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Human Mutation|May 12, 2009
Modeling ATM mutant proteins from missense changes confirms retained kinase activityGiancarlo Barone, Alix Groom, Anne Reiman, et al.
Protein Science : a Publication of the Protein Society|April 13, 2026
An ALS-associated mutation in the C-terminal α-helix of TDP-43 uncouples condensate formation and amyloid assemblyEmily J Byrd, Joel A Crossley, Chalmers C C Chau, et al.
BMC Microbiology|October 17, 2008
Acid stress damage of DNA is prevented by Dps binding in Escherichia coli O157:H7Kwang Cheol Jeong, Kai Foong Hung, David J Baumler, et al.
Pediatric Nephrology (Berlin, Germany)|August 1, 1996
Oxalate elimination via hemodialysis or peritoneal dialysis in children with chronic renal failureB Hoppe, D Graf, G Offner, et al.
The Journal of Surgical Research|March 16, 2025
Development and Validation of a Discharge Disposition Prediction Model in Injured AdultsLiling Lu, David Silver, Jamison Beiriger, et al.
Transplantation|July 1, 1988
Effect of cyclosporine on the renal tubular amino acid handling after kidney transplantationP F Hoyer, J Brodehl, D J Byrd, et al.
Developmental Medicine and Child Neurology|May 17, 2006
Atypical presentation of ataxia-oculomotor apraxia type 1Amre Shahwan, Philip J Byrd, A Malcolm R Taylor, et al.
Lancet (London, England)|May 26, 1990
Evidence suggesting hyperoxaluria as a cause of nephrocalcinosis in phosphate-treated hypophosphataemic ricketsG S Reusz, K Latta, P F Hoyer, et al.
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