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The European Respiratory Journal|August 21, 2025
Genetics of Interstitial Lung Diseases: A State-of-the-Art ReviewNicole Ng, Maria Molina-Molina, Ayodeji Adegunsoye, et al.
Cell Reports|September 14, 2022
Inhibition of Th1 activation and differentiation by dietary guar gum ameliorates experimental autoimmune encephalomyelitisNaomi M Fettig, Hannah G Robinson, Jessica R Allanach, et al.
Blood Advances|February 9, 2021
Restoring RUNX1 deficiency in RUNX1 familial platelet disorder by inhibiting its degradationMichelle C Krutein, Matthew R Hart, Donovan J Anderson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2009
Mutations in a gene encoding a midbody kelch protein in familial and sporadic classical Hodgkin lymphoma lead to binucleated cellsStephen J Salipante, Matthew E Mealiffe, Jeremy Wechsler, et al.
Plos One|September 6, 2014
Genome sequencing of idiopathic pulmonary fibrosis in conjunction with a medical school human anatomy courseAkash Kumar, Max Dougherty, Gregory M Findlay, et al.
Biochemical Pharmacology|February 15, 2017
Prolonged pharmacological inhibition of cathepsin C results in elimination of neutrophil serine proteasesCarla Guarino, Yveline Hamon, Cécile Croix, et al.
BMC Genomics|August 2, 2008
Integrative analysis of RUNX1 downstream pathways and target genesJoëlle Michaud, Ken M Simpson, Robert Escher, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
Ultra-deep duplex sequencing reveals unique features of somatic evolution in the normal tissues of a family with Li-Fraumeni syndromeHunter L Colegrove, Marianne E Dubard-Gault, Henry Marshall, et al.
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