Robert Steiner

University of Washington, Seattle, Seattle, WA 
Neuroendocrinology, Reproductive physiology, Regulation of neuropeptide gene expression
"Robert Steiner"
Mean distance: 17.15 (cluster 19)
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McCarthy EA, Dischino D, Maguire C, et al. (2021) Inhibiting Kiss1 Neurons with Kappa Opioid Receptor Agonists to Treat Polycystic Ovary Syndrome and Vasomotor Symptoms. The Journal of Clinical Endocrinology and Metabolism
Schaefer EJ, Tint GS, Duell PB, et al. (2021) Cerebrotendinous xanthomatosis, sitosterolemia, Smith-Lemli-Opitz syndrome and the seminal contributions of Gerald Salen, MD (1935-2020). Journal of Clinical Lipidology
Danovitch G, Bunnapradist S, Cohen D, et al. (2021) Tests for the non-invasive diagnosis of kidney transplant rejection should be evaluated by kidney transplant programs. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons
Škrlec I, Talapko J, Juzbašić M, et al. (2021) Sex Differences in Circadian Clock Genes and Myocardial Infarction Susceptibility. Journal of Cardiovascular Development and Disease. 8
Baker KM, Parikh NS, Salsbery KT, et al. (2021) A 17-Month-old Boy With Pancytopenia Caused by a Rare Genetic Defect of Vitamin B12 Malabsorption. Journal of Pediatric Hematology/Oncology
Steiner RW. (2021) How Many Disparate Measurements of Kidney Function Unfairly Allow Selected Candidates to Accumulate Time on the Deceased Donor Kidney Transplant Waiting List? Journal of the American Society of Nephrology : Jasn. 32: 1539-1540
Steiner RW. (2021) How MDRD (and CKD-epi and Cystatin C) eGFRs Obscure Interpretation of Kidney Transplant Studies. Transplantation
Essex RM, Williams RW, Treinen KC, et al. (2020) A highly‑enriched Pu reference material for nuclear safeguards and nuclear forensics measurements. Journal of Radioanalytical and Nuclear Chemistry. 324
Reinhard A, Inglis J, Steiner R, et al. (2020) Isotopic analysis of sub-nanogram Nd loads using new ATONA amplifiers. Rapid Communications in Mass Spectrometry : Rcm. e9032
Martin EMMA, Enriquez A, Sparrow DB, et al. (2020) Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice. Human Molecular Genetics
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