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 *

170 related articles for article (PubMed ID: 3969155)

  • 21. A beta-thalassemia lesion abolishes the same Mst II site as the sickle mutation.
    Chang JC; Alberti A; Kan YW
    Nucleic Acids Res; 1983 Nov; 11(22):7789-94. PubMed ID: 6316272
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Double-strand cleavage at a two-base deletion mismatch in a DNA heteroduplex by nuclease S1.
    Burdon MG; Lees JH
    Biosci Rep; 1985 Aug; 5(8):627-32. PubMed ID: 2998501
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Heteroduplex formation: a potential source of genotyping error from PCR products.
    Hatcher SL; Lambert QT; Teplitz RL; Carlson JR
    Prenat Diagn; 1993 Mar; 13(3):171-7. PubMed ID: 8506218
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Rapid detection of point mutations and polymorphisms of the alpha-globin genes by DGGE and SSCA.
    Harteveld KL; Heister AJ; Giordano PC; Losekoot M; Bernini LF
    Hum Mutat; 1996; 7(2):114-22. PubMed ID: 8829628
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Comparison of RNase A, a chemical cleavage and GC-clamped denaturing gradient gel electrophoresis for the detection of mutations in exon 9 of the human acid beta-glucosidase gene.
    Theophilus BD; Latham T; Grabowski GA; Smith FI
    Nucleic Acids Res; 1989 Oct; 17(19):7707-22. PubMed ID: 2508065
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A general method for saturation mutagenesis of cloned DNA fragments.
    Myers RM; Lerman LS; Maniatis T
    Science; 1985 Jul; 229(4710):242-7. PubMed ID: 2990046
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [New single point mutation at the initiation codon (ATG-AGG) identified in amplified genomic DNA of a Chinese with beta-thalassaemia].
    Xie S
    Zhonghua Yi Xue Za Zhi; 1990 May; 70(5):258-61, 20. PubMed ID: 1975769
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Denaturing gradient gel analysis of single-base substitutions at a mouse adenine phosphoribosyltransferase splice acceptor site.
    Dlouhy SR; Schaff DA; Trofatter JA; Liu HS; Stambrook PJ; Tischfield JA
    Mol Carcinog; 1989; 2(4):217-25. PubMed ID: 2803521
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular defects in beta-thalassemia.
    Nienhuis AW; Ley T; Pepe G; Tam J; Kantor J
    Birth Defects Orig Artic Ser; 1982; 18(7):69-79. PubMed ID: 6186315
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detection of beta-globin gene mutations by polymerase chain reaction.
    Lee HH; Chang JG; Lee LS; Lin ST; Ko TM; Choo KB
    Proc Natl Sci Counc Repub China B; 1991 Apr; 15(2):97-100. PubMed ID: 1682965
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvases.
    Mashal RD; Koontz J; Sklar J
    Nat Genet; 1995 Feb; 9(2):177-83. PubMed ID: 7719346
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular basis of beta (0)-thalassemia/HbE disease in Thailand.
    Petmitr S; Wilairat P; Kownkon J; Winichagoon P; Fucharoen S
    Biochem Biophys Res Commun; 1989 Jul; 162(2):846-51. PubMed ID: 2757643
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutation detection by denaturing DNA chromatography using fluorescently labeled polymerase chain reaction products.
    Hecker KH; Taylor PD; Gjerde DT
    Anal Biochem; 1999 Aug; 272(2):156-64. PubMed ID: 10415084
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An improved method for the detection of genetic variations in DNA with denaturing gradient gel electrophoresis.
    Takahashi N; Hiyama K; Kodaira M; Satoh C
    Mutat Res; 1990 Apr; 234(2):61-70. PubMed ID: 2183038
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterization of beta-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA.
    Wong C; Dowling CE; Saiki RK; Higuchi RG; Erlich HA; Kazazian HH
    Nature; 1987 Nov 26-Dec 2; 330(6146):384-6. PubMed ID: 3683554
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Rapid classification of phenylketonuria genotypes by analysis of heteroduplexes generated by PCR-amplifiable synthetic DNA.
    Wood N; Tyfield L; Bidwell J
    Hum Mutat; 1993; 2(2):131-7. PubMed ID: 8318990
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Detection of 81 of 81 known mouse beta-globin promoter mutations with T4 endonuclease VII--the EMC method.
    Youil R; Kemper B; Cotton RG
    Genomics; 1996 Mar; 32(3):431-5. PubMed ID: 8838807
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Highly selective isolation of unknown mutations in diverse DNA fragments: toward new multiplex screening in cancer.
    Chakrabarti S; Price BD; Tetradis S; Fox EA; Zhang Y; Maulik G; Makrigiorgos GM
    Cancer Res; 2000 Jul; 60(14):3732-7. PubMed ID: 10919642
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A new codon 31 (-C) mutant resulting in beta zero-thalassemia.
    Lin LI; Lin KS; Lin KH
    Proc Natl Sci Counc Repub China B; 1992 Jan; 16(1):6-9. PubMed ID: 1631246
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Influence of nearest neighbor sequence on the stability of base pair mismatches in long DNA; determination by temperature-gradient gel electrophoresis.
    Ke SH; Wartell RM
    Nucleic Acids Res; 1993 Nov; 21(22):5137-43. PubMed ID: 8255768
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.