Results 241 to 250 of about 71,498 (314)
Loss of U11/U12 spliceosome gene <i>ZCRB1</i> leads to aberrant ciliogenesis and WNT signaling. [PDF]
Pirzada MUR +8 more
europepmc +1 more source
The Evolving Landscape of CHD Genetics: A Contemporary Guide to Genetic Testing and Management
ABSTRACT Congenital heart disease (CHD) is the most common birth defect, affecting an estimated 9.4/1000 infants globally. The genetics of CHD is complex, with most cases thought to have multifactorial aetiology, implicating both genetic and environmental factors.
Bridget R. O'Malley +3 more
wiley +1 more source
A light-off response characterised by body contraction and ciliary arrest in Acropora coral larvae. [PDF]
Brodrick EA +6 more
europepmc +1 more source
Comparative genomics reveals novel genes associated with sensory cilia
O'Flaherety, B +6 more
core +1 more source
ABSTRACT Background Trauma‐informed care (TIC) is widely recognised in psychiatric practice, yet the trauma specialist nurse role remains undefined in Israel. Aims This study aimed to examine mental health nurses' attitudes and perceptions of the trauma specialist nurse role and to identify predictors of support for its implementation.
Merav Ben Natan +3 more
wiley +1 more source
Primary Cilia Are Required for Efficient BMP Signaling in Traumatic Heterotopic Ossification. [PDF]
Yuan X +9 more
europepmc +1 more source
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
Disruption of primary ciliary prostaglandin E<sub>2</sub> signaling by transforming growth factor-β1 impairs endometrial receptivity. [PDF]
Hou HT +10 more
europepmc +1 more source
Setmelanotide in Bardet‐Biedl Syndrome: A Case Report
ABSTRACT Setmelanotide is a melanocortin‐4‐receptor agonist used for the treatment of hyperphagia in the genetic obesity syndrome Bardet‐Biedl. Presented is a case of diffuse hyperpigmentation in a patient treated with setmelanotide, which represents the most common side effect of this medication.
Shelby Smith +2 more
wiley +1 more source
Pathophysiological significance of cholesterol in ciliopathies. [PDF]
Itabashi T +7 more
europepmc +1 more source

