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Josef T Prchal

Showing results (91-100 of 241) with videos related to

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Blood|December 4, 2013
RUNX1 and NF-E2 upregulation is not specific for MPNs, but is seen in polycythemic disorders with augmented HIF signalingKatarina Kapralova, Lucie Lanikova, Felipe Lorenzo, et al.
Journal of Molecular Medicine (Berlin, Germany)|December 27, 2015
Delayed hemoglobin switching and perinatal neocytolysis in mice with gain-of-function erythropoietin receptorVladimir Divoky, Jihyun Song, Monika Horvathova, et al.
Blood|January 8, 2003
Discrimination of polycythemias and thrombocytoses by novel, simple, accurate clonality assays and comparison with PRV-1 expression and BFU-E response to erythropoietinEnli Liu, Jaroslav Jelinek, Yves D Pastore, et al.
Haematologica|June 21, 2006
Idiopathic myelofibrosis without dacryocytesGeorge L Chen, Enli Liu, Kubendran Naidoo, et al.
Blood Cells, Molecules & Diseases|February 28, 2012
Hemolysis and Mediterranean G6PD mutation (c.563 C>T) and c.1311 C>T polymorphism among Palestinians at Gaza StripMahmoud Sirdah, N Scott Reading, Sherrie L Perkins, et al.
Blood|March 30, 2013
Novel homozygous VHL mutation in exon 2 is associated with congenital polycythemia but not with cancerLucie Lanikova, Felipe Lorenzo, Chunzhang Yang, et al.
Ebiomedicine|June 8, 2021
Gain-of-function Tibetan PHD2<sup>D4E;C127S</sup> variant suppresses monocyte function: A lesson in inflammatory response to inspired hypoxiaSulagna Bhattacharya, Nishith M Shrimali, Ghulam Mohammad, et al.
Human Genome Variation|April 16, 2016
Somatic mosaicism of EPAS1 mutations in the syndrome of paraganglioma and somatostatinoma associated with polycythemiaChunzhang Yang, Christopher S Hong, Josef T Prchal, et al.
Haematologica|November 4, 2006
A novel mutation of the cytochrome-b5 reductase gene in an Indian patient: the molecular basis of type I methemoglobinemiaRoberto H Nussenzveig, H Bindu Lingam, Amos Gaikwad, et al.
Neonatology|October 4, 2014
Novel α-spectrin mutation in trans with α-spectrin causing severe neonatal jaundice from hereditary spherocytosisRoberto H Nussenzveig, Robert D Christensen, Josef T Prchal, et al.
Pageof 25

Showing results (91-100 of 241) with videos related to

Sort By:
Pageof 25
Blood|December 4, 2013
RUNX1 and NF-E2 upregulation is not specific for MPNs, but is seen in polycythemic disorders with augmented HIF signalingKatarina Kapralova, Lucie Lanikova, Felipe Lorenzo, et al.
Journal of Molecular Medicine (Berlin, Germany)|December 27, 2015
Delayed hemoglobin switching and perinatal neocytolysis in mice with gain-of-function erythropoietin receptorVladimir Divoky, Jihyun Song, Monika Horvathova, et al.
Blood|January 8, 2003
Discrimination of polycythemias and thrombocytoses by novel, simple, accurate clonality assays and comparison with PRV-1 expression and BFU-E response to erythropoietinEnli Liu, Jaroslav Jelinek, Yves D Pastore, et al.
Haematologica|June 21, 2006
Idiopathic myelofibrosis without dacryocytesGeorge L Chen, Enli Liu, Kubendran Naidoo, et al.
Blood Cells, Molecules & Diseases|February 28, 2012
Hemolysis and Mediterranean G6PD mutation (c.563 C>T) and c.1311 C>T polymorphism among Palestinians at Gaza StripMahmoud Sirdah, N Scott Reading, Sherrie L Perkins, et al.
Blood|March 30, 2013
Novel homozygous VHL mutation in exon 2 is associated with congenital polycythemia but not with cancerLucie Lanikova, Felipe Lorenzo, Chunzhang Yang, et al.
Ebiomedicine|June 8, 2021
Gain-of-function Tibetan PHD2<sup>D4E;C127S</sup> variant suppresses monocyte function: A lesson in inflammatory response to inspired hypoxiaSulagna Bhattacharya, Nishith M Shrimali, Ghulam Mohammad, et al.
Human Genome Variation|April 16, 2016
Somatic mosaicism of EPAS1 mutations in the syndrome of paraganglioma and somatostatinoma associated with polycythemiaChunzhang Yang, Christopher S Hong, Josef T Prchal, et al.
Haematologica|November 4, 2006
A novel mutation of the cytochrome-b5 reductase gene in an Indian patient: the molecular basis of type I methemoglobinemiaRoberto H Nussenzveig, H Bindu Lingam, Amos Gaikwad, et al.
Neonatology|October 4, 2014
Novel α-spectrin mutation in trans with α-spectrin causing severe neonatal jaundice from hereditary spherocytosisRoberto H Nussenzveig, Robert D Christensen, Josef T Prchal, et al.
Pageof 25