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N Constantinescu

Showing results (121-130 of 180) with videos related to

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Blood|February 24, 2007
The myeloproliferative disorder-associated JAK2 V617F mutant escapes negative regulation by suppressor of cytokine signaling 3Michelle B Hookham, Joanne Elliott, Yvonne Suessmuth, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2009
A helix-to-coil transition at the epsilon-cut site in the transmembrane dimer of the amyloid precursor protein is required for proteolysisTakeshi Sato, Tzu-Chun Tang, Gabriella Reubins, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 1995
Expression and signaling specificity of the IFNAR chain of the type I interferon receptor complexS N Constantinescu, E Croze, A Murti, et al.
Blood|November 27, 2015
Calreticulin mutants in mice induce an MPL-dependent thrombocytosis with frequent progression to myelofibrosisCaroline Marty, Christian Pecquet, Harini Nivarthi, et al.
Blood|November 17, 2020
Hematoxylin binds to mutant calreticulin and disrupts its abnormal interaction with thrombopoietin receptorRuochen Jia, Thomas Balligand, Vasyl Atamanyuk, et al.
Blood|January 25, 2020
MPL mutations in essential thrombocythemia uncover a common path of activation with eltrombopag dependent on W491Gabriel Levy, Serge Carillo, Benjamin Papoular, et al.
Structure (London, England : 1993)|January 28, 2014
Conformational changes induced by the A21G Flemish mutation in the amyloid precursor protein lead to increased Aβ productionTzu-Chun Tang, Yi Hu, Pascal Kienlen-Campard, et al.
Blood|October 12, 2007
The ubiquitin-mediated degradation of Jak1 modulates osteoclastogenesis by limiting interferon-beta-induced inhibitory signalingYoungkyun Lee, Seok-Won Hyung, Hee Jung Jung, et al.
Blood|July 9, 2016
Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypiaKatarina Kapralova, Monika Horvathova, Christian Pecquet, et al.
Oncogene|March 9, 2019
Rare type 1-like and type 2-like calreticulin mutants induce similar myeloproliferative neoplasms as prevalent type 1 and 2 mutants in miceKatte Rao Toppaldoddi, Maira da Costa Cacemiro, Olivier Bluteau, et al.
Pageof 18

Showing results (121-130 of 180) with videos related to

Sort By:
Pageof 18
Blood|February 24, 2007
The myeloproliferative disorder-associated JAK2 V617F mutant escapes negative regulation by suppressor of cytokine signaling 3Michelle B Hookham, Joanne Elliott, Yvonne Suessmuth, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2009
A helix-to-coil transition at the epsilon-cut site in the transmembrane dimer of the amyloid precursor protein is required for proteolysisTakeshi Sato, Tzu-Chun Tang, Gabriella Reubins, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 1995
Expression and signaling specificity of the IFNAR chain of the type I interferon receptor complexS N Constantinescu, E Croze, A Murti, et al.
Blood|November 27, 2015
Calreticulin mutants in mice induce an MPL-dependent thrombocytosis with frequent progression to myelofibrosisCaroline Marty, Christian Pecquet, Harini Nivarthi, et al.
Blood|November 17, 2020
Hematoxylin binds to mutant calreticulin and disrupts its abnormal interaction with thrombopoietin receptorRuochen Jia, Thomas Balligand, Vasyl Atamanyuk, et al.
Blood|January 25, 2020
MPL mutations in essential thrombocythemia uncover a common path of activation with eltrombopag dependent on W491Gabriel Levy, Serge Carillo, Benjamin Papoular, et al.
Structure (London, England : 1993)|January 28, 2014
Conformational changes induced by the A21G Flemish mutation in the amyloid precursor protein lead to increased Aβ productionTzu-Chun Tang, Yi Hu, Pascal Kienlen-Campard, et al.
Blood|October 12, 2007
The ubiquitin-mediated degradation of Jak1 modulates osteoclastogenesis by limiting interferon-beta-induced inhibitory signalingYoungkyun Lee, Seok-Won Hyung, Hee Jung Jung, et al.
Blood|July 9, 2016
Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypiaKatarina Kapralova, Monika Horvathova, Christian Pecquet, et al.
Oncogene|March 9, 2019
Rare type 1-like and type 2-like calreticulin mutants induce similar myeloproliferative neoplasms as prevalent type 1 and 2 mutants in miceKatte Rao Toppaldoddi, Maira da Costa Cacemiro, Olivier Bluteau, et al.
Pageof 18