Results 1 to 10 of about 26,469 (137)
Human FUS is toxic via association with RNA polymerase II in Drosophila [PDF]
The RNA-binding protein FUS is commonly mutated in familial cases of amyotrophic lateral sclerosis (ALS-FUS), where it forms cytoplasmic inclusions. In addition, non-mutated FUS is a constituent component of protein inclusions in approximately 5–10% of ...
Thomas G. Moens +7 more
doaj +2 more sources
In tokamak and other fusion devices, magnetic control is the main tool that allows to regulate the plasma current, position and shape; it is in charge of actuating the desired plasma current waveform, steering the plasma position to a given set point and
Domenica Corona +6 more
doaj +1 more source
Heterogeneidad del tratamiento para cándida parapsilosis en endocarditis micótica de válvula nativa
Las infecciones por cándida en el ámbito intrahospitalario han ido en ascenso en las últimas décadas en especial en las unidades de cuidado intensivo (UCI), dado el uso cada vez más frecuente de antibióticos de amplio espectro y de procedimientos ...
Gary Andrés Baquero +4 more
doaj +1 more source
Genetics of familial amyotrophic lateral sclerosis
To analyze results of the studies covering modern scientific views on the genetics of familial amyotrophic lateral sclerosis (FALS).We searched for full-text publications containing the key words “amyotrophic lateral sclerosis”, “FALS”, and “genetics” in
A. V. Savinova +2 more
doaj +1 more source
The article describes the requirements for the lubricant used in injection molding of non-ferrous alloys. A methodology for conducting research to determine the sedimentation stability of a prepared lubricant is presented, as well as the results of a ...
A. A. Pivovarchyk +2 more
doaj +1 more source
Objective To compare the clearance rate of high-risk human papillomavirus (HR-HPV) in patients with a high-grade squamous intraepithelial lesion (HSIL) 12 months after focused ultrasound (FUS) or loop electrosurgical excision procedure (LEEP), and ...
Yi Qin +7 more
doaj +1 more source
Summary of neuromuscular junction (NMJ) changes across ALS mouse models. ALS mouse models show different levels of NMJ pathology depending on gene targets: SOD1, TDP‐43 and FUS models all show initial NMJ dysfunction prior to motor neuron death (arrows), supporting a ‘dying‐back’ theory, while C9orf72 NMJ pathology is less clear. Terminal Schwann cells
Abrar Alhindi +2 more
wiley +1 more source
DF402, a fluorine derivative of Dimebon/Latrepirdine, delays the onset and slows the progression of pathology in the transgenic model of ALS‐FUS. An original CatWalk analysis protocol allowing detection of gait changes in FUS transgenic mice long before manifestation of clinical signs reveals effects of DF402 on their gait at early pre‐symptomatic ...
Kirill Chaprov +10 more
wiley +1 more source
Objective This study was aimed at investigating the clinical efficacy and studying the possible mechanism of FUS applications to treat cervical intraepithelial neoplasia 1 (CIN1).
Zhenhua Fu +6 more
doaj +1 more source
Focused ultrasound on the thalamus is employed to relieve tremor in movement disorders. The treatment efficacy is currently assessed by subjective observation of patient tremor during hand movements.
Aharonson Vered +4 more
doaj +1 more source

