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Jun Ishikawa

Researcher at Osaka University

Publications -  61
Citations -  4490

Jun Ishikawa is an academic researcher from Osaka University. The author has contributed to research in topics: Haematopoiesis & Bone marrow. The author has an hindex of 28, co-authored 61 publications receiving 4335 citations. Previous affiliations of Jun Ishikawa include University of California, Irvine.

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Adiponectin, a new member of the family of soluble defense collagens, negatively regulates the growth of myelomonocytic progenitors and the functions of macrophages

TL;DR: The results suggest that adiponectin is an important negative regulator in hematopoiesis and immune systems and raise the possibility that it may be involved in ending inflammatory responses through its inhibitory functions.
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Expression and functional role of the proto-oncogene c-kit in acute myeloblastic leukemia cells

TL;DR: Results indicate that c-kit proto-oncogene is expressed in most cases of AML and is functional in terms of supporting proliferation.
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Molecular cloning and chromosomal mapping of a bone marrow stromal cell surface gene, BST2, that may be involved in pre-B-cell growth.

TL;DR: BST-2 surface expression on fibroblast cell lines facilitated the stromal cell-dependent growth of a murine bone marrow-derived pre-B-cell line, DW34, and the results suggest that BST-2 may be involved in pre- B-cell growth.
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BST-1, a surface molecule of bone marrow stromal cell lines that facilitates pre-B-cell growth.

TL;DR: BST-1 expression was enhanced in rheumatoid arthritis patient-derived bone marrow stromal cell lines that were previously shown to have an enhanced ability to support the growth of a pre-B-cell line as compared with stromAL cell lines derived from healthy donors.
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Thrombopoietin-induced differentiation of a human megakaryoblastic leukemia cell line, CMK, involves transcriptional activation of p21(WAF1/Cip1) by STAT5.

TL;DR: In this paper, a human megakaryoblastic leukemia cell line, CMK, was transfected with the p21, p27, or p16 gene, together with a marker gene, beta-galactosidase, and were cultured with medium alone for 5 days.