نتایج جستجو برای: p15ink4b gene

تعداد نتایج: 1141459  

2011
Jin He Anh Tram Nguyen Yi Zhang

The histone H3 lysine 36 dimethyl– specific demethylase KDM2b/JHDM1b, which is highly expressed in various human leukemias, was previously found to be important in regulating cell proliferation and cellular senescence. However, its functions in leukemia development and maintenance are unclear. Here, we demonstrate that ectopic expression of Kdm2b/Jhdm1b is sufficient to transform hematopoietic ...

Journal: :Cancer research 1999
C N Parris J D Harris D K Griffin A P Cuthbert A J Silver R F Newbold

Losses of heterozygosity involving chromosomes 9 and 10 are frequent events in the development and progression of cutaneous malignant melanoma. To investigate whether specifically deleted chromosomal regions encode tumor suppressor genes (TSGs), we introduced normal chromosome 10 into the tumorigenic human metastatic melanoma cell line UACC-903 by microcell fusion. In addition, two chromosome 9...

Journal: :Blood 2002
Anna Dimberg Fredrik Oberg

Retinoic acid-induced terminal differentiation of myeloid cells involves the sequential regulation of cell cycle regulatory genes, coordinating the process of differentiation with arrest in the G0/G1 phase of the cell cycle. In this review we have summarized changes in expression and activity of cell cycle regulatory proteins associated with retinoic acid induced-growth arrest in human myeloid ...

Journal: :Cancer research 2010
Jaap Kool Anthony G Uren Carla P Martins Daoud Sie Jeroen de Ridder Geoffrey Turner Miranda van Uitert Konstantin Matentzoglu Wendy Lagcher Paul Krimpenfort Jules Gadiot Colin Pritchard Jack Lenz Anders H Lund Jos Jonkers Jane Rogers David J Adams Lodewyk Wessels Anton Berns Maarten van Lohuizen

The cyclin dependent kinase (CDK) inhibitors p15, p16, p21, and p27 are frequently deleted, silenced, or downregulated in many malignancies. Inactivation of CDK inhibitors predisposes mice to tumor development, showing that these genes function as tumor suppressors. Here, we describe high-throughput murine leukemia virus insertional mutagenesis screens in mice that are deficient for one or two ...

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