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The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|February 7, 2024
Sociodemographic Associations With Blood Pressure in 10-14-Year-Old AdolescentsJason M Nagata, Joan E Shim, Priyadharshini Balasubramanian, et al.DNA Repair|October 29, 2008
XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptomsSikandar G Khan, Kyu-Seon Oh, Steffen Emmert, et al.Journal of Medical Primatology|February 3, 2015
Initial gene vector dosing for studying symptomatology of amyotrophic lateral sclerosis in non-human primatesKasey L Jackson, Robert D Dayton, Jeanne M Fisher-Perkins, et al.Frontiers in Genetics|August 22, 2022
DNA methylation patterns and gene expression from amygdala tissue of mature Brahman cows exposed to prenatal stressEmilie C Baker, Audrey L Earnhardt, Kubra Z Cilkiz, et al.Injury Epidemiology|February 14, 2024
Military community engagement to prevent firearm-related violence: adaptation of project safe guard for service membersS Rachel Kennedy, Jessica Buck-Atkinson, Jayna Moceri-Brooks, et al.Biology of Reproduction|May 13, 2021
PRG2 and AQPEP are misexpressed in fetal membranes in placenta previa and percreta†Elisa T Zhang, Roberta L Hannibal, Keyla M Badillo Rivera, et al.Journal of the American College of Radiology : JACR|November 5, 2025
ACR Appropriateness Criteria® Suspected Osteomyelitis of the Foot in Patients With Diabetes Mellitus: 2025 Update, Jonathan C Baker, Benjamin E Northrup, et al.JAMA Network Open|May 21, 2025
Social Media Use and Depressive Symptoms During Early AdolescenceJason M Nagata, Christopher D Otmar, Joan Shim, et al.Acta Neuropathologica|April 29, 2015
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degenerationMasataka Nakamura, Kevin F Bieniek, Wen-Lang Lin, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 3, 2013
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementiaMarka van Blitterswijk, Matthew C Baker, Kevin F Bieniek, et al.Pageof 236