Showing results (1031-1040 of 1,237) with videos related to

Sort By:
Pageof 124
Human Gene Therapy|October 6, 2021
Intra-Articular Adeno-Associated Virus-Mediated Proteoglycan 4 Gene Therapy for Preventing Posttraumatic OsteoarthritisDongrim Seol, Hyeong Hun Choe, Hongjun Zheng, et al.
Frontiers in Cell and Developmental Biology|January 21, 2025
Curcumin encapsulated in PAMAM dendrimers for the therapeutic treatment of ischemic stroke in ratsJustin Stadler, Lucas G Garmo, David Doyle, et al.
International Journal of Molecular Sciences|August 14, 2025
Extracellular Vesicles-Induced Cell Homing and Odontogenesis via microRNA Signaling for Dentin RegenerationVenkateswaran Ganesh, Douglas C Fredericks, Emily B Petersen, et al.
The American Journal of Psychiatry|August 1, 1989
The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counselingE R Ritvo, L B Jorde, A Mason-Brothers, et al.
American Journal of Obstetrics and Gynecology|May 25, 2018
Preoperative obstructive sleep apnea screening in gynecologic oncology patientsRoss F Harrison, Erin E Medlin, Chase B Petersen, et al.
Leukemia Research|November 29, 2019
A phase I study of panobinostat and ruxolitinib in patients with primary myelofibrosis (PMF) and post--polycythemia vera/essential thrombocythemia myelofibrosis (post--PV/ET MF)J Mascarenhas, B K Marcellino, M Lu, et al.
American Journal of Medical Genetics. Part A|January 12, 2013
Pure de novo partial trisomy 6p in a girl with craniosynostosisKonstantinos Varvagiannis, Amalia Stefanidou, Yolanda Gyftodimou, et al.
Journal of the American Chemical Society|June 26, 2025
The Swiss Army Knife of Alginate Metabolism: Mechanistic Analysis of a Mixed-Function Polysaccharide Lyase/Epimerase of the Human Gut MicrobiotaTobias Tandrup, José Pablo Rivas-Fernández, Mikkel Madsen, et al.
Children (Basel, Switzerland)|December 23, 2022
Prenatal Identification of a Novel Mutation in the <i>MCPH1</i> Gene Associated with Autosomal Recessive Primary Microcephaly (MCPH) Using Next Generation Sequencing (NGS): A Case Report and Review of the LiteratureIoannis Papoulidis, Makarios Eleftheriades, Emmanouil Manolakos, et al.
Molecular Cytogenetics|February 25, 2011
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boyEmmanouil Manolakos, Catherine Sarri, Annalisa Vetro, et al.
Pageof 124