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Josef T Prchal

Showing results (121-130 of 241) with videos related to

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Neonatology|November 7, 2013
Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosisRobert D Christensen, Roberto H Nussenzveig, N Scott Reading, et al.
Experimental Hematology|June 15, 2015
Comparative long-term effects of interferon α and hydroxyurea on human hematopoietic progenitor cellsKatherine Y King, Katie A Matatall, Ching-Chieh Shen, et al.
Clinical Pediatrics|January 17, 2017
Three Novel Spectrin Variants in Jaundiced NeonatesRobert D Christensen, Archana M Agarwal, Hassan M Yaish, et al.
Pediatric Blood & Cancer|April 15, 2014
The homozygous VHL(D126N) missense mutation is associated with dramatically elevated erythropoietin levels, consequent polycythemia, and early onset severe pulmonary hypertensionSusmita Sarangi, Lucie Lanikova, Katarina Kapralova, et al.
American Journal of Hematology|July 11, 2022
Developmental changes in iron metabolism and erythropoiesis in mice with human gain-of-function erythropoietin receptorBarbora Kralova, Lucie Sochorcova, Jihyun Song, et al.
Blood|September 21, 2016
Coexistence of gain-of-function JAK2 germ line mutations with JAK2V617F in polycythemia veraLucie Lanikova, Olga Babosova, Sabina Swierczek, et al.
Leukemia Research Reports|September 13, 2023
Allogeneic stem cell transplant for multiple myeloma & myelofibrosis with split-dose busulfan, fludarabine & cyclophosphamideAndrew D Trunk, Sagar S Patel, Josef T Prchal, et al.
Blood|October 24, 2002
Mutations in the VHL gene in sporadic apparently congenital polycythemiaYves D Pastore, Jaroslav Jelinek, Sonny Ang, et al.
American Journal of Human Genetics|July 5, 2003
Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemiaYves Pastore, Katerina Jedlickova, Yongli Guan, et al.
Haematologica|January 12, 2005
Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patientsMaria Celeste Bento, Ko Tung Chang, Yongli Guan, et al.
Pageof 25

Showing results (121-130 of 241) with videos related to

Sort By:
Pageof 25
Neonatology|November 7, 2013
Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosisRobert D Christensen, Roberto H Nussenzveig, N Scott Reading, et al.
Experimental Hematology|June 15, 2015
Comparative long-term effects of interferon α and hydroxyurea on human hematopoietic progenitor cellsKatherine Y King, Katie A Matatall, Ching-Chieh Shen, et al.
Clinical Pediatrics|January 17, 2017
Three Novel Spectrin Variants in Jaundiced NeonatesRobert D Christensen, Archana M Agarwal, Hassan M Yaish, et al.
Pediatric Blood & Cancer|April 15, 2014
The homozygous VHL(D126N) missense mutation is associated with dramatically elevated erythropoietin levels, consequent polycythemia, and early onset severe pulmonary hypertensionSusmita Sarangi, Lucie Lanikova, Katarina Kapralova, et al.
American Journal of Hematology|July 11, 2022
Developmental changes in iron metabolism and erythropoiesis in mice with human gain-of-function erythropoietin receptorBarbora Kralova, Lucie Sochorcova, Jihyun Song, et al.
Blood|September 21, 2016
Coexistence of gain-of-function JAK2 germ line mutations with JAK2V617F in polycythemia veraLucie Lanikova, Olga Babosova, Sabina Swierczek, et al.
Leukemia Research Reports|September 13, 2023
Allogeneic stem cell transplant for multiple myeloma & myelofibrosis with split-dose busulfan, fludarabine & cyclophosphamideAndrew D Trunk, Sagar S Patel, Josef T Prchal, et al.
Blood|October 24, 2002
Mutations in the VHL gene in sporadic apparently congenital polycythemiaYves D Pastore, Jaroslav Jelinek, Sonny Ang, et al.
American Journal of Human Genetics|July 5, 2003
Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemiaYves Pastore, Katerina Jedlickova, Yongli Guan, et al.
Haematologica|January 12, 2005
Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patientsMaria Celeste Bento, Ko Tung Chang, Yongli Guan, et al.
Pageof 25