Dynamic changes in the subcellular localization of Drosophila beta-sarcoglycan during the cell cycle.

No abstract is available for this paper.

• Publication year

  2006

• Venue

  Cell Structure and Function

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1247/CSF.06025PMID 17159290
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Genetic link between β - sarcoglycan and the Egfr signaling pathway

  2006cited by this paper
• Genetic link between beta-sarcoglycan and the Egfr signaling pathway.

  2006cited by this paper
• 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.

  2006cited by this paper
• Phosphorylation of dystrophin Dp71d by Ca2+/calmodulin‐dependent protein kinase II modulates the Dp71d nuclear localization in PC12 cells

  2006cited by this paper
• Delta-sarcoglycan is necessary for early heart and muscle development in zebrafish.

  2006cited by this paper
• Expression of α-dystrobrevin in blood-tissue barriers: sub-cellular localisation and molecular characterisation in normal and dystrophic mice

  2006cited by this paper
• Identification of functional domains in sarcoglycans essential for their interaction and plasma membrane targeting.

  2006cited by this paper
• Drosophila: a "model" model system to study neurodegeneration.

  2005cited by this paper
• Delta-sarcoglycan is required for early zebrafish muscle organization.

  2005cited by this paper
• ϵ‐Sarcoglycan immunoreactivity and mRNA expression in mouse brain

  2005cited by this paper
• The sarcoglycan-sarcospan complex localization in mouse retina is independent from dystrophins.

  2005cited by this paper
• Epsilon-sarcoglycan immunoreactivity and mRNA expression in mouse brain.

  2005cited by this paper
• Molecular and cell biology of the sarcoglycan complex

  2005influential reference
• The role of dystrophin in the central nervous system: a mini review.

  2005cited by this paper
• Expression Analysis of the SG-SSPN Complex in Smooth Muscle and Endothelial Cells of Human Umbilical Cord Vessels

  2005cited by this paper
• Embryonic expression patterns of the Drosophila dystrophin-associated glycoprotein complex orthologs.

  2004cited by this paper
• Genetic compensation for sarcoglycan loss by integrin α7β1 in muscle

  2004cited by this paper
• Genetic compensation for sarcoglycan loss by integrin alpha7beta1 in muscle.

  2004cited by this paper
• Characterization of the ATP-hydrolysing activity of α-sarcoglycan

  2004cited by this paper
• Specific assembly pathway of sarcoglycans is dependent on beta‐ and delta‐sarcoglycan

  2004cited by this paper
• Characterization of the ATP-hydrolysing activity of alpha-sarcoglycan.

  2004cited by this paper
• The zebrafish as a model for muscular dystrophy and congenital myopathy.

  2003cited by this paper
• Differential expression and subcellular distribution of dystrophin Dp71 isoforms during differentiation process.

  2003cited by this paper
• Modelling human diseases in Drosophila and Caenorhabditis.

  2003cited by this paper
• Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.

  2002cited by this paper
• Genetic evidence for a dystrophin-glycoprotein complex (DGC) in Caenorhabditis elegans.

  2002cited by this paper
• Zeta-sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy.

  2002cited by this paper
• Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.

  2001cited by this paper
• Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome

  2001cited by this paper
• Differential distribution of the members of the dystrophin glycoprotein complex in mouse retina: effect of the mdx(3Cv) mutation.

  2001cited by this paper
• Characterization of the intermolecular associations of the dystrophin-associated glycoprotein complex in retinal Müller glial cells.

  2000cited by this paper
• Conservation of components of the dystrophin complex in Drosophila 1

  2000cited by this paper
• Differential expression of dystrophin, utrophin, and dystrophin-associated proteins in human muscle culture

  2000cited by this paper
• Muscular dystrophy: the worm turns to genetic disease.

  2000cited by this paper
• Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.

  2000cited by this paper
• Membrane Targeting and Stabilization of Sarcospan Is Mediated by the Sarcoglycan Subcomplex

  1999cited by this paper
• Developmental expression of sarcoglycan gene products in cultured myocytes.

  1999cited by this paper
• Ecto-ATPase Activity of α-Sarcoglycan (Adhalin)*

  1999cited by this paper
• Molecular Pathogenesis of Muscle Degeneration in the δ-Sarcoglycan-Deficient Hamster

  1998cited by this paper
• Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster.

  1998cited by this paper
• Role of dystrophin isoforms and associated proteins in muscular dystrophy (review).

  1998cited by this paper
• ε-Sarcoglycan, a Broadly Expressed Homologue of the Gene Mutated in Limb-Girdle Muscular Dystrophy 2D*

  1997cited by this paper
• Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene

  1996cited by this paper
• Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).

  1996cited by this paper
• The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.

  1996cited by this paper
• Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.

  1996cited by this paper
• Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12.

  1995cited by this paper
• Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy.

  1995cited by this paper
• Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy

  1995cited by this paper
• β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

  1995cited by this paper
• Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy.

  1994cited by this paper
• An adenovirus glycoprotein binds heavy chains of class I transplantation antigens from man and mouse

  1982cited by this paper
• Direct evidence of homology between human DC-1 antigen and murine I-A molecules

  1982cited by this paper

• Pharmacogenetics of response to neoadjuvant paclitaxel treatment for locally advanced breast cancer

  2017cites this paper
• Structural characterization and subcellular localization of Drosophila organic solute carrier partner 1

  2014cites this paper
• Sarcoglycan complex formation is involved in regulation of EGFR signaling during Drosophila eye development

  2012cites this paper
• Genetic Variations Associated with Resistance to Doxorubicin and Paclitaxel in Breast Cancer

  2012cites this paper
• Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines

  2011cites this paper