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 *

81 related articles for article (PubMed ID: 17994268)

  • 21. The breakdown of the word symmetry in the human genome.
    Afreixo V; Bastos CA; Garcia SP; Rodrigues JM; Pinho AJ; Ferreira PJ
    J Theor Biol; 2013 Oct; 335():153-9. PubMed ID: 23831271
    [TBL] [Abstract][Full Text] [Related]  

  • 22. High-resolution copy number arrays in cancer and the problem of normal genome copy number variation.
    Gorringe KL; Campbell IG
    Genes Chromosomes Cancer; 2008 Nov; 47(11):933-8. PubMed ID: 18663746
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Survival of replicators with parabolic growth tendency and exponential decay.
    Scheuring I; Szathmáry E
    J Theor Biol; 2001 Sep; 212(1):99-105. PubMed ID: 11527448
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Estimation of SNP allele frequencies by SSCP analysis of pooled DNA.
    Tahira T; Kukita Y; Higasa K; Okazaki Y; Yoshinaga A; Hayashi K
    Methods Mol Biol; 2009; 578():193-207. PubMed ID: 19768595
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A rebuttal to the comments on the genome order index.
    Zhang R
    Comput Biol Chem; 2009 Aug; 33(4):350. PubMed ID: 19097944
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Necessary relations for nucleotide frequencies.
    Sinclair R
    J Theor Biol; 2015 Jun; 374():179-82. PubMed ID: 25843217
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Codon evolution is governed by linear formulas.
    Sorimachi K; Okayasu T
    Amino Acids; 2008 May; 34(4):661-8. PubMed ID: 18180868
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel look at DNA and life-Symmetry as evolutionary forcing.
    Rosandić M; Vlahović I; Paar V
    J Theor Biol; 2019 Dec; 483():109985. PubMed ID: 31469987
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Single nucleotide polymorphism screening with denaturing gradient gel electrophoresis.
    Knapp LA
    Methods Mol Biol; 2009; 578():137-51. PubMed ID: 19768591
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prediction of replication time zones at single nucleotide resolution in the human genome.
    Gao F; Zhang CT
    FEBS Lett; 2008 Jul; 582(16):2441-4. PubMed ID: 18555015
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Structural variation in the human genome contributes to variation of traits].
    Barøy T; Misceo D; Frengen E
    Tidsskr Nor Laegeforen; 2008 Sep; 128(17):1951-5. PubMed ID: 18787571
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Analysis of bilateral inverse symmetry in whole bacterial chromosomes.
    Sánchez J; José MV
    Biochem Biophys Res Commun; 2002 Nov; 299(1):126-34. PubMed ID: 12435398
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Ensuring the fidelity of recombination in mammalian chromosomes.
    Waldman AS
    Bioessays; 2008 Nov; 30(11-12):1163-71. PubMed ID: 18937366
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Recombination frequency in plasmid DNA containing direct repeats--predictive correlation with repeat and intervening sequence length.
    Oliveira PH; Lemos F; Monteiro GA; Prazeres DM
    Plasmid; 2008 Sep; 60(2):159-65. PubMed ID: 18647618
    [TBL] [Abstract][Full Text] [Related]  

  • 35. PoooL: an efficient method for estimating haplotype frequencies from large DNA pools.
    Zhang H; Yang HC; Yang Y
    Bioinformatics; 2008 Sep; 24(17):1942-8. PubMed ID: 18573795
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Symmetry observations in long nucleotide sequences: a commentary on the Discovery Note of Qi and Cuticchia.
    Forsdyke DR
    Bioinformatics; 2002 Jan; 18(1):215-7. PubMed ID: 11836239
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genome-wide association analyses of expression phenotypes.
    Chen GK; Zheng T; Witte JS; Goode EL; Gao L; Hu P; Suh YJ; Suktitipat B; Szymczak S; Woo JH; Zhang W
    Genet Epidemiol; 2007; 31 Suppl 1():S7-S11. PubMed ID: 18046762
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cataloging coding sequence variations in human genome databases.
    Won HH; Kim HJ; Lee KA; Kim JW
    PLoS One; 2008; 3(10):e3575. PubMed ID: 18974781
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel approach reveals genomic landscapes of single-strand DNA breaks with nucleotide resolution in human cells.
    Cao H; Salazar-García L; Gao F; Wahlestedt T; Wu CL; Han X; Cai Y; Xu D; Wang F; Tang L; Ricciardi N; Cai D; Wang H; Chin MPS; Timmons JA; Wahlestedt C; Kapranov P
    Nat Commun; 2019 Dec; 10(1):5799. PubMed ID: 31862872
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Increased gene coverage and Alu frequency in large linkage disequilibrium blocks of the human genome.
    Wang Y; Fong PY; Leung FC; Mak W; Sham PC
    Genet Mol Res; 2007 Dec; 6(4):1131-41. PubMed ID: 18273807
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.