Ron Korstanje

The University of Maine, Orono, MN, United States 
Genetics, Molecular Biology, Cell Biology
"Ron Korstanje"
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Khan AA, Kim N, Korstanje R, et al. (2022) Loss-of-function mutation in Pcsk1 increases serum APOA1 level and LCAT activity in mice. Laboratory Animal Research. 38: 1
Bitto A, Lee MB, Hill CM, et al. (2021) The AGE Presents Introduction to Geroscience video lecture series. Geroscience
Garrett MR, Korstanje R. (2020) Using Genetic and Species Diversity to Tackle Kidney Disease. Trends in Genetics : Tig
de Groot T, Ebert LK, Christensen BM, et al. (2019) Identification of as a First Susceptibility Gene for Lithium-Induced Nephrogenic Diabetes Insipidus in Mice. Journal of the American Society of Nephrology : Jasn
Olinger E, Lake J, Sheehan S, et al. (2019) Hepsin-mediated Processing of Uromodulin is Crucial for Salt-sensitivity and Thick Ascending Limb Homeostasis. Scientific Reports. 9: 12287
Bubier JA, Sutphin GL, Reynolds TJ, et al. (2019) Integration of heterogeneous functional genomics data in gerontology research to find genes and pathway underlying aging across species. Plos One. 14: e0214523
Srivastava A, Kumar Sarsani V, Fiddes I, et al. (2018) Genome assembly and gene expression in the American black bear provides new insights into the renal response to hibernation. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes
Backer G, Eddy S, Sheehan SM, et al. (2018) FAR2 is Associated with Kidney Disease in Mice and Humans. Physiological Genomics
Raghupathy N, Choi K, Vincent MJ, et al. (2018) Hierarchical Analysis of RNA-Seq Reads Improves the Accuracy of Allele-specific Expression. Bioinformatics (Oxford, England)
Tian C, Gagnon LH, Longo-Guess C, et al. (2017) Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts. Human Molecular Genetics. 26: 3722-3735
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