Results 211 to 220 of about 2,474,551 (357)

Amino acid sequence of crab metallothionein [PDF]

open access: yesFEBS Letters, 1981
Lerch, K., Ammer, D., Olafson, R.W.
openaire   +2 more sources

Neurochemical Endpoints to Inform Early‐Stage Trials of Spinocerebellar Ataxia 2 and 3 in a Multisite Setting

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Neurochemical levels measured by brain MR spectroscopy (MRS) have been proposed as endpoints for clinical trials in early‐stage spinocerebellar ataxia (SCA) trials. We tested their trial‐readiness by quantifying neurochemicals in three affected brain regions in early‐stage cohorts of SCA2 and SCA3, examining their reproducibility in ...
James M. Joers   +19 more
wiley   +1 more source

A first attempt to elucidate the amino acid sequence of some lichen lectins

open access: yes, 2008
Secreted arginases from Evernia prunastri and Xanthoria parietina thalii, exhibiting lectin activity, have been purified to homogeneity. Analyses of both amino acid and glycoside composition are reported.
Legaz González, María Estrella   +4 more
core  

Bayes empirical bayes inference of amino acid sites under positive selection.

open access: yesMolecular biology and evolution, 2005
Ziheng Yang   +2 more
semanticscholar   +1 more source

Cognitive and Neuroimaging Divergence Between Juvenile and Adult FUS Amyotrophic Lateral Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by progressive motor neuron degeneration. Fused in sarcoma (FUS)‐associated juvenile ALS (jALS) represents a distinct and aggressive subgroup with rapid deterioration and poor prognosis.
Alexandra V. Jürs   +7 more
wiley   +1 more source

A 57‐Year‐Old Male With Behavioral Variant Frontotemporal Dementia and MATR3 and NOS3 Mutations

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This report presents a case of behavioral variant frontotemporal dementia caused by mutations in the MATR3 and NOS3 genes, aiming to analyze its clinical manifestations and genetic characteristics. For a case presenting with personality changes and gait abnormalities as the initial symptoms, this study conducted a comprehensive analysis of its
Feifei Lin, Saie Huang
wiley   +1 more source

Amino acid sequence encodes protein abundance shaped by protein stability at reduced synthesis cost. [PDF]

open access: yesProtein Sci
Buric F   +9 more
europepmc   +1 more source

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