Results 151 to 160 of about 19,007 (252)

A Next-Generation ELISA for the Detection of Anti-(Para)Nodal Antibodies in Autoimmune Nodopathy and COVID-19 Vaccinated Individuals. [PDF]

open access: yesJ Peripher Nerv Syst
Appeltshauser L   +9 more
europepmc   +1 more source

High Prevalence of Metabolic Dysfunction–Associated Steatohepatitis With Significant Fibrosis in Primary Care and Endocrinology Clinics

open access: yesDiabetes, Obesity and Metabolism, Volume 28, Issue 7, Page 6184-6193, July 2026.
ABSTRACT Aims Metabolic dysfunction‐associated steatohepatitis (MASH) is a leading cause of cirrhosis. NIS2+ is a recently approved serum‐based test combining two biomarkers (miR‐34a‐5p and YKL‐40) to identify at‐risk MASH (i.e., MASH and significant fibrosis). Objective To assess the prevalence of at‐risk MASH by NIS2+ in individuals from primary care
Srilaxmi Kalavalapalli   +12 more
wiley   +1 more source

Alternative splicing regulates PACC1 function and promotes acidosis-induced cytotoxicity. [PDF]

open access: yesFront Cell Dev Biol
Tamburro S   +8 more
europepmc   +1 more source

‘EINEN FILM DREHEN’: TECHNOPOLITICAL TURNS AND THE RENDERING OPERATIONAL OF SUBJECTIVITY IN FAROCKI'S LEBEN–BRD (1990) AND PETZOLD'S BARBARA (2012)

open access: yesGerman Life and Letters, Volume 79, Issue 3, Page 396-418, July 2026.
ABSTRACT This article analyses the ‘Gestus’ of turning in films by Harun Farocki and Christian Petzold, in light of a central claim of Andrew Webber's esteemed theoretical work on film: that film has the power to uncover unconscious processes through which subjects come into being and are made operational for political regimes.
Annie Ring
wiley   +1 more source

Translating Human Prototype Liver Implant Technology from Academia to Industry for Third-Party Transplant and In Vivo Validation. [PDF]

open access: yesCells
Szkolnicka D   +8 more
europepmc   +1 more source

Pubertal development and hypothalamic–pituitary–gonadal axis are altered in male mice lacking Mecp2

open access: yesJournal of Neuroendocrinology, Volume 38, Issue 7, July 2026.
Abstract Mutations in the MECP2 gene, encoding the epigenetic reader Methyl‐CpG binding protein 2, are the main cause of Rett syndrome, a rare neurodevelopmental disorder. Besides severe symptoms such as profound intellectual disability, loss of speech and motor skills, and epilepsy, loss of function of MECP2 has been associated with pubertal ...
Ana Martín‐Sánchez   +6 more
wiley   +1 more source

Molecular Characterization of the Effect of Glucagon-Like Peptide-1 Receptor Agonist Semaglutide in the Nephrotoxic Serum Nephritis Mouse Model. [PDF]

open access: yesKidney360
Martinez JM   +9 more
europepmc   +1 more source

Therapeutic manipulation and spatial quantification of the tumor microenvironment in colorectal cancer. [PDF]

open access: yesiScience
Mulholland-Illingworth EJ   +19 more
europepmc   +1 more source

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