Results 141 to 150 of about 216,058 (291)
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
SPG4 and Dementia: Expanding the Clinical Spectrum
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
The accretion-ejection connection in the asymmetric Th 28 jet revealed by MUSE-NFM★
Context. Mass loss through stellar jets is closely tied to the process of accretion through the disk. Understanding mass loss phenomena such as episodic ejections and outflow asymmetries can shed light on the mechanism of jet launching and its connection
Murphy A. +7 more
doaj +1 more source
ABSTRACT Objective Considerable efforts have been dedicated to developing effective treatments for post‐stroke executive impairment (PSEI), among which repetitive transcranial magnetic stimulation (rTMS) has shown great potential. This study aimed to investigate the therapeutic effects of high‐frequency rTMS on working memory (WM) and response ...
Mengting Lao +6 more
wiley +1 more source
Circumstellar Disks in pre-Main Sequence Stars
This review covers the properties of disks around pre-main--sequence stars. It is at this time in the evolution that planets form, and it is important to understand the properties of these disks to understand planet formation. I discuss disk shapes, masses and temperatures, the properties of the host stars, disk lifetimes and dissipation processes ...
openaire +2 more sources
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
Choroid Plexus Enlargement and USPIO‐Based Inflammatory Feature in Cerebral Small Vessel Disease
ABSTRACT Objective The choroid plexus (CP) is a key component of the blood–cerebrospinal fluid barrier (BCSFB), but its mechanism of action in cerebral small vessel disease (CSVD) remains unclear. This study investigated CP volume (CPV) alterations and their association with conventional imaging markers in CSVD and explored the underlying role of ...
Yongqiang Qu +11 more
wiley +1 more source
Starspots and Undetected Binary Stars Have Distinct Signatures in Young Stellar Associations
Young stars form in associations, meaning that young stellar associations provide an ideal environment to measure the age of a nominally coeval population.
Kendall Sullivan, Adam L. Kraus
doaj +1 more source
A Systematic Comparison of Alpha‐Synuclein Seed Amplification Assays for Increasing Reproducibility
ABSTRACT Seed amplification assays (SAAs) enable ultrasensitive detection of misfolded α‐synuclein across biofluids and tissues. Yet, heterogeneity in protocols limits cross‐study comparability and clinical translation. Here, we review α‐synuclein SAA methods and their performance across various biological matrices.
Manuela Amaral‐do‐Nascimento +3 more
wiley +1 more source
Gaia Data Release 3 (DR3) has provided the largest and most astrometrically precise catalog of nearby stars to date, allowing for a more complete membership census of nearby, young stellar moving groups. These loose associations of young (age
Attila Varga +3 more
doaj +1 more source

