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Josef T Prchal

Showing results (151-160 of 241) with videos related to

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Cancer Research|February 3, 2006
Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American womenMartha P Mims, Teresa G Hayes, Shiyan Zheng, et al.
Journal of Molecular Medicine (Berlin, Germany)|October 24, 2012
A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paragangliomaFelipe R Lorenzo, Chunzhang Yang, Mark Ng Tang Fui, et al.
Blood Cells, Molecules & Diseases|November 13, 2021
Thirty-five males with severe (Class 1) G6PD deficiency (c.637G>T) in a North American family of European ancestryTimothy M Bahr, Archana M Agarwal, Jessica A Meznarich, et al.
Hemasphere|December 9, 2025
VHL, transferrin, and erythropoietin in the regulation of hepcidinIvan Sergeev, Josef T Prchal, Seyed Mehdi Nouraie, et al.
The New England Journal of Medicine|August 31, 2012
Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemiaZhengping Zhuang, Chunzhang Yang, Felipe Lorenzo, et al.
Haematologica|July 11, 2019
Thrombotic risk in congenital erythrocytosis due to up-regulated hypoxia sensing is not associated with elevated hematocritVictor R Gordeuk, Galina Y Miasnikova, Adelina I Sergueeva, et al.
Plos One|August 5, 2016
A Genome-Wide Search for Greek and Jewish Admixture in the Kashmiri PopulationJonathan M Downie, Tsewang Tashi, Felipe Ramos Lorenzo, et al.
American Journal of Hematology|November 8, 2021
Tissue factor activity is increased in neutrophils from JAK2 V617F-mutated essential thrombocythemia and polycythemia vera patientsBrandi N Reeves, Soo Jin Kim, Jihyun Song, et al.
American Journal of Hematology|April 17, 2024
Novel germline JAK2<sup>R715T</sup> mutation causing PV-like erythrocytosis in 3 generations. Amelioration by Ropeg-InterferonJihyun Song, Lucie Lanikova, Soo Jin Kim, et al.
Blood|January 31, 2013
Novel HIF2A mutations disrupt oxygen sensing, leading to polycythemia, paragangliomas, and somatostatinomasChunzhang Yang, Michael G Sun, Joey Matro, et al.
Pageof 25

Showing results (151-160 of 241) with videos related to

Sort By:
Pageof 25
Cancer Research|February 3, 2006
Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American womenMartha P Mims, Teresa G Hayes, Shiyan Zheng, et al.
Journal of Molecular Medicine (Berlin, Germany)|October 24, 2012
A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paragangliomaFelipe R Lorenzo, Chunzhang Yang, Mark Ng Tang Fui, et al.
Blood Cells, Molecules & Diseases|November 13, 2021
Thirty-five males with severe (Class 1) G6PD deficiency (c.637G>T) in a North American family of European ancestryTimothy M Bahr, Archana M Agarwal, Jessica A Meznarich, et al.
Hemasphere|December 9, 2025
VHL, transferrin, and erythropoietin in the regulation of hepcidinIvan Sergeev, Josef T Prchal, Seyed Mehdi Nouraie, et al.
The New England Journal of Medicine|August 31, 2012
Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemiaZhengping Zhuang, Chunzhang Yang, Felipe Lorenzo, et al.
Haematologica|July 11, 2019
Thrombotic risk in congenital erythrocytosis due to up-regulated hypoxia sensing is not associated with elevated hematocritVictor R Gordeuk, Galina Y Miasnikova, Adelina I Sergueeva, et al.
Plos One|August 5, 2016
A Genome-Wide Search for Greek and Jewish Admixture in the Kashmiri PopulationJonathan M Downie, Tsewang Tashi, Felipe Ramos Lorenzo, et al.
American Journal of Hematology|November 8, 2021
Tissue factor activity is increased in neutrophils from JAK2 V617F-mutated essential thrombocythemia and polycythemia vera patientsBrandi N Reeves, Soo Jin Kim, Jihyun Song, et al.
American Journal of Hematology|April 17, 2024
Novel germline JAK2<sup>R715T</sup> mutation causing PV-like erythrocytosis in 3 generations. Amelioration by Ropeg-InterferonJihyun Song, Lucie Lanikova, Soo Jin Kim, et al.
Blood|January 31, 2013
Novel HIF2A mutations disrupt oxygen sensing, leading to polycythemia, paragangliomas, and somatostatinomasChunzhang Yang, Michael G Sun, Joey Matro, et al.
Pageof 25