KIA

(redirected from MKI67)
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Related to MKI67: Ki-67

KIA

 (kā′ī-ā′)
n.
A member of the armed services who is reported killed during a combat mission.

[k(illed) i(n) a(ction).]

KIA

1. Also, K.I.A. killed in action.
2.
pl. KIA's, KIAs. a member of the military services who has been killed in action.
References in periodicals archive ?
Gene symbols: ALPI, intestinal-type alkaline phosphatase; CHGA, chromogranin A; DEFA5, defensin [alpha] 5; FFA4R, free fatty acid receptor 4; GAPDH, glyceraldehyde- 3-phosphate dehydrogenase; LGR5, leucin-rich repeat-containing G-protein-couple receptor 5; LYZ, lysosyme; MKI67, marker of proliferation Ki-67; MUC2, mucin 2; SI, sucrose isomaltase; SYP, synaptophysin; TFF3, trefoil factor 3.
Three sections per uterus were stained for histological analysis with antibodies to GR (1:500; Cell Signaling Technologies) or MKi67 (1:400; Cell Signaling Technologies) overnight at 4[degrees]C (see Table S2).
Han et al., "Genome-wide association study of mki67 expression and its clinical implications in hbv-related hepatocellular carcinoma in southern china," in Proceedings of the Cellular Physiology Biochemistry International Journal of Experimental Cellular Physiology Biochemistry Pharmacology, vol.
Conversely, we found a mild inverse correlation of CXCR4 and CXCL12 with MKI67 (rs = -0.1262; rs = -0.2076, resp.), thus confirming the lack of association between the CXCR4/CXCL12 axis and proliferation in luminal B BC (Figures 4(a) and 4(b)).
As reported in Table 2, 14 genes (KRT19, FLT1, EGER, EPCAM, MET, PGR, CD24, KIT, PLAU, ALDH1A1, CTSD, MKI67, TWIST1, and ERBB2) were evaluated as significantly differentially expressed in the tested sample cohorts between CTC+ and CTC- samples.
Antigen Ki67 is a nuclear protein, encoded by MKI67 gene that is mapped at 10q26.2.
This group was marked by high activation of the cell proliferation marker Mki67. In addition, this group is comprised of interferon-induced GTPases such as Gbp6 and Gbp10, which are involved in the innate response to protect against a bacterial infection [17] and Iigp1.
The expression of other genes from the cell cycle functional group was altered: APC (-3.79), CCND1 (-1.90), CCNE1 (-2.38), MKI67 (-1.51), MYC (2.04) and TP53 (2.05).
After 3 injections of docetaxel (once a week), 7 mice were sacrificed to analyze MKI67 gene and protein expressions and the rest were monitored for diet consumption, tumor growth and survival rates.
(25) The authors found a strong correlation between FDG uptake and mitotic counts; and the percentage of cells positive for the Ki-67 protein, which is a product of the MKI67 gene, and nuclear grade.
Among the 1485 DEGs, neuroendocrine-associated genes SYP (Syn; FC=1.5, FDR = 0.04), CHGA (CgA; FC = 3.02, FDR=0.04), NCAM1 (CD56; FC=18.10, FDR=0.006), ASCL1 (FC=619.23, FDR=0.0005), and GRP (FC=5.33, FDR= 0.03) and proliferation-associated genes MKI67 (Ki-67; FC=9.35, FDR=0.007) and PCNA (FC=4.20, FDR= 0.006) were overexpressed.
E2 had a significant effect on the expression of genes associated with cell division (Top2a, Mki67, Ccnbl, Ccnb2; Figure 5A) and cytokinesis (Kifll, Kf2c, Kif18a; Figure 5B).