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Consecutive signaling pathways are activated in progression of Duchenne muscular dystrophy in C. elegans

https://doi.org/10.1101/532465
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/dvdy.21578openalex-snapshot
Differential expression pattern of the four mitochondrial adenine nucleotide transporter ant genes and their roles during the development of Caenorhabditis elegans
inferredcites →https://doi.org/10.1007/978-1-4939-2842-2_5openalex-snapshot
Transposon-Assisted Genetic Engineering with Mos1-Mediated Single-Copy Insertion (MosSCI)
inferredcites →https://doi.org/10.1007/pl00012490openalex-snapshot
Nascent-polypeptide-associated complex
inferredcites →https://doi.org/10.1007/s100480050053openalex-snapshot
Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission
inferredcites →https://doi.org/10.1016/0022-510x(86)90003-1openalex-snapshot
The association of cardiac muscle necrosis and inflammation with the degenerative and persistent myopathy of MDX mice
inferredcites →https://doi.org/10.1016/0888-7543(92)90210-jopenalex-snapshot
An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy
inferredcites →https://doi.org/10.1016/j.bbrc.2009.06.053openalex-snapshot
Mutation in dystrophin-encoding gene affects energy metabolism in mouse myoblasts
inferredcites →https://doi.org/10.1016/j.mehy.2015.08.015openalex-snapshot
Revisiting the dystrophin-ATP connection: How half a century of research still implicates mitochondrial dysfunction in Duchenne Muscular Dystrophy aetiology
inferredcites →https://doi.org/10.1016/s0070-2153(08)00609-1openalex-snapshot
Chapter 9 The Value of Mammalian Models for Duchenne Muscular Dystrophy in Developing Therapeutic Strategies
inferredcites →https://doi.org/10.1016/s0960-8966(01)00273-5openalex-snapshot
Creatine supplementation reduces skeletal muscle degeneration and enhances mitochondrial function in mdx mice
inferredcites →https://doi.org/10.1016/s0960-8966(01)00278-4openalex-snapshot
A quantitative study of bioenergetics in skeletal muscle lacking utrophin and dystrophin
inferredcites →https://doi.org/10.1016/s0960-8966(02)00093-7openalex-snapshot
A web-accessible complete transcriptome of normal human and DMD muscle
inferredcites →https://doi.org/10.1016/s0960-9822(00)00691-6openalex-snapshot
Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans
inferredcites →https://doi.org/10.1023/a:1006868130002openalex-snapshot
Impaired mitochondrial oxidative phosphorylation in skeletal muscle of the dystrophin-deficient mdx mouse
inferredcites →https://doi.org/10.1038/333466a0openalex-snapshot
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle
inferredcites →https://doi.org/10.1038/35042517openalex-snapshot
Functional genomic analysis of C. elegans chromosome I by systematic RNA interference
inferredcites →https://doi.org/10.1038/cdd.2016.127openalex-snapshot
Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy
inferredcites →https://doi.org/10.1038/nature01012openalex-snapshot
Chromosomal clustering of muscle-expressed genes in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/nature01920openalex-snapshot
Suppression of CED-3-independent apoptosis by mitochondrial βNAC in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/nbt.1621openalex-snapshot
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1042/bj3040649openalex-snapshot
Defective regulation of energy metabolism in mdx-mouse skeletal muscles
inferredcites →https://doi.org/10.1073/pnas.1308866110openalex-snapshot
Reduced IGF signaling prevents muscle cell death in a Caenorhabditis elegans model of muscular dystrophy
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/hmg/ddh033openalex-snapshot
Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy
inferredcites →https://doi.org/10.1093/nar/gni149openalex-snapshot
Isolation of mRNA from specific tissues of Drosophila by mRNA tagging
inferredcites →https://doi.org/10.1111/j.1440-1681.2006.04394.xopenalex-snapshot
MUSCLE DAMAGE IN MDX (DYSTROPHIC) MICE: ROLE OF CALCIUM AND REACTIVE OXYGEN SPECIES
inferredcites →https://doi.org/10.1111/nyas.13500openalex-snapshot
The molecular cross talk of the dystrophin–glycoprotein complex
inferredcites →https://doi.org/10.1126/scitranslmed.aaf5504openalex-snapshot
NAD + repletion improves muscle function in muscular dystrophy and counters global PARylation
inferredcites →https://doi.org/10.1128/aem.07486-11openalex-snapshot
Caenorhabditis elegans, a Model Organism for Investigating Immunity
inferredcites →https://doi.org/10.1128/mcb.01509-08openalex-snapshot
Adenine Nucleotide Translocator Cooperates with Core Cell Death Machinery To Promote Apoptosis in Caenorhabditis elegans
inferredcites →https://doi.org/10.1186/1471-2474-7-23openalex-snapshot
Transcriptome-scale similarities between mouse and human skeletal muscles with normal and myopathic phenotypes
inferredcites →https://doi.org/10.1186/s12915-015-0116-6openalex-snapshot
Comparative RNA-Seq analysis reveals pervasive tissue-specific alternative polyadenylation in Caenorhabditis elegans intestine and muscles
inferredcites →https://doi.org/10.1242/dev.125.13.2479openalex-snapshot
MyoD and the specification of muscle and non-muscle fates during postembryonic development of the C. elegans mesoderm
inferredcites →https://doi.org/10.1242/dmm.036137openalex-snapshot
Muscle strength deficiency and mitochondrial dysfunction in a muscular dystrophy model of Caenorhabditis elegans and its functional response to drugs
inferredcites →https://doi.org/10.1371/journal.pone.0115763openalex-snapshot
Defects in Mitochondrial ATP Synthesis in Dystrophin-Deficient Mdx Skeletal Muscles May Be Caused by Complex I Insufficiency
inferredcites →https://doi.org/10.14348/molcells.2017.0017openalex-snapshot
Survival assays using Caenorhabditis elegans
inferredcites →https://doi.org/10.1534/genetics.116.196774openalex-snapshot
Alternative Polyadenylation Directs Tissue-Specific miRNA Targeting in Caenorhabditis elegans Somatic Tissues
inferredcites →https://doi.org/10.1534/genetics.117.202101openalex-snapshot
Alternative Poly(A) Tails Meet miRNA Targeting in Caenorhabditis elegans
inferredcites →https://doi.org/10.1895/wormbook.1.101.1openalex-snapshot
Maintenance of C. elegans
inferredcites →https://doi.org/10.1895/wormbook.1.181.1openalex-snapshot
History of research on C. elegans and other free-living nematodes as model organisms
inferredcites →https://doi.org/10.1895/wormbook.1.81.2openalex-snapshot
Development, structure, and maintenance of C. elegans body wall muscle
inferredcites →https://doi.org/10.4161/rna.7.3.11649openalex-snapshot
Crossing the borders: Poly(A)-binding proteins working on both sides of the fence
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