On the public citation graph

Chromatin accessibility dynamics of myogenesis at single cell resolution

0 signed · 64 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/0092-8674(90)90214-yopenalex-snapshot
The protein Id: A negative regulator of helix-loop-helix DNA binding proteins
inferredcites →https://doi.org/10.1016/0092-8674(95)90139-6openalex-snapshot
Cooperative activation of muscle gene expression by MEF2 and myogenic bHLH proteins
inferredcites →https://doi.org/10.1016/0092-8674(95)90385-2openalex-snapshot
The retinoblastoma protein and cell cycle control
inferredcites →https://doi.org/10.1016/j.ajhg.2014.10.004openalex-snapshot
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
inferredcites →https://doi.org/10.1016/j.cell.2014.11.021openalex-snapshot
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
inferredcites →https://doi.org/10.1016/j.cell.2015.11.024openalex-snapshot
CTCF-Mediated Human 3D Genome Architecture Reveals Chromatin Topology for Transcription
inferredcites →https://doi.org/10.1016/j.celrep.2015.02.055openalex-snapshot
Conversion of MyoD to a Neurogenic Factor: Binding Site Specificity Determines Lineage
inferredcites →https://doi.org/10.1016/j.devcel.2010.02.014openalex-snapshot
Genome-wide MyoD Binding in Skeletal Muscle Cells: A Potential for Broad Cellular Reprogramming
inferredcites →https://doi.org/10.1016/j.molcel.2007.08.021openalex-snapshot
Functional Interdependence at the Chromatin Level between the MKK6/p38 and IGF1/PI3K/AKT Pathways during Muscle Differentiation
inferredcites →https://doi.org/10.1016/s1097-2765(00)80005-2openalex-snapshot
Differential Roles of p300 and PCAF Acetyltransferases in Muscle Differentiation
inferredcites →https://doi.org/10.1016/s1097-2765(02)00781-5openalex-snapshot
Looping and Interaction between Hypersensitive Sites in the Active β-globin Locus
inferredcites →https://doi.org/10.1016/s1097-2765(04)00260-6openalex-snapshot
Pbx Marks Genes for Activation by MyoD Indicating a Role for a Homeodomain Protein in Establishing Myogenic Potential
inferredcites →https://doi.org/10.1023/a:1024922626726openalex-snapshot
Spatial organization of gene expression: the active chromatin hub
inferredcites →https://doi.org/10.1038/nature11232openalex-snapshot
The accessible chromatin landscape of the human genome
inferredcites →https://doi.org/10.1038/nature11247openalex-snapshot
An integrated encyclopedia of DNA elements in the human genome
inferredcites →https://doi.org/10.1038/nbt.2859openalex-snapshot
The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells
inferredcites →https://doi.org/10.1038/nbt.3199openalex-snapshot
Epigenome editing by a CRISPR-Cas9-based acetyltransferase activates genes from promoters and enhancers
inferredcites →https://doi.org/10.1038/ng1378openalex-snapshot
p38 pathway targets SWI-SNF chromatin-remodeling complex to muscle-specific loci
inferredcites →https://doi.org/10.1038/nmeth.3033openalex-snapshot
Sets and intersections
inferredcites →https://doi.org/10.1038/nmeth.4402openalex-snapshot
Reversed graph embedding resolves complex single-cell trajectories
inferredcites →https://doi.org/10.1038/nprot.2012.101openalex-snapshot
Identifying ChIP-seq enrichment using MACS
inferredcites →https://doi.org/10.1038/nrg3454openalex-snapshot
Exploring the three-dimensional organization of genomes: interpreting chromatin interaction data
inferredcites →https://doi.org/10.1073/pnas.0404192101openalex-snapshot
In vitro transcription system delineates the distinct roles of the coactivators pCAF and p300 during MyoD/E47-dependent transactivation
inferredcites →https://doi.org/10.1073/pnas.1518552112openalex-snapshot
Chromatin extrusion explains key features of loop and domain formation in wild-type and engineered genomes
inferredcites →https://doi.org/10.1073/pnas.93.18.9384openalex-snapshot
Chromatin structure and gene expression.
inferredcites →https://doi.org/10.1080/01621459.2012.737745openalex-snapshot
Optimal Detection of Changepoints With a Linear Computational Cost
inferredcites →https://doi.org/10.1088/1742-5468/2008/10/p10008openalex-snapshot
Fast unfolding of communities in large networks
inferredcites →https://doi.org/10.1093/bib/bbu034openalex-snapshot
Predictive modelling of gene expression from transcriptional regulatory elements
inferredcites →https://doi.org/10.1093/bioinformatics/btr064openalex-snapshot
FIMO: scanning for occurrences of a given motif
inferredcites →https://doi.org/10.1093/biostatistics/kxm045openalex-snapshot
Sparse inverse covariance estimation with the graphical lasso
inferredcites →https://doi.org/10.1093/nar/27.18.3752openalex-snapshot
A conserved motif N-terminal to the DNA-binding domains of myogenic bHLH transcription factors mediates cooperative DNA binding with Pbx-Meis1/Prep1
inferredcites →https://doi.org/10.1093/nar/gkt111openalex-snapshot
Enriching the gene set analysis of genome-wide data by incorporating directionality of gene expression and combining statistical hypotheses and methods
inferredcites →https://doi.org/10.1093/nar/gkt374openalex-snapshot
Enhancer networks revealed by correlated DNAse hypersensitivity states of enhancers
inferredcites →https://doi.org/10.1093/nar/gkv1176openalex-snapshot
JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles
inferredcites →https://doi.org/10.1101/086025openalex-snapshot
A unified encyclopedia of human functional DNA elements through fully automated annotation of 164 human cell types
inferredcites →https://doi.org/10.1111/j.1467-9868.2005.00503.xopenalex-snapshot
Regularization and Variable Selection Via the Elastic Net
inferredcites →https://doi.org/10.1126/science.1222794openalex-snapshot
Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
inferredcites →https://doi.org/10.1126/science.aab1601openalex-snapshot
Multiplex single-cell profiling of chromatin accessibility by combinatorial cellular indexing
inferredcites →https://doi.org/10.1128/mcb.00916-12openalex-snapshot
Comparison of Genome-Wide Binding of MyoD in Normal Human Myogenic Cells and Rhabdomyosarcomas Identifies Regional and Local Suppression of Promyogenic Transcription Factors
inferredcites →https://doi.org/10.1128/mcb.17.2.1010openalex-snapshot
Molecular Mechanisms of Myogenic Coactivation by p300: Direct Interaction with the Activation Domain of MyoD and with the MADS Box of MEF2C
inferredcites →https://doi.org/10.1128/mcb.25.10.3997-4009.2005openalex-snapshot
MyoD Targets Chromatin Remodeling Complexes to the Myogenin Locus Prior to Forming a Stable DNA-Bound Complex
inferredcites →https://doi.org/10.1186/gb-2008-9-9-r137openalex-snapshot
Model-based Analysis of ChIP-Seq (MACS)
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1242/dev.003905openalex-snapshot
Pbx homeodomain proteins direct Myod activity to promote fast-muscle differentiation
inferredcites →https://doi.org/10.1242/jcs.111.6.769openalex-snapshot
Cell heterogeneity upon myogenic differentiation: down-regulation of MyoD and Myf-5 generates ‘reserve cells’
inferredcites →https://doi.org/10.1242/jcs.114.2.303openalex-snapshot
A calcineurin- and NFAT-dependent pathway regulates Myf5 gene expression in skeletal muscle reserve cells
inferredcites →https://doi.org/10.1371/journal.pone.0009425openalex-snapshot
The Core Binding Factor CBF Negatively Regulates Skeletal Muscle Terminal Differentiation
inferredcites →https://doi.org/10.1371/journal.pone.0013984openalex-snapshot
Enrichment Map: A Network-Based Method for Gene-Set Enrichment Visualization and Interpretation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/978-1-4939-9802-9_3openalex-snapshot
Chromatin Epigenomics in Muscle Development and Disease
inferred← citeshttps://doi.org/10.1016/j.cels.2020.02.003openalex-snapshot
Inferring Causal Gene Regulatory Networks from Coupled Single-Cell Expression Dynamics Using Scribe
inferred← citeshttps://doi.org/10.1016/j.tig.2018.06.001openalex-snapshot
Single-Cell Multi-omics: An Engine for New Quantitative Models of Gene Regulation
inferred← citeshttps://doi.org/10.1038/nature25981openalex-snapshot
The cis-regulatory dynamics of embryonic development at single-cell resolution
inferred← citeshttps://doi.org/10.1038/s41467-018-04629-3openalex-snapshot
Unsupervised clustering and epigenetic classification of single cells
inferred← citeshttps://doi.org/10.1038/s41467-019-09483-5openalex-snapshot
Dynamics of genome reorganization during human cardiogenesis reveal an RBM20-dependent splicing factory
inferred← citeshttps://doi.org/10.1038/s41467-019-09670-4openalex-snapshot
Single-cell trajectories reconstruction, exploration and mapping of omics data with STREAM
inferred← citeshttps://doi.org/10.1038/s41586-019-0969-xopenalex-snapshot
The single-cell transcriptional landscape of mammalian organogenesis
inferred← citeshttps://doi.org/10.1038/s41586-021-03933-1openalex-snapshot
Genetic and epigenetic coordination of cortical interneuron development
inferred← citeshttps://doi.org/10.1093/bfgp/elx046openalex-snapshot
Mapping gene regulatory networks from single-cell omics data
inferred← citeshttps://doi.org/10.1093/nar/gky950openalex-snapshot
Classifying cells with Scasat, a single-cell ATAC-seq analysis tool
inferred← citeshttps://doi.org/10.1101/370346openalex-snapshot
Cis-topic modelling of single-cell epigenomes
inferred← citeshttps://doi.org/10.1101/438937openalex-snapshot
Building gene regulatory networks from scATAC-seq and scRNA-seq using Linked Self-Organizing Maps
inferred← citeshttps://doi.org/10.1186/s43556-020-00009-wopenalex-snapshot
Profiling chromatin regulatory landscape: insights into the development of ChIP-seq and ATAC-seq
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1006555openalex-snapshot
Building gene regulatory networks from scATAC-seq and scRNA-seq using Linked Self Organizing Maps
inferred← citeshttps://doi.org/10.15252/msb.20178046openalex-snapshot
Using single‐cell genomics to understand developmental processes and cell fate decisions
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.