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Neoplasia (New York, N.Y.)|September 15, 2019
VCAM-1 Density and Tumor Perfusion Predict T-cell Infiltration and Treatment Response in Preclinical ModelsJohannes Riegler, Herman Gill, Annie Ogasawara, et al.
The Lancet. Digital Health|June 11, 2022
COVID-19 trajectories among 57 million adults in England: a cohort study using electronic health recordsJohan H Thygesen, Christopher Tomlinson, Sam Hollings, et al.
European Journal of Human Genetics : EJHG|August 9, 2012
The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathyStephanie Fehr, Meredith Wilson, Jenny Downs, et al.
Orphanet Journal of Rare Diseases|March 5, 2022
Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasiaRachel L Taylor, Carla Sanjuro Soriano, Simon Williams, et al.
Molecular Genetics & Genomic Medicine|December 10, 2017
A review of structural brain abnormalities in Pallister-Killian syndromeCathryn Poulton, Gareth Baynam, Clarissa Yates, et al.
American Journal of Medical Genetics. Part A|January 21, 2016
Exploring the genetic basis of 3MC syndrome: Findings in 12 further familiesJill Urquhart, Rebecca Roberts, Deepthi de Silva, et al.
Atherosclerosis|October 2, 2018
Familial hypercholesterolaemia patient support groups and advocacy: A multinational perspectiveJules Payne, Simon Williams, Diana Maxwell, et al.
Cancer Research|July 4, 2003
Cyclooxygenase-2 is up-regulated by interleukin-1 beta in human colorectal cancer cells via multiple signaling pathwaysWenbiao Liu, Niels Reinmuth, Oliver Stoeltzing, et al.
European Journal of Heart Failure|January 8, 2020
Impact of remote monitoring on clinical outcomes for patients with heart failure and atrial fibrillation: results from the REM-HF trialRosita Zakeri, John M Morgan, Patrick Phillips, et al.
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