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Scientific Reports|June 18, 2017
Regulation of Angiopoietin Signalling by Soluble Tie2 Ectodomain and Engineered Ligand TrapDeborah O A Alawo, Tariq A Tahir, Marlies Fischer, et al.
Human Nature (Hawthorne, N.Y.)|July 22, 2025
Are Higher-Order Constructs in Evolutionary Psychology Attributable to Omitted Cross-Loading Bias? An Exploratory Structural Equation Modeling ApproachGeorge B Richardson, Daniel G Bates, Laura E McLaughlin, et al.
American Journal of Human Genetics|October 7, 2000
Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34A H Németh, E Bochukova, E Dunne, et al.
Molecular Biosystems|May 23, 2009
Computational modelling suggests dynamic interactions between Ca2+, IP3 and G protein-coupled modules are key to robust Dictyostelium aggregationNajl V Valeyev, Jung-Su Kim, J S Pat Heslop-Harrison, et al.
Small Methods|February 18, 2026
From Millimeters to Microns: A Hybrid Strategy for Reconfigurable Liquid-Crystal PatterningAdithya Pradeep, Yunuen Montelongo, Jun-Seok Ma, et al.
CPT: Pharmacometrics & Systems Pharmacology|July 3, 2018
Inhaled sGC Modulator Can Lower PH in Patients With COPD Without Deteriorating OxygenationSina Saffaran, Wenfei Wang, Anup Das, et al.
Annals of Neurology|January 13, 2000
Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouseS J Tabrizi, J Workman, P E Hart, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|September 10, 2022
Why Reduced Inspiratory Pressure Could Determine Success of Non-Invasive Ventilation in Acute Hypoxic Respiratory FailureLiam Weaver, Sina Saffaran, Marc Chikhani, et al.
Experimental Neurology|January 6, 1999
Striatal transplantation in a transgenic mouse model of Huntington's diseaseS B Dunnett, R J Carter, C Watts, et al.
Nature Genetics|May 1, 1995
Comparative sequence analysis of the human and pufferfish Huntington's disease genesS Baxendale, S Abdulla, G Elgar, et al.
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