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culture cellulaireSynonyme(s)cultured cell cell cultures |
Documents disponibles dans cette catégorie (1042)


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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
Revue : The International Journal of Biochemistry & Cell Biology, 120 Titre : Ubiquitin ligase LRSAM1 suppresses neurodegenerative diseases linked aberrant proteins induced cell death Type de document : Article Auteurs : Mishra R ; Amanullah A ; Upadhyay A ; Dhiman R ; Dubey AR ; Singh S ; Prasad A ; Mishra A Editeur : Netherlands Année de publication : 03/2020 Langues : Anglais (eng) Mots-clés : biologie moléculaire ; culture cellulaire ; maladie de Charcot-Marie-Tooth ; maladie du système nerveux périphérique ; physiopathologie ; RECHERCHE Pubmed / DOI : Pubmed : 31982566 / DOI : 10.1016/j.biocel.2020.105697
N° Profil MNM : 2020013 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31982566 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Glia Titre : Loss-of-function of EBP50 is a new cause of hereditary peripheral neuropathy: EBP50 functions in peripheral nerve system Type de document : Article Auteurs : Song GJ ; Gupta DP ; Rahman MH ; Park HT ; Al Ghouleh I ; Bisello A ; Lee MG ; Park JY ; Park HH ; Jun JH ; Chung KW ; Choi BO ; Suk K Editeur : United States Année de publication : 02/2020 Langues : Anglais (eng) Mots-clés : corrélation génotype-phénotype ; culture cellulaire ; identification du gène ; maladie de Charcot-Marie-Tooth ; maladie du système nerveux périphérique ; recherche génétique ; souris Pubmed / DOI : Pubmed : 32077526 / DOI : 10.1002/glia.23805
N° Profil MNM : 2020022 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32077526 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Molecular therapy : the journal of the American Society of Gene Therapy Titre : AMPK Complex Activation Promotes Sarcolemmal Repair in Dysferlinopathy Type de document : Article Auteurs : Ono H ; Suzuki N ; Kanno SI ; Kawahara G ; Izumi R ; Takahashi T ; Kitajima Y ; Osana S ; Nakamura N ; Akiyama T ; Ikeda K ; Shijo T ; Mitsuzawa S ; Nagatomi R ; Araki N ; Yasui A ; Warita H ; Hayashi YK ; Miyake K ; Aoki M Editeur : United States Année de publication : 02/2020 Langues : Anglais (eng) Mots-clés : culture cellulaire ; dysferline (maladie neuromusculaire liée à) ; dystrophie musculaire ; physiopathologie ; poisson zèbre ; RECHERCHE ; souris Pubmed / DOI : Pubmed : 32087766 / DOI : 10.1016/j.ymthe.2020.02.006
N° Profil MNM : 2020022 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32087766 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Scientific Reports, 10, 1 Titre : Inhibition of cyclooxygenase-1 by nonsteroidal anti-inflammatory drugs demethylates MeR2 enhancer and promotes Mbnl1 transcription in myogenic cells Type de document : Article Auteurs : Huang K ; Masuda A ; Chen G ; Bushra S ; Kamon M ; Araki T ; Kinoshita M ; Ohkawara B ; Ito M ; Ohno K Editeur : England Année de publication : 02/2020 Langues : Anglais (eng) Mots-clés : culture cellulaire ; dystrophie myotonique de type 1 ; maladie neuromusculaire ; myoblaste ; recherche thérapeutique ; souris Pubmed / DOI : Pubmed : 32054946 / DOI : 10.1038/s41598-020-59517-y
N° Profil MNM : 2020021 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32054946 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : ACS chemical biology Titre : Structure-Specific Cleavage of an RNA Repeat Expansion with a Dimeric Small Molecule Is Advantageous over Sequence-Specific Recognition by an Oligonucleotide Type de document : Article Auteurs : Benhamou RI ; Angelbello AJ ; Andrews RJ ; Wang ET ; Moss WN ; Disney MD Editeur : United States Année de publication : 01/2020 Langues : Anglais (eng) Mots-clés : culture cellulaire ; dystrophie myotonique ; dystrophie myotonique de type 2 ; in vitro ; maladie neuromusculaire ; oligonucléotide antisens ; recherche thérapeutique Pubmed / DOI : Pubmed : 31927948 / DOI : 10.1021/acschembio.9b00958
N° Profil MNM : 2020012 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31927948 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
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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
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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
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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
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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
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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
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Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells
Earle AJ, Kirby TJ, Fedorchak GR, et al.
Nature materials, 2019
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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The Use of Antisense Oligonucleotides for the Treatment of Duchenne Muscular Dystrophy
Relizani K, Goyenvalle A
Methods in molecular biology, 2018, 1687, p 171
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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
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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
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