Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Yulia Okhotina"'
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