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 *

141 related articles for article (PubMed ID: 9538515)

  • 61. Simultaneous detection of methylenetetrahydrofolate reductase gene polymorphisms, C677T and A1298C, by melting curve analysis with LightCycler.
    Nakamura S; Aoshima T; Ikeda M; Sekido Y; Shimokata K; Niwa T
    Anal Biochem; 2002 Jul; 306(2):340-3. PubMed ID: 12123675
    [No Abstract]   [Full Text] [Related]  

  • 62. Methylenetetrahydrofolate reductase 677C > T mutation and epilepsy.
    Ono H; Sakamoto A; Mizoguchi N; Sakura N
    J Inherit Metab Dis; 2000 Jul; 23(5):525-6. PubMed ID: 10947212
    [No Abstract]   [Full Text] [Related]  

  • 63. A common mutation of the methylenetetrahydrofolate reductase gene as a risk factor for diabetic nephropathy.
    Odawara M; Yamashita K
    Diabetologia; 1999 May; 42(5):631-2. PubMed ID: 10333059
    [No Abstract]   [Full Text] [Related]  

  • 64. MTHFR gene polymorphism as a risk factor for diabetic retinopathy in type 2 diabetic patients without serum creatinine elevation.
    Maeda M; Yamamoto I; Fukuda M; Nishida M; Fujitsu J; Nonen S; Igarashi T; Motomura T; Inaba M; Fujio Y; Azuma J
    Diabetes Care; 2003 Feb; 26(2):547-8. PubMed ID: 12547903
    [No Abstract]   [Full Text] [Related]  

  • 65. The frequency of the C677T substitution in the methylenetetrahydrofolate reductase gene in Manitoba.
    Mogk RL; Rothenmund H; Evans JA; Carson N; Dawson AJ
    Clin Genet; 2000 Nov; 58(5):406-8. PubMed ID: 11140843
    [No Abstract]   [Full Text] [Related]  

  • 66. Differences in methylenetetrahydrofolate reductase genotype frequencies, between Whites and Blacks.
    Stevenson RE; Schwartz CE; Du YZ; Adams MJ
    Am J Hum Genet; 1997 Jan; 60(1):229-30. PubMed ID: 8981967
    [No Abstract]   [Full Text] [Related]  

  • 67. The 1298(A-->C) mutation of methylenetetrahydrofolate reductase should be designated to the 1289 position of the gene.
    Donnelly JG
    Am J Hum Genet; 2000 Feb; 66(2):744-5. PubMed ID: 10677336
    [No Abstract]   [Full Text] [Related]  

  • 68. Absence of association of fetal MTHFR C677T polymorphism with prenatal Down syndrome pregnancies.
    Yanamandra K; Bocchini JA; Thurmon TF
    Eur J Hum Genet; 2003 Jan; 11(1):5. PubMed ID: 12529699
    [No Abstract]   [Full Text] [Related]  

  • 69. Genotyping method for methylenetetrahydrofolate reductase (C677T thermolabile variant) using heteroduplex technology.
    Clark ZE; Bowen DJ; Whatley SD; Bellamy MF; Collins PW; McDowell IF
    Clin Chem; 1998 Nov; 44(11):2360-2. PubMed ID: 9799766
    [No Abstract]   [Full Text] [Related]  

  • 70. V677 mutation of methylenetetrahydrofolate reductases and cardiovascular disease in Canadian Inuit.
    Hegele RA; Tully C; Young TK; Connelly PW
    Lancet; 1997 Apr; 349(9060):1221-2. PubMed ID: 9130949
    [No Abstract]   [Full Text] [Related]  

  • 71. Association between the methylenetetrahydrofolate reductase 677C>T polymorphism and the risk of secondary lymphoproliferative disease in patients with a first idiopathic thrombosis.
    Gris JC; Mercier E; Quéré I; Dauzat M
    Blood; 2002 Jul; 100(2):735. PubMed ID: 12123235
    [No Abstract]   [Full Text] [Related]  

  • 72. Worldwide distribution of a common methylenetetrahydrofolate reductase mutation.
    Schneider JA; Rees DC; Liu YT; Clegg JB
    Am J Hum Genet; 1998 May; 62(5):1258-60. PubMed ID: 9545406
    [No Abstract]   [Full Text] [Related]  

  • 73. Relevance to spina bifida of mutated methylenetetrahydrofolate reductase.
    Wilcken DE; Wang XL
    Lancet; 1996 Feb; 347(8997):340. PubMed ID: 8569408
    [No Abstract]   [Full Text] [Related]  

  • 74. High-speed prothrombin G-->A 20210 and methylenetetrahydrofolate reductase C-->T 677 mutation detection using real-time fluorescence PCR and melting curves.
    Aslanidis C; Nauck M; Schmitz G
    Biotechniques; 1999 Aug; 27(2):234-6, 238. PubMed ID: 10457821
    [No Abstract]   [Full Text] [Related]  

  • 75. 677-->CT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey.
    Boduroglu K; Alikasifoglu M; Anar B; Tuncbilek E
    Arch Dis Child Fetal Neonatal Ed; 1998 May; 78(3):F235. PubMed ID: 9713045
    [No Abstract]   [Full Text] [Related]  

  • 76. [Is the thermolabile variant of methylenetetrahydrofolate reductase a risk factor of arterial and venous thrombosis?].
    Trillot N; Jude B
    Rev Med Interne; 1997; 18 Suppl 6():657s-659s. PubMed ID: 9515147
    [No Abstract]   [Full Text] [Related]  

  • 77. Spontaneous cervical artery dissection: from risk factors toward pathogenesis.
    Brandt T; Grond-Ginsbach C
    Stroke; 2002 Mar; 33(3):657-8. PubMed ID: 11872881
    [No Abstract]   [Full Text] [Related]  

  • 78. The methylenetetrahydrofolate reductase (Mthfr) gene maps to distal mouse chromosome 4.
    Frosst P; Zhang Z; Pai A; Rozen R
    Mamm Genome; 1996 Nov; 7(11):864-5. PubMed ID: 8875901
    [No Abstract]   [Full Text] [Related]  

  • 79. Molecular beacons: a new approach for semiautomated mutation analysis.
    Giesendorf BA; Vet JA; Tyagi S; Mensink EJ; Trijbels FJ; Blom HJ
    Clin Chem; 1998 Mar; 44(3):482-6. PubMed ID: 9510851
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Methylene tetrahydrofolate reductase mutation and stroke in a monozygotic twin.
    Eikelboom JW; Saharay I; Baker RI; Hankey GJ
    Aust N Z J Med; 1998 Dec; 28(6):849-50. PubMed ID: 9972427
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.