Igor Slukvin

Affiliations: 
Cellular & Molecular Pathology University of Wisconsin, Madison, Madison, WI 
Area:
Cell Biology, Medicine and Surgery
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"Igor Slukvin"
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Publications

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Kumar A, Lee JH, Suknuntha K, et al. (2018) NOTCH Activation at the Hematovascular Mesoderm Stage Facilitates Efficient Generation of T Cells with High Proliferation Potential from Human Pluripotent Stem Cells. Journal of Immunology (Baltimore, Md. : 1950)
Slukvin II, Kumar A. (2018) The mesenchymoangioblast, mesodermal precursor for mesenchymal and endothelial cells. Cellular and Molecular Life Sciences : Cmls
Park MA, Kumar A, Jung HS, et al. (2018) Activation of the Arterial Program Drives Development of Definitive Hemogenic Endothelium with Lymphoid Potential. Cell Reports. 23: 2467-2481
Uenishi GI, Jung HS, Kumar A, et al. (2018) NOTCH signaling specifies arterial-type definitive hemogenic endothelium from human pluripotent stem cells. Nature Communications. 9: 1828
D'Souza SS, Kumar A, Slukvin II. (2018) Functional Heterogeneity of Endothelial Cells Derived from Human Pluripotent Stem Cells. Stem Cells and Development
Suknuntha K, Tao L, Brok-Volchanskaya V, et al. (2018) Optimization of Synthetic mRNA for Highly Efficient Translation and its Application in the Generation of Endothelial and Hematopoietic Cells from Human and Primate Pluripotent Stem Cells. Stem Cell Reviews
Kumar A, D'Souza SS, Moskvin OV, et al. (2017) Specification and Diversification of Pericytes and Smooth Muscle Cells from Mesenchymoangioblasts. Cell Reports. 19: 1902-1916
Jung HS, Uenishi G, Kumar A, et al. (2016) A human VE-cadherin-tdTomato and CD43-green fluorescent protein dual reporter cell line for study endothelial to hematopoietic transition. Stem Cell Research. 17: 401-405
Suknuntha K, Thita T, Togarrati PP, et al. (2016) Wnt signaling inhibitor FH535 selectively inhibits cell proliferation and potentiates imatinib-induced apoptosis in myeloid leukemia cell lines. International Journal of Hematology
Hafner AL, Contet J, Ravaud C, et al. (2016) Brown-like adipose progenitors derived from human induced pluripotent stem cells: Identification of critical pathways governing their adipogenic capacity. Scientific Reports. 6: 32490
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