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Jim Vadolas

Showing results (31-40 of 51) with videos related to

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British Journal of Haematology|October 12, 2022
A comprehensive study of immune function and immunophenotyping of white blood cells from β-thalassaemia/HbE patients on hydroxyurea supports the safety of the drugSirikwan Siriworadetkun, Chayada Thiengtavor, Rattanawan Thubthed, et al.
American Journal of Physiology. Endocrinology and Metabolism|June 2, 2016
Hepcidin and 1,25(OH)2D3 effectively restore Ca2+ transport in β-thalassemic mice: reciprocal phenomenon of Fe2+ and Ca2+ absorptionKamonshanok Kraidith, Saovaros Svasti, Jarinthorn Teerapornpuntakit, et al.
British Journal of Haematology|August 6, 2020
Elevated levels of circulating monocytic myeloid derived suppressor cells in splenectomised β-thalassaemia/HbE patientsSirikwan Siriworadetkun, Rattanawan Thubthed, Chayada Thiengtavor, et al.
Scientific Reports|November 4, 2022
Increased autophagy leads to decreased apoptosis during β-thalassaemic mouse and patient erythropoiesisPornthip Chaichompoo, Ramaneeya Nithipongvanitch, Wasinee Kheansaard, et al.
Stem Cell Reports|August 9, 2016
A Cas9 Variant for Efficient Generation of Indel-Free Knockin or Gene-Corrected Human Pluripotent Stem CellsSara E Howden, Bradley McColl, Astrid Glaser, et al.
International Journal of Cancer|May 30, 2009
Accumulation of lipid peroxidation-derived DNA lesions in iron-overloaded thalassemic mouse livers: comparison with levels in the lymphocytes of thalassemia patientsMayura Meerang, Jagadeesan Nair, Pornpan Sirankapracha, et al.
Scientific Reports|April 21, 2021
Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at <sup>G</sup>γ-globin gene promoterKhanita Nuamsee, Thipphawan Chuprajob, Wachirachai Pabuprapap, et al.
Genomics|April 25, 2006
A humanized BAC transgenic/knockout mouse model for HbE/beta-thalassemiaDuangporn Jamsai, Faten Zaibak, Jim Vadolas, et al.
Genomics|March 23, 2005
A humanized mouse model for a common beta0-thalassemia mutationDuangporn Jamsai, Faten Zaibak, Wantana Khongnium, et al.
British Journal of Haematology|May 4, 2021
SLN124, a GalNac-siRNA targeting transmembrane serine protease 6, in combination with deferiprone therapy reduces ineffective erythropoiesis and hepatic iron-overload in a mouse model of β-thalassaemiaJim Vadolas, Garrett Z Ng, Kai Kysenius, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
British Journal of Haematology|October 12, 2022
A comprehensive study of immune function and immunophenotyping of white blood cells from β-thalassaemia/HbE patients on hydroxyurea supports the safety of the drugSirikwan Siriworadetkun, Chayada Thiengtavor, Rattanawan Thubthed, et al.
American Journal of Physiology. Endocrinology and Metabolism|June 2, 2016
Hepcidin and 1,25(OH)2D3 effectively restore Ca2+ transport in β-thalassemic mice: reciprocal phenomenon of Fe2+ and Ca2+ absorptionKamonshanok Kraidith, Saovaros Svasti, Jarinthorn Teerapornpuntakit, et al.
British Journal of Haematology|August 6, 2020
Elevated levels of circulating monocytic myeloid derived suppressor cells in splenectomised β-thalassaemia/HbE patientsSirikwan Siriworadetkun, Rattanawan Thubthed, Chayada Thiengtavor, et al.
Scientific Reports|November 4, 2022
Increased autophagy leads to decreased apoptosis during β-thalassaemic mouse and patient erythropoiesisPornthip Chaichompoo, Ramaneeya Nithipongvanitch, Wasinee Kheansaard, et al.
Stem Cell Reports|August 9, 2016
A Cas9 Variant for Efficient Generation of Indel-Free Knockin or Gene-Corrected Human Pluripotent Stem CellsSara E Howden, Bradley McColl, Astrid Glaser, et al.
International Journal of Cancer|May 30, 2009
Accumulation of lipid peroxidation-derived DNA lesions in iron-overloaded thalassemic mouse livers: comparison with levels in the lymphocytes of thalassemia patientsMayura Meerang, Jagadeesan Nair, Pornpan Sirankapracha, et al.
Scientific Reports|April 21, 2021
Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at <sup>G</sup>γ-globin gene promoterKhanita Nuamsee, Thipphawan Chuprajob, Wachirachai Pabuprapap, et al.
Genomics|April 25, 2006
A humanized BAC transgenic/knockout mouse model for HbE/beta-thalassemiaDuangporn Jamsai, Faten Zaibak, Jim Vadolas, et al.
Genomics|March 23, 2005
A humanized mouse model for a common beta0-thalassemia mutationDuangporn Jamsai, Faten Zaibak, Wantana Khongnium, et al.
British Journal of Haematology|May 4, 2021
SLN124, a GalNac-siRNA targeting transmembrane serine protease 6, in combination with deferiprone therapy reduces ineffective erythropoiesis and hepatic iron-overload in a mouse model of β-thalassaemiaJim Vadolas, Garrett Z Ng, Kai Kysenius, et al.
Pageof 6