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 *

164 related articles for article (PubMed ID: 7333455)

  • 21. The DNA sequence of sea urchin (S. purpuratus) H2A, H2B and H3 histone coding and spacer regions.
    Sures I; Lowry J; Kedes LH
    Cell; 1978 Nov; 15(3):1033-44. PubMed ID: 728984
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The eta-globin gene. Its long evolutionary history in the beta-globin gene family of mammals.
    Goodman M; Koop BF; Czelusniak J; Weiss ML
    J Mol Biol; 1984 Dec; 180(4):803-23. PubMed ID: 6527390
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Characterization of two nonallelic pairs of late histone H2A and H2B genes of the sea urchin: differential regulation in the embryo and tissue-specific expression in the adult.
    Kemler I; Busslinger M
    Mol Cell Biol; 1986 Nov; 6(11):3746-54. PubMed ID: 3025611
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Direct demonstration of termination signals for RNA polymerase II from the sea urchin H2A histone gene.
    Briggs D; Jackson D; Whitelaw E; Proudfoot NJ
    Nucleic Acids Res; 1989 Oct; 17(20):8061-71. PubMed ID: 2813057
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Stimulation of sea urchin H2B histone gene transcription by a chromatin-associated protein fraction depends on gene sequences downstream of the transcription start site.
    Mous J; Stunnenberg H; Georgiev O; Birnstiel ML
    Mol Cell Biol; 1985 Oct; 5(10):2764-9. PubMed ID: 3837183
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Estimation of average number of nucleotide substitutions when the rate of substitution varies with nucleotide.
    Gojobori T; Ishii K; Nei M
    J Mol Evol; 1982; 18(6):414-23. PubMed ID: 7175958
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The five cleavage-stage (CS) histones of the sea urchin are encoded by a maternally expressed family of replacement histone genes: functional equivalence of the CS H1 and frog H1M (B4) proteins.
    Mandl B; Brandt WF; Superti-Furga G; Graninger PG; Birnstiel ML; Busslinger M
    Mol Cell Biol; 1997 Mar; 17(3):1189-200. PubMed ID: 9032246
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Isolation and nucleotide sequence analysis of the beta-type globin pseudogene from human, gorilla and chimpanzee.
    Chang LY; Slightom JL
    J Mol Biol; 1984 Dec; 180(4):767-84. PubMed ID: 6098690
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Evolution of alpha q- and beta-tubulin genes as inferred by the nucleotide sequences of sea urchin cDNA clones.
    Alexandraki D; Ruderman JV
    J Mol Evol; 1983; 19(6):397-410. PubMed ID: 6317873
    [TBL] [Abstract][Full Text] [Related]  

  • 30. An unusual transposon with long terminal inverted repeats in the sea urchin Strongylocentrotus purpuratus.
    Liebermann D; Hoffman-Liebermann B; Weinthal J; Childs G; Maxson R; Mauron A; Cohen SN; Kedes L
    Nature; 1983 Nov 24-30; 306(5941):342-7. PubMed ID: 6316151
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Variability of evolutionary rates of DNA.
    Gillespie JH
    Genetics; 1986 Aug; 113(4):1077-91. PubMed ID: 3744027
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Fetal recruitment of anthropoid gamma-globin genes. Findings from phylogenetic analyses involving the 5'-flanking sequences of the psi gamma 1 globin gene of spider monkey Ateles geoffroyi.
    Hayasaka K; Fitch DH; Slightom JL; Goodman M
    J Mol Biol; 1992 Apr; 224(3):875-81. PubMed ID: 1569563
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A genetic code Boolean structure. I. The meaning of Boolean deductions.
    Sánchez R; Morgado E; Grau R
    Bull Math Biol; 2005 Jan; 67(1):1-14. PubMed ID: 15691536
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Nonallelic histone gene clusters of individual sea urchins (Lytechinus pictus): polarity and gene organization.
    Cohn RH; Kedes LH
    Cell; 1979 Nov; 18(3):843-53. PubMed ID: 519757
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [The loss of CpG dinucleotides from DNA. III. Methylation and evolution of histone genes].
    Mazin AL; Vaniushin BF
    Mol Biol (Mosk); 1987; 21(3):678-87. PubMed ID: 3657769
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Extraordinarily high evolutionary rate of pseudogenes: evidence for the presence of selective pressure against changes between synonymous codons.
    Miyata T; Hayashida H
    Proc Natl Acad Sci U S A; 1981 Sep; 78(9):5739-43. PubMed ID: 6795634
    [TBL] [Abstract][Full Text] [Related]  

  • 37. DNA and the neutral theory.
    Kimura M
    Philos Trans R Soc Lond B Biol Sci; 1986 Jan; 312(1154):343-54. PubMed ID: 2870526
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Evidence from nuclear sequences that invariable sites should be considered when sequence divergence is calculated.
    Shoemaker JS; Fitch WM
    Mol Biol Evol; 1989 May; 6(3):270-89. PubMed ID: 2622335
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The primate psi beta 1 gene. An ancient beta-globin pseudogene.
    Harris S; Barrie PA; Weiss ML; Jeffreys AJ
    J Mol Biol; 1984 Dec; 180(4):785-801. PubMed ID: 6527389
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Nonneutral evolution of the transcribed pseudogene Makorin1-p1 in mice.
    Podlaha O; Zhang J
    Mol Biol Evol; 2004 Dec; 21(12):2202-9. PubMed ID: 15306660
    [TBL] [Abstract][Full Text] [Related]  

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