نتایج جستجو برای: csf gene

تعداد نتایج: 1165569  

Journal: :Experimental hematology 2008
Eun Wha Choi Il Seob Shin Young Jin Chae Hye Cheong Koo Jong Hwa Lee Tae Ho Chung Yong Ho Park Dae Yong Kim Cheol Yong Hwang Chang Woo Lee Hwa Young Youn

OBJECTIVE We sought to test two concepts: that nanoparticles can be used for in vivo gene delivery and that canine granulocyte-macrophage colony-stimulating factor (GM-CSF)/nanoparticles can have possibility to be used to treat transient (acute) canine leukopenia. MATERIALS AND METHODS We have generated a novel fluorescent-silica nanoparticle binding of canine GM-CSF gene; canine GM-CSF gene ...

Journal: :Blood 1987
A Rambaldi D C Young J D Griffin

Monocyte colony-stimulating factor (M-CSF, CSF-1) is a macrophage lineage-specific growth factor. Northern blot analysis using a human M-CSF cDNA probe and a specific bioassay for human M-CSF were used to investigate the cellular sources of M-CSF. Expression of the M-CSF gene was induced in blood mononuclear cells stimulated by phorbol myristate acetate (PMA) or gamma-interferon. When mononucle...

Journal: :Blood 1992
W M Roberts L H Shapiro R A Ashmun A T Look

Receptors for macrophage colony-stimulating factor (CSF-1R) are expressed not only by monocytes, macrophages, and their progenitors, but also by placental trophoblasts during fetal development. In monocytes, CSF-1R gene transcripts originate at multiple sites immediately upstream of the gene's coding sequences, whereas in placental cells the transcripts include an additional noncoding exon, loc...

Journal: :Blood 1994
D M Bodine N E Seidel M S Gale A W Nienhuis D Orlic

Cytokine-mobilized peripheral blood cells have been shown to participate in hematopoietic recovery after bone marrow (BM) transplantation, and are proposed to be useful targets for retrovirus-mediated gene transfer protocols. We treated mice with granulocyte colony-stimulating factor (G-CSF) and stem cell factor (SCF) to mobilize hematopoietic progenitor cells into the peripheral blood. These c...

Journal: :The Journal of clinical investigation 1997
M Kochetkova P O Iversen A F Lopez M F Shannon

Juvenile myelomonocytic leukemia (JMML) is a severe childhood malignancy. The autocrine production of GMCSF is believed to be responsible for the spontaneous proliferation of JMML cells. A nuclear factor-kappaB (NF-kappaB)/Rel binding site within the GM-CSF gene promoter, termed the kappaB element, plays an important role in controlling transcription from the GM-CSF gene. We investigated the ef...

Journal: :Nucleic Acids Research 1989

Journal: :European Journal of Neurology 2021

Background Parkinson´s disease (PD) has a large phenotypic variability, which may, at least partly, be genetically driven including alterations of gene products. Candidates might not only proteins associated with risk but also pathways that play role in aging. Objective To evaluate phenotype-modifying effects genetic variants Klotho, longevity gene. Methods We analyzed two longitudinal cohorts:...

Journal: :Leukemia research 1996
I P Touw F Dong

Severe congenital neutropenia (SCN) is a heterogeneous disease condition with a variable family history and a propensity to progress towards myelodysplastic syndrome (MDS) and acute myeloblastic leukemia (AML). In a subgroup of patients, point mutations in the G-CSF-R gene have been found. These nonsense mutations result in the truncation of the C-terminal cytoplasmic region, a subdomain that i...

Journal: :Alzheimers & Dementia 2023

Background IFITM3, an innate immune response protein and inhibitor of viral infection, was reported to modulate amyloid-β production in Alzheimer’s disease (AD). We aimed identify single-nucleotide polymorphisms (SNPs) IFITM3 associated with cognition AD biomarkers. Method used genetic, longitudinal biomarker data from Disease Neuroimaging Initiative (ADNI; N = 1,565) AddNeuroMed (N 633) as dis...

Journal: :Stroke 2001
H Nakane Y Chu F M Faraci L W Oberley D D Heistad

BACKGROUND AND PURPOSE Copper-zinc superoxide dismutase (CuZnSOD) is expressed intracellularly, while extracellular SOD (EC-SOD) is released from cells. The purpose of this study was to determine whether gene transfer of CuZnSOD increases SOD activity predominantly in tissues, and gene transfer of EC-SOD increases SOD activity in cerebrospinal fluid (CSF). We also determined whether heparin or ...

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