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Abbreviation : DGC
Long Form : dystrophin-glycoprotein complex
No. Year Title Co-occurring Abbreviation
2021 Enterovirus 71 infection induced Aquaporin-4 depolarization by increasing matrix metalloproteinase-9 activity. AQP4, beta-DG, CSF, EV71, MMP-9
2021 Essential roles of the dystrophin-glycoprotein complex in different cardiac pathologies. ---
2021 Loss of sarcospan exacerbates pathology in mdx mice, but does not affect utrophin amelioration of disease. DMD, SSPN, UGC, UTRN
2021 Phosphorylation of ERK and dystrophin S3059 protects against inflammation-associated C2C12 myotube atrophy. PMA
2021 Sarcoglycanopathies: an update. AAV, LGMDs
2020 A signaling hub of insulin receptor, dystrophin glycoprotein complex and plakoglobin regulates muscle size. ---
2020 Agrin-Mediated Cardiac Regeneration: Some Open Questions. CMs, ECM
2020 Caveolin-3: A Causative Process of Chicken Muscular Dystrophy. Cav-3, WWP1
2020 Dystroglycan Mediates Clustering of Essential GABAergic Components in Cerebellar Purkinje Cells. ---
10  2020 Genome Editing-Mediated Utrophin Upregulation in Duchenne Muscular Dystrophy Stem Cells. DMD, DMD-hiPSCs, IMTR, miRNAs, SBOs
11  2020 Impaired Regeneration in Dystrophic Muscle-New Target for Therapy. ECM, MuSCs, SCs
12  2020 Mitochondrial dysfunction in skeletal muscle of fukutin-deficient mice is resistant to exercise- and 5-aminoimidazole-4-carboxamide ribonucleotide-induced rescue. AICAR, AMPK, Fktn KO, LM, PGC-1alpha
13  2020 Pathological evaluation of rats carrying in-frame mutations in the dystrophin gene: a new model of Becker muscular dystrophy. BMD, IF rats
14  2020 The role of the dystrophin glycoprotein complex on the neuromuscular system. AChRs, NMJs
15  2019 Distinct mechanical properties in homologous spectrin-like repeats of utrophin. AFM, DMD
16  2019 Exogenous expression of the glycosyltransferase LARGE1 restores alpha-dystroglycan matriglycan and laminin binding in rhabdomyosarcoma. ECM, LG, RMS
17  2019 Regulation of the dystrophin-associated glycoprotein complex composition by the metabolic properties of muscle fibres. ---
18  2019 Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex. MRI
19  2018 Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical Phenotype. BMD, DCM, DMD, XLDCM
20  2018 Syntrophins entangled in cytoskeletal meshwork: Helping to hold it all together. ---
21  2018 The Dystrophin Glycoprotein Complex Regulates the Epigenetic Activation of Muscle Stem Cell Commitment. ---
22  2018 The enzymatic processing of alpha-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site. alpha-DG, beta-DG, cdMMP-2, DG
23  2018 Towards a better understanding of AQP4's role in astrocytic process extension: An Editorial for 'Involvement of aquaporin-4 in laminin-enhanced process formation of mouse astrocytes in 2D culture: Roles of dystroglycan and a-syntrophin in aquaporin-4 expression' on page 495. AQP4, BBB
24  2017 ABC of multifaceted dystrophin glycoprotein complex (DGC). ---
25  2017 Dystrophin-glycoprotein complex sequesters Yap to inhibit cardiomyocyte proliferation. Dag1
26  2017 Heart Regeneration 4.0: Matrix Medicine. ---
27  2017 Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophy. DMD
28  2017 SU9516 Increases alpha7beta1 Integrin and Ameliorates Disease Progression in the mdx Mouse Model of Duchenne Muscular Dystrophy. DMD, SPAK
29  2017 Targeting Nfix to fix muscular dystrophies. MDs, SCs
30  2017 The molecular cross talk of the dystrophin-glycoprotein complex. ECM, NMJs
31  2016 Actin depolymerization mediated loss of SNTA1 phosphorylation and Rac1 activity has implications on ROS production, cell migration and apoptosis. ROS, SNTA1
32  2016 Age-related alterations in the sarcolemmal environment are attenuated by lifelong caloric restriction and voluntary exercise. CR, nNOS, NOX2, OAL
33  2016 Genetic overexpression of Serpina3n attenuates muscular dystrophy in mice. MD
34  2016 Mechanistic aspects of the formation of alpha-dystroglycan and therapeutic research for the treatment of alpha-dystroglycanopathy: A review. alpha-DG, FCMD, LGMD2I, MEB, WWS
35  2016 Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy. ---
36  2016 Skeletal muscle-specific overexpression of IGFBP-2 promotes a slower muscle phenotype in healthy but not dystrophic mdx mice and does not affect the dystrophic pathology. DMD, IGFBPs, TA
37  2015 Characterization of the dystrophin-glycoprotein complex in airway smooth muscle: role of delta-sarcoglycan in airway responsiveness. ASM, delta-SG, MCh
38  2015 Dystrophin hydrophobic regions in the pathogenesis of Duchenne and Becker muscular dystrophies. ABD
39  2015 Dystrophin-glycoprotein complex regulates muscle nitric oxide production through mechanoregulation of AMPK signaling. AMPK, nNOS, NO
40  2015 Genetic Engineering of Dystroglycan in Animal Models of Muscular Dystrophy. DG
41  2015 Neuronal nitric oxide synthase localizes to utrophin expressing intercalated discs and stabilizes their structural integrity. DMD, IDs, KO, nNOS, NO, sGC
42  2015 Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains. ECM, NMJ, nNOS
43  2015 Progress and prospects of gene therapy clinical trials for the muscular dystrophies. LGMDs, MD's
44  2015 Role of gelatinases in pathological and physiological processes involving the dystrophin-glycoprotein complex. ---
45  2014 Absence of γ-sarcoglycan alters the response of p70S6 kinase to mechanical perturbation in murine skeletal muscle. ---
46  2014 Phosphorylation within the cysteine-rich region of dystrophin enhances its association with β-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting. ---
47  2013 A new look at cytoskeletal NOS-1 and beta-dystroglycan changes in developing muscle and brain in control and mdx dystrophic mice. bDG
48  2013 Bortezomib (PS-341) treatment decreases inflammation and partially rescues the expression of the dystrophin-glycoprotein complex in GRMD dogs. CD, DMD, GRMD
49  2013 Dynamics of nicotinic acetylcholine receptors and receptor-associated proteins at the vertebrate neuromuscular junction. nAChRs, NMJ
50  2012 Costameric proteins: from benchside to future translational cardiovascular research. ---
51  2012 Dg-Dys-Syn1 signaling in Drosophila regulates the microRNA profile. ---
52  2012 Dystrophin-compromised sarcoglycan-δ-knockout diaphragm requires full wild-type embryonic stem cell reconstitution for correction. ESCs, KO, LGMD-2F, SGC, SGdelta, WT
53  2012 Expression of sarcoglycans in the human cerebral cortex: an immunohistochemical and molecular study. CNS, SG
54  2012 Hyperthermic seizures and aberrant cellular homeostasis in Drosophila dystrophic muscles. Dg, Dys, MDs
55  2012 Pre-clinical drug tests in the mdx mouse as a model of dystrophinopathies: an overview. ---
56  2012 Presynaptic dystroglycan-pikachurin complex regulates the proper synaptic connection between retinal photoreceptor and bipolar cells. DG, DG CKO
57  2012 Preventing phosphorylation of dystroglycan ameliorates the dystrophic phenotype in mdx mouse. ---
58  2012 Successful regional delivery and long-term expression of a dystrophin gene in canine muscular dystrophy: a preclinical model for human therapies. AAV, c-dys, DMD, IM
59  2012 The AChE membrane-binding tail PRiMA is down-regulated in muscle and nerve of mice with muscular dystrophy by merosin deficiency. AChE, BuChE
60  2012 The dystrophin-glycoprotein complex in brain development and disease. AQP4, ECM, MCI
61  2011 A second Ig-like domain identified in dystroglycan by molecular modelling and dynamics. DG, Ig-like
62  2011 Age-related changes in dystrophin-glycoprotein complex and in utrophin are not correlated with intrinsic laryngeal muscles protection in mdx mice. ILM
63  2011 Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice. ---
64  2011 Lateral transmission of force is impaired in skeletal muscles of dystrophic mice and very old rats. WT
65  2011 Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers. DMD, MMPs, VEGFA
66  2011 Mitigation of muscular dystrophy in mice by SERCA overexpression in skeletal muscle. AAV-SERCA2a, MDs, SERCA1
67  2011 New dystrophin/dystroglycan interactors control neuron behavior in Drosophila eye. Dg, Dys
68  2011 Stress and muscular dystrophy: a genetic screen for dystroglycan and dystrophin interactors in Drosophila identifies cellular stress response components. ---
69  2011 The role of α-dystrobrevin in striated muscle. ---
70  2011 Three-dimensional regulation of radial glial functions by Lis1-Nde1 and dystrophin glycoprotein complexes. RGCs
71  2010 Analysis by two-dimensional Blue Native/SDS-PAGE of membrane protein alterations in rat soleus muscle after hindlimb unloading. AQP4, HU
72  2010 beta-Dystroglycan binds caveolin-1 in smooth muscle: a functional role in caveolae distribution and Ca2+ release. ---
73  2010 Biological role of dystroglycan in Schwann cell function and its implications in peripheral nervous system diseases. ---
74  2010 Disruption of sarcolemmal dystrophin and beta-dystroglycan may be a potential mechanism for myocardial dysfunction in severe sepsis. CLP, MSI
75  2010 Drosophila Syntrophins are involved in locomotion and regulation of synaptic morphology. Syn1, Syn2
76  2010 Possible molecular mechanisms underlying age-related cardiomyocyte apoptosis in the F344XBN rat heart. F344XBN
77  2009 Calcium influx is sufficient to induce muscular dystrophy through a TRPC-dependent mechanism. SCGD, TRPC3
78  2009 Distribution of costameric proteins in normal human ventricular and atrial cardiac muscle. ---
79  2009 Dystrophin glycoprotein complex-associated Gbetagamma subunits activate phosphatidylinositol-3-kinase/Akt signaling in skeletal muscle in a laminin-dependent manner. PI3K
80  2009 Dystrophin-glycoprotein complex and vinculin-talin-integrin system in human adult cardiac muscle. ---
81  2009 Immune-mediated mechanisms potentially regulate the disease time-course of duchenne muscular dystrophy and provide targets for therapeutic intervention. ---
82  2009 MLC1 trafficking and membrane expression in astrocytes: role of caveolin-1 and phosphorylation. MLC
83  2009 Several dystrophin-glycoprotein complex members are present in crude surface membranes but they are sodium dodecyl sulphate invisible in KCl-washed microsomes from mdx mouse muscle. ---
84  2009 Syntrophin-2 is required for eye development in Drosophila. Syn2
85  2009 The conserved WW-domain binding sites in Dystroglycan C-terminus are essential but partially redundant for Dystroglycan function. Dg, Dys
86  2008 Aberrantly spliced alpha-dystrobrevin alters alpha-syntrophin binding in myotonic dystrophy type 1. DM1, mRNA
87  2008 An ankyrin-based mechanism for functional organization of dystrophin and dystroglycan. DG
88  2008 Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies. AQP4, LGMDs
89  2008 Biochemical characterization of MLC1 protein in astrocytes and its association with the dystrophin-glycoprotein complex. MLC, MLC1
90  2008 Correlation of dystrophin-glycoprotein complex and focal adhesion complex with myosin heavy chain isoforms in rat skeletal muscle. FAC, MHC, SOL
91  2008 Destabilization of the dystrophin-glycoprotein complex without functional deficits in alpha-dystrobrevin null muscle. ---
92  2008 Isoproterenol induces primary loss of dystrophin in rat hearts: correlation with myocardial injury. ---
93  2008 Microutrophin delivery through rAAV6 increases lifespan and improves muscle function in dystrophic dystrophin/utrophin-deficient mice. AAV, DMD
94  2008 Muscle dystroglycan organizes the postsynapse and regulates presynaptic neurotransmitter release at the Drosophila neuromuscular junction. Dg, NMJ
95  2008 Plectin 1 links intermediate filaments to costameric sarcolemma through beta-synemin, alpha-dystrobrevin and actin. IFs
96  2008 Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex. SSPN, UGC
97  2008 The ABCA1 cholesterol transporter associates with one of two distinct dystrophin-based scaffolds in Schwann cells. ---
98  2007 A mutation in CHN-1/CHIP suppresses muscle degeneration in Caenorhabditis elegans. DMD
99  2007 Altered biomechanical properties of carotid arteries in two mouse models of muscular dystrophy. ---
100  2007 Complete deletion of all alpha-dystrobrevin isoforms does not reveal new neuromuscular junction phenotype. NMJ