.
    Kanwar YS, Manaligod JR, Wong PW.
    Pediatr Res; 1976 Jun 25; 10(6):598-609. PubMed ID: 1272636
    [Abstract] [Full Text] [Related]

  • 35. The rise and fall of MTHF as a methyl donor in biogenic amine metabolism.
    Fuller RW.
    Life Sci; 1976 Sep 01; 19(5):625-8. PubMed ID: 785140
    [No Abstract] [Full Text] [Related]

  • 36. MTHFD2--a new twist?
    Tedeschi PM, Scotto KW, Kerrigan J, Bertino JR.
    Oncotarget; 2016 Feb 16; 7(7):7368-9. PubMed ID: 26848977
    [No Abstract] [Full Text] [Related]

  • 37. Advances in Nutritional Epigenetics-A Fresh Perspective for an Old Idea. Lessons Learned, Limitations, and Future Directions.
    Sedley L.
    Epigenet Insights; 2020 Feb 16; 13():2516865720981924. PubMed ID: 33415317
    [Abstract] [Full Text] [Related]

  • 38. CblE type of homocystinuria due to methionine synthase reductase deficiency: clinical and molecular studies and prenatal diagnosis in two families.
    Zavadakova P, Fowler B, Zeman J, Suormala T, Pristoupilová K, Kozich V, Zavad'áková P.
    J Inherit Metab Dis; 2002 Oct 16; 25(6):461-76. PubMed ID: 12555939
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemia.
    Mudd SH, Cerone R, Schiaffino MC, Fantasia AR, Minniti G, Caruso U, Lorini R, Watkins D, Matiaszuk N, Rosenblatt DS, Schwahn B, Rozen R, LeGros L, Kotb M, Capdevila A, Luka Z, Finkelstein JD, Tangerman A, Stabler SP, Allen RH, Wagner C.
    J Inherit Metab Dis; 2001 Aug 16; 24(4):448-64. PubMed ID: 11596649
    [Abstract] [Full Text] [Related]

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