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Journal of Medicinal Chemistry|November 7, 2000
Inhibition of protein synthesis by didemnins: cell potency and SARD Ahuja, A Geiger, J M Ramanjulu, et al.American Journal of Medical Genetics. Part A|December 25, 2009
A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21Chad R Haldeman-Englert, Kimberly A Chapman, Hillary Kruger, et al.Human Molecular Genetics|May 15, 2015
Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain developmentPeter M Van Laarhoven, Leif R Neitzel, Anita M Quintana, et al.Arthritis and Rheumatism|July 15, 1998
Fcgamma receptor IIa polymorphism in Caucasian patients with systemic lupus erythematosus: association with clinical symptomsK Manger, R Repp, B M Spriewald, et al.Journal of Neurosurgery|September 17, 2022
Use of heparin to rescue immunosuppressive monocyte reprogramming by glioblastoma-derived extracellular vesiclesBenjamin T Himes, Cori E Fain, Zachariah P Tritz, et al.European Journal of Medical Genetics|December 23, 2008
A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delayChad R Haldeman-Englert, Xiaowu Gai, Juan Carlos Perin, et al.Cancer Research|September 19, 2007
Identification and biological evaluation of a novel and potent small molecule radiation sensitizer via an unbiased screen of a chemical libraryBrian E Lally, Geoffrey A Geiger, Steven Kridel, et al.Neurosurgery|June 11, 2020
Evaluating the Effects of Cerebrospinal Fluid Protein Content on the Performance of Differential Pressure Valves and Antisiphon Devices Using a Novel Benchtop Shunting ModelNoah L Gorelick, Riccardo Serra, Rajiv Iyer, et al.Journal of Neurosurgery|December 2, 2014
Stereotactic radiosurgery to the resection bed for intracranial metastases and risk of leptomeningeal carcinomatosisEric Ojerholm, John Y K Lee, Jayesh P Thawani, et al.Genetics|March 16, 2021
Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variationYulia Mostovoy, Feyza Yilmaz, Stephen K Chow, et al.Pageof 16