نتایج جستجو برای: s100β

تعداد نتایج: 209  

2012
Yasunori Okabe Tomoyuki Takahashi Chiaki Mitsumasu Ken-ichiro Kosai Eiichiro Tanaka Toyojiro Matsuishi

Rett syndrome (RTT) is a neurodevelopmetal disorder associated with mutations in the methyl-CpG-binding protein 2 (MeCP2) gene. MeCP2-deficient mice recapitulate the neurological degeneration observed in RTT patients. Recent studies indicated a role of not only neurons but also glial cells in neuronal dysfunction in RTT. We cultured astrocytes from MeCP2-null mouse brain and examined astroglial...

2017
Chiara Traini Stefano Evangelista Vincent Girod Maria Simonetta Faussone‐Pellegrini Maria Giuliana Vannucchi

Otilonium bromide (OB) is a spasmolytic drug successfully used for the treatment of irritable bowel syndrome (IBS). Its efficacy has been attributed to the block of L- and T-type Ca2+ channels and muscarinic and tachykinin receptors in the smooth muscle. Furthermore, in healthy rats, repeated OB administration modified neurotransmitter expression and function suggesting other mechanisms of acti...

2017
Ingrid Morales Alberto Sanchez Clara Rodriguez-Sabate Manuel Rodriguez

The role of astrocytes in Parkinson's disease is still not well understood. This work studied the astrocytic response to the dopaminergic denervation. Rats were injected in the lateral ventricles with 6-hydroxydopamine (25μg), inducing a dopaminergic denervation of the striatum not accompanied by non-selective tissue damage. The dopaminergic debris were found within spheroids (free-spheroids) w...

2017
Guimei Ran Yixuan Wang Haochen Liu Chunxiang Wei Tao Zhu Haidong Wang Hua He Xiaoquan Liu

PURPOSE The study was designed to evaluate the disease outcome based on multiple biomarkers related to cerebral ischemia. METHODS Rats were randomly divided into sham, permanent middle cerebral artery occlusion, and edaravone-treated groups. Cerebral ischemia was induced by permanent middle cerebral artery occlusion surgery in rats. To form a simplified crosstalk network, the related multiple...

Journal: :Human molecular genetics 2015
Wei Zhao Baichun Jiang Huili Hu Shuqian Zhang Shuaishuai Lv Jupeng Yuan Yanyan Qian Yongxin Zou Xi Li Hong Jiang Fang Liu Changshun Shao Yaoqin Gong

Astrocytes are the most abundant cell type in the mammalian brain and are important for the functions of the central nervous system. Glial fibrillary acidic protein (GFAP) is regarded as a hallmark of mature astrocytes, though some GFPA-positive cells may act as neural stem cells. Missense heterozygous mutations in GFAP cause Alexander disease that manifests leukodystrophy and intellectual disa...

2012
Martha Douglas-Escobar Michael D. Weiss

The term "encephalopathy of prematurity" encompasses not only the acute brain injury [such as intraventricular hemorrhage (IVH)] but also complex disturbance on the infant's subsequent brain development. In premature infants, the most frequent recognized source of brain injury is IVH and periventricular leukomalacia (PVL). Furthermore 20-25% infants with birth weigh less than 1,500 g will have ...

2013
Emiliano Trias Pablo Díaz-Amarilla Silvia Olivera-Bravo Eugenia Isasi Derek A. Drechsel Nathan Lopez C. Samuel Bradford Kyle E. Ireton Joseph S. Beckman Luis Barbeito

Microglia and reactive astrocytes accumulate in the spinal cord of rats expressing the Amyotrophic lateral sclerosis (ALS)-linked SOD1 (G93A) mutation. We previously reported that the rapid progression of paralysis in ALS rats is associated with the appearance of proliferative astrocyte-like cells that surround motor neurons. These cells, designated as Aberrant Astrocytes (AbA cells) because of...

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