Nuclear and nuclear envelope localization of dystrophin Dp71 and dystrophin‐associated proteins (DAPs) in the C2C12 muscle cells: DAPs nuclear localization is modulated during myogenesis
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B. Cisneros | D. Mornet | R. González-Ramírez | B. Cisneros | R. González‐Ramírez | S.L. Morales‐Lázaro | V. Tapia‐Ramírez | D. Mornet | S. Morales-Lázaro | V. Tapia-Ramírez
[1] B. Cisneros,et al. Differential expression and subcellular distribution of dystrophin Dp71 isoforms during differentiation process , 2003, Neuroscience.
[2] N. Amariglio,et al. Gene silencing at the nuclear periphery , 2007, The FEBS journal.
[3] A. Monaco. Dystrophin, the protein product of the Duchenne/Becker muscular dystrophy gene. , 1989, Trends in biochemical sciences.
[4] G. Lyons,et al. MyoD, myogenin independent differentiation of primordial myoblasts in mouse somites , 1992, The Journal of cell biology.
[5] K. Davies,et al. Characterisation of alpha-dystrobrevin in muscle. , 1998, Journal of cell science.
[6] E. Friauf,et al. A subcellular prefractionation protocol for minute amounts of mammalian cell cultures and tissue , 2005, Proteomics.
[7] M. Matunis. Isolation and fractionation of rat liver nuclear envelopes and nuclear pore complexes. , 2006, Methods.
[8] Derek J. Blake,et al. Different Dystrophin-like Complexes Are Expressed in Neurons and Glia , 1999, The Journal of cell biology.
[9] H. Baumgarten,et al. Nitric oxide synthase in skeletal muscle fibers: a signaling component of the dystrophin-glycoprotein complex. , 1999, Histology and histopathology.
[10] J. Ervasti,et al. Purification of dystrophin from skeletal muscle. , 1991, The Journal of biological chemistry.
[11] M. Topham,et al. Interaction of gamma 1-syntrophin with diacylglycerol kinase-zeta. Regulation of nuclear localization by PDZ interactions. , 2001, The Journal of biological chemistry.
[12] K. Campbell,et al. Expression of dystrophin-associated glycoproteins during human fetal muscle development: A preliminary immunocytochemical study , 1994, Neuromuscular Disorders.
[13] H. Klamut,et al. Dystrophin isoforms Dp71 and Dp427 have distinct roles in myogenic cells , 1999, Muscle & nerve.
[14] H. Worman,et al. How do mutations in lamins A and C cause disease? , 2004, The Journal of clinical investigation.
[15] D. Bulman,et al. Myogenic regulation of dystrophin gene expression. , 1989, British medical bulletin.
[16] B. Chait,et al. Proteomic analysis of the mammalian nuclear pore complex , 2002, The Journal of cell biology.
[17] M. Shigekawa,et al. Bidirectional Signaling between Sarcoglycans and the Integrin Adhesion System in Cultured L6 Myocytes* , 1998, The Journal of Biological Chemistry.
[18] T. Bergman,et al. Characterization of human alpha-dystrobrevin isoforms in HL-60 human promyelocytic leukemia cells undergoing granulocytic differentiation. , 2002, Molecular biology of the cell.
[19] K. Wilson. The nuclear envelope, muscular dystrophy and gene expression. , 2000, Trends in cell biology.
[20] B. Cisneros,et al. Characterization of a novel Dp71 dystrophin-associated protein complex (DAPC) present in the nucleus of HeLa cells: members of the nuclear DAPC associate with the nuclear matrix. , 2006, Experimental cell research.
[21] U. Francke,et al. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations. , 1988, American journal of human genetics.
[22] S. Carbonetto,et al. Dystroglycan contributes to the formation of multiple dystrophin‐like complexes in brain , 2001, Journal of neurochemistry.
[23] R. Coral-Vázquez,et al. Partial characterization of the mouse α-sarcoglycan promoter and its responsiveness to MyoD , 2006 .
[24] G. Macchia,et al. Association of the Dystroglycan Complex Isolated from Bovine Brain Synaptosomes with Proteins Involved in Signal Transduction , 1999, Journal of neurochemistry.
[25] K. Davies,et al. Assembly of multiple dystrobrevin-containing complexes in the kidney. , 2000, Journal of cell science.
[26] J. Sahel,et al. Characterization of the intermolecular associations of the dystrophin-associated glycoprotein complex in retinal Müller glial cells. , 2000, Journal of cell science.
[27] O. Ibraghimov-Beskrovnaya,et al. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix , 1992, Nature.
[28] J. Towbin,et al. Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy. , 2000, The Journal of clinical investigation.
[29] Eric P. Hoffman,et al. Dystrophin: The protein product of the duchenne muscular dystrophy locus , 1987, Cell.
[30] S. Carbonetto,et al. α-Dystroglycan Is a Laminin Receptor Involved in Extracellular Matrix Assembly on Myotubes and Muscle Cell Viability , 1999, The Journal of cell biology.
[31] L. Kunkel,et al. The Three Human Syntrophin Genes Are Expressed in Diverse Tissues, Have Distinct Chromosomal Locations, and Each Bind to Dystrophin and Its Relatives (*) , 1996, The Journal of Biological Chemistry.
[32] K. Davies,et al. beta-dystrobrevin, a member of the dystrophin-related protein family. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[33] F. Rivier,et al. Dystrophin and Utrophin Complexed with Different Associated Proteins in Cardiac Purkinje Fibres , 1999, The Histochemical Journal.
[34] A. Levey,et al. Cell-specific Sorting of Biogenic Amine Transporters Expressed in Epithelial Cells* , 1996, The Journal of Biological Chemistry.
[35] Mutations in the human δ-sarcoglycan gene in familial and sporadic dilated cardiomyopathy , 2000 .
[36] K. Campbell,et al. Sarcospan, the 25-kDa Transmembrane Component of the Dystrophin-Glycoprotein Complex* , 1997, The Journal of Biological Chemistry.
[37] Y. Sunada,et al. Characterization of the Transmembrane Molecular Architecture of the Dystroglycan Complex in Schwann Cells* , 1999, The Journal of Biological Chemistry.
[38] M. Topham,et al. Interaction of γ1-Syntrophin with Diacylglycerol Kinase-ζ , 2001, The Journal of Biological Chemistry.
[39] U. Nudel,et al. Specificity of expression of the muscle and brain dystrophin gene promoters in muscle and brain cells , 1990, Neuron.
[40] R. Foisner,et al. Nuclear envelope and nuclear matrix: interactions and dynamics , 2001, Cellular and Molecular Life Sciences CMLS.
[41] M. Lisanti,et al. Expression of Caveolin-3 in Skeletal, Cardiac, and Smooth Muscle Cells , 1996, The Journal of Biological Chemistry.
[42] V. Sartorelli,et al. Mechanisms underlying the transcriptional regulation of skeletal myogenesis. , 2005, Current opinion in genetics & development.
[43] K. Davies,et al. The dystrophin-associated protein complex. , 2002, Journal of cell science.
[44] S. Noguchi,et al. Identification of myogenesis-dependent transcriptional enhancers in promoter region of mouse gamma-sarcoglycan gene. , 2001, European journal of biochemistry.
[45] P. Gómez,et al. Dystrophin Dp71 Expression Is Down-regulated during Myogenesis , 2005, Journal of Biological Chemistry.