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interaction protéine-protéineSynonyme(s)liaison entre protéines ;protein protein binding ;protein-protein interactions interactome |
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Force Generation by Myosin Motors: A Structural Perspective
Robert-Paganin J, Pylypenko O, Kikuti C, et al.
Chemical reviews, 2019
The molecular cross talk of the dystrophin-glycoprotein complex
Gawor M, Proszynski TJ
Annals of the New York Academy of Sciences, 2018, 1412, 1, p 62
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
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
Linking Amyotrophic Lateral Sclerosis and Spinal Muscular Atrophy through RNA-transcriptome homeostasis: a genomics perspective
Gama-Carvalho M, Garcia-Vaquero ML, Pinto FR, et al.
Journal of neurochemistry, 2017, 141, 1, p 12
Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice
Reinhard JR, Lin S, McKee KK, et al.
Science translational medicine, 2017, 9, 396
Nuclear poly(A) binding protein 1 (PABPN1) and Matrin3 interact in muscle cells and regulate RNA processing
Banerjee A, Vest KE, Pavlath GK, et al.
Nucleic acids research, 2017, 45, 18, p 10706
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy
Rossi D, Palmio J, Evila A, et al.
PLoS ONE, 2017, 12, 10
Duchenne Muscular Dystrophy (DMD) Protein-Protein Interaction Mapping
Rezaei Tavirani M, OkHOVATIAN F, Zamanian Azodi M, et al.
Iranian journal of child neurology, 2017, 11, 4, p 7
The reason for a high Ca2+-sensitivity associated with Arg91Gly substitution in TPM2 gene is the abnormal behavior and high flexibility of tropomyosin during the ATPase cycle
Borovikov YS, Simonyan AO, Karpicheva OE, et al.
Biochemical and biophysical research communications, 2017, 494, 3-4, p 681
Gènes impliqués dans les alpha-dystroglycanopathies. Le point en 2016 : [Les cahiers de Myologie]
Bouchet-Seraphin C, Chelbi-Viallon M, Vuillaumier-Barrot S, et al.
Les Cahiers de Myologie, 2016, Vol.32, Hors série n°2, p.40-45
La dystrophine présente plusieurs sites indépendants pour son ancrage membranaire : [Les cahiers de Myologie]
Mornet D
Les Cahiers de Myologie, 2016, Vol.32, Hors série n°2, p.49
Myology 2016 : 5th International Congress of Myology ; Posters n° 104 to 156 - Dystrophinopathies (Duchenne, Becker, others)
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 72-97
Myology 2016 : 5th International Congress of Myology ; Posters n° 219 to 237 - Inflammatory myopathies
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 127-137
Myology 2016 : 5th International Congress of Myology ; Posters n° 238 to 255 - Limb girdle muscular dystrophies / OPMD
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 137-146
Myology 2016 : 5th International Congress of Myology ; Posters n° 256 to 274 - Miscellaneous
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 146-156
Myology 2016 : 5th International Congress of Myology ; Posters n° 275 to 283 - Muscle function
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 156-159
Myology 2016 : 5th International Congress of Myology ; Posters n° 323 to 330 - Nuclear envelopathies (lamin A/C, emerin, others)
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 178-181
Myology 2016 : 5th International Congress of Myology ; Posters n° 388 to 423 - Young Investigator Posters
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 205-222
The sarcoglycan complex in skeletal muscle
Tarakci H, Berger J
Frontiers in bioscience, 2016, 21, p 744
Homologous Transcription Factors DUX4 and DUX4c Associate with Cytoplasmic Proteins during Muscle Differentiation
Ansseau E, Eidahl JO, Lancelot C, et al.
PLoS ONE, 2016, 11, 1
Deep RNA profiling identified clock and molecular clock genes as pathophysiological signatures in collagen VI myopathy
Scotton C, Bovolenta M, Schwartz E, et al.
Journal of cell science, 2016, 129, 8, p 1671
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Winter L, Türk M, Harter PN, et al.
Acta neuropathologica communications, 2016, 4, 1
Roles of collagen Q in MuSK antibody-positive myasthenia gravis
Ohno K, Otsuka K, Ito M
Chemico-biological interactions, 2016, 259, Pt B, p 266
Molecular signatures of membrane protein complexes underlying muscular dystrophy
Turk R, Hsiao JJ, Smits MM, et al.
Molecular & cellular proteomics : MCP, 2016, 15, 6, p 2169
