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PIWIL4 belongs to the Argonaute family of proteins, which function in development and maintenance of germline stem cells (Sasaki et al., 2003 [PubMed 12906857]).[supplied by OMIM, Mar 2008].. Zusätzlich bieten wir Ihnen PIWIL4 Antikörper (73) und viele weitere Produktgruppen zu diesem Protein an.
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HIWI2 is aberrantly expressed in cells of the Retinoblastoma (RB) line (Y79) and silencing of HIWI2 downregulates OTX2 (zeige OTX2 Proteine), suggesting that HIWI2 might affects cell cycle and plays a role in the progression of RB.
data delineate MIWI2-dependent functions outside of the germline and demonstrate the presence of distinct subsets of airway multiciliated cells that can be discriminated by MIWI2 expression.
PIWIL2 and PIWIL4 genes expression in synovial fibroblasts of the rheumatoid arthritis patients.PIWIL4 does not regulate methylation or expression of LINE-1.
MiR (zeige MLXIP Proteine)-384 functioned as tumor suppressor by decreasing PIWIL4 in glioma cell lines.
study demonstrates the presence of PIWI (zeige PIWIL1 Proteine)-like proteins in somatic cells and the possible role of HIWI2 in preserving the functional integrity of epithelial cells probably by modulating the phosphorylation status of Akt (zeige AKT1 Proteine).
PIWIL4 is highly expressed in both breast cancer tissues and the cytoplasm of MDA-MB-231 cells derived from breast cancer. Reducing PIWIL4 expression drastically impairs the migration ability of MDA-MB-231 cells, significantly increases their apoptosis, and mildly affects their proliferation.
Results show that three CpG loci within FYN (zeige FYN Proteine) were hypermethylated in obese individuals, while obesity was associated with lower methylation of CpG loci within PIWIL4 and TAOK3 (zeige TAOK3 Proteine).
study to evaluate frequency of PIWIL4 genetic variants in order to better define the relationship between PIWIL4 SNPs and defective spermatogenesis and specific spermatogenic disorders; results suggest genetic and epigenetic alterations that affect the PIWI pathway contribute to unsuccessful sperm production
Data suggest that MIWI2 and MIWI2-associated piRNAs have functions beyond TE suppression.
associations were determined between the Piwi-like family member expression levels and clinicopathological parameters of ccRCC, suggesting a potential role for these genes/proteins in ccRCC diagnostics and tumorigenesis
MIWI2 functions as an effector of de novo DNA methylation (zeige HELLS Proteine) of the retrotransposon.
Miwi2 deficiency had only a minor impact on piRNA biogenesis. Miwi2-knockout mice indicated overexpression of several LINE1 TE families.
piRNA biogenesis triggered by PIWI slicing, and promoted by EXD1, ensures that the same guides instruct PIWI proteins in the nucleus and cytoplasm.
MIWI2 is not solely necessary for hematopoiesis within the normal life span of a mouse.
Mice with a global deletion of all three piwi (zeige PIWIL1 Proteine) genes, Miwi (zeige PIWIL1 Proteine), Mili, and Miwi2, are able to maintain long-term hematopoiesis with no observable effect on the homeostatic hematopoietic stem cells compartment in adult mice.
Icariin induced a decrease in piwil4 protein expression and piwil4 silencing significantly enhanced the cytotoxic effects of icariin in MLTC-1 cells.
Results identify TDRD9 as a functional partner of MIWI2 and indicate that the tudor-piwi association is a conserved feature, while two separate axes, TDRD9-MIWI2 and TDRD1-MILI, cooperate in the piwi-small RNA pathway in the mouse male germline.
Data strongly suggest that MILI and MIWI2 play essential roles in establishing de novo DNA methylation (zeige HELLS Proteine) of retrotransposons in fetal male germ cells.
purified the three murine Piwi (zeige PIWIL1 Proteine) family proteins, MILI, MIWI (zeige PIWIL1 Proteine), and MIWI2, from mouse germ cells and characterized their interacting protein partners
PIWIL4 belongs to the Argonaute family of proteins, which function in development and maintenance of germline stem cells (Sasaki et al., 2003
, piwi-like protein 4
, piwi-like homolog 4