Zobrazeno 1 - 5
of 5
pro vyhledávání: '"David Okhotin"'
Autor:
Todd Maddox, Charisse Sparks, Liesl Oldstone, Roselani Maddox, Kelsey Ffrench, Heidy Garcia, Parthasarathy Krishnamurthy, David Okhotin, Laura M Garcia, Brandon J Birckhead, Josh Sackman, Ian Mackey, Robert Louis, Vafi Salmasi, Alexis Oyao, Beth D Darnall
Publikováno v:
Pain Medicine.
Trial Registration Information ClinicalTrials.gov NCT04415177; https://clinicaltrials.gov/ct2/show/NCT04415177 International Registered Report Identifier (IRRID) RR2-10.2196/25291
Autor:
Todd Maddox, Heidy Garcia, Kelsey Ffrench, Roselani Maddox, Laura Garcia, Parthasarathy Krishnamurthy, David Okhotin, Charisse Sparks, Liesl Oldstone, Brandon Birckhead, Josh Sackman, Ian Mackey, Robert Louis, Vafi Salmasi, Alexis Oyao, Beth D Darnall
Publikováno v:
Regional Anesthesia & Pain Medicine. :rapm-2022
Autor:
Juan Salomon-Andonie, Donghoon Yoon, Sabina Swierczek, Donald A. McClain, Lydia A. Polyakova, Khadega A. Abuelgasim, Galina Y. Miasnikova, Rabia Cherqaoui, Xiaomei Niu, Daniel J. Okhotin, Adelina I. Sergueeva, M. Celeste Simon, Victor R. Gordeuk, Mehdi Nouraie, Jingyu Huang, James E. Cox, Josef T. Prchal, Jihyun Song, Judith Simcox, David Okhotin
Publikováno v:
Journal of Molecular Medicine. 91:59-67
In Chuvash polycythemia, a homozygous 598CT mutation in the von Hippel-Lindau gene (VHL) leads to an R200W substitution in VHL protein, impaired degradation of α-subunits of hypoxia-inducible factor (HIF)-1 and HIF-2, and augmented hypoxic responses
Autor:
Daniel J. Okhotin, Josef T. Prchal, Galina Y. Miasnikova, Donghoon Yoon, Yong Gu Lee, Yulia Okhotina, Gregg L. Semenza, Bum Jun Kim, David Okhotin, Adelina I. Sergueeva, Alexei Maslow, Victor R. Gordeuk, Lydia A. Polyakova
Publikováno v:
Journal of Molecular Medicine. 88:523-530
Chuvash polycythemia, the first hereditary disease associated with dysregulated oxygen-sensing to be recognized, is characterized by a homozygous germ-line loss-of-function mutation of the VHL gene (VHL(R200W)) resulting in elevated hypoxia inducible
Autor:
Alexei Maslow, Galina Y. Miasnikova, Daniel J. Okhotin, Victor R. Gordeuk, Adelina I. Sergueeva, David Okhotin, Gregg L. Semenza, Donghoon Yoon, Josef T. Prchal, Yong Gu Lee, Lydia A. Polyakova, Bum Jun Kim, Yulia Okhotina
Publikováno v:
Blood. 114:5039-5039
Abstract 5039 Chuvash polycythemia, the first hereditary disease associated with dysregulated oxygen sensing, is characterized by homozygous germ-line loss-of-function mutation of VHL (598C>T) resulting in elevated hypoxia inducible factor (HIF)-1 an