نتایج جستجو برای: مخلوطهای sma

تعداد نتایج: 19226  

Journal: :Neuromuscular disorders : NMD 2007
P Kaufmann F Muntoni

Advances in preclinical SMA research have identified several candidate treatments. Early clinical trials evaluating these medications are underway or in the planning stage. At the NINDS Workshop on SMA in September 2004 in Washington DC, discussions started within the international SMA community to identify features that should be common to SMA clinical trials [1]. Having a set of design featur...

Journal: :Genes & development 2015
Yimin Hua Ying Hsiu Liu Kentaro Sahashi Frank Rigo C Frank Bennett Adrian R Krainer

Survival of motor neuron (SMN) deficiency causes spinal muscular atrophy (SMA), but the pathogenesis mechanisms remain elusive. Restoring SMN in motor neurons only partially rescues SMA in mouse models, although it is thought to be therapeutically essential. Here, we address the relative importance of SMN restoration in the central nervous system (CNS) versus peripheral tissues in mouse models ...

2009
WILLIAM C. ORR

138. 9. Guda N, Partington S, Vakil N. Symptomatic gastrooesophageal reflux, arousals and sleep quality in patients undergoing polysomnography for possible obstructive sleep apnoea. Aliment Pharm Ther. 2004;20:1153-1159.Indeed, results of a recent Internet survey showed thatGERD-related symptom severity was strongly associatedwith work impairment, and that nighttime GERD wasasso...

Journal: :Journal of neurophysiology 2011
Sayuki Takara Nobuhiko Hatanaka Masahiko Takada Atsushi Nambu

Activity patterns of projection neurons in the putamen were investigated in behaving monkeys. Stimulating electrodes were implanted chronically into the proximal (MI(proximal)) and distal (MI(distal)) forelimb regions of the primary motor cortex (MI) and the forelimb region of the supplementary motor area (SMA). Cortical inputs to putaminal neurons were identified by excitatory orthodromic resp...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2010
Katherine Wilson Scangos Veit Stuphorn

Voluntary control of behavior implies the ability to select what action is performed. The supplementary motor area (SMA) and pre-SMA are widely considered to be of central importance for this ability because of their role in movement initiation and inhibition. To test this hypothesis, we recorded from neurons in SMA and pre-SMA of monkeys performing an arm countermanding task. Temporal analysis...

Journal: :Development 2003
Jun Liang Robyn Lints Marisa L Foehr Rafal Tokarz Ling Yu Scott W Emmons Jun Liu Cathy Savage-Dunn

In Caenorhabditis elegans, the DBL-1 pathway, a BMP/TGFbeta-related signaling cascade, regulates body size and male tail development. We have cloned a new gene, sma-9, that encodes the C. elegans homolog of Schnurri, a large zinc finger transcription factor that regulates dpp target genes in Drosophila. Genetic interactions, the sma-9 loss-of-function phenotype, and the expression pattern sugge...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
Noritoshi Arai Florian Müller-Dahlhaus Takenobu Murakami Barbara Bliem Ming-Kuei Lu Yoshikazu Ugawa Ulf Ziemann

The supplementary motor area (SMA-proper) plays a key role in the preparation and execution of voluntary movements. Anatomically, SMA-proper is densely reciprocally connected to primary motor cortex (M1), but neuronal coordination within the SMA-M1 network and its modification by external perturbation are not well understood. Here we modulated the SMA-M1 network using MR-navigated multicoil ass...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2014
Francesco Vergani Luis Lacerda Juan Martino Johannes Attems Christopher Morris Patrick Mitchell Michel Thiebaut de Schotten Flavio Dell'Acqua

INTRODUCTION The supplementary motor area (SMA) is frequently involved by brain tumours (particularly WHO grade II gliomas). Surgery in this area can be followed by the 'SMA syndrome', characterised by contralateral akinesia and mutism. Knowledge of the connections of the SMA can provide new insights on the genesis of the SMA syndrome, and a better understanding of the challenges related to ope...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2015
Nimrod Miller Zhihua Feng Brittany M Edens Ben Yang Han Shi Christie C Sze Benjamin Taige Hong Susan C Su Jorge A Cantu Jacek Topczewski Thomas O Crawford Chien-Ping Ko Charlotte J Sumner Long Ma Yong-Chao Ma

Mechanisms underlying motor neuron degeneration in spinal muscular atrophy (SMA), the leading inherited cause of infant mortality, remain largely unknown. Many studies have established the importance of hyperphosphorylation of the microtubule-associated protein tau in various neurodegenerative disorders, including Alzheimer's and Parkinson's diseases. However, tau phosphorylation in SMA pathoge...

2012
Fernanda Marques de Souza Godinho Hugo Bock Tailise Conte Gheno Maria Luiza Saraiva-Pereira

Spinal muscular atrophy (SMA) is an autosomal recessive inherited disorder caused by alterations in the survival motor neuron I (SMN1) gene. SMA patients are classified as type I-IV based on severity of symptoms and age of onset. About 95% of SMA cases are caused by the homozygous absence of SMN1 due to gene deletion or conversion into SMN2. PCR-based methods have been widely used in genetic te...

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