Showing results (31-40 of 40) with videos related to
Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
The Journal of Biological Chemistry|May 30, 1997
The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expressionJ N Feder, Z Tsuchihashi, A Irrinki, et al.Blood|February 14, 2012
Polycombs and microRNA-223 regulate human granulopoiesis by transcriptional control of target gene expressionGiuseppe Zardo, Alberto Ciolfi, Laura Vian, et al.Scientific Reports|March 21, 2017
DEK is required for homologous recombination repair of DNA breaksEric A Smith, Boris Gole, Nicholas A Willis, et al.Journal of Occupational and Environmental Medicine|February 10, 2026
The Respiratory Effects of Jet Fuel Exposure: A Fit-for-Purpose Systematic Literature Review and Evidence SynthesisEmma C Bowers, Elizabeth M Martin, Meredith Clemons, et al.Journal of Occupational and Environmental Medicine|February 10, 2026
Understanding the Neurologic and Cognitive and Behavioral Effects Associated with Exposures to Jet Fuels: A Fit-for-Purpose Systematic Literature ReviewJenna L N Sprowles, Barrett D Allen, Alex J Lindahl, et al.Genes & Development|January 9, 2016
A PTIP-PA1 subcomplex promotes transcription for IgH class switching independently from the associated MLL3/MLL4 methyltransferase complexLinda M Starnes, Dan Su, Laura M Pikkupeura, et al.Cell|June 4, 2013
53BP1 mediates productive and mutagenic DNA repair through distinct phosphoprotein interactionsElsa Callen, Michela Di Virgilio, Michael J Kruhlak, et al.Journal of Occupational and Environmental Medicine|February 10, 2026
Jet Fuel Effects on Hepatic and Renal Health: A Fit-for-Purpose Systematic Literature ReviewManasi Kotulkar, Lisa M Prince, Anastasia N Freedman, et al.Nature|July 23, 2016
Replication fork stability confers chemoresistance in BRCA-deficient cellsArnab Ray Chaudhuri, Elsa Callen, Xia Ding, et al.Nature Genetics|August 1, 1996
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosisJ N Feder, A Gnirke, W Thomas, et al.Pageof 4