Results 91 to 100 of about 871,588 (266)
Cyclin‐dependent kinase 13 is indispensable for normal mouse heart development
Congenital heart disease (CHD) is the most common defect in live births. The role of cyclin‐dependent kinase (CDK13) in cardiogenesis and CHD was studied using a transgenic mouse model (Cdk13tm1b) carrying deletion of exons 3 and 4, causing loss of function.
Qazi Waheed‐Ullah +8 more
wiley +1 more source
Evidence of a chlorophyll “tongue” in the Malacca Strait from satellite observations
S. Mandal +4 more
semanticscholar +1 more source
CHARGE Syndrome: A Narrative Review and Update on Diagnosis, Assessment and Management
ABSTRACT Background CHARGE syndrome (CS) is a rare multisystemic genetic condition caused by a pathogenic variant in the DNA‐binding protein‐7 CHD7 gene. The condition affects the development of neural crest cells, which give rise to craniofacial structures, cranial nerves, ears, eyes and the heart, resulting in diverse and complex clinical features ...
Eleni M. van Gelder +7 more
wiley +1 more source
CASE REPORT: Enteric Duplication Cyst of Caecum Presenting with Intestinal Obstruction - A Case Report [PDF]
Background: Enteric duplication cyst is a rare congenital anomaly. It can occur anywhere along the alimentary tract from the tongue to the anus, more common in ileum but rare in the caecum.
Vijay Dombale +3 more
doaj
A graphical abstract recapping the different sources of dental, periodontal, and other oral‐derived mesenchymal stromal cells (MSCs) and their regenerative mechanisms and potentials. The review's article findings bridge fundamental biological science with translational advances, highlighting the significance of MSCs in craniofacial regenerative ...
Karim M. Fawzy El‐Sayed +6 more
wiley +1 more source
Hydrogel‐based therapies have proven to be valuable tools to address the unique regeneration challenges of complex multi‐domain periodontal and craniofacial tissues. This review highlights and classifies clinically approved and emerging hydrogel therapies indicated for the regeneration of periodontal and craniofacial tissues.
Z. Gouveia +5 more
wiley +1 more source
Characterisation of sleep apneas and respiratory circuitry in mice lacking CDKL5
Summary CDKL5 deficiency disorder is a rare genetic disease caused by mutations in the CDKL5 gene. Central apneas during wakefulness have been reported in patients with CDKL5 deficiency disorder. Studies on CDKL5‐knockout mice, a CDKL5 deficiency disorder model, reported sleep apneas, but it is still unclear whether these events are central (central ...
Gabriele Matteoli +12 more
wiley +1 more source
Nonsyndromic Mandibular Symphysis Cleft
Median cleft of lower lip and mandible is a rare congenital anomaly described as cleft number 30 of Tessier’s classification. In minor forms only lower lip cleft is seen.
Leela Krishna Guttikonda +4 more
doaj +1 more source
Abstract Do immersion and nonimmersion learners’ English grammaticality judgment test (GJT) scores reflect the same underlying processes in language learning? Drawing on data from Chen and Hartshorne's (2021) study, we argue that they do not. Using generalized additive mixed models (GAMMs), we found that age of onset was the strongest predictor of GJT ...
Frans van der Slik, Roeland van Hout
wiley +1 more source
Reproducing National Distinction: How Cultural Capital Shapes Estonia's Russian School Field
ABSTRACT Research on nationalism has long emphasized the homogenizing role of education in producing shared language, history and identity, while studies in the sociology of education have examined how cultural capital and social class structure school hierarchies.
Léo Henry
wiley +1 more source

