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Journal of Animal Science|December 8, 2015
The direct-maternal genetic correlation has little impact on genetic evaluationsI David, F Bouvier, M Banville, et al.
American Journal of Physiology. Renal Physiology|January 10, 2022
Acid-base effects of combined renal deletion of NBCe1-A and NBCe1-BHyun-Wook Lee, Jill W Verlander, Gary E Shull, et al.
American Journal of Physiology. Renal Physiology|May 1, 2015
Effect of dietary protein restriction on renal ammonia metabolismHyun-Wook Lee, Gunars Osis, Mary E Handlogten, et al.
Cureus|April 8, 2024
Leptomeningeal Dissemination Complicated With Acute Tetraplegia From a Supratentorial Multicentric Isocitrate Dehydrogenase (IDH)-Wildtype Glioblastoma: A Case ReportDan M Visarion, Ionut Cale, Ioana Miron, et al.
Metabolic Engineering|September 2, 2003
Analysis of metabolic networks using a pathway distance metric through linear programmingEvangelos Simeonidis, Stuart C G Rison, Janet M Thornton, et al.
Animal : an International Journal of Animal Bioscience|September 26, 2025
Transmissibility model to evaluate transgenerational transmission of environmental effects in quailsK Karami, S Rousse, F Pitel, et al.
The Journal of Biological Chemistry|September 7, 2020
A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformationHe-Qin Zhan, Mitra Najmi, Kai Lin, et al.
Histochemistry and Cell Biology|October 1, 1996
Localization, expression, and characterization of guanylin in the rat adrenal medullaM Reinecke, I David, D Loffing-Cueni, et al.
The Journal of Biological Chemistry|April 25, 2009
The functional roles of the His247 and His281 residues in folate and proton translocation mediated by the human proton-coupled folate transporter SLC46A1Ersin Selcuk Unal, Rongbao Zhao, Min-Hwang Chang, et al.
The Journal of Pediatrics|August 23, 2008
The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorptionSang Hee Min, Sun Young Oh, George I Karp, et al.
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