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 *

143 related articles for article (PubMed ID: 10953951)

  • 1. Novel method for molecular detection of the two common hereditary hemochromatosis mutations.
    Kaler SG; Devaney JM; Pettit EL; Kirshman R; Marino MA
    Genet Test; 2000; 4(2):125-9. PubMed ID: 10953951
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotyping of two mutations in the HFE gene using single-base extension and high-performance liquid chromatography.
    Devaney JM; Pettit EL; Kaler SG; Vallone PM; Butler JM; Marino MA
    Anal Chem; 2001 Feb; 73(3):620-4. PubMed ID: 11217771
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations.
    Stott MK; Fellowes AP; Upton JD; Burt MJ; George PM
    Clin Chem; 1999 Mar; 45(3):426-8. PubMed ID: 10053052
    [No Abstract]   [Full Text] [Related]  

  • 4. Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC.
    Le Gac G; Mura C; Férec C
    Clin Chem; 2001 Sep; 47(9):1633-40. PubMed ID: 11514397
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High-performance liquid chromatography multiplex detection of two single nucleotide mutations associated with hereditary hemochromatosis.
    Liang Q; Davis PA; Thompson BH; Simpson JT
    J Chromatogr B Biomed Sci Appl; 2001 Apr; 754(1):265-70. PubMed ID: 11318424
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An improved real time PCR method for simultaneous detection of C282Y and H63D mutations in the HFE gene associated with hereditary hemochromatosis.
    Walburger DK; Afonina IA; Wydro R
    Mutat Res; 2001 Jan; 432(3-4):69-78. PubMed ID: 11465544
    [TBL] [Abstract][Full Text] [Related]  

  • 7. HFE genotyping by amplification refractory mutation system-denaturing HPLC.
    Pissard S; Huynh LT; Martin J; Goossens M
    Clin Chem; 2002 May; 48(5):769-72. PubMed ID: 11978606
    [No Abstract]   [Full Text] [Related]  

  • 8. A reverse-hybridization assay for the rapid and simultaneous detection of nine HFE gene mutations.
    Oberkanins C; Moritz A; de Villiers JN; Kotze MJ; Kury F
    Genet Test; 2000; 4(2):121-4. PubMed ID: 10953950
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technology.
    Restagno G; Gomez AM; Sbaiz L; De Gobbi M; Roetto A; Bertino E; Fabris C; Fiorucci GC; Fortina P; Camaschella C
    Genet Test; 2000; 4(2):177-81. PubMed ID: 10953958
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of C282Y and H63D in the HFE gene.
    Pointon JJ; Merryweather-Clarke AT; Carella M; Robson KJ
    Genet Test; 2000; 4(2):115-20. PubMed ID: 10953949
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotyping of hemochromatosis-associated mutations in the HFE gene by PCR-RFLP and a novel reverse hybridization method.
    Koeken A; Cobbaert C; Quint W; van Doorn LJ
    Clin Chem Lab Med; 2002 Feb; 40(2):122-5. PubMed ID: 11939483
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary hemochromatosis in Spain.
    Sánchez M; Bruguera M; Quintero E; Barrio Y; Mazzara R; Rodés J; Oliva R
    Genet Test; 2000; 4(2):171-6. PubMed ID: 10953957
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Detection of HFE polymorphism in German patients with hereditary hemochromatosis].
    Burggraf S; Olgemöller B
    Dtsch Med Wochenschr; 2000 Nov; 125(44):1346; author reply 1347. PubMed ID: 11109419
    [No Abstract]   [Full Text] [Related]  

  • 14. HFE genotyping using multiplex allele-specific polymerase chain reaction and capillary electrophoresis.
    Lubin IM; Yamada NA; Stansel RM; Pace RG; Rohlfs EM; Silverman LM
    Arch Pathol Lab Med; 1999 Dec; 123(12):1177-81. PubMed ID: 10583922
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Large-scale screening for HFE mutations: methodology and cost.
    Beutler E; Gelbart T
    Genet Test; 2000; 4(2):131-42. PubMed ID: 10953952
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Clinical usefulness of the detection of mutations of the HFE gene in hemochromatosis].
    Oliva R; Sánchez M; Bruguera M; Rodés J
    Gastroenterol Hepatol; 2000 Nov; 23(9):433-5. PubMed ID: 11126040
    [No Abstract]   [Full Text] [Related]  

  • 17. Rapid single-tube screening of the C282Y hemochromatosis mutation by real-time multiplex allele-specific PCR without fluorescent probes.
    Donohoe GG; Laaksonen M; Pulkki K; Rönnemaa T; Kairisto V
    Clin Chem; 2000 Oct; 46(10):1540-7. PubMed ID: 11017930
    [TBL] [Abstract][Full Text] [Related]  

  • 18. LightCycler PCR assay for simultaneous detection of the H63D and S65C mutations in the HFE hemochromatosis gene based on opposite melting temperature shifts.
    Bollhalder M; Mura C; Landt O; Maly FE
    Clin Chem; 1999 Dec; 45(12):2275-8. PubMed ID: 10585367
    [No Abstract]   [Full Text] [Related]  

  • 19. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Noll WW; Belloni DR; Stenzel TT; Grody WW
    Nat Genet; 1999 Nov; 23(3):271-2. PubMed ID: 10610176
    [No Abstract]   [Full Text] [Related]  

  • 20. Haemochromatosis: automated detection of the two point mutations in the HFE gene: Cys282Tyr and His63Asp.
    Klingler KR; Zech D; Wielckens K
    Clin Chem Lab Med; 2000 Dec; 38(12):1225-30. PubMed ID: 11205685
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.