Results 171 to 180 of about 63,717 (277)

Exploring the sub-Neptune frontier with JWST. [PDF]

open access: yesProc Natl Acad Sci U S A
Madhusudhan N   +3 more
europepmc   +1 more source

STELLAR MASS FUNCTIONS OF GALAXIES AT 4 <z< 7 FROM ANIRAC-SELECTED SAMPLE IN COSMOS/ULTRAVISTA: LIMITS ON THE ABUNDANCE OF VERY MASSIVE GALAXIES [PDF]

open access: bronze, 2015
Mauro Stefanon   +18 more
openalex   +1 more source

Systemic T Cell Receptor Profiling Reveals Adaptive Immune Activation and Potential Immune Signatures of Diagnosis and Brain Atrophy in Epilepsy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Epilepsy is increasingly associated with immune dysregulation and inflammation. The T cell receptor (TCR), a key mediator of adaptive immunity, shows repertoire alterations in various immune‐mediated diseases. The unique TCR sequence serves as a molecular barcode for T cells, and clonal expansion accompanied by reduced overall TCR ...
Yong‐Won Shin   +12 more
wiley   +1 more source

A hot white dwarf merger remnant revealed by an ultraviolet detection of carbon. [PDF]

open access: yesNat Astron
Sahu S   +9 more
europepmc   +1 more source

The Metal Content of Bulge Field Stars from FLAMES-GIRAFFE Spectra. I. Stellar parameters and Iron Abundances

open access: green, 2008
M. Zoccali   +7 more
openalex   +1 more source

Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam   +6 more
wiley   +1 more source

A precise metallicity and carbon-to-oxygen ratio for a warm giant exoplanet from its panchromatic JWST emission spectrum. [PDF]

open access: yesProc Natl Acad Sci U S A
Wiser LS   +13 more
europepmc   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas   +18 more
wiley   +1 more source

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