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Cell|April 30, 2026
Proteostasis sustains T cell differentiation potential and tumor-infiltrating lymphocyte functionNicole E Scharping, Xuezhen Ge, Maria Inês Matias, et al.Nature Communications|May 18, 2025
Electroconvulsive therapy generates a postictal wave of spreading depolarization in mice and humansZachary P Rosenthal, Joseph B Majeski, Ala Somarowthu, et al.Frontiers in Veterinary Science|February 19, 2019
British Red Squirrels Remain the Only Known Wild Rodent Host for Leprosy BacilliAnna-Katarina Schilling, Charlotte Avanzi, Rainer G Ulrich, et al.Thorax|February 14, 2026
Clinical, molecular and microbial characterisation of the eosinophilic endotype of bronchiectasis: data from the EMBARC-BRIDGE studyJennifer Pollock, Jeffrey T J Huang, Morven Shuttleworth, et al.Inflammatory Bowel Diseases|August 21, 2023
Safety, Effectiveness, and Treatment Persistence of Subcutaneous Vedolizumab in IBD: A Multicenter Study From the United KingdomSamuel Hsiang Lim, Beatriz Gros, Esha Sharma, et al.American Journal of Human Genetics|October 24, 2001
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndromeS Kenwrick, H Woffendin, T Jakins, et al.Bioorganic & Medicinal Chemistry Letters|January 6, 2012
AMG 837: a potent, orally bioavailable GPR40 agonistJonathan B Houze, Liusheng Zhu, Ying Sun, et al.Molecular Cancer Therapeutics|July 9, 2009
Biological properties of potent inhibitors of class I phosphatidylinositide 3-kinases: from PI-103 through PI-540, PI-620 to the oral agent GDC-0941Florence I Raynaud, Suzanne A Eccles, Sonal Patel, et al.American Journal of Respiratory and Critical Care Medicine|September 12, 2025
Upper-Airway Microbiome, Mucociliary Function, and Clinical Outcomes in Bronchiectasis: Data from the EMBARC-BRIDGE StudyHayoung Choi, Hollian Richardson, Chandani Hennayake, et al.Scientific Reports|February 9, 2017
Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's diseaseRobert M Bragg, Sydney R Coffey, Rory M Weston, et al.Pageof 83