Cargando…

Decrease in Prosaposin in the Dystrophic mdx Mouse Brain

BACKGROUND: Duchenne muscular dystrophy caused by a mutation in the X-linked dystrophin gene induces metabolic and structural disorders in the brain. A lack of dystrophin in brain structures is involved in impaired cognitive function. Prosaposin (PS), a neurotrophic factor, is abundant in the choroi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gao, Hui-ling, Li, Cheng, Nabeka, Hiroaki, Shimokawa, Tetsuya, Kobayashi, Naoto, Saito, Shouichiro, Wang, Zhan-You, Cao, Ya-ming, Matsuda, Seiji
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828254/ https://www.ncbi.nlm.nih.gov/pubmed/24244600 http://dx.doi.org/10.1371/journal.pone.0080032

Ejemplares similares

Temporal Changes in Prosaposin Expression in the Rat Dentate Gyrus after Birth
por: Morishita, Midori, et al.
Publicado: (2014)

A Prosaposin-Derived Peptide Alleviates Kainic Acid-Induced Brain Injury
por: Nabeka, Hiroaki, et al.
Publicado: (2015)

Prosaposin Overexpression following Kainic Acid-Induced Neurotoxicity
por: Nabeka, Hiroaki, et al.
Publicado: (2014)

Interneurons secrete prosaposin, a neurotrophic factor, to attenuate kainic acid-induced neurotoxicity
por: Nabeka, Hiroaki, et al.
Publicado: (2017)

Expression of prosaposin and its receptors in the rat cerebellum after kainic acid injection
por: Li, Xuan, et al.
Publicado: (2017)

Prosaposin and its receptors GRP37 and GPR37L1 show increased immunoreactivity in the facial nucleus following facial nerve transection
por: Kunihiro, Joji, et al.
Publicado: (2020)

The expression of prosaposin and its receptors, GRP37 and GPR37L1, are increased in the developing dorsal root ganglion
por: Taniguchi, Miho, et al.
Publicado: (2021)

Administration of prosaposin-derived neurotrophic factor to neural tube defects facilitates regeneration and restores neurological functions
por: Khan, Sakirul, et al.
Publicado: (2023)

Early neonatal loss of inhibitory synaptic input to the spinal motor neurons confers spina bifida-like leg dysfunction in a chicken model
por: Khan, Md. Sakirul Islam, et al.
Publicado: (2017)

Expression of the G protein-coupled receptor (GPR) 37 and GPR37L1 in the mouse digestive system
por: SARKAR, Sonjoy, et al.
Publicado: (2020)

Expression of prosaposin and its G protein-coupled receptor (GPR) 37 in mouse cochlear and vestibular nuclei
por: FUYUKI, Aimi, et al.
Publicado: (2023)

Rho kinase inhibitors stimulate the migration of human cultured osteoblastic cells by regulating actomyosin activity
por: Zhang, Xuejiao, et al.
Publicado: (2011)

Regional expression of prosaposin in the wild-type and saposin D-deficient mouse brain detected by an anti-mouse prosaposin-specific antibody
por: Yoneshige, Azusa, et al.
Publicado: (2009)

Mutation Types and Aging Differently Affect Revertant Fiber Expansion in Dystrophic Mdx and Mdx52 Mice
por: Echigoya, Yusuke, et al.
Publicado: (2013)

Proteome Profiling of the Dystrophic mdx Mice Diaphragm
por: Mucha, Olga, et al.
Publicado: (2023)

Hormonal Receptors in Skeletal Muscles of Dystrophic Mdx Mice
por: Feder, David, et al.
Publicado: (2013)

Erythropoietin reduces the expression of myostatin in mdx dystrophic mice
por: Feder, D., et al.
Publicado: (2014)

Dysfunctional Muscle and Liver Glycogen Metabolism in mdx Dystrophic Mice
por: Stapleton, David I., et al.
Publicado: (2014)

Dystrophic phenotype improvement in the diaphragm muscle of mdx mice by diacerhein
por: Mâncio, Rafael Dias, et al.
Publicado: (2017)

Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers
por: Vandebrouck, Clarisse, et al.
Publicado: (2002)

Decreased Prosaposin and Progranulin in the Cingulate Cortex Are Associated with Schizophrenia Pathophysiology
por: He, Yachao, et al.
Publicado: (2022)

Neurolysosomal pathology in human prosaposin deficiency suggests essential neurotrophic function of prosaposin
por: Sikora, Jakub, et al.
Publicado: (2006)

Six weeks of N-acetylcysteine antioxidant in drinking water decreases pathological fiber branching in MDX mouse dystrophic fast-twitch skeletal muscle
por: Redwan, Asma, et al.
Publicado: (2023)

Extensive but Coordinated Reorganization of the Membrane Skeleton in Myofibers of Dystrophic (mdx) Mice
por: Williams, McRae W., et al.
Publicado: (1999)

A proteasome inhibitor fails to attenuate dystrophic pathology in mdx mice
por: Selsby, Joshua, et al.
Publicado: (2012)

The FVB Background Does Not Dramatically Alter the Dystrophic Phenotype of Mdx Mice
por: Wasala, Nalinda B., et al.
Publicado: (2015)

Increased levels of interleukin-6 exacerbate the dystrophic phenotype in mdx mice
por: Pelosi, Laura, et al.
Publicado: (2015)

Lipidomic Analyses Reveal Specific Alterations of Phosphatidylcholine in Dystrophic Mdx Muscle
por: Valentine, William J., et al.
Publicado: (2022)

Investigating the Potential for Sulforaphane to Attenuate Gastrointestinal Dysfunction in mdx Dystrophic Mice
por: Swiderski, Kristy, et al.
Publicado: (2021)

Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene
por: Koppanati, Bhanu Munil, et al.
Publicado: (2010)

A Reduction in Selenoprotein S Amplifies the Inflammatory Profile of Fast-Twitch Skeletal Muscle in the mdx Dystrophic Mouse
por: Wright, Craig Robert, et al.
Publicado: (2017)

Chronic Dosing with Membrane Sealant Poloxamer 188 NF Improves Respiratory Dysfunction in Dystrophic Mdx and Mdx/Utrophin(-/-) Mice
por: Markham, Bruce E., et al.
Publicado: (2015)

Interplay between Exonic Splicing Enhancers, mRNA Processing, and mRNA Surveillance in the Dystrophic Mdx Mouse
por: Buvoli, Massimo, et al.
Publicado: (2007)

Dystrophic Changes in Extraocular Muscles after Gamma Irradiation in mdx:utrophin(+/−) Mice
por: McDonald, Abby A., et al.
Publicado: (2014)

Subproteomic profiling of sarcolemma from dystrophic mdx-4cv skeletal muscle
por: Murphy, Sandra, et al.
Publicado: (2018)

Cardioprotective Effect of Whole Body Periodic Acceleration in Dystrophic Phenotype mdx Rodent
por: Uryash, Arkady, et al.
Publicado: (2021)

Pharmacological activation of SERCA ameliorates dystrophic phenotypes in dystrophin-deficient mdx mice
por: Nogami, Ken'ichiro, et al.
Publicado: (2021)

P2X7 purinoceptor alterations in dystrophic mdx mouse muscles: relationship to pathology and potential target for treatment
por: Young, Christopher N J, et al.
Publicado: (2012)

Muscle Pathology in Dystrophic Rats and Zebrafish Is Unresponsive to Taurine Treatment, Compared to the mdx Mouse Model for Duchenne Muscular Dystrophy
por: Terrill, Jessica R., et al.
Publicado: (2023)

Risk of congenital birth defects during COVID-19 pandemic: Draw attention to the physicians and policymakers
por: Khan, Md Sakirul Islam, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_fvn7tt7jj9mn8go29t9oadvpmf