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 *

76 related articles for article (PubMed ID: 10464599)

  • 1. A simple system for automated two-dimensional electrophoresis: applications to genetic testing.
    Dhanda RK; Smith WM; Scott CB; Eng C; Vijg J
    Genet Test; 1998; 2(1):67-70. PubMed ID: 10464599
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Accurate, high-throughput "snapshot" detection of hMLH1 mutations by two-dimensional DNA electrophoresis.
    Smith WM; Van Orsouw NJ; Fox EA; Kolodner RD; Vijg J; Eng C
    Genet Test; 1998; 2(1):43-53. PubMed ID: 10464596
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutational analysis of the hMLH1 gene using an automated two-dimensional DNA typing system.
    Sasaki S; Tokino T; Miyatsu T; Muto T; Nakamura Y
    Hum Mutat; 1997; 9(2):164-71. PubMed ID: 9067757
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-speed, multicolor fluorescent two-dimensional gene scanning.
    McGrath SB; Bounpheng M; Torres L; Calavetta M; Scott CB; Suh Y; Rines D; van Orsouw N; Vijg J
    Genomics; 2001 Nov; 78(1-2):83-90. PubMed ID: 11707076
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rapid design of denaturing gradient-based two-dimensional electrophoretic gene mutational scanning tests.
    van Orsouw NJ; Dhanda RK; Rines RD; Smith WM; Sigalas I; Eng C; Vijg J
    Nucleic Acids Res; 1998 May; 26(10):2398-406. PubMed ID: 9580692
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Design and application of 2-D DGGE-based gene mutational scanning tests.
    Van Orsouw NJ; Vijg J
    Genet Anal; 1999 Feb; 14(5-6):205-13. PubMed ID: 10084116
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Various mutation screening techniques in the DNA mismatch repair genes hMSH2 and hMLH1.
    Wahlberg S; Liu T; Lindblom P; Lindblom A
    Genet Test; 1999; 3(3):259-64. PubMed ID: 10495924
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mutations of the hMSH2 and hMlH1 genes are responsible for 90% of hereditary colorectal carcinomas].
    Hahn SA; Schmiegel WH
    Z Gastroenterol; 1995 Feb; 33(2):135-7. PubMed ID: 7725761
    [No Abstract]   [Full Text] [Related]  

  • 9. Rapid diagnostic test for hereditary nonpolyposis colon cancer kindred using polymerase chain reaction.
    Faragher IG; Whitehead RH
    Dis Colon Rectum; 1998 Jul; 41(7):938-40. PubMed ID: 9678385
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unbalanced germ-line expression of hMLH1 and hMSH2 alleles in hereditary nonpolyposis colorectal cancer.
    Curia MC; Palmirotta R; Aceto G; Messerini L; Verì MC; Crognale S; Valanzano R; Ficari F; Fracasso P; Stigliano V; Tonelli F; Casale V; Guadagni F; Battista P; Mariani-Costantini R; Cama A
    Cancer Res; 1999 Aug; 59(15):3570-5. PubMed ID: 10446963
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identifying hereditary nonpolyposis colorectal cancer.
    Lynch HT; Smyrk TC
    N Engl J Med; 1998 May; 338(21):1537-8. PubMed ID: 9593794
    [No Abstract]   [Full Text] [Related]  

  • 12. Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.
    Wijnen JT; Vasen HF; Khan PM; Zwinderman AH; van der Klift H; Mulder A; Tops C; Møller P; Fodde R
    N Engl J Med; 1998 Aug; 339(8):511-8. PubMed ID: 9709044
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A yeast two-hybrid assay provides a simple way to evaluate the vast majority of hMLH1 germ-line mutations.
    Kondo E; Suzuki H; Horii A; Fukushige S
    Cancer Res; 2003 Jun; 63(12):3302-8. PubMed ID: 12810663
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Record no. 23: hMLH1].
    Soussi T
    Bull Cancer; 1999 Mar; 86(3):245-6. PubMed ID: 10847718
    [No Abstract]   [Full Text] [Related]  

  • 15. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.
    Bronner CE; Baker SM; Morrison PT; Warren G; Smith LG; Lescoe MK; Kane M; Earabino C; Lipford J; Lindblom A
    Nature; 1994 Mar; 368(6468):258-61. PubMed ID: 8145827
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae.
    Shimodaira H; Filosi N; Shibata H; Suzuki T; Radice P; Kanamaru R; Friend SH; Kolodner RD; Ishioka C
    Nat Genet; 1998 Aug; 19(4):384-9. PubMed ID: 9697702
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis.
    Wu Y; Nyström-Lahti M; Osinga J; Looman MW; Peltomäki P; Aaltonen LA; de la Chapelle A; Hofstra RM; Buys CH
    Genes Chromosomes Cancer; 1997 Apr; 18(4):269-78. PubMed ID: 9087566
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease.
    Aaltonen LA; Salovaara R; Kristo P; Canzian F; Hemminki A; Peltomäki P; Chadwick RB; Kääriäinen H; Eskelinen M; Järvinen H; Mecklin JP; de la Chapelle A
    N Engl J Med; 1998 May; 338(21):1481-7. PubMed ID: 9593786
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome.
    Risinger JI; Barrett JC; Watson P; Lynch HT; Boyd J
    Cancer; 1996 May; 77(9):1836-43. PubMed ID: 8646682
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two types of sporadic multiple colorectal cancers with and without HNPCC-like genetic instability.
    Komura K; Masuda H; Esumi M
    Hepatogastroenterology; 1999; 46(30):3115-20. PubMed ID: 10626171
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.