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Sequence Complexity of Histone H1 Subtypes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0134(19991101)37:2<284::aid-prot13>3.0.co;2-4openalex-snapshot
Local-scale repetitiveness in amino acid use in eukaryote protein sequences: A genomic factor in protein evolution
inferredcites →https://doi.org/10.1002/bies.950180512openalex-snapshot
Simple sequences and the expanding genome
inferredcites →https://doi.org/10.1002/bies.950190311openalex-snapshot
What do linker histones do in chromatin?
inferredcites →https://doi.org/10.1002/j.1460-2075.1989.tb03440.xopenalex-snapshot
SPKK, a new nucleic acid‐binding unit of protein found in histone.
inferredcites →https://doi.org/10.1002/j.1460-2075.1989.tb03536.xopenalex-snapshot
Comparison of the gap segmentation gene hunchback between Drosophila melanogaster and Drosophila virilis reveals novel modes of evolutionary change.
inferredcites →https://doi.org/10.1002/pro.5560030406openalex-snapshot
A proposal for a coherent mammalian histone H1 nomenclature correlated with amino acid sequences
inferredcites →https://doi.org/10.1007/bf02337357openalex-snapshot
Sequence simplicity and evolution of the 3′ untranslated region of the histone H1° Gene
inferredcites →https://doi.org/10.1007/bf02342746openalex-snapshot
Length polymorphism in the threonine-glycine-encoding repeat region of theperiod gene inDrosophila
inferredcites →https://doi.org/10.1007/bf02406725openalex-snapshot
Adaptive nature of interspecies variation of histone H1 in insects
inferredcites →https://doi.org/10.1016/0006-291x(69)90237-xopenalex-snapshot
A new histone found only in mammalian tissues with little cell division
inferredcites →https://doi.org/10.1016/0014-4827(82)90162-8openalex-snapshot
Distribution and synthesis of histone 1 subfractions during spermatogenesis in the rat
inferredcites →https://doi.org/10.1016/0022-2836(86)90006-9openalex-snapshot
The silkmoth late chorion locus
inferredcites →https://doi.org/10.1016/0022-2836(90)90355-popenalex-snapshot
The Balbiani ring 3 gene in Chironomus tentans has a diverged repetitive structure split by many introns
inferredcites →https://doi.org/10.1016/0968-0004(91)90040-3openalex-snapshot
Protein motifs that recognize structural features of DNA
inferredcites →https://doi.org/10.1016/s0021-9258(17)43713-6openalex-snapshot
Differences in evolutionary stability among mammalian H1 subtypes. Implications for the roles of H1 subtypes in chromatin.
inferredcites →https://doi.org/10.1016/s0021-9258(18)33359-3openalex-snapshot
Characterization of highly phosphorylated subcomponents of rat thymus H1 histone.
inferredcites →https://doi.org/10.1016/s0021-9258(18)34653-2openalex-snapshot
The H1 histones and their interphase phosphorylated states in differentiated and undifferentiated cell lines derived from murine teratocarcinomas.
inferredcites →https://doi.org/10.1016/s0092-8674(00)80120-8openalex-snapshot
Linker Histone H1 Regulates Specific Gene Expression but Not Global Transcription In Vivo
inferredcites →https://doi.org/10.1016/s0960-9822(98)70206-4openalex-snapshot
The globular domain of histone H1 is sufficient to direct specific gene repression in early Xenopus embryos
inferredcites →https://doi.org/10.1016/s1097-2765(00)80215-4openalex-snapshot
Phosphorylation of Linker Histone H1 Regulates Gene Expression In Vivo by Mimicking H1 Removal
inferredcites →https://doi.org/10.1021/bi00048a025openalex-snapshot
DNA- and chromatin-condensing properties of rat testes H1a and H1t compared to those of rat liver H1bdec: H1t is a poor condenser of chromatin
inferredcites →https://doi.org/10.1038/322652a0openalex-snapshot
Cryptic simplicity in DNA is a major source of genetic variation
inferredcites →https://doi.org/10.1073/pnas.86.21.8447openalex-snapshot
Vectorial expansion of the involucrin gene and the relatedness of the hominoids.
inferredcites →https://doi.org/10.1073/pnas.87.8.2887openalex-snapshot
AlgR3, a protein resembling eukaryotic histone H1, regulates alginate synthesis in Pseudomonas aeruginosa.
inferredcites →https://doi.org/10.1074/jbc.273.48.32236openalex-snapshot
In Vitro Binding of H1 Histone Subtypes to Nucleosomal Organized Mouse Mammary Tumor Virus Long Terminal Repeat Promotor
inferredcites →https://doi.org/10.1074/jbc.m104189200openalex-snapshot
Induction of Secondary Structure in a COOH-terminal Peptide of Histone H1 by Interaction with the DNA
inferredcites →https://doi.org/10.1074/jbc.m106952200openalex-snapshot
DNA-induced α-Helical Structure in the NH2-terminal Domain of Histone H1
inferredcites →https://doi.org/10.1093/bioinformatics/10.1.67openalex-snapshot
SIMPLE34: an improved and enhanced implementation for VAX and Sun computers of the SIMPLE algorithm for analysis of clustered repetitive motifs in nucleotide sequences
inferredcites →https://doi.org/10.1093/bioinformatics/18.5.672openalex-snapshot
Detecting cryptically simple protein sequences using the SIMPLE algorithm
inferredcites →https://doi.org/10.1093/emboj/17.5.1454openalex-snapshot
Prolonged glucocorticoid exposure dephosphorylates histone H1 and inactivates the MMTV promoter
inferredcites →https://doi.org/10.1093/nar/20.2.211openalex-snapshot
Slippage synthesis of simple sequence DNA
inferredcites →https://doi.org/10.1093/nar/21.12.2823openalex-snapshot
Evolution of sequence repetition and gene duplications in the TATA-binding protein TBP (TFIID)
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025973openalex-snapshot
Evolution of the vertebrate H1 histone class: evidence for the functional differentiation of the subtypes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040442openalex-snapshot
Slipped-strand mispairing: a major mechanism for DNA sequence evolution.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040505openalex-snapshot
Molecular coevolution among cryptically simple expansion segments of eukaryotic 26S/28S rRNAs.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040662openalex-snapshot
Evolution of the cetacean mitochondrial D-loop region.
inferredcites →https://doi.org/10.1101/gad.8.10.1147openalex-snapshot
Specific regulation of Xenopus chromosomal 5S rRNA gene transcription in vivo by histone H1.
inferredcites →https://doi.org/10.1101/gr.152201openalex-snapshot
Low-Complexity Regions in Plasmodium falciparum Proteins
inferredcites →https://doi.org/10.1110/ps.29602openalex-snapshot
An inducible helix–Gly–Gly–helix motif in the N‐terminal domain of histone H1e: A CD and NMR study
inferredcites →https://doi.org/10.1110/ps.9.4.627openalex-snapshot
A helix‐turn motif in the C‐terminal domain of histone H1
inferredcites →https://doi.org/10.1111/j.1365-2958.1995.tb02357.xopenalex-snapshot
A novel chromatin‐forming histone H1 homologue is encoded by a dispensable and growth‐regulated gene in Bordetella pertussis
inferredcites →https://doi.org/10.1111/j.1432-1033.1994.00501.xopenalex-snapshot
Developmentally regulated expression of linker‐histone variants in vertebrates
inferredcites →https://doi.org/10.1111/j.1432-1033.1995.744_3.xopenalex-snapshot
A Precursor‐product Relationship in Molluscan Sperm Proteins from Ensis minor
inferredcites →https://doi.org/10.1242/dev.128.5.655openalex-snapshot
A mammalian oocyte-specific linker histone gene H1oo: homology with the genes for the oocyte-specific cleavage stage histone (cs-H1) of sea urchin and the B4/H1M histone of the frog
inferredcites →https://doi.org/10.1242/jcs.103.4.889openalex-snapshot
Histone H1 and transcription: still an enigma?
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s13127-022-00565-9zenodo-depositor-declared
Estimating range disjunction time of the Palearctic Admirals (Limenitis L.) with COI and histone H1 genes
inferred← citeshttps://doi.org/10.1007/978-1-4614-0659-4_2openalex-snapshot
Dynamic Fuzziness During Linker Histone Action
inferred← citeshttps://doi.org/10.1007/s00239-004-2647-2openalex-snapshot
Evolution of the Regular Zone of Histone H1 in Fabaceae Plants
inferred← citeshttps://doi.org/10.1007/s11033-012-1959-3openalex-snapshot
Polymorphism in a histone H1 subtype with a short N-terminal domain in three legume species (Fabaceae, Fabaeae)
inferred← citeshttps://doi.org/10.1007/s13127-014-0195-1openalex-snapshot
Range of a Palearctic uraniid moth Eversmannia exornata (Lepidoptera: Uraniidae: Epipleminae) was split in the Holocene, as evaluated using histone H1 and COI genes with reference to the Beringian disjunction in the genus Oreta (Lepidoptera: Drepanidae)
inferred← citeshttps://doi.org/10.1016/j.bpc.2013.08.005openalex-snapshot
Calorimetric studies of the interactions of linker histone H10 and its carboxyl (H10–C) and globular (H10–G) domains with calf-thymus DNA
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.11.038openalex-snapshot
Linker Histone H1.2 Cooperates with Cul4A and PAF1 to Drive H4K31 Ubiquitylation-Mediated Transactivation
inferred← citeshttps://doi.org/10.1016/j.crvi.2010.10.006openalex-snapshot
Two polymorphic linker histone loci in Guinea fowl erythrocytes
inferred← citeshttps://doi.org/10.1016/j.dib.2014.10.002openalex-snapshot
Sequence conservation of linker histones between chicken and mammalian species
inferred← citeshttps://doi.org/10.1016/j.dnarep.2022.103301openalex-snapshot
Histone variants: The unsung guardians of the genome
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2011.01.034openalex-snapshot
Ex vivo detection of histone H1 modified with advanced glycation end products
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.166734openalex-snapshot
Towards understanding the Regulation of Histone H1 Somatic Subtypes with OMICs
inferred← citeshttps://doi.org/10.1021/cr400525mopenalex-snapshot
Classification of Intrinsically Disordered Regions and Proteins
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800650openalex-snapshot
Structure of allelic variants of subtype 5 of histone H1 in pea Pisum sativum L.
inferred← citeshttps://doi.org/10.1038/srep16714openalex-snapshot
Linker histone H1.2 establishes chromatin compaction and gene silencing through recognition of H3K27me3
inferred← citeshttps://doi.org/10.1073/pnas.2519770123openalex-snapshot
A bacterial translation activator with an intrinsically disordered RNA-binding region
inferred← citeshttps://doi.org/10.1074/jbc.m400070200openalex-snapshot
The C-terminal Domain Is the Primary Determinant of Histone H1 Binding to Chromatin in Vivo
inferred← citeshttps://doi.org/10.1074/jbc.m505636200openalex-snapshot
DNA-induced Secondary Structure of the Carboxyl-terminal Domain of Histone H1
inferred← citeshttps://doi.org/10.1074/jbc.m708205200openalex-snapshot
Isolation and Characterization of a Novel H1.2 Complex That Acts as a Repressor of p53-mediated Transcription
inferred← citeshttps://doi.org/10.1093/molbev/msk021openalex-snapshot
Common Phylogenetic Origin of Protamine-like (PL) Proteins and Histone H1: Evidence from Bivalve PL Genes
inferred← citeshttps://doi.org/10.1093/molbev/msw241openalex-snapshot
Complex Evolutionary History of the Mammalian Histone H1.1–H1.5 Gene Family
inferred← citeshttps://doi.org/10.1093/nar/gku491openalex-snapshot
Dynamic condensation of linker histone C-terminal domain regulates chromatin structure
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2006.05147.xopenalex-snapshot
Sequence variants of chicken linker histone H1.a
inferred← citeshttps://doi.org/10.1128/mmbr.00037-16openalex-snapshot
Yeast HMO1: Linker Histone Reinvented
inferred← citeshttps://doi.org/10.1134/s0006297913020053openalex-snapshot
Interaction of short peptides with FITC-labeled wheat histones and their complexes with deoxyribooligonucleotides
inferred← citeshttps://doi.org/10.1134/s000629791305009xopenalex-snapshot
Modulation of action of wheat seedling endonucleases WEN1 and WEN2 by histones
inferred← citeshttps://doi.org/10.1134/s0006350918060064openalex-snapshot
The Role of Linker Histones in Chromatin Structural Organization. 1. H1 Family Histones
inferred← citeshttps://doi.org/10.1139/o08-127openalex-snapshot
Molecular dynamics of histone H1This paper is one of a selection of papers published in this Special Issue, entitled CSBMCB’s 51st Annual Meeting – Epigenetics and Chromatin Dynamics, and has undergone the Journal’s usual peer review process.
inferred← citeshttps://doi.org/10.1139/o10-024openalex-snapshot
Structure of the H1 C-terminal domain and function in chromatin condensationThis paper is one of a selection of papers published in a Special Issue entitled 31st Annual International Asilomar Chromatin and Chromosomes Conference, and has undergone the Journal’s usual peer review process.
inferred← citeshttps://doi.org/10.1371/journal.pone.0001553openalex-snapshot
Fine Mapping of Posttranslational Modifications of the Linker Histone H1 from Drosophila melanogaster
inferred← citeshttps://doi.org/10.1529/biophysj.107.104513openalex-snapshot
Macromolecular Crowding Induces a Molten Globule State in the C-Terminal Domain of Histone H1
inferred← citeshttps://doi.org/10.3390/ijerph15102170openalex-snapshot
Characterization of Histone Genes from the Bivalve Lucina Pectinata
inferred← citeshttps://doi.org/10.5324/cjcr.v0i26.1657openalex-snapshot
Chironomus Newsletter on Chironomidae Research
inferred← citeshttps://doi.org/10.53846/goediss-258openalex-snapshot
Expressionsanalyse des humanen Histonsubtyps H1x
inferred← citeshttps://doi.org/10.53846/goediss-3806openalex-snapshot
Molecular characterization of Mst77F and implication in Drosophila spermatogenesis
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