BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 8569042)

  • 1. Non-radioactive mismatch analysis to detect small mutations in human hypoxanthine-guanine phosphoribosyl transferase cDNA.
    Tsuboi K; Nose T; Okinaka RT; Chen DJ
    Jpn J Med Sci Biol; 1995 Aug; 48(4):163-75. PubMed ID: 8569042
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A mouse model for the study of in vivo mutational spectra: sequence specificity of ethylene oxide at the hprt locus.
    Walker VE; Skopek TR
    Mutat Res; 1993 Jul; 288(1):151-62. PubMed ID: 7686258
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening for mutations in human HPRT cDNA using the polymerase chain reaction (PCR) in combination with constant denaturant gel electrophoresis (CDGE).
    Smith-Sørensen B; Hovig E; Andersson B; Børresen AL
    Mutat Res; 1992 Sep; 269(1):41-53. PubMed ID: 1381470
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rapid characterization of mutations in amplified human hprt cDNA by polyacrylamide gel electrophoresis.
    Garganta F; Krause G; Scherer G
    Mutat Res; 1998 Nov; 406(1):33-43. PubMed ID: 9920053
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular analysis of mutations in the human HPRT gene.
    Keohavong P; Xi L; Grant SG
    Methods Mol Biol; 2014; 1105():291-301. PubMed ID: 24623237
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hypoxanthine phosphoribosyltransferase cDNA in gerbils (Meriones unguiculatus).
    Mai Z; Horohov DW; Klei TR
    Lab Anim Sci; 1998 Apr; 48(2):179-83. PubMed ID: 10090010
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The gene encoding hypoxanthine-guanine phosphoribosyltransferase as target for mutational analysis: PCR cloning and sequencing of the cDNA from the rat.
    Jansen JG; Vrieling H; van Zeeland AA; Mohn GR
    Mutat Res; 1992 Apr; 266(2):105-16. PubMed ID: 1373820
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic analysis of the HPRT mutation of Lesch-Nyhan syndrome in a Chinese family.
    Lee WJ; Lee HM; Chi CS; Yang MT; Lin HY; Lin WH
    Zhonghua Yi Xue Za Zhi (Taipei); 1995 Dec; 56(6):359-66. PubMed ID: 8851475
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A germ line mutation within the coding sequence for the putative 5-phosphoribosyl-1-pyrophosphate binding site of hypoxanthine-guanine phosphoribosyltransferase (HPRT) in a Lesch-Nyhan patient: missense mutations within a functionally important region probably cause disease.
    Fujimori S; Tagaya T; Kamatani N; Akaoka I
    Hum Genet; 1992 Dec; 90(4):385-8. PubMed ID: 1282899
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of point mutations induced by ultraviolet light in human cells.
    Keohavong P; Liu VF; Thilly WG
    Mutat Res; 1991 Jul; 249(1):147-59. PubMed ID: 2067529
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutational spectra at the hypoxanthine-guanine phosphoribosyltransferase (HPRT) locus in T-lymphocytes of nonsmoking and smoking lung cancer patients.
    Hackman P; Hou SM; Nyberg F; Pershagen G; Lambert B
    Mutat Res; 2000 Jun; 468(1):45-61. PubMed ID: 10863157
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spectrum of point mutations in the coding region of the hypoxanthine-guanine phosphoribosyltransferase (hprt) gene in human T-lymphocytes in vivo.
    Podlutsky A; Osterholm AM; Hou SM; Hofmaier A; Lambert B
    Carcinogenesis; 1998 Apr; 19(4):557-66. PubMed ID: 9600338
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sequence of the rat hypoxanthine guanine phosphoribosyl transferase (HPRT) transcriptional promoter region in wild-type and mutant rat liver epithelial cell lines.
    Lazarus P; Calcagnotto A; Williams GM; Alvi N
    Mutat Res; 1994 Dec; 325(4):117-23. PubMed ID: 7527902
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel types of mutation identified at the hprt locus of human T-lymphocytes.
    Hou SM
    Mutat Res; 1994 Jul; 308(1):23-31. PubMed ID: 7516483
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular analysis of five independent Japanese mutant genes responsible for hypoxanthine guanine phosphoribosyltransferase (HPRT) deficiency.
    Yamada Y; Goto H; Suzumori K; Adachi R; Ogasawara N
    Hum Genet; 1992 Dec; 90(4):379-84. PubMed ID: 1483694
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Resolution of a missense mutant in human genomic DNA by denaturing gradient gel electrophoresis and direct sequencing using in vitro DNA amplification: HPRT Munich.
    Cariello NF; Scott JK; Kat AG; Thilly WG; Keohavong P
    Am J Hum Genet; 1988 May; 42(5):726-34. PubMed ID: 3358423
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of in vivo mutation in exon 8 of the rat hprt gene.
    Mittelstaedt RA; Heflich RH
    Mutat Res; 1994 Nov; 311(1):139-48. PubMed ID: 7526167
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular Analysis of Mutations in the Human HPRT Gene.
    Keohavong P; Xi L; Grant SG
    Methods Mol Biol; 2020; 2102():349-359. PubMed ID: 31989566
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency: identification of point mutations in Japanese patients with Lesch-Nyhan syndrome and hereditary gout and their permanent expression in an HPRT-deficient mouse cell line.
    Tohyama J; Nanba E; Ohno K
    Hum Genet; 1994 Feb; 93(2):175-81. PubMed ID: 8112742
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of large X-ray-induced mutant populations by denaturing gradient gel electrophoresis.
    Okinaka RT; Anzick SL; Oller A; Thilly WG
    Radiat Res; 1993 Aug; 135(2):212-21. PubMed ID: 8367592
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.