Results 101 to 110 of about 21,889,530 (328)

Data reduction in protein serial crystallography

open access: yesIUCrJ
Serial crystallography (SX) has become an established technique for protein structure determination, especially when dealing with small or radiation-sensitive crystals and investigating fast or irreversible protein dynamics. The advent of newly developed
Marina Galchenkova   +9 more
doaj   +1 more source

Bioengineering facets of the tumor microenvironment in 3D tumor models: insights into cellular, biophysical and biochemical interactions

open access: yesFEBS Open Bio, EarlyView.
The tumor microenvironment is a dynamic, multifaceted complex system of interdependent cellular, biochemical, and biophysical components. Three‐dimensional in vitro models of the tumor microenvironment enable a better understanding of these interactions and their impact on cancer progression and therapeutic resistance.
Salma T. Rafik   +3 more
wiley   +1 more source

Earthing effects on mitochondrial function: ATP production and ROS generation

open access: yesFEBS Open Bio, EarlyView.
In contrast to sham and naive controls, grounded mitochondria not only exhibit significantly enhanced energy production but also demonstrate a remarkable reduction in membrane potential and oxidative stress. This suggests a profound improvement in mitochondrial health, presenting a promising avenue for therapeutic interventions.
Cecilia Giulivi, Richard Kotz
wiley   +1 more source

Big Data-Based Improved Data Acquisition and Storage System for Designing Industrial Data Platform

open access: yesIEEE Access, 2019
Big data-based acquisition and storage system (ASS) plays an important role in the design of industrial data platform. Many big data frameworks have been integrated compression and serialization method.
Daoqu Geng   +5 more
doaj   +1 more source

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra   +17 more
wiley   +1 more source

Analyzing Data Reduction Techniques: An Experimental Perspective

open access: yesApplied Sciences
The exponential growth in data generation has become a ubiquitous phenomenon in today’s rapidly growing digital technology. Technological advances and the number of connected devices are the main drivers of this expansion. However, the exponential growth
Vítor Fernandes   +3 more
doaj   +1 more source

Concept of Entire Boolean Values Recalculation From Aggregates in the Preprocessed Category of Incomplete Soft Sets

open access: yesIEEE Access, 2017
Soft set is a mathematical tool for dealing with vague and imprecise data. It is used in many applications and decision-making after representing the uncertain data in the Boolean-valued information system (BIS). BISs become incomplete because of various
Muhammad Sadiq Khan   +4 more
doaj   +1 more source

Demonstration of a Quantile System for Compression of Data from Deep Space Probes [PDF]

open access: green, 1967
T. O. Anderson   +3 more
openalex   +1 more source

Discontinuation of Immunotherapy in Patients With Relapsing Myelitis Without AQP4/MOG Antibodies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This study assesses the outcomes of immunotherapy discontinuation in patients with relapsing seronegative idiopathic myelitis (SIM), a condition that remains uninvestigated due to its rarity. We reviewed records from 77 patients with relapsing SIM at the National Cancer Center of Korea, focusing on 11 who discontinued treatment after a median ...
Ki Hoon Kim   +4 more
wiley   +1 more source

Fetal Akinesia/Hypokinesia and Arthrogryposis of Neuromuscular Origin: Etiologic Groups, Genetics, and Phenotypic Spectrum

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To provide a comprehensive clinical and genetic characterization of individuals with arthrogryposis multiplex congenita (AMC), focusing on the distribution of genetic etiologies across the neuromuscular spectrum and comparing myogenic and neurogenic subtypes. Methods A total of 105 individuals with AMC were clinically and genetically
Florencia Pérez‐Vidarte   +13 more
wiley   +1 more source

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