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References from Dysregulation of the Schwann cell GABAergic system and Aβ-fibers conduction abnormalities in the sciatic nerve of the mdx mouse model of Duchenne muscular dystrophy. Local targets link to admitted publications; unresolved targets remain external evidence.
Role of neuregulins in glial cell development
10.1002/(sici)1098-1136(20000115)29:2<104::aid-glia2>3.0.co;2-2 · 2000 · External reference
Advances in sciatic nerve regeneration: a review of contemporary techniques
10.1016/j.reth.2025.04.016 · 2025 · External reference
Perisynaptic Schwann cells - the multitasking cells at the developing neuromuscular junctions
10.1016/j.semcdb.2020.02.011 · 2020 · External reference
Functional regeneration in the hindlimb skeletal muscle of the mdx mouse
10.1007/bf01738755 · 1988 · External reference
Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophy
10.1186/s12868-017-0381-0 · 2017 · External reference
Truncated dystrophins can influence neuromuscular synapse structure
10.1016/j.mcn.2008.12.011 · 2009 · External reference
Function and genetics of dystrophin and dystrophin-related proteins in muscle
10.1152/physrev.00028.2001 · 2002 · External reference
Nerve excitability changes after intravenous immunoglobulin infusions in multifocal motor neuropathy and chronic inflammatory demyelinating neuropathy
10.1016/j.jns.2010.02.002 · 2010 · External reference
Axonal GABAA stabilizes excitability in unmyelinated sensory axons secondary to NKCC1 activity
10.1113/jp279664 · 2021 · External reference
Threshold tracking techniques in the study of human peripheral nerve
10.1002/(sici)1097-4598(199802)21:2<137::aid-mus1>3.0.co;2-c · 1998 · External reference
Role of gelatinases in pathological and physiological processes involving the dystrophin-glycoprotein complex
10.1016/j.matbio.2015.02.005 · 2015 · External reference
Absence of dystrophin-related protein-2 disrupts Cajal bands in a patient with Charcot-Marie-tooth disease
10.1016/j.nmd.2015.07.001 · 2015 · External reference
Excitability of human axons
10.1016/s1388-2457(01)00595-8 · 2001 · External reference
An alternative dystrophin transcript specific to peripheral nerve
10.1038/ng0593-77 · 1993 · External reference
Expression of neuregulins and their putative receptors, ErbB2 and ErbB3, is induced during Wallerian degeneration
10.1523/jneurosci.17-05-01642.1997 · 1997 · External reference
Schwann cell development, maturation and regeneration: A focus on classic and emerging intracellular signaling pathways
10.4103/1673-5374.211172 · 2017 · External reference
Regulation of matrix metalloproteinase-9 (MMP-9) in TNF-stimulated neutrophils: novel pathways for tertiary granule release
10.1189/jlb.0605353 · 2006 · External reference
Proteolytic cleavage, trafficking, and functions of nuclear receptor tyrosine kinases
10.1111/febs.13342 · 2015 · External reference
A G+1-->A transversion at the 5′ splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient
10.1093/hmg/4.11.2171 · 1995 · External reference
GABA and its B-receptor are present at the node of Ranvier in a small population of sensory fibers, implicating a role in myelination
10.1002/jnr.23489 · 2015 · External reference
MMP2-9 cleavage of dystroglycan alters the size and molecular composition of Schwann cell domains
10.1523/jneurosci.0141-11.2011 · 2011 · External reference
Elevated levels of active matrix metalloproteinase-9 cause hypertrophy in skeletal muscle of normal and dystrophin-deficient mdx mice
10.1093/hmg/ddr362 · 2011 · External reference
Persistent inflammation and nutritional status in Duchenne muscular dystrophy
10.1016/j.clnesp.2024.04.014 · 2024 · External reference
Dystrophin and its isoforms in a sympathetic ganglion of normal and dystrophic mdx mice: immunolocalization by electron microscopy and biochemical characterization
10.1016/s0306-4522(97)00003-1 · 1997 · External reference
Synaptic alterations as a neurodevelopmental trait of Duchenne muscular dystrophy
10.1016/j.nbd.2022.105718 · 2022 · External reference
Motor axonopathies in a mouse model of Duchenne muscular dystrophy
10.1038/s41598-020-65824-1 · 2020 · External reference
Duchenne muscular dystrophy
10.1038/s41572-021-00248-3 · 2021 · External reference
Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-tooth disease 4H
10.1093/brain/awac402 · 2023 · External reference
Comparative localization of two forms of glutamic acid decarboxylase and their mRNAs in rat brain supports the concept of functional differences between the forms
10.1523/jneurosci.14-03-01834.1994 · 1994 · External reference
Matrix metalloproteinases: evolution, gene regulation and functional analysis in mouse models
10.1016/j.bbamcr.2009.07.004 · 2010 · External reference
Schwann-like adult stem cells derived from bone marrow and adipose tissue express γ-aminobutyric acid type B receptors
10.1002/jnr.22652 · 2011 · External reference
Deletion of GABA-B receptor in Schwann cells regulates Remak bundles and small nociceptive C-fibers
10.1002/glia.22625 · 2014 · External reference
GABA-B1 receptor-null Schwann cells exhibit compromised in vitro myelination
10.1007/s12035-018-1158-x · 2019 · External reference
Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ)
10.1186/1471-2474-8-54 · 2007 · External reference
A dual role of erbB2 in myelination and in expansion of the Schwann cell precursor pool
10.1083/jcb.148.5.1035 · 2000 · External reference
Neuregulin, a factor with many functions in the life of a Schwann cell
10.1002/1521-1878(200011)22:11<987::aid-bies5>3.0.co;2-5 · 2000 · External reference
The classification of nerve fibers
1941 · External reference
Multiple measures of axonal excitability in peripheral sensory nerves: an in vivo rat model
10.1002/mus.20851 · 2007 · External reference
Impaired muscle spindle function in murine models of muscular dystrophy
10.1113/jp278563 · 2020 · External reference
The enzymatic processing of α-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site
10.1371/journal.pone.0192651 · 2018 · External reference
Molecular signaling mechanisms of axon-glia communication in the peripheral nervous system
10.1002/bies.201400172 · 2015 · External reference
The tyrosine phosphatase Shp2 (PTPN11) directs Neuregulin-1/ErbB signaling throughout Schwann cell development
10.1073/pnas.0904336106 · 2009 · External reference
Cycles of myofibers degeneration and regeneration lead to remodeling of the neuromuscular junction in two mammalian models of Duchenne muscular dystrophy
10.1371/journal.pone.0205926 · 2018 · External reference
Postinjury induction of activated ErbB2 selectively hyperactivates denervated Schwann cells and promotes robust dorsal root axon regeneration
10.1523/jneurosci.0903-17.2017 · 2017 · External reference
Effect of beta-dystroglycan processing on utrophin/Dp116 anchorage in normal and mdx mouse Schwann cell membrane
10.1016/j.neuroscience.2006.04.043 · 2006 · External reference
Mek/ERK1/2-MAPK and PI3K/Akt/mTOR signaling plays both independent and cooperative roles in Schwann cell differentiation, myelination and dysmyelination
10.1002/glia.24049 · 2021 · External reference
Aberrant neuregulin 1/ErbB signaling in Charcot-Marie-tooth type 4D disease
10.1128/mcb.00559-21 · 2022 · External reference
Evolution of life expectancy of patients with Duchenne muscular dystrophy at AFM Yolaine de Kepper centre between 1981 and 2011
10.1016/j.rehab.2013.06.002 · 2013 · External reference
Differences in the recovery of excitability in sensory and motor axons of human median nerve
10.1093/brain/119.4.1099 · 1996 · External reference
Multiple measures of axonal excitability: a new approach in clinical testing
10.1002/(sici)1097-4598(200003)23:3<399::aid-mus12>3.0.co;2-g · 2000 · External reference
Effects of temperature on the excitability properties of human motor axons
10.1093/brain/124.4.816 · 2001 · External reference
Dystrophin-glycoprotein complex and laminin colocalize to the sarcolemma and transverse tubules of cardiac muscle
10.1161/01.res.72.2.349 · 1993 · External reference
Investigation of the relationship between upper extremity proprioception and upper extremity functions in children with Duchenne muscular dystrophy
10.1080/17518423.2026.2665086 · 2025 · External reference
On the dependency of cellular protein levels on mRNA abundance
10.1016/j.cell.2016.03.014 · 2016 · External reference
Pre-synaptic GABAA in NaV1.8+ primary afferents is required for the development of punctate but not dynamic mechanical allodynia following CFA inflammation
10.3390/cells11152390 · 2022 · External reference
Alterations of neuromuscular junctions in Duchenne muscular dystrophy
10.1016/j.neulet.2020.135304 · 2020 · External reference
Impact of atorvastatin on skeletal muscle mitochondrial activity, locomotion and axonal excitability – evidence from ApoE−/− mice
10.3390/ijms23105415 · 2022 · External reference
GABAB receptors in Schwann cells influence proliferation and myelin protein expression
10.1111/j.0953-816x.2004.03368.x · 2004 · External reference
GABA receptor-mediated effects in the peripheral nervous system: a cross-interaction with neuroactive steroids
10.1385/jmn:28:1:89 · 2006 · External reference
Altered peripheral myelination in mice lacking GABAB receptors
10.1016/j.mcn.2007.12.009 · 2008 · External reference
GABA synthesis in Schwann cells is induced by the neuroactive steroid allopregnanolone
10.1111/j.1471-4159.2009.06512.x · 2010 · External reference
Prevalence of smooth muscle dysfunction among children with Duchenne muscular dystrophy
10.1002/mus.27077 · 2020 · External reference
Biological role of dystroglycan in Schwann cell function and its implications in peripheral nervous system diseases
10.1155/2010/740403 · 2010 · External reference
Anti-HER2 antibody therapy using gene-transduced adipocytes for HER2-positive breast cancer
10.1007/s10549-020-05581-x · 2020 · External reference
Differential expression of dystrophin, utrophin and dystrophin-associated proteins in peripheral nerve
10.1016/0014-5793(93)80695-q · 1993 · External reference
Dystrophin Dp116: a yet to be investigated product of the Duchenne muscular dystrophy gene
10.3390/genes8100251 · 2017 · External reference
Modeling the excitability of mammalian nerve fibers: influence of afterpotentials on the recovery cycle
10.1152/jn.00353.2001 · 2002 · External reference
Neuregulin-ERBB signaling in the nervous system and neuropsychiatric diseases
10.1016/j.neuron.2014.06.007 · 2014 · External reference
Src and phospho-FAK kinases are activated by allopregnanolone promoting Schwann cell motility, morphology and myelination
10.1111/jnc.13951 · 2017 · External reference
Decreased electrical excitability of peripheral nerves in demyelinating polyneuropathies
10.1136/jnnp.62.4.398 · 1997 · External reference
Axonal neuregulin-1 regulates myelin sheath thickness
10.1126/science.1095862 · 2004 · External reference
Muscle damage in dystrophic mdx mice is influenced by the activity of Ca2+−activated KCa3.1 channels
2022 · External reference
Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD)
10.1016/j.nmd.2011.05.011 · 2011 · External reference
Dystrophin Dp71 and the neuropathophysiology of Duchenne muscular dystrophy
10.1007/s12035-019-01845-w · 2020 · External reference
Phosphorylation of serine residues 3, 6, 10, and 13 distinguishes membrane anchored from soluble glutamic acid decarboxylase 65 and is restricted to glutamic acid decarboxylase 65alpha
10.1074/jbc.272.3.1548 · 1997 · External reference
Myelination of the nervous system: mechanisms and functions
10.1146/annurev-cellbio-100913-013101 · 2014 · External reference
Bringing nerve excitability out of the research laboratory into the clinic
10.1016/j.cnp.2022.10.001 · 2022 · External reference
Recent insights into neuromuscular junction biology in Duchenne muscular dystrophy: impacts, challenges, and opportunities
10.1016/j.ebiom.2020.103032 · 2020 · External reference
Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier
10.1523/jneurosci.2068-05.2005 · 2005 · External reference
Opposing extracellular signal–regulated kinase (ERK) and Akt pathways control Schwann cell myelination
10.1523/jneurosci.5520-03.2004 · 2004 · External reference
Complexity of skeletal muscle degeneration: multi-systems pathophysiology and organ crosstalk in dystrophinopathy
10.1007/s00424-021-02623-1 · 2021 · External reference
Terminal Schwann cell structure is altered in diaphragm of mdx mice
10.1002/mus.20405 · 2005 · External reference
Notch signal mediates the cross-interaction between M2 muscarinic acetylcholine receptor and neuregulin/ErbB pathway: effects on Schwann cell proliferation
10.3390/biom12020239 · 2022 · External reference
Pre- and postsynaptic changes in the neuromuscular junction in dystrophic mice
10.3389/fphys.2015.00252 · 2015 · External reference
Recovery of altered neuromuscular junction morphology and muscle function in mdx mice after injury
10.1007/s00018-014-1663-7 · 2015 · External reference
GABA-B receptors in the PNS have a role in Schwann cells differentiation?
10.3389/fncel.2012.00068 · 2013 · External reference
The proprioceptive senses: their roles in signaling body shape, body position and movement, and muscle force
10.1152/physrev.00048.2011 · 2012 · External reference
The burden, epidemiology, costs and treatment for Duchenne muscular dystrophy: an evidence review
10.1186/s13023-017-0631-3 · 2017 · External reference
Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization
10.1016/s0896-6273(03)00301-5 · 2003 · External reference
Recent progress on the molecular organization of myelinated axons
10.1046/j.1529-8027.2002.02001.x · 2002 · External reference
Metabolism and functions of lipids in myelin
10.1016/j.bbalip.2014.12.016 · 2015 · External reference
Expression and function of GABA receptors in myelinating cells
10.3389/fncel.2020.00256 · 2020 · External reference
Muscular fatigue in Duchenne muscular dystrophy
10.1212/wnl.45.2.306 · 1995 · External reference
Specific disruption of a Schwann cell dystrophin-related protein complex in a demyelinating neuropathy
10.1016/s0896-6273(01)00327-0 · 2001 · External reference
The molecular basis of muscular dystrophy in the mdx mouse: a point mutation
10.1126/science.2662404 · 1989 · External reference
Two isoforms of glutamate decarboxylase: why?
10.1016/s0165-6147(98)01270-x · 1998 · External reference
Proteolytic and non-proteolytic roles of membrane type-1 matrix metalloproteinase in malignancy
10.1016/j.bbamcr.2009.04.009 · 2010 · External reference
Histomorphology of neuromuscular junction in Duchenne muscular dystrophy
10.1111/j.1460-9592.2008.02411.x · 2008 · External reference
The shortest isoform of dystrophin (Dp40) interacts with a group of presynaptic proteins to form a presumptive novel complex in the mouse brain
10.1007/s12035-012-8233-5 · 2012 · External reference
The influence of visual and tactile perception on hand control in children with Duchenne muscular dystrophy
10.1111/dmcn.12469 · 2014 · External reference
Insights into the regulation of protein abundance from proteomic and transcriptomic analyses
10.1038/nrg3185 · 2012 · External reference
Increased mRNA expression of tissue inhibitors of metalloproteinase-1 and -2 in Duchenne muscular dystrophy
10.1007/s00401-004-0941-0 · 2005 · External reference
In vivo electrophysiological measurement of the rat ulnar nerve with axonal excitability testing
2018 · External reference
Schwann cell interactions during the development of the peripheral nervous system
10.1002/dneu.22744 · 2021 · External reference
Regulation of matrix metalloproteinase gene expression
10.1002/jcp.20948 · 2007 · External reference
Animal models for researching approaches to therapy of Duchenne muscular dystrophy
10.1007/s11248-021-00278-3 · 2021 · External reference
