scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1012952873 |
P356 | DOI | 10.1186/GB-2010-11-12-R120 |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1186/gb-2010-11-12-r120 |
P932 | PMC publication ID | 3046480 |
P698 | PubMed publication ID | 21176223 |
P5875 | ResearchGate publication ID | 49700483 |
P50 | author | Jason D Lieb | Q109084133 |
Susan Strome | Q65088229 | ||
P2093 | author name string | Thea A Egelhofer | |
Kohta Ikegami | |||
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Protruding vulva mutants identify novel loci and Wnt signaling factors that function during Caenorhabditis elegans vulva development | Q34610825 | ||
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P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Caenorhabditis elegans | Q91703 |
P304 | page(s) | R120 | |
P577 | publication date | 2010-12-23 | |
P1433 | published in | Genome Biology | Q5533480 |
P1476 | title | Caenorhabditis elegans chromosome arms are anchored to the nuclear membrane via discontinuous association with LEM-2 | |
P478 | volume | 11 |
Q35976800 | A streamlined tethered chromosome conformation capture protocol. |
Q93213323 | A study of the impact of DNA helical rise on protein-DNA interaction |
Q33574854 | A team of heterochromatin factors collaborates with small RNA pathways to combat repetitive elements and germline stress |
Q36466883 | A transgenerational role of the germline nuclear RNAi pathway in repressing heat stress-induced transcriptional activation in C. elegans |
Q92227197 | Active chromatin marks drive spatial sequestration of heterochromatin in C. elegans nuclei |
Q37099127 | An Abundant Class of Non-coding DNA Can Prevent Stochastic Gene Silencing in the C. elegans Germline. |
Q37349779 | An H4K16 histone acetyltransferase mediates decondensation of the X chromosome in C. elegans males |
Q36150010 | Anchoring of Heterochromatin to the Nuclear Lamina Reinforces Dosage Compensation-Mediated Gene Repression. |
Q36178359 | Beyond Tethering and the LEM domain: MSCellaneous functions of the inner nuclear membrane Lem2. |
Q34548272 | Broad chromosomal domains of histone modification patterns in C. elegans |
Q38170221 | C. elegans epigenetic regulation in development and aging |
Q47645730 | Caenorhabditis elegans Dosage Compensation: Insights into Condensin-Mediated Gene Regulation |
Q34384139 | Caenorhabditis elegans RSD-2 and RSD-6 promote germ cell immortality by maintaining small interfering RNA populations |
Q90848690 | Caenorhabditis elegans as an emerging model system in environmental epigenetics |
Q48911542 | Caenorhabditis elegans: an old genetic model can learn new epigenetic tricks. |
Q39042190 | Cell Biology of the Caenorhabditis elegans Nucleus |
Q64081772 | Characterization of a Unique Form of Arrhythmic Cardiomyopathy Caused by Recessive Mutation in LEMD2 |
Q26798007 | Chromatin states and nuclear organization in development--a view from the nuclear lamina |
Q89946693 | Chromosome-Level Assembly of the Caenorhabditis remanei Genome Reveals Conserved Patterns of Nematode Genome Organization |
Q34670135 | Condensin-driven remodelling of X chromosome topology during dosage compensation. |
Q50131745 | Consequences of Lamin B1 and Lamin B Receptor Downregulation in Senescence. |
Q34309873 | Constitutive nuclear lamina-genome interactions are highly conserved and associated with A/T-rich sequence |
Q42687369 | Control of heterochromatin localization and silencing by the nuclear membrane protein Lem2. |
Q37412741 | Crossover heterogeneity in the absence of hotspots in Caenorhabditis elegans |
Q33879043 | Crossover recombination mediated by HIM-18/SLX4-associated nucleases. |
Q41735227 | Defining heterochromatin in C. elegans through genome-wide analysis of the heterochromatin protein 1 homolog HPL-2. |
Q34590236 | Differential spatial and structural organization of the X chromosome underlies dosage compensation in C. elegans |
Q38991463 | Diseases of the Nucleoskeleton. |
Q36791375 | Emerin and histone deacetylase 3 (HDAC3) cooperatively regulate expression and nuclear positions of MyoD, Myf5, and Pax7 genes during myogenesis. |
Q35259539 | Emerin in health and disease |
Q36012704 | Enrichment of H3K9me2 on Unsynapsed Chromatin in Caenorhabditis elegans Does Not Target de Novo Sites |
Q37871545 | Epigenetics in C. elegans: facts and challenges |
Q37958966 | Evolvement of LEM proteins as chromatin tethers at the nuclear periphery |
Q36958215 | Fine-Scale Crossover Rate Variation on the Caenorhabditis elegans X Chromosome. |
Q50487328 | Fine-tuning of chromatin composition and Polycomb recruitment by two Mi2 homologues during C. elegans early embryonic development. |
Q33741805 | Genome-wide analysis links emerin to neuromuscular junction activity in Caenorhabditis elegans. |
Q34690818 | Global remodeling of nucleosome positions in C. elegans |
Q50278958 | Histone H3K9 methylation is dispensable for Caenorhabditis elegans development but suppresses RNA:DNA hybrid-associated repeat instability. |
Q26770526 | Histones and histone modifications in perinuclear chromatin anchoring: from yeast to man |
Q37719263 | Identification of an RNA Polymerase III Regulator Linked to Disease-Associated Protein Aggregation |
Q42961294 | Integral nuclear pore proteins bind to Pol III-transcribed genes and are required for Pol III transcript processing in C. elegans |
Q28301622 | Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project |
Q28513559 | Interplay between structure-specific endonucleases for crossover control during Caenorhabditis elegans meiosis |
Q37207889 | Lamin A/C-promoter interactions specify chromatin state-dependent transcription outcomes |
Q64064616 | Lamina Associated Domains and Gene Regulation in Development and Cancer |
Q39318399 | Lamina-Associated Domains: Links with Chromosome Architecture, Heterochromatin, and Gene Repression |
Q89916726 | Lamina-Dependent Stretching and Unconventional Chromosome Compartments in Early C. elegans Embryos |
Q36191743 | Linking dosage compensation and X chromosome nuclear organization in C. elegans. |
Q33698066 | Locking the genome: nuclear organization and cell fate |
Q64295438 | Loss of CRWN Nuclear Proteins Induces Cell Death and Salicylic Acid Defense Signaling |
Q90089208 | Loss of an H3K9me anchor rescues laminopathy-linked changes in nuclear organization and muscle function in an Emery-Dreifuss muscular dystrophy model |
Q37371435 | Meiotic recombination and the crossover assurance checkpoint in Caenorhabditis elegans |
Q35908957 | Networking in the nucleus: a spotlight on LEM-domain proteins |
Q38565289 | Nuclear architecture: the cell biology of a laminopathy |
Q35194606 | Nuclear envelope and genome interactions in cell fate |
Q64104480 | Nuclear lamina integrity is required for proper spatial organization of chromatin in Drosophila |
Q41958139 | Nuclear lamins: making contacts with promoters |
Q27318643 | Nucleo-cytoplasmic shuttling of the endonuclease ankyrin repeats and LEM domain-containing protein 1 (Ankle1) is mediated by canonical nuclear export- and nuclear import signals |
Q30410148 | O-Linked β-N-acetylglucosamine (O-GlcNAc) regulates emerin binding to barrier to autointegration factor (BAF) in a chromatin- and lamin B-enriched "niche". |
Q26799890 | One, Two, Three: Polycomb Proteins Hit All Dimensions of Gene Regulation |
Q90621864 | Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria |
Q96135696 | Predicting gene essentiality in Caenorhabditis elegans by feature engineering and machine-learning |
Q30537180 | Promoter- and RNA polymerase II-dependent hsp-16 gene association with nuclear pores in Caenorhabditis elegans |
Q46244949 | Regulation of Crossover Frequency and Distribution during Meiotic Recombination. |
Q64055118 | Repression of Germline Genes in Somatic Tissues by H3K9 Dimethylation of Their Promoters |
Q48148054 | Repressive Chromatin in Caenorhabditis elegans: Establishment, Composition, and Function |
Q41106921 | Role of Inner Nuclear Membrane Protein Complex Lem2-Nur1 in Heterochromatic Gene Silencing |
Q34505026 | Role of histone deacetylases in gene regulation at nuclear lamina. |
Q92542928 | Roles for Non-coding RNAs in Spatial Genome Organization |
Q37723762 | Something silent this way forms: the functional organization of the repressive nuclear compartment |
Q92190852 | Spatial chromatin organization and gene regulation at the nuclear lamina |
Q38987148 | Spatial organization of the Schizosaccharomyces pombe genome within the nucleus |
Q37189656 | Spatial segregation of heterochromatin: Uncovering functionality in a multicellular organism. |
Q38203362 | Stochastic genome-nuclear lamina interactions: modulating roles of Lamin A and BAF. |
Q28088652 | Structural and functional diversity of Topologically Associating Domains |
Q35583845 | The Fun30 chromatin remodeler Fft3 controls nuclear organization and chromatin structure of insulators and subtelomeres in fission yeast. |
Q35683964 | The Inner Nuclear Membrane Protein Src1 Is Required for Stable Post-Mitotic Progression into G1 in Aspergillus nidulans |
Q64243970 | The Nuclear Lamina as an Organizer of Chromosome Architecture |
Q51033425 | The gastrula transition reorganizes replication-origin selection in Caenorhabditis elegans. |
Q44273923 | The inner nuclear membrane proteins Man1 and Ima1 link to two different types of chromatin at the nuclear periphery in S. pombe |
Q58551419 | The large fraction of heterochromatin in Drosophila neurons is bound by both B-type lamin and HP1a |
Q26826857 | The nuclear envelope LEM-domain protein emerin |
Q36052491 | The nuclear envelope protein emerin binds directly to histone deacetylase 3 (HDAC3) and activates HDAC3 activity |
Q37958962 | The nuclear lamina and heterochromatin: a complex relationship |
Q35914454 | Tools for DNA adenine methyltransferase identification analysis of nuclear organization during C. elegans development |
Q92523616 | Transcription-independent TFIIIC-bound sites cluster near heterochromatin boundaries within lamina-associated domains in C. elegans |
Q26863161 | Transcriptional regulation at the yeast nuclear envelope |
Q38117116 | Transcriptional regulation of gene expression in C. elegans |
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