نتایج جستجو برای: gm csf

تعداد نتایج: 42918  

Journal: :Cancer research 1996
C A Armstrong R Botella T H Galloway N Murray J M Kramp I S Song J C Ansel

The use of immunomodulating gene therapy in the treatment of malignant disease is under intensive investigation. In this study, we examined the potential of melanoma-derived granulocyte-macrophage colony-stimulating factor (GM-CSF) to inhibit melanoma progression in a murine model. The HGH18 murine melanoma cell line was transfected with the murine GM-CSF gene in a SV40 expression vector that r...

Journal: :Blood 1995
C B Brown P Beaudry T D Laing S Shoemaker K Kaushansky

We have cloned, expressed, and partially purified a naturally occurring, truncated, soluble form of the human granulocyte-macrophage colony-stimulating factor (GM-CSF) receptor alpha subunit to investigate its biochemical and biologic properties. The soluble receptor species lacks the transmembrane and cytoplasmic domains that are presumably removed from the intact receptor cDNA by a mechanism ...

Journal: :Blood 1992
A Suzuki T Takahashi K Nakamura R Tsuyuoka Y Okuno T Enomoto M Fukumoto H Imura

We investigated the cause of thrombocytosis in 14 patients with tumors producing colony-stimulating factor (CSF). Of the 14 patients, 10 had tumors producing granulocyte-CSF (G-CSF) and 4 had tumors producing granulocyte-macrophage--CSF (GM-CSF). Thrombocytosis of greater than 400 x 10(9)/L was noted in 8 of 10 patients with G-CSF-producing tumors and all 4 patients with GM-CSF-producing tumors...

1999
JACQUELYN A. REED MACHIKO IKEGAMI ELI R. CIANCIOLO WEI LU PATRICIA S. CHO WILLIAM HULL ALAN H. JOBE JEFFREY A. WHITSETT Machiko Ikegami Eli R. Cian Wei Lu Patricia S. Cho William Hull Alan H. Jobe

Reed, Jacquelyn A., Machiko Ikegami, Eli R. Cianciolo, Wei Lu, Patricia S. Cho, William Hull, Alan H. Jobe, and JeffreyA. Whitsett. Aerosolized GM-CSF ameliorates pulmonary alveolar proteinosis in GM-CSF-deficient mice. Am. J. Physiol. 276 (Lung Cell. Mol. Physiol. 20): L556–L563, 1999.—Surfactant proteins and phospholipids accumulate in the alveolar spaces and lung tissues of mice deficient in...

Journal: :Blood 1989
K Yamato Z El-Hajjaoui J F Kuo H P Koeffler

Granulocyte-monocyte colony-stimulating factor (GM-CSF) is an important hematopoietic growth factor. Mesenchymal cells produce abundant GM-CSF in response to tumor necrosis factor alpha (TNF). We wished to determine (1) what cellular pathways enhanced levels of GM-CSF mRNA, and (2) if TNF used any of these pathways. Modulation in levels of GM-CSF mRNA in human fibroblasts (WI-38) was studied by...

2002
Pierre-Yves Berclaz Yoko Shibata Jeffrey A. Whitsett Bruce C. Trapnell

Severely impaired pulmonary microbial clearance was observed in granulocytemacrophage colony-stimulating factor (GM-CSF)–deficient mice. To determine mechanisms by which GM-CSF mediates lung host defense, Fc R-mediated phagocytosis (opsonophagocytosis) by alveolar macrophages (AMs) was assessed in GM-CSF–sufficient (GM / ) and –deficient (GM / ) mice and in GM / mice expressing GM-CSF only in t...

2017
Tatjana Scholz Andreas Weigert Bernhard Brüne Christian D Sadik Beate Böhm Harald Burkhardt

Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a pleiotropic, Th17-derived cytokine thought to critically contribute to the pathogenesis of diverse autoimmune diseases, including rheumatoid arthritis and psoriasis. Treatment with monoclonal antibodies that block GM-CSF activity is associated with favorable therapeutic effects in patients with rheumatoid arthritis. We evaluated the...

Journal: :Blood 1999
D Metcalf N A Nicola S Mifsud L Di Rago

Marrow cells from mice lacking high-affinity receptors for granulocyte-macrophage colony-stimulating factor (GM-CSF; betac-/- mice) were shown to bind and internalize much less GM-CSF than cells from normal (betac+/+) mice. betac-/- mice were used to determine the effect of negligible receptor-mediated clearance on detectible GM-CSF responses to the intravenous injection of endotoxin or the int...

Journal: :Blood 2001
L Houzet D Morello P Defrance P Mercier G Huez V Kruys

In vitro studies have indicated that the granulocyte-macrophage colony-stimulating factor (GM-CSF) gene expression is regulated at the posttranscriptional level by the AU-rich element (ARE) sequence present in its 3' untranslated region (UTR). This study investigated the importance of the ARE in the control of GM-CSF gene expression in vivo. For this purpose, transgenic mice bearing GM-CSF gene...

Journal: :Biology of reproduction 1997
A A de Moraes P J Hansen

The objective was to determine whether granulocyte-macrophage colony-stimulating factor (GM-CSF) stimulates development of bovine embryos. In each experiment, oocytes were fertilized in vitro, GM-CSF was added to embryo culture medium at 8-10 h or 5 days after insemination, and development was monitored as the proportion of oocytes that formed blastocysts. Addition of recombinant bovine GM-CSF ...

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