BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

278 related articles for article (PubMed ID: 7433115)

  • 21. [Structural transformations of oligonucleosomes from pigeon erythrocyte chromatin].
    Osipova TN; Karpova EV; Ramm EI; Svetrlikova SB; Pospelov VA
    Mol Biol (Mosk); 1986; 20(3):853-60. PubMed ID: 3724755
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Major role of the histones H3-H4 in the folding of the chromatin fiber.
    Moore SC; Ausió J
    Biochem Biophys Res Commun; 1997 Jan; 230(1):136-9. PubMed ID: 9020030
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Nucleosomes containing histones H1 or H5 are closely interspersed in chromatin.
    Torres-Martinez S; Ruiz-Carrillo A
    Nucleic Acids Res; 1982 Apr; 10(7):2323-35. PubMed ID: 6178082
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Localization of histone H5 in the subunit organization of chromatin using immunoelectron microscopy.
    Mazen A; De Murcia G; Bernard S; Pouyet J; Champagne M
    Eur J Biochem; 1982 Sep; 127(1):169-76. PubMed ID: 7140753
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Dependence of mononucleosome deoxyribonucleic acid conformation on the deoxyribonucleic acid length and H1/H5 content. Circular dichroism and thermal denaturation studies.
    Cowman MK; Fasman GD
    Biochemistry; 1980 Feb; 19(3):532-41. PubMed ID: 7356945
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Solubility and structure of domains of chicken erythrocyte chromatin containing transcriptionally competent and inactive genes.
    Komaiko W; Felsenfeld G
    Biochemistry; 1985 Feb; 24(5):1186-93. PubMed ID: 4096899
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Differences among chicken erythrocyte histones H1 and H5 in associating with H1-depleted polynucleosomes.
    Klingholz R; Strätling WH
    Int J Biochem; 1988; 20(11):1321-5. PubMed ID: 3248684
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Immunochemical analysis of histone H1 and H5 from pigeon erythroid cells].
    Bers EP; Andreeva NB; Gazarian KG; Kozlov AV; Lipskaia AA
    Biokhimiia; 1979 Jul; 44(7):1264-73. PubMed ID: 91388
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Exchange of histones H1 and H5 between chromatin fragments. A preference of H5 for higher-order structures.
    Thomas JO; Rees C
    Eur J Biochem; 1983 Jul; 134(1):109-15. PubMed ID: 6861754
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Linker histones stabilize the intrinsic salt-dependent folding of nucleosomal arrays: mechanistic ramifications for higher-order chromatin folding.
    Carruthers LM; Bednar J; Woodcock CL; Hansen JC
    Biochemistry; 1998 Oct; 37(42):14776-87. PubMed ID: 9778352
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Chicken erythrocyte nucleus contains two classes of chromatin that differ in micrococcal nuclease susceptibility and solubility at physiological ionic strength.
    Fulmer AW; Bloomfield VA
    Proc Natl Acad Sci U S A; 1981 Oct; 78(10):5968-72. PubMed ID: 6947211
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Erythroid-specific gene chromatin has an altered association with linker histones.
    Ridsdale JA; Rattner JB; Davie JR
    Nucleic Acids Res; 1988 Jul; 16(13):5915-26. PubMed ID: 3399383
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Histone H5 promotes the association of condensed chromatin fragments to give pseudo-higher-order structures.
    Thomas JO; Rees C; Pearson EC
    Eur J Biochem; 1985 Feb; 147(1):143-51. PubMed ID: 3971973
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Histone acetylation alters the capacity of the H1 histones to condense transcriptionally active/competent chromatin.
    Ridsdale JA; Hendzel MJ; Delcuve GP; Davie JR
    J Biol Chem; 1990 Mar; 265(9):5150-6. PubMed ID: 2318888
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Differential compaction of transcriptionally competent and repressed chromatin reconstituted with histone H1 subtypes.
    Nagaraja S; Delcuve GP; Davie JR
    Biochim Biophys Acta; 1995 Jan; 1260(2):207-14. PubMed ID: 7841198
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Involvement of the domains of histones H1 and H5 in the structural organization of soluble chromatin.
    Thoma F; Losa R; Koller T
    J Mol Biol; 1983 Jul; 167(3):619-40. PubMed ID: 6876160
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Histone accessibility determined by lysine-specific acetylation in chicken erythrocyte nuclei.
    Lewis PN; Guillemette JG; Chan S
    Eur J Biochem; 1988 Feb; 172(1):135-45. PubMed ID: 3126068
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Generation of different nucleosome spacing periodicities in vitro. Possible origin of cell type specificity.
    Stein A; Mitchell M
    J Mol Biol; 1988 Oct; 203(4):1029-43. PubMed ID: 2463368
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Role of serine-rich histone (H5) in bird erythrocyte genome inactivation].
    Andreeva NB; Vishnevskaia TIu; Gazarian KG
    Mol Biol (Mosk); 1978; 12(1):123-34. PubMed ID: 634279
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Separation of nucleosomes containing histones H1 and H5.
    Bakayeva TG; Bakayev VV
    Mol Biol Rep; 1978 Oct; 4(3):185-9. PubMed ID: 739986
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.