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 *

174 related articles for article (PubMed ID: 9482872)

  • 1. High-throughput genetic analysis using microfabricated 96-sample capillary array electrophoresis microplates.
    Simpson PC; Roach D; Woolley AT; Thorsen T; Johnston R; Sensabaugh GF; Mathies RA
    Proc Natl Acad Sci U S A; 1998 Mar; 95(5):2256-61. PubMed ID: 9482872
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High speed single nucleotide polymorphism typing of a hereditary haemochromatosis mutation with capillary array electrophoresis microplates.
    Medintz I; Wong WW; Sensabaugh G; Mathies RA
    Electrophoresis; 2000 Jul; 21(12):2352-8. PubMed ID: 10939445
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High-speed DNA genotyping using microfabricated capillary array electrophoresis chips.
    Woolley AT; Sensabaugh GF; Mathies RA
    Anal Chem; 1997 Jun; 69(11):2181-6. PubMed ID: 9183181
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-performance genetic analysis using microfabricated capillary array electrophoresis microplates.
    Medintz IL; Paegel BM; Blazej RG; Emrich CA; Berti L; Scherer JR; Mathies RA
    Electrophoresis; 2001 Oct; 22(18):3845-56. PubMed ID: 11700713
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genotyping by microdevice electrophoresis.
    Schmalzing D; Koutny L; Adourian A; Chisholm D; Matsudaira P; Ehrlich D
    Methods Mol Biol; 2001; 163():163-73. PubMed ID: 11242941
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. A cheaper and more rapid polymerase chain reaction-restriction fragment length polymorphism method for the detection of the HLA-H gene mutations occurring in hereditary hemochromatosis.
    Lynas C
    Blood; 1997 Nov; 90(10):4235-6. PubMed ID: 9354698
    [No Abstract]   [Full Text] [Related]  

  • 8. High-performance multiplex SNP analysis of three hemochromatosis-related mutations with capillary array electrophoresis microplates.
    Medintz I; Wong WW; Berti L; Shiow L; Tom J; Scherer J; Sensabaugh G; Mathies RA
    Genome Res; 2001 Mar; 11(3):413-21. PubMed ID: 11230165
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Denaturing gradient gel electrophoresis analysis of the hemochromatosis (HFE) gene: impact of HFE gene mutations on the manifestation of porphyria cutanea tarda.
    Christiansen L; Bygum A; Thomsen K; Brandrup F; Hørder M; Petersen NE
    Clin Chem; 1999 Nov; 45(11):2025-6. PubMed ID: 10545080
    [No Abstract]   [Full Text] [Related]  

  • 10. Targeted disruption of the HFE gene.
    Beutler E
    Proc Natl Acad Sci U S A; 1998 Mar; 95(5):2033-4. PubMed ID: 9482831
    [No Abstract]   [Full Text] [Related]  

  • 11. Hemochromatosis-related mutation detection.
    Merryweather-Clarke AT; Shearman JD; Robson KJ; Pointon JJ; Liu YT; Bomford A; Dooley J; Walker AP; Worwood M
    Blood; 1998 Apr; 91(7):2620-1. PubMed ID: 9516166
    [No Abstract]   [Full Text] [Related]  

  • 12. Rapid diagnosis of the HLA-H gene Cys 282 Tyr mutation in hemochromatosis by polymerase chain reaction--a very rare mutation in the Chinese population.
    Chang JG; Liu TC; Lin SF
    Blood; 1997 May; 89(9):3492-3. PubMed ID: 9129062
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
    Hellerbrand C; Bosserhoff AK; Seegers S; Lingner G; Wrede C; Lock G; Schölmerich J; Büttner R
    Scand J Gastroenterol; 2001 Nov; 36(11):1211-6. PubMed ID: 11686223
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Evaluation of a nucleic acid-based cross-linking assay to screen for hereditary hemochromatosis in healthy blood donors.
    Wylenzek C; Engelmann M; Holten D; Van Atta R; Wood M; Gathof B
    Clin Chem; 2000 Nov; 46(11):1853-5. PubMed ID: 11067829
    [No Abstract]   [Full Text] [Related]  

  • 18. Rapid diagnosis of hemochromatosis gene Cys282Tyr mutation by SSCP analysis.
    Hertzberg MS; McDonald D; Mirochnik O
    Am J Hematol; 1998 Mar; 57(3):260-1. PubMed ID: 9495384
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Efficient large-scale screening for the hemochromatosis susceptibility gene mutation.
    Takeuchi T; Soejima H; Faed JM; Yun K
    Blood; 1997 Oct; 90(7):2848-9. PubMed ID: 9326257
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.