نتایج جستجو برای: neurodegeneration

تعداد نتایج: 14504  

2017
Hironobu Endo Takeshi Uenaka Wataru Satake Yutaka Suzuki Hisatsugu Tachibana Norio Chihara Takehiro Ueda Kenji Sekiguchi Taniguchi-Ikeda Mariko Hisatomo Kowa Fumio Kanda Tatsushi Toda

A 40-year-old Japanese woman presented with slowly progressing parkinsonism in adulthood. She had a history of epilepsy with intellectual disability in childhood. In a head magnetic resonance scan, T2-weighted imaging showed low signal intensity areas in the globus pallidus and the substantia nigra; T1-weighted imaging showed a halo in the nigra. Because the patient's symptoms and history were ...

2013
Yunting Lin Chengyuan Tang Hua He Ranhui Duan

Fragile X associated tremor/ataxia syndrome (FXTAS) is a late onset neurodegenerative disorder caused by aberrant expansion of CGG repeats in 5' UTR of FMR1 gene. The elevated mRNA confers a toxic gain-of-function thought to be the critical event of pathogenesis. Expressing rCGG90 repeats of the human FMR1 5'UTR in Drosophila is sufficient to induce neurodegeneration. Rapamycin has been demonst...

Journal: :Frontiers in Endocrinology 2023

Diabetic retinopathy (DR) is a microvascular lesion that occurs as complication of diabetes mellitus. Many studies reveal retinal neurodegeneration early in its pathogenesis, and abnormal function can occur patients without any signs abnormalities. The gut microbiota large, diverse colony microorganisms colonize the human intestine. Studies indicated involved pathophysiological processes DR pla...

Journal: :Journal of neurotrauma 2005
Edward D Hall Patrick G Sullivan Tonya R Gibson Krissi M Pavel Brian M Thompson Stephen W Scheff

The present study examined the neuropathology of the lateral controlled cortical impact (CCI) traumatic brain injury (TBI) model in mice utilizing the de Olmos silver staining method that selectively identifies degenerating neurons and their processes. The time course of ipsilateral and contralateral neurodegeneration was assessed at 6, 24, 48, 72, and 168 h after a severe (1.0 mm, 3.5 M/sec) i...

2015
Timothy Cutler Ankita Sarkar Michael Moran Andrew Steffensmeier Oorvashi Roy Puli Greg Mancini Meghana Tare Neha Gogia Amit Singh Udai Pandey

BACKGROUND The progressive neurodegenerative disorder Alzheimer's disease (AD) manifests as loss of cognitive functions, and finally leads to death of the affected individual. AD may result from accumulation of amyloid plaques. These amyloid plaques comprising of amyloid-beta 42 (Aβ42) polypeptides results from the improper cleavage of amyloid precursor protein (APP) in the brain. The Aβ42 plaq...

2016
Rebekah M Ahmed Emma M Devenney Muireann Irish Arne Ittner Sharon Naismith Lars M Ittner Jonathan D Rohrer Glenda M Halliday Andrew Eisen John R Hodges Matthew C Kiernan

Neurodegeneration refers to a heterogeneous group of brain disorders that progressively evolve. It has been increasingly appreciated that many neurodegenerative conditions overlap at multiple levels and therefore traditional clinicopathological correlation approaches to better classify a disease have met with limited success. Neuronal network disintegration is fundamental to neurodegeneration, ...

2016
Chiara De Lucia Adeline Rinchon Adrian Olmos-Alonso Kristoffer Riecken Boris Fehse Delphine Boche V. Hugh Perry Diego Gomez-Nicola

Neurogenesis is altered in neurodegenerative disorders, partly regulated by inflammatory factors. We have investigated whether microglia, the innate immune brain cells, regulate hippocampal neurogenesis in neurodegeneration. Using the ME7 model of prion disease we applied gain- or loss-of CSF1R function, as means to stimulate or inhibit microglial proliferation, respectively, to dissect the con...

Journal: :Human molecular genetics 2012
Lauren R Kett Daniela Boassa Cherry Cheng-Ying Ho Hardy J Rideout Junru Hu Masako Terada Mark Ellisman William T Dauer

Dominant missense mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic causes of Parkinson disease (PD) and genome-wide association studies identify LRRK2 sequence variants as risk factors for sporadic PD. Intact kinase function appears critical for the toxicity of LRRK2 PD mutants, yet our understanding of how LRRK2 causes neurodegeneration remains limited. We find tha...

Journal: :Science 2014
Sarah Mizielinska Sebastian Grönke Teresa Niccoli Charlotte E Ridler Emma L Clayton Anny Devoy Thomas Moens Frances E Norona Ione O C Woollacott Julian Pietrzyk Karen Cleverley Andrew J Nicoll Stuart Pickering-Brown Jacqueline Dols Melissa Cabecinha Oliver Hendrich Pietro Fratta Elizabeth M C Fisher Linda Partridge Adrian M Isaacs

An expanded GGGGCC repeat in C9orf72 is the most common genetic cause of frontotemporal dementia and amyotrophic lateral sclerosis. A fundamental question is whether toxicity is driven by the repeat RNA itself and/or by dipeptide repeat proteins generated by repeat-associated, non-ATG translation. To address this question, we developed in vitro and in vivo models to dissect repeat RNA and dipep...

2014
Diego Gomez-Nicola Stefano Suzzi Mariana Vargas-Caballero Nina L. Fransen Hussain Al-Malki Arantxa Cebrian-Silla Jose Manuel Garcia-Verdugo Kristoffer Riecken Boris Fehse V. Hugh Perry

The study of neurogenesis during chronic neurodegeneration is crucial in order to understand the intrinsic repair mechanisms of the brain, and key to designing therapeutic strategies. In this study, using an experimental model of progressive chronic neurodegeneration, murine prion disease, we define the temporal dynamics of the generation, maturation and integration of new neurons in the hippoc...

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