Results 241 to 250 of about 224,712 (352)
Abstract Hidden Markov diagnostic classification models capture how students' cognitive attributes evolve over time. This paper introduces a Bayesian Markov chain Monte Carlo algorithm for diagnostic classification models that jointly estimates time‐varying Q matrices, latent attributes, item parameters, attribute class proportions and transition ...
Chen‐Wei Liu
wiley +1 more source
Evidence for a lipofibroblast-to-<i>Cthrc1</i> <sup>+</sup> myofibroblast reversible switch during the development and resolution of lung fibrosis in young mice. [PDF]
Lingampally A +33 more
europepmc +1 more source
Background While numerous studies have explored factors contributing to poor mental health, few have examined the combined influence of multiple health and social factors and their cumulative effect. This study specifically aimed to analyze the cumulative effect of multiple health and social factors associated with poor mental well‐being in school‐aged
Marina Robles‐Muñoz +7 more
wiley +1 more source
CRISPR activation of NEB in fibroblasts, followed by RNA‐sequencing, documents spliceogenic effects of a NEB intronic variant. The assay enabled variant reclassification as likely pathogenic, providing molecular diagnosis in fetuses with Arthrogryposis multiplex congenita 6.
Doriana Misceo +7 more
wiley +1 more source
Oral, Vaginal, and Stool Microbial Signatures in Patients With Endometriosis as Potential Diagnostic Non-Invasive Biomarkers: A Prospective Cohort Study. [PDF]
Hicks C +7 more
europepmc +1 more source
GOVERNMENT LANGUAGES OF THE REPUBLIC OF MARI EL (HISTORY OF LEGAL REGULATION OF LANGUAGE PROBLEMS)
Elena A. Kondrashkina
openalex +2 more sources
Mary Bell, en el país de las miserias
"Este Artículo pertenece a la sección En punto. "
openaire +1 more source
Chromatinopathies (CP) are a growing group of rare genetic disorders characterized by cognitive deficits and growth abnormalities. This is the largest collection of CP to date, contributing to a deeper understanding of the landscape and diagnosis of these rare diseases, strongly improved by the use of large‐scale sequencing technologies.
Giulia Bruna Marchetti +16 more
wiley +1 more source

