Pages that link to "Q54749218"
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The following pages link to Changes in chromatin folding in solution. (Q54749218):
Displaying 50 items.
- EM measurements define the dimensions of the "30-nm" chromatin fiber: evidence for a compact, interdigitated structure (Q24542512) (← links)
- Footprinting of linker histones H5 and H1 on the nucleosome (Q24564110) (← links)
- What determines the folding of the chromatin fiber? (Q24602085) (← links)
- A metastable structure for the compact 30-nm chromatin fibre (Q27343084) (← links)
- Histone H1 subtypes differentially modulate chromatin condensation without preventing ATP-dependent remodeling by SWI/SNF or NURF. (Q33507902) (← links)
- Direct detection of linker DNA bending in defined-length oligomers of chromatin (Q33821984) (← links)
- Replacement of histone H1 by H5 in vivo does not change the nucleosome repeat length of chromatin but increases its stability (Q33919824) (← links)
- Chromatin structure of transcriptionally competent and repressed genes (Q33923306) (← links)
- Correlation between endogenous nucleosomal hyper(ADP-ribosyl)ation of histone H1 and the induction of chromatin relaxation (Q33933862) (← links)
- Use of histone antibodies for studying chromatin topography and the phosphorylation of chromatin subunits (Q33940001) (← links)
- Analytical ultracentrifugation and the characterization of chromatin structure (Q34057400) (← links)
- Effect of DNA groove binder distamycin A upon chromatin structure (Q34064478) (← links)
- Histones: Controlling Tumor Signaling Circuitry (Q34109472) (← links)
- Small angle x-ray scattering of chromatin. Radius and mass per unit length depend on linker length (Q34127193) (← links)
- Chromatin fiber structure: morphology, molecular determinants, structural transitions. (Q34167910) (← links)
- Chromatin fibers are left-handed double helices with diameter and mass per unit length that depend on linker length. (Q34196678) (← links)
- Molecular modeling of the chromatosome particle (Q34213222) (← links)
- Assembly of chromatin fibers into metaphase chromosomes analyzed by transmission electron microscopy and scanning electron microscopy (Q34258032) (← links)
- Differences of supranucleosomal organization in different kinds of chromatin: cell type-specific globular subunits containing different numbers of nucleosomes (Q34267736) (← links)
- Higher-order structure of Saccharomyces cerevisiae chromatin (Q34314952) (← links)
- Chromatin higher-order structure studied by neutron scattering and scanning transmission electron microscopy (Q34362137) (← links)
- X-ray structure of a tetranucleosome and its implications for the chromatin fibre (Q34431881) (← links)
- 30 nm chromatin fibre decompaction requires both H4-K16 acetylation and linker histone eviction (Q34800325) (← links)
- The high mobility group proteins, HMG 14 and 17, do not prevent the formation of chromatin higher order structure (Q35497438) (← links)
- Control of 5S RNA transcription in Xenopus somatic cell chromatin: activation with an oocyte extract. (Q35668861) (← links)
- Histone hyperacetylation has little effect on the higher order folding of chromatin (Q35677784) (← links)
- Histories H1 and H5: one or two molecules per nucleosome? (Q35745519) (← links)
- Identification of two DNA-binding sites on the globular domain of histone H5. (Q35900412) (← links)
- Periodic binding of individual core histones to DNA: inadvertent purification of the core histone H2B as a putative enhancer-binding factor (Q35938795) (← links)
- Formation of higher-order secondary and tertiary chromatin structures by genomic mouse mammary tumor virus promoters (Q35966066) (← links)
- Low angle x-ray diffraction studies of HeLa metaphase chromosomes: effects of histone phosphorylation and chromosome isolation procedure (Q36206808) (← links)
- Higher order structure in a short repeat length chromatin (Q36210481) (← links)
- Chromatin conformation and salt-induced compaction: three-dimensional structural information from cryoelectron microscopy (Q36236348) (← links)
- Chicken erythrocyte nucleus contains two classes of chromatin that differ in micrococcal nuclease susceptibility and solubility at physiological ionic strength (Q36373008) (← links)
- Treatment with sodium butyrate inhibits the complete condensation of interphase chromatin (Q36449939) (← links)
- The higher-order structure of chromatin: evidence for a helical ribbon arrangement (Q36510381) (← links)
- Chromatin structure outside and inside the nucleus (Q36570241) (← links)
- Regulation of the higher-order structure of chromatin by histones H1 and H5 (Q36659577) (← links)
- Conformation of chromatin oligomers. A new argument for a change with the hexanucleosome (Q36660512) (← links)
- Hydrodynamic studies on defined heterochromatin fragments support a 30-nm fiber having six nucleosomes per turn (Q37413887) (← links)
- Packaged DNA. An elastic model (Q38148554) (← links)
- High-level transgene expression in plant cells: effects of a strong scaffold attachment region from tobacco. (Q38358283) (← links)
- The superstructure of chromatin and its condensation mechanism. II. Theoretical analysis of the X-ray scattering patterns and model calculations (Q38591182) (← links)
- The superstructure of chromatin and its condensation mechanism. I. Synchrotron radiation X-ray scattering results (Q38591185) (← links)
- Circle ligation of in vitro assembled chromatin indicates a highly flexible structure (Q39689822) (← links)
- Transcriptionally active chromatin (Q40156200) (← links)
- Salt-dependent compaction of di- and trinucleosomes studied by small-angle neutron scattering (Q40167668) (← links)
- The Folding of Chromatin (Q40167976) (← links)
- Proteases as structural probes for chromatin: The domain structure of histones (Q40179478) (← links)
- Purification of genomic DNA using heparin to remove nuclear proteins (Q40408077) (← links)