Results 81 to 90 of about 54,356 (248)

Progressive myoclonus epilepsy associated with SACS gene mutations

open access: yes, 2016
Pathogenic variants in the SACS gene (OMIM #604490) cause autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). ARSACS is a neurodegenerative early-onset progressive disorder, originally described in French Canadians, but later observed ...
Andrade, DM   +7 more
core   +1 more source

Xavier Nogués

open access: yes
Avant-títol: La nostra gentBiografia de Xavier Nogués escrita per Joan Sacs i publicada dins la col·lecció La nostra gent dels Quaderns blaus. Il·lustrada amb reproduccions d'obres de l'artista.Biography of Xavier Nogués written by Joan Sacs and ...
Sacs, Joan,
core   +1 more source

A minimal cellulosome‐like system in Cellulosilyticum lentocellum

open access: yesFEBS Open Bio, EarlyView.
Cellulose‐degrading bacteria typically use cellulosomes, large multi‐enzyme complexes on a scaffold protein. In Cellulosilyticum lentocellum, we characterise a far smaller arrangement, a single scaffold bound to one cellulase through a single cohesin‐dockerin interaction.
John Allan   +2 more
wiley   +1 more source

SACS

open access: yes, 2023
The South Atlantic Coastal Study Vision Meeting 2 : Creating a Shared Vision to Address Coastal Vulnerability a [11Jf,!;l@lf US Army Corps of Engineers ® AG ENDA INTRODUCTIONS MEETING PURPOSE TIER 1 TIER 2 NEXT STEPS SACS VISION MEETING 2 : AGENDA ...
United States. Army; United States. Army. Corps of Engineers;
core  

The C‐terminal domain of yeast Arginyltransferase1 is essential for its catalytic activity

open access: yesFEBS Open Bio, EarlyView.
Arginyltransferase 1 (Ate1), a eukaryotic enzyme, catalyses arginylation, transferring arginine from tRNA‐Arg to the amino terminus of the target protein. Overexpression of Ate1 in yeast is lethal and is dependent on arginylation. This study elucidates how mutations in the cofactor‐binding and active site of Ate1 and truncation of its structural ...
Vikas Kumar Yadav   +4 more
wiley   +1 more source

The perceptual effect of air sacs

open access: yes, 2010
This paper presents work on air sacs that extends the work presented by de Boer, (2008a). In that paper, and before (Fitch, 2000) air sacs were identified as a likely feature of our evolutionary ancestors that may have been lost because of the evolution ...
Smith, A.D.M.   +3 more
core   +2 more sources

Genetic dissection of human ABCE1 in yeast reveals separable requirements for ribosome recycling and suppression of aberrant reinitiation

open access: yesFEBS Open Bio, EarlyView.
Human ABCE1 cannot functionally replace its yeast ortholog. Yeast–human chimera analysis identified NBD1 as a major interspecies barrier. Genetic screening yielded hABCE1 revertants that rescue yeast viability but fail to suppress aberrant translation reinitiation in the 3′ UTR.
Eriko Nakata   +3 more
wiley   +1 more source

Modulating the Structure and Composition of Single‐Atom Electrocatalysts for CO2 reduction

open access: yesAdvanced Science
Electrochemical CO2 reduction reaction (eCO2RR) is a promising strategy to achieve carbon cycling by converting CO2 into value‐added products under mild reaction conditions.
Weiren Chen   +4 more
doaj   +1 more source

Advanced Characterization Techniques and Theoretical Calculation for Single Atom Catalysts in Fenton-like Chemistry

open access: yesMolecules
Single-atom catalysts (SACs) have attracted extensive attention due to their unique catalytic properties and wide range of applications. Advanced characterization techniques, such as energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy,
Zhaokun Xiong   +5 more
doaj   +1 more source

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach   +23 more
wiley   +1 more source

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