M
Malcolm A.S. Moore
Researcher at Memorial Sloan Kettering Cancer Center
Publications - 549
Citations - 42338
Malcolm A.S. Moore is an academic researcher from Memorial Sloan Kettering Cancer Center. The author has contributed to research in topics: Haematopoiesis & Stem cell. The author has an hindex of 97, co-authored 548 publications receiving 41147 citations. Previous affiliations of Malcolm A.S. Moore include University of Oxford & Amgen.
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Journal ArticleDOI
Expression of VEGFR-2 and AC133 by circulating human CD34+ cells identifies a population of functional endothelial precursors
Mario Peichev,Afzal J. Naiyer,Daniel S. Pereira,Zhenping Zhu,William J. Lane,Mathew R. Williams,Mehmet C. Oz,Daniel J. Hicklin,Larry Witte,Malcolm A.S. Moore,Shahin Rafii +10 more
TL;DR: In an in vivo human model, it is found that the neo-intima formed on the surface of left ventricular assist devices is colonized with AC133(+)VEGFR-2(+) cells, suggesting a phenotypically and functionally distinct population of circulating endothelial cells that may play a role in neo-angiogenesis.
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Impaired recruitment of bone-marrow–derived endothelial and hematopoietic precursor cells blocks tumor angiogenesis and growth
David Lyden,Koichi Hattori,Koichi Hattori,Sergio Dias,Carla Costa,Pamela Blaikie,Linda J. Butros,Amy Chadburn,Beate Heissig,Willy Marks,Larry Witte,Yan Wu,Daniel J. Hicklin,Zhenping Zhu,Neil R. Hackett,Ronald G. Crystal,Malcolm A.S. Moore,Katherine A. Hajjar,Katia Manova,Robert Benezra,Shahin Rafii +20 more
TL;DR: It is demonstrated that recruitment of VEGF-responsive BM-derived precursors is necessary and sufficient for tumor angiogenesis and suggested new clinical strategies to block tumor growth are suggested.
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Recruitment of Stem and Progenitor Cells from the Bone Marrow Niche Requires MMP-9 Mediated Release of Kit-Ligand
Beate Heissig,Koichi Hattori,Sergio Dias,Matthias Friedrich,Barbara Ferris,Neil R. Hackett,Ronald G. Crystal,Peter Besmer,David Lyden,Malcolm A.S. Moore,Zena Werb,Shahin Rafii +11 more
TL;DR: In this article, BM ablation induces SDF-1, which upregulates MMP-9 expression, and causes shedding of sKitL and recruitment of c-Kit+ stem/progenitors.
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Recombinant human granulocyte colony-stimulating factor: effects on normal and leukemic myeloid cells
Lawrence M. Souza,Thomas C. Boone,Janice Gabrilove,Por H. Lai,Krisztina M. Zsebo,Murdock Douglas C,Vicki R. Chazin,Joan Bruszewski,Hsieng Sen Lu,Kenneth Chen,Jean M. Barendt,Erich Platzer,Malcolm A.S. Moore,Roland Mertelsmann,Karl Welte +14 more
TL;DR: Experiments were conducted to isolate and characterize the gene and gene product of a human hematopoietic colony-stimulating factor with pluripotent biological activities, which has the ability to induce differentiation of a murine myelomonocytic leukemia cell line WEHI-3B(D+) and cells from patients with newly diagnosed acute nonlymphocytic cancer.
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Ontogeny of the haemopoietic system: yolk sac origin of in vivo and in vitro colony forming cells in the developing mouse embryo.
TL;DR: The mouse yolk sac has been shown to contain in‐vivo colony forming cells capable of producing granulocytic, megakaryocytic and erythroid spleen colonies, and haemopoietic precursor cells demonstrated in the blood at the time of initiation of the circulation and in the early embryonic liver.