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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 18, 2021
Brain dysfunction in tubular and tubulointerstitial kidney diseasesDavide Viggiano, Annette Bruchfeld, Sol Carriazo, et al.
Physical Review Letters|July 15, 2003
Coulomb dissociation of 8B and the low-energy cross section of the 7Be(p,gamma)8B solar fusion reactionF Schümann, F Hammache, S Typel, et al.
Journal of the American Society of Nephrology : JASN|June 7, 2015
Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile HypercalcemiaKarl P Schlingmann, Justyna Ruminska, Martin Kaufmann, et al.
Nature Genetics|August 3, 2004
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorderRobert Kleta, Elisa Romeo, Zorica Ristic, et al.
The Journal of Clinical Investigation|August 3, 2013
Myeloperoxidase, paraoxonase-1, and HDL form a functional ternary complexYing Huang, Zhiping Wu, Meliana Riwanto, et al.
Nature Communications|January 13, 2026
Magneto-ionic control of magnetism through voltage-driven carbon transportZ Tan, Z Ma, S Privitera, et al.
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