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Genes|February 26, 2025
Analysis of Short Tandem Repeat Expansions in a Cohort of 12,496 Exomes from Patients with Neurological Diseases Reveals Variable Genotyping Rate Dependent on Exome Capture KitsClarissa Rocca, David Murphy, Chris Clarkson, et al.Trials|August 29, 2013
Dose-related effects of vitamin D on immune responses in patients with clinically isolated syndrome and healthy control participants: study protocol for an exploratory randomized double- blind placebo-controlled trialKaren O'Connell, Siobhan Kelly, Katie Kinsella, et al.Lancet (London, England)|October 22, 2013
Clinical and cost-effectiveness of cognitive behaviour therapy for health anxiety in medical patients: a multicentre randomised controlled trialPeter Tyrer, Sylvia Cooper, Paul Salkovskis, et al.Digital Health|August 22, 2025
A scoping review of frameworks evaluating digital health applicationsOrla Deegan, Eoghan O Riain, Denis Martin, et al.Communications Biology|September 23, 2022
Transcriptomic plasticity of the hypothalamic osmoregulatory control centre of the Arabian dromedary camelPanjiao Lin, Benjamin T Gillard, Audrys G Pauža, et al.Biology of Sex Differences|January 8, 2026
The impact of testosterone on paraventricular nucleus gene expression in male and female spontaneously hypertensive ratsAlex Paterson, Su-Yi Loh, Shadi Kadijeh Gholami, et al.Frontiers in Physiology|April 5, 2021
Transcriptome Analysis Reveals Downregulation of Urocortin Expression in the Hypothalamo-Neurohypophysial System of Spontaneously Hypertensive RatsAndrew Martin, Andre S Mecawi, Vagner R Antunes, et al.Social Cognitive and Affective Neuroscience|October 25, 2011
An fMRI study of the brain responses of traumatized mothers to viewing their toddlers during separation and playDaniel S Schechter, Dominik A Moser, Zhishun Wang, et al.Journal of Advanced Nursing|March 7, 2024
Youth, caregiver and healthcare professional perspectives on planning the implementation of a trauma-informed care programme: A qualitative studyYehudis Stokes, Paula Cloutier, Dhiraj Aggarwal, et al.Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Partial loss of FITM2 function causes hereditary spastic paraplegiaAinara Salazar-Villacorta, Laura M Bond, Leehyeon Kim, et al.Pageof 33