Results 51 to 60 of about 282,573 (230)
Long non‐coding RNAs (lncRNAs) occupy an abundant fraction of the eukaryotic transcriptome and an emerging area in cancer research. Regulation by lncRNAs is based on their subcellular localization in HNSCC. This cartoon shows the various functions of lncRNAs in HNSCC discussed in this review.
Ellen T. Tran+3 more
wiley +1 more source
Exoplanets imaging with a Phase-Induced Amplitude Apodization Coronagraph - I. Principle
Using 2 aspheric mirrors, it is possible to apodize a telescope beam without losing light or angular resolution: the output beam is produced by ``remapping'' the entrance beam to produce the desired light intensity distribution in a new pupil. We present
Eugene A. Pluzhnik+6 more
core +1 more source
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
CSF Biomarker‐Based Cognitive Trajectories in Parkinson's Disease‐Subjective Cognitive Decline
ABSTRACT Objective Cognitive complaints without objective cognitive impairment in Parkinson's Disease, termed Parkinson's Disease‐Subjective Cognitive Decline (PD‐SCD), have been associated with cognitive decline. However, its progression is heterogeneous, highlighting the need for improved identification of patients at greater risk for deterioration ...
Jon Rodriguez‐Antiguedad+7 more
wiley +1 more source
Gravitomagnetism and gravitational waves
After extensively reviewing general relativistic gravitomagnetism, both historically and phenomenologically, we review in detail the so-called magnetic components of gravitational waves (GWs), which have to be taken into account in the context of the ...
Corda, Christian, Iorio, Lorenzo
core +1 more source
Translating Muscle RNAseq Into the Clinic for the Diagnosis of Muscle Diseases
ABSTRACT Objective Approximately half of patients with hereditary myopathies remain without a definitive genetic diagnosis after DNA next‐generation sequencing (NGS). Here, we implemented transcriptome analysis of muscle biopsies as a complementary diagnostic tool for patients with muscle disease but no definitive genetic diagnosis after exome ...
Alba Segarra‐Casas+24 more
wiley +1 more source
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large‐Scale Exome Sequencing
ABSTRACT Objective Dystonia is one of the most prevalent movement disorders, characterized by significant clinical and etiological heterogeneity. Despite considerable heritability (~25%), the etiology in most patients remains elusive. Moreover, understanding correlations between clinical manifestations and genetic variants has become increasingly ...
Mirja Thomsen+47 more
wiley +1 more source
La lutte contre les micropolluants métalliques urbains représente un enjeu véritablement majeur et complexe, en particulier dans les zones côtières, du fait d’une urbanisation croissante et de l’émission de formes émergentes de contaminants métalliques comme les Terres Rares.
openaire +1 more source
Clinical Characteristics of Parkinsonism in HTLV‐1‐Associated Myelopathy
ABSTRACT Objective Human T‐lymphotropic virus type 1 (HTLV‐1)‐associated myelopathy/tropical spastic paraparesis (HAM/TSP) is the classic neurological manifestation of HTLV‐1 infection; however, this virus has also been associated with other neurological disorders. Concurrent parkinsonism is relatively rare and presents diagnostic challenges.
Mika Dozono+8 more
wiley +1 more source
A limestone cave filled with montmorillonite clay was found in a hill above the karst plateau on the north‐eastern edge of the Adriatic Sea. The cave fill shows no correlation with sediments found in the surrounding caves or other known caves of the ...
Nadja Zupan Hajna+12 more
doaj +1 more source