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Journal of Clinical Microbiology|September 6, 2003
Detection of infectious human immunodeficiency virus type 1 in female genital secretions by a short-term culture methodJames E Cummins, Julie M Villanueva, Tammy Evans-Strickfaden, et al.JACS Au|September 26, 2025
Stabilizing a Native Fold of Alpha-Synuclein with Short Helix-Constrained PeptidesRichard M Meade, Scott G Allen, Amy J Lopez, et al.Biomaterials|March 16, 2021
Stable oxime-crosslinked hyaluronan-based hydrogel as a biomimetic vitreous substituteAlexander E G Baker, Hong Cui, Brian G Ballios, et al.Cancers|January 8, 2025
Evaluation of Anti-Angiogenic Therapy Combined with Immunotherapy and Chemotherapy as a Strategy to Treat Locally Advanced and Metastatic Non-Small-Cell Lung CancerMahmoud Abdallah, Rick Voland, Malcolm Decamp, et al.Investigative Ophthalmology & Visual Science|June 4, 2016
Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal RetinoschisisAjoy Vincent, Judith Ng, Christina Gerth-Kahlert, et al.Phlebology|May 29, 2021
Standard of care for lipedema in the United StatesKaren L Herbst, Linda Anne Kahn, Emily Iker, et al.The Journal of Physiology|February 12, 2024
Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuseLaura C Sommerfeld, Andrew P Holmes, Ting Y Yu, et al.Journal of Shoulder and Elbow Surgery|March 7, 2021
Predictors of acromial and scapular stress fracture after reverse shoulder arthroplasty: a study by the ASES Complications of RSA Multicenter Research Group, Kuhan A Mahendraraj, Joseph Abboud, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2022
Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxiaHeba Morsy, Mehdi Benkirane, Elisa Cali, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 28, 2022
SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profileReem Al-Jawahiri, Aidin Foroutan, Jennifer Kerkhof, et al.Pageof 28