DP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient-Reference-Cited by-同舟云学术

DP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient

Published:2019-01-15 Issue:1 Volume:10 Page:
ISSN:1757-6512
Container-title:Stem Cell Research & Therapy
language:en
Short-container-title:Stem Cell Res Ther

Author:

Ruggieri Simona,Viggiano Luigi,Annese Tiziana,Rubolino Carmela,Gerbino Andrea,De Zio Roberta,Corsi Patrizia,Tamma Roberto,Ribatti Domenico,Errede Mariella,Operto Francesca,Margari Lucia,Resta Nicoletta,Di Tommaso Silvia,Rosati Jessica,Trojano Maria,Nico Beatrice

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Biochemistry, Genetics and Molecular Biology (miscellaneous),Molecular Medicine,Medicine (miscellaneous)

Link

http://link.springer.com/content/pdf/10.1186/s13287-018-1125-5.pdf

Reference23 articles.

1. Ervasti JM, Campbell KP. Membrane organization of the dystrophin-glycoprotein complex. Cell. 1991;66:1121–31.

2. Desguerre I, Christov C, Mayer M, et al. Clinical heterogeneity of duchenne muscular dystrophy (DMD): definition of sub-phenotypes and predictive criteria by long-term follow-up. PLoS One. 2009;4:e4347.

3. Jung D, Filliol D, Metz-Boutigue MH, et al. Characterization and subcellular localization of the dystrophin-protein 71 (Dp71) from brain. Neuromuscul Disord. 1993;3:515–8.

4. Austin RC, Morris GE, Howard PL, et al. Expression and synthesis of alternatively spliced variants of Dp71 in adult human brain. Neuromuscul Dis. 2000;10:187–93.

5. Bresolin N, Castelli E, Comi GP, et al. Cognitive impairment in Duchenne muscular dystrophy. Neuromuscul Dis. 1994;4:359–69.

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1. Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells;International Journal of Molecular Sciences;2022-10-06

2. Neuromuscular Development and Disease: Learning From in vitro and in vivo Models;Frontiers in Cell and Developmental Biology;2021-10-27

3. Disrupted Calcium Homeostasis in Duchenne Muscular Dystrophy: A Common Mechanism behind Diverse Consequences;International Journal of Molecular Sciences;2021-10-13

4. The variability in neurological deficits in Duchenne muscular dystrophy patients may be explained by differences in dystrophin glycoprotein complexes in the brain and muscle;NeuroReport;2021-09-07

5. Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy;Molecular Neurobiology;2019-12-13