Cargando…

The dystrotelin, dystrophin and dystrobrevin superfamily: new paralogues and old isoforms

BACKGROUND: Dystrophins and dystrobrevins are distantly related proteins with important but poorly understood roles in the function of metazoan muscular and neuronal tissues. Defects in them and their associated proteins cause a range of neuromuscular disorders. Members of this superfamily have been...

Descripción completa

Detalles Bibliográficos
Autores principales:	Jin, Hong, Tan, Sipin, Hermanowski, Jane, Böhm, Sabrina, Pacheco, Sabrina, McCauley, Joanna M, Greener, Marc J, Hinits, Yaniv, Hughes, Simon M, Sharpe, Paul T, Roberts, Roland G
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2007
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1790709/ https://www.ncbi.nlm.nih.gov/pubmed/17233888 http://dx.doi.org/10.1186/1471-2164-8-19

Ejemplares similares

Dystrophins and dystrobrevins
por: Roberts, Roland G
Publicado: (2001)

Profound human/mouse differences in alpha-dystrobrevin isoforms: a novel syntrophin-binding site and promoter missing in mouse and rat
por: Böhm, Sabrina V, et al.
Publicado: (2009)

Destabilization of the Dystrophin-Glycoprotein Complex without Functional Deficits in α-Dystrobrevin Null Muscle
por: Bunnell, Tina M., et al.
Publicado: (2008)

Differential Membrane Localization and Intermolecular Associations of α-Dystrobrevin Isoforms in Skeletal Muscle
por: Peters, Matthew F., et al.
Publicado: (1998)

The Role of Alpha-Dystrobrevin in Striated Muscle
por: Nakamori, Masayuki, et al.
Publicado: (2011)

Tyrosine-phosphorylated and nonphosphorylated isoforms of α-dystrobrevin: roles in skeletal muscle and its neuromuscular and myotendinous junctions
por: Grady, R. Mark, et al.
Publicado: (2003)

Morpholino Oligomer-Induced Dystrophin Isoforms to Map the Functional Domains in the Dystrophin Protein
por: Li, Dunhui, et al.
Publicado: (2020)

Development of mandibular, hyoid and hypobranchial muscles in the zebrafish: homologies and evolution of these muscles within bony fishes and tetrapods
por: Diogo, Rui, et al.
Publicado: (2008)

Nuclear Small Dystrophin Isoforms during Muscle Differentiation
por: Donandt, Tina, et al.
Publicado: (2023)

Neuregulin/ErbB regulate neuromuscular junction development by phosphorylation of α-dystrobrevin
por: Schmidt, Nadine, et al.
Publicado: (2011)

Arhgef5 Binds α-Dystrobrevin 1 and Regulates Neuromuscular Junction Integrity
por: Bernadzki, Krzysztof M., et al.
Publicado: (2020)

Unique tasks for ribosomal paralogues
por: Leslie, Mitch
Publicado: (2007)

Subcellular Localization of Dystrophin Isoforms in Cardiomyocytes and Phenotypic Analysis of Dystrophin-deficient Mice Reveal Cardiac Myopathy is Predominantly Caused by a Deficiency in Full-length Dystrophin
por: Masubuchi, Nami, et al.
Publicado: (2013)

A Drosophila model for Meniere’s disease: Dystrobrevin is required for support cell function in hearing and proprioception
por: Requena, T., et al.
Publicado: (2022)

eIF4EBP3L Acts as a Gatekeeper of TORC1 In Activity-Dependent Muscle Growth by Specifically Regulating Mef2ca Translational Initiation
por: Yogev, Orli, et al.
Publicado: (2013)

Mef2c factors are required for early but not late addition of cardiomyocytes to the ventricle
por: Kula-Alwar, Duvaraka, et al.
Publicado: (2021)

Diversification of hAT transposase paralogues in the sugarcane genome
por: de Jesus, Erika M., et al.
Publicado: (2012)

Revisiting the methionine salvage pathway and its paralogues
por: Sekowska, Agnieszka, et al.
Publicado: (2018)

Detection of a specific isoform of alpha-actinin with antisera directed against dystrophin
Publicado: (1989)

Investigating the role of dystrophin isoform deficiency in motor function in Duchenne muscular dystrophy
por: Chesshyre, Mary, et al.
Publicado: (2022)

Natural History of a Mouse Model Overexpressing the Dp71 Dystrophin Isoform
por: Lim, Kenji Rowel Q., et al.
Publicado: (2021)

Distinct functions of alternatively spliced isoforms encoded by zebrafish mef2ca and mef2cb
por: Ganassi, M., et al.
Publicado: (2014)

Genetic association of single nucleotide polymorphisms in dystrobrevin binding protein 1 gene with schizophrenia in a Malaysian population
por: Tan, Grace Kang Ning, et al.
Publicado: (2015)

Identification of β-Dystrobrevin as a Direct Target of miR-143: Involvement in Early Stages of Neural Differentiation
por: Quaranta, Maria Teresa, et al.
Publicado: (2016)

Tissue- and cell-specific whole-transcriptome meta-analysis from brain and retina reveals differential expression of dystrophin complexes and new dystrophin spliced isoforms
por: García-Cruz, César, et al.
Publicado: (2022)

A transcriptomics analysis of the Tbx5 paralogues in zebrafish
por: Boyle Anderson, Erin A. T., et al.
Publicado: (2018)

Functional differentiation of Sec13 paralogues in the euglenozoan protists
por: Faktorová, Drahomíra, et al.
Publicado: (2023)

α-Dystrobrevin knockout mice have increased motivation for appetitive reward and altered brain cannabinoid receptor 1 expression
por: Hawkes, Cheryl A., et al.
Publicado: (2022)

A beta-spectrin isoform from Drosophila (beta H) is similar in size to vertebrate dystrophin
Publicado: (1990)

Duchenne Muscular Dystrophy from Brain to Muscle: The Role of Brain Dystrophin Isoforms in Motor Functions
por: Wijekoon, Nalaka, et al.
Publicado: (2023)

Evolution and regulation of cellular periodic processes: a role for paralogues
por: Trachana, Kalliopi, et al.
Publicado: (2010)

Combinatorial CRISPR screen identifies fitness effects of gene paralogues
por: Thompson, Nicola A., et al.
Publicado: (2021)

The α-dystrobrevins play a key role in maintaining the structure and function of the extracellular matrix–significance for protein elimination failure arteriopathies
por: Sharp, Matthew MacGregor, et al.
Publicado: (2021)

S-nitrosylation in TNF superfamily signaling pathway: Implication in cancer()
por: Plenchette, Stéphanie, et al.
Publicado: (2015)

Myogenin promotes myocyte fusion to balance fibre number and size
por: Ganassi, Massimo, et al.
Publicado: (2018)

Complete restoration of multiple dystrophin isoforms in genetically corrected Duchenne muscular dystrophy patient–derived cardiomyocytes
por: Zatti, Susi, et al.
Publicado: (2014)

Novel Nuclear Protein Complexes of Dystrophin 71 Isoforms in Rat Cultured Hippocampal GABAergic and Glutamatergic Neurons
por: Rodríguez-Muñoz, Rafael, et al.
Publicado: (2015)

Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy
por: Doorenweerd, Nathalie, et al.
Publicado: (2017)

Presynaptic BK channel localization is dependent on the hierarchical organization of alpha-catulin and dystrobrevin and fine-tuned by CaV2 calcium channels
por: Oh, Kelly H, et al.
Publicado: (2015)

The importance of dystrophin and the dystrophin associated proteins in vascular smooth muscle
por: Kaplan, Katherine M., et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_sp095hdmr36otr0hq65huhe67b