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European Journal of Medical Genetics|January 3, 2013
A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial featuresElise Boudry-Labis, Bénédicte Demeer, Cédric Le Caignec, et al.
Free Radical Biology & Medicine|April 24, 2013
Biomarkers of oxidative stress study V: ozone exposure of rats and its effect on lipids, proteins, and DNA in plasma and urineMaria B Kadiiska, Samar Basu, Nathan Brot, et al.
Scientific Reports|February 21, 2024
Environmental enrichment promotes adaptive responding during tests of behavioral regulation in male heterogeneous stock ratsKeita Ishiwari, Christopher P King, Connor D Martin, et al.
Human Genetics|May 11, 2005
SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defectsKristen L Deak, Abee L Boyles, Heather C Etchevers, et al.
The Lancet. Respiratory Medicine|December 17, 2023
High-resolution CT phenotypes in pulmonary sarcoidosis: a multinational Delphi consensus studySujal R Desai, Nishanth Sivarasan, Kerri A Johannson, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 18, 2023
Pragmatic approaches to handling practice effects in longitudinal cognitive aging researchRuijia Chen, Camilla Calmasini, Kaitlin Swinnerton, et al.
The International Journal of Neuropsychopharmacology|April 3, 2020
A Randomized Trial of the N-Methyl-d-Aspartate Receptor Glycine Site Antagonist Prodrug 4-Chlorokynurenine in Treatment-Resistant DepressionLawrence T Park, Bashkim Kadriu, Todd D Gould, et al.
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