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The Journal of Clinical Investigation|May 3, 2000
Proinflammatory consequences of transgenic fas ligand expression in the heartD P Nelson, E Setser, D G Hall, et al.
Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|October 22, 2023
Challenges simulating the AMOC in climate modelsLaura C Jackson, Helene T Hewitt, Diego Bruciaferri, et al.
Hormones and Behavior|September 19, 2020
Characterizing the effects of tonic 17β-estradiol administration on spatial learning and memory in the follicle-deplete middle-aged female ratStephanie V Koebele, Sarah E Mennenga, Mallori L Poisson, et al.
Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|June 3, 2015
A seamless approach to understanding and predicting Arctic sea ice in Met Office modelling systemsHelene T Hewitt, Jeff K Ridley, Ann B Keen, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|September 1, 1996
Recent progress in engineering the Pittsburgh intravenous membrane oxygenatorW J Federspiel, T Hewitt, M S Hout, et al.
Genetics|October 16, 2025
Identification of sisters separate (ssep), a gene required for meiotic centromere cohesion in Drosophila melanogasterSanay T Hewitt, Sarah Pellizzari, Sean Thornton, et al.
Frontiers in Neuroscience|December 24, 2016
Benefits of Hormone Therapy Estrogens Depend on Estrogen Type: 17β-Estradiol and Conjugated Equine Estrogens Have Differential Effects on Cognitive, Anxiety-Like, and Depressive-Like Behaviors and Increase Tryptophan Hydroxylase-2 mRNA Levels in Dorsal Raphe Nucleus SubregionsRyoko Hiroi, Giulia Weyrich, Stephanie V Koebele, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1986
Macular corneal dystrophy. Lack of keratan sulfate in serum and corneaG K Klintworth, R Meyer, R Dennis, et al.
American Journal of Ophthalmology|November 15, 1986
Absence of normal keratan sulfate in the blood of patients with macular corneal dystrophyE J Thonar, R F Meyer, R F Dennis, et al.
Plos Genetics|April 25, 2019
The Noonan Syndrome-linked Raf1L613V mutation drives increased glial number in the mouse cortex and enhanced learningMichael C Holter, Lauren T Hewitt, Stephanie V Koebele, et al.
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