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We unexpectedly found that p19INK4d plays an important role in human terminal erythropoiesis
p19(INK4D) is one of the key mediators of miR (zeige MLXIP ELISA Kits)-125b activity during the onset of megakaryocyte polyploidization.
p19 may play an important role in the ototoxic effects of cisplatin and is probably involved in the pathogenesis of hearing loss.
MiR (zeige MLXIP ELISA Kits)-451 inhibited the proliferation of esophageal squamous cell carcinoma cells by targeting CDKN2D and MAP3K1 (zeige MAP3K1 ELISA Kits) expression.
Data indicate that upon oxidative DNA damage, cyclin-dependent kinase (zeige CDK1 ELISA Kits) inhibitor p19INK4d strongly binds to and relaxes chromatin.
CDKN2D repression by PML (zeige PML ELISA Kits)/RARalpha (zeige RARA ELISA Kits) disrupts both cell proliferation and differentiation in the pathogenesis of acute promyelocytic leukemia (zeige PML ELISA Kits).
p19-INK4d inhibits neuroblastoma (zeige ARHGEF16 ELISA Kits) cell growth, induces differentiation and is hypermethylated and downregulated in MYCN (zeige MYCN ELISA Kits)-amplified neuroblastomas.
CDKN2D-WDFY2 (zeige ZFYVE22 ELISA Kits) fusion could be an important molecular signature for understanding and classifying sub-lineages among heterogeneous high-grade serous ovarian carcinomas.
Mutations in CDKN2D is associated with sporadic parathyroid adenoma.
P19(INK4d) expression is a poor prognostic factor in ovarian cancer patients.
The expression of three tumor suppressor genes encoded in the INK4/ARF locus (p15(INK4b (zeige CDKN2B ELISA Kits)), p16(INK4a), and p19(ARF)) was decreased in E6AP (zeige ube3a ELISA Kits)(-/-) embryo fibroblasts.
TWIST1 (zeige TWIST1 ELISA Kits)-E protein heterodimeric complexes may thus constitute the main active forms of TWIST1 (zeige TWIST1 ELISA Kits) with regard to senescence inhibition over the time course of breast tumorigenesis.
Rescue from early-onset hearing loss in a mouse model lacking the cyclin-dependent kinase (zeige CDK1 ELISA Kits) inhibitor p19Ink4d.
p19 INK4d controls hematopoietic stem cells in a cell-autonomous manner during genotoxic stress and through the microenvironment during aging
Cdk4 (zeige CDK4 ELISA Kits) and Cdk6 (zeige CDK6 ELISA Kits) cooperate in hematopoietic tumor development and suggest a role for Cdk6 (zeige CDK6 ELISA Kits) in sequestering INK4 proteins away from Cdk4 (zeige CDK4 ELISA Kits).
Deletion of p19(Ink4d) (p19), a cyclin-dependent kinase (zeige CDK1 ELISA Kits) CDK (zeige CDK4 ELISA Kits) inhibitor gene, in mice results in spontaneous development of tumors in multiple organs and tissues.
We propose that p19INK4d participates in the cellular mechanisms that trigger senescence by contributing to chromatin compaction
CDK5 (zeige CDK5 ELISA Kits)-mediated phosphorylation of p19INK4d avoids DNA damage-induced neurodegeneration in mouse hippocampus and prevents loss of cognitive functions.
an asymmetrical distribution pattern for Cdkn2d transcripts in 2-cell embryos.
Ectopic expression of RUVBL2 decreases the levels of ARF, whereas knockdown of RUVBL2 results in a marked increase in ARF levels. In addition, RUVBL2 down-regulates the levels of p53 in an ARF-dependent manner.
The protein encoded by this gene is a member of the INK4 family of cyclin-dependent kinase inhibitors. This protein has been shown to form a stable complex with CDK4 or CDK6, and prevent the activation of the CDK kinases, thus function as a cell growth regulator that controls cell cycle G1 progression. The abundance of the transcript of this gene was found to oscillate in a cell-cycle dependent manner with the lowest expression at mid G1 and a maximal expression during S phase. The negative regulation of the cell cycle involved in this protein was shown to participate in repressing neuronal proliferation, as well as spermatogenesis. Two alternatively spliced variants of this gene, which encode an identical protein, have been reported.
cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)
, cyclin-dependent kinase 4 inhibitor D
, Cyclin-dependent kinase 4 inhibitor D
, CDK inhibitor p19INK4d
, cell cycle inhibitor, Nur77 associating protein
, cyclin-dependent kinase 4 inhibitor D p19
, inhibitor of cyclin-dependent kinase 4d