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The Journal of Biological Chemistry|June 25, 2002
Characterization of a heparan sulfate octasaccharide that binds to herpes simplex virus type 1 glycoprotein DJian Liu, Zach Shriver, R Marshall Pope, et al.Neuropathology and Applied Neurobiology|May 18, 2018
Expression of myxovirus-resistance protein A: a possible marker of muscle disease activity and autoantibody specificities in juvenile dermatomyositisS Soponkanaporn, C T Deakin, P W Schutz, et al.Clinical Genetics|March 30, 2010
Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from PakistanM A Rafiq, M Ansar, C R Marshall, et al.Scientific Reports|October 2, 2020
The neurophysiological architecture of semantic dementia: spectral dynamic causal modelling of a neurodegenerative proteinopathyElia Benhamou, Charles R Marshall, Lucy L Russell, et al.ESMO Open|September 20, 2021
Osimertinib plus platinum-pemetrexed in newly diagnosed epidermal growth factor receptor mutation-positive advanced/metastatic non-small-cell lung cancer: safety run-in results from the FLAURA2 studyD Planchard, P-H Feng, N Karaseva, et al.Chemical Communications (Cambridge, England)|June 13, 2020
Synthesis of protected 3-aminopiperidine and 3-aminoazepane derivatives using enzyme cascadesGrayson J Ford, Nico Kress, Ashley P Mattey, et al.Journal of Cognitive Neuroscience|November 27, 2023
EEGManyPipelines: A Large-scale, Grassroots Multi-analyst Study of Electroencephalography Analysis Practices in the WildDarinka Trübutschek, Yu-Fang Yang, Claudia Gianelli, et al.Human Molecular Genetics|September 7, 2018
Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in miceSandra C P De Castro, Peter Gustavsson, Abigail R Marshall, et al.Journal of the American Dietetic Association|March 3, 2004
Low energy reporting may increase in intervention participants enrolled in dietary intervention trialsBette Caan, Rachel Ballard-Barbash, Martha L Slattery, et al.American Journal of Medical Genetics. Part A|March 6, 2007
Duplication of 17(p11.2p11.2) in a male child with autism and severe language delayAlisa Nakamine, Leonid Ouchanov, Patricia Jiménez, et al.Pageof 201