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culture cellulaireSynonyme(s)cultured cell cell cultures |
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Ubiquitin ligase LRSAM1 suppresses neurodegenerative diseases linked aberrant proteins induced cell death
Mishra R, Amanullah A, Upadhyay A, et al.
The International Journal of Biochemistry & Cell Biology, 2020, 120
Loss-of-function of EBP50 is a new cause of hereditary peripheral neuropathy: EBP50 functions in peripheral nerve system
Song GJ, Gupta DP, Rahman MH, et al.
Glia, 2020
AMPK Complex Activation Promotes Sarcolemmal Repair in Dysferlinopathy
Ono H, Suzuki N, Kanno SI, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2020
Inhibition of cyclooxygenase-1 by nonsteroidal anti-inflammatory drugs demethylates MeR2 enhancer and promotes Mbnl1 transcription in myogenic cells
Huang K, Masuda A, Chen G, et al.
Scientific Reports, 2020, 10, 1
Structure-Specific Cleavage of an RNA Repeat Expansion with a Dimeric Small Molecule Is Advantageous over Sequence-Specific Recognition by an Oligonucleotide
Benhamou RI, Angelbello AJ, Andrews RJ, et al.
ACS chemical biology, 2020
Novel HDAC6 Inhibitors Increase Tubulin Acetylation and Rescue Axonal Transport of Mitochondria in a Model of Charcot-Marie-Tooth Type 2F
Adalbert R, Kaieda A, Antoniou C, et al.
ACS chemical neuroscience, 2020
Mitochondrial function in skeletal myofibers is controlled by a TRF2-SIRT3 axis over lifetime
Robin JD, Jacome Burbano MS, Peng H, et al.
Aging cell, 2020
ZPR1 prevents R-loop accumulation, upregulates SMN2 expression and rescues spinal muscular atrophy
Kannan A, Jiang X, He L, et al.
Brain : a journal of neurology, 2020, 143, 1, p 69
Intravenous immunoglobulin mediates anti-inflammatory effects in peripheral blood mononuclear cells by inducing autophagy
Das M, Karnam A, Stephen-Victor E, et al.
Cell death & disease, 2020, 11, 1, p 50
AdipoRon, a new therapeutic prospect for Duchenne muscular dystrophy
Abou-Samra M, Selvais CM, Boursereau R, et al.
Journal of cachexia, sarcopenia and muscle, 2020
Defects in G-Actin Incorporation into Filaments in Myoblasts Derived from Dysferlinopathy Patients Are Restored by Dysferlin C2 Domains
Baez-Matus X, Figueroa-Cares C, González-Jamett AM, et al.
International Journal of molecular sciences, 2019, 21, 1
Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells
Earle AJ, Kirby TJ, Fedorchak GR, et al.
Nature materials, 2019
Antisense-Mediated Skipping of Dysferlin Exons in Control and Dysferlinopathy Patient-Derived Cells
Verwey N, Gazzoli I, Krause S, et al.
Nucleic acid therapeutics, 2019
Identification of the hyaluronic acid pathway as a therapeutic target for facioscapulohumeral muscular dystrophy
DeSimone AM, Leszyk J, Wagner K, et al.
Science advances, 2019, 5, 12
MYO9A deficiency in motor neurons is associated with reduced neuromuscular agrin secretion
O'Connor E, Phan V, Cordts I, et al.
Human molecular genetics, 2018, 27, 8, p 1434
Cell endogenous activities of fukutin and FKRP coexist with the ribitol xylosyltransferase, TMEM5
Nishihara R, Kobayashi K, Imae R, et al.
Biochemical and biophysical research communications, 2018, 497, 4, p 1025
Stem cell derived phenotypic human neuromuscular junction model for dose response evaluation of therapeutics
Santhanam N, Kumanchik L, Guo X, et al.
Biomaterials, 2018, 166, p 64
Activin A amplifies dysregulated BMP signaling and induces chondro-osseous differentiation of primary connective tissue progenitor cells in patients with fibrodysplasia ossificans progressiva (FOP)
Wang H, Shore EM, Pignolo RJ, et al.
Bone, 2018, 109, p 218
Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next-generation human artificial chromosomes for Duchenne muscular dystrophy
Benedetti S, Uno N, Hoshiya H, et al.
EMBO Molecular Medicine, 2018, 10, 2, p 254
PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease
Juneja M, Azmi A, Baets J, et al.
Journal of neurology, neurosurgery, and psychiatry, 2018, 89, 8, p 870
Advanced Methods to Study the Cross Talk Between Fibro-Adipogenic Progenitors and Muscle Stem Cells
Tucciarone L, Etxaniz U, Sandona M, et al.
Methods in molecular biology, 2018, 1687, p 231
Test of Antifibrotic Drugs in a Cellular Model of Fibrosis Based on Muscle-Derived Fibroblasts from Duchenne Muscular Dystrophy Patients
Zanotti S, Mora M
Methods in molecular biology, 2018, 1687, p 205
The Use of Antisense Oligonucleotides for the Treatment of Duchenne Muscular Dystrophy
Relizani K, Goyenvalle A
Methods in molecular biology, 2018, 1687, p 171
Measurement of Chaperone-Mediated Effects on Polyglutamine Protein Aggregation by the Filter Trap Assay
van Waarde-Verhagen MAWH, Kampinga HH
Methods in molecular biology, 2018, 1709, p 59
From gRNA Identification to the Restoration of Dystrophin Expression: A Dystrophin Gene Correction Strategy for Duchenne Muscular Dystrophy Mutations Using the CRISPR-Induced Deletion Method
Duchêne B, Iyombe-Engembe JP, Rousseau J, et al.
Methods in molecular biology (Clifton, N.J.), 2018, 1687, p 267
