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 *

132 related articles for article (PubMed ID: 6135251)

  • 21. Methylmalonyl-CoA mutase activity of leukocytes in variants and heterozygotes of methylmalonic acidemia.
    Narisawa K; Saito T; Hisa S; Suzuki H; Hayasaka K
    Tohoku J Exp Med; 1977 Sep; 123(1):1-8. PubMed ID: 21471
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Methylmalonyl-CoA mutase (EC 5.4.99.2) and methionine synthetase (EC 2.1.1.13) in the tissues of cobalt-vitamin B12 deficient sheep.
    Kennedy DG; Cannavan A; Molloy A; O'Harte F; Taylor SM; Kennedy S; Blanchflower WJ
    Br J Nutr; 1990 Nov; 64(3):721-32. PubMed ID: 1979918
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Methylmalonic aciduria without vitamin B12 deficiency in an adult sibship.
    Giorgio AJ; Trowbridge M; Boone AW; Patten RS
    N Engl J Med; 1976 Aug; 295(6):310-3. PubMed ID: 6909
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Identification and perturbation of mutant human fibroblasts based on measurements of methylmalonic acid and total homocysteine in the culture media.
    Kolhouse JF; Stabler SP; Allen RH
    Arch Biochem Biophys; 1993 Jun; 303(2):355-60. PubMed ID: 8099783
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Perturbation of methionine metabolism in sheep with nitrous-oxide-induced inactivation of cobalamin.
    Xue GP; Snoswell AM; Runciman WB
    Biochem Int; 1986 Jan; 12(1):61-9. PubMed ID: 2868723
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The inherited methylmalonic acidemias.
    Rosenberg LE
    Prog Clin Biol Res; 1982; 103 Pt B():187-209. PubMed ID: 6131428
    [No Abstract]   [Full Text] [Related]  

  • 27. Studies on cultured fibroblasts in a case of methylmalonic aciduria.
    Davidson JS; Lloyd A; Christianson A; Harley EH; Berger GM
    S Afr Med J; 1984 Feb; 65(7):257-60. PubMed ID: 6141644
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Screening for methylmalonic aciduria in Alberta: a voluntary program with particular significance for the Hutterite Brethren.
    Fowlow SB; Holmes TM; Morgan K; Snyder FF
    Am J Med Genet; 1985 Nov; 22(3):513-9. PubMed ID: 2865895
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)].
    Saudubray JM; Charpentier C; Coude FX; Ogier H; Pham Dinh D; Bartlett K; Gompertz D
    Arch Fr Pediatr; 1980; 37 Suppl 2():IX-XIV. PubMed ID: 6108749
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Methylmalonic acidaemia due to mutase apoenzyme defect: responsive to vitamin B12 in intact fibroblasts but not in vivo.
    Baumgartner R; Giardini O; Cantani A; Sabetta G; Castro M
    J Inherit Metab Dis; 1982; 5(3):137-41. PubMed ID: 6133033
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Effect of N2O treatment/vitamin B12 deficiency in pigs on tissue concentrations of odd-numbered, branched-chain fatty acids.
    Young PB; Kennedy S; Molloy AM; Scott JM; Weir DG; Kennedy DG
    Int J Vitam Nutr Res; 1995; 65(4):255-60. PubMed ID: 8789622
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression test.
    Carmel R; Bedros AA; Mace JW; Goodman SI
    Blood; 1980 Apr; 55(4):570-9. PubMed ID: 7357085
    [No Abstract]   [Full Text] [Related]  

  • 33. Deranged isoleucine metabolism during ketotic attacks in patients with methylmalonic acidaemia.
    Duran M; Bruinvis L; Ketting D; Wadman SK
    J Inherit Metab Dis; 1978; 1(3):105-7. PubMed ID: 116077
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Effect of nitrous oxide on human bone marrow cells and its synergistic effect with methionine and methotrexate on functional folate deficiency.
    Kano Y; Sakamoto S; Sakuraya K; Kubota T; Hida K; Suda K; Takaku F
    Cancer Res; 1981 Nov; 41(11 Pt 1):4698-701. PubMed ID: 7306986
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood.
    Carmel R; Watkins D; Goodman SI; Rosenblatt DS
    N Engl J Med; 1988 Jun; 318(26):1738-41. PubMed ID: 2897628
    [No Abstract]   [Full Text] [Related]  

  • 36. Cobalamins in fibroblasts cultured from normal control subjects and patients with methylmalonic aciduria.
    Linnell JC; Matthews DM; Mudd SH; Uhlendorf BW; Wise IJ
    Pediatr Res; 1976 Mar; 10(3):179-83. PubMed ID: 2896
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Studies on the urinary acidic metabolites from three patients with methylmalonic aciduria.
    Kuhara T; Matsumoto I
    Biomed Mass Spectrom; 1980 Oct; 7(10):424-8. PubMed ID: 6111361
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Methylmalonic aciduria. Classification, diagnosis and therapy (author's transl)].
    Leupold D
    Klin Wochenschr; 1977 Jan; 55(2):57-63. PubMed ID: 319293
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The influence of nitrous oxide on methionine, S-adenosylmethionine, and other amino acids.
    ViƱa JR; Davis DW; Hawkins RA
    Anesthesiology; 1986 Apr; 64(4):490-5. PubMed ID: 2870665
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Urinary methylmalonic acid excretion.
    Chanarin I
    Blood; 1983 Jan; 61(1):208-9. PubMed ID: 6848145
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.