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Cycling hypoxia could induce significant changes in CLDN1 (zeige CLDN1 Proteine) and CLDN7 (zeige CLDN7 Proteine) expression in nasopharyngeal cancer cells, indirectly regulation P18 expression and affecting cell invasion/proliferation.
genetic association studies in population in Houston TX: Data suggest that CDKN2C copy number variations are associated with sporadic medullary thyroid carcinoma; these associations include presence of distant metastasis at presentation and decreased overall survival.
CDKN2C gene deletion is associated with plasma cell post-transplantation lymphoproliferative disorders.
The differences in p18(INK4c)and p57(Kip2 (zeige CDKN1C Proteine))activities in chronic myeloid leukemia (zeige BCL11A Proteine) and normal stem cells suggest a different cell cycle regulation.
Our study suggests that p18 is a limiting factor for the noncanonical HSC (zeige FUT1 Proteine) differentiation path in lymphoid lineages.
CDKN2C inactivation contributes to the leukemogenesis in acute promyelocytic leukemia (zeige PML Proteine).
DNA methyltransferase 3A (zeige DNMT3A Proteine) promotes cell proliferation by silencing CDK (zeige CDK4 Proteine) inhibitor p18INK4C in gastric carcinogenesis
Data suggest that cell cycle-dependent kinase inhibitors CDKN2C/p18 and CDKN1A/p21 (zeige CDKN1A Proteine) facilitate cell cycle entry/cell proliferation of quiescent adult human pancreatic beta cells in primary culture (from tissues obtained from organ donors).
this studydemonstrated abundant levels of the critical negative cell-cycle regulators, p27(Kip1 (zeige CDKN1B Proteine)), its phosphorylated form, p-p27 (zeige PAK2 Proteine)(S10 (zeige L1CAM Proteine)), p18Ink4c, and GSK-3, in beta-cells of both adult human and mouse pancreatic islets, which contribute to maintenance of beta-cell quiescence.
in 85 sporadic parathyroid adenomas, study identified alterations in 5 adenomas: 2 contained heterozygous changes in CDKN1A, 1 germline and 1 of undetermined germline status; 1 had a CDKN2B (zeige CDKN2B Proteine) germline alteration, accompanied by loss of the normal allele in the tumor (LOH); 2 had variants of CDKN2C, 1 somatic and 1 germline with LOH
Gata3 (zeige GATA3 Proteine) deficiency promotes B cell differentiation and proliferation, and cooperates with p18 loss to induce B cell lymphomas
These results indicate that p18 blocks reprogramming by targeting Cdk4/6 (zeige CDK4 Proteine)-mediated cell cycle regulation.
Host Tumor Suppressor p18(INK4c) Functions as a Potent Cell-Intrinsic Inhibitor of Murine Gammaherpesvirus 68 Reactivation and Pathogenesis.
Specifically, the proteins p18INK4C, p21CIP1 (zeige CDKN1A Proteine) and p27KIP1 (zeige CDKN1B Proteine) seem to play an outstanding role in the maintenance of the differentiated state of adipocytes.
CD4 (zeige CD4 Proteine)+ T cells from mice genetically deficient for p18ink4c divide more rapidly than wild-type cells in response to antigenic, costimulatory and growth factor signals.
p18 represents a potent and specific target for enhancing the self-renewal property of HSC (zeige FUT1 Proteine), as demonstrated the effect of inhibitors
p18 may play protective roles and may be associated with or partially account for the cytoprotective effects of HO-1 (zeige HMOX1 Proteine) in cisplatin-induced acute kidney injury.
Cdk4 (zeige CDK4 Proteine) and Cdk6 (zeige CDK6 Proteine) cooperate in hematopoietic tumor development and suggest a role for Cdk6 (zeige CDK6 Proteine) in sequestering INK4 proteins away from Cdk4 (zeige CDK4 Proteine).
Gata3 (zeige GATA3 Proteine)/Ruvbl2 (zeige RUVBL2 Proteine) complex regulates T helper 2 cell proliferation via repression of Cdkn2c expression.
deletion of P18 results in a deacreased proliferation of hematopoietic progenitor cells (HPCs) suggesting a positive role for P18 on HPCs in vivo
The protein encoded by this gene is a member of the INK4 family of cyclin-dependent kinase inhibitors. This protein has been shown to interact 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. Ectopic expression of this gene was shown to suppress the growth of human cells in a manner that appears to correlate with the presence of a wild-type RB1 function. Studies in the knockout mice suggested the roles of this gene in regulating spermatogenesis, as well as in suppressing tumorigenesis. Two alternatively spliced transcript variants of this gene, which encode an identical protein, have been reported.
cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
, cyclin-dependent kinase 4 inhibitor C
, CDK6 inhibitor p18
, cyclin-dependent inhibitor
, cyclin-dependent kinase 6 inhibitor p18
, cyclin-dependent kinase 6 inhibitor