LIM and Senescent Cell Antigen-Like Domains 1 (LIMS1) ELISA Kits

Human LIM and Senescent Cell Antigen-Like Domains 1 (LIMS1) Interaktionspartner

1. that PINCH-1 may be playing an important role in etiopathogenesis of both subtypes breast cancer

2. Mammalian cells have two functional PINCH proteins, PINCH1 and PINCH2. PINCH not only binds to Nck2 and engages in the signaling of growth factor receptors, but also forms a ternary complex with ILK (zeige ILK ELISA Kits) and parvin (IPP (zeige IPP ELISA Kits) complex).

3. our data suggest an essential role of PINCH1, ILK (zeige ILK ELISA Kits) and ILKAP (zeige ILKAP ELISA Kits) for the radioresistance of p53 (zeige TP53 ELISA Kits)-wildtype glioblastoma multiforme cells

4. Data suggest that PINCH1 and Nck2 critically participate in the regulation of cellular radiosensitivity and EGFR (zeige EGFR ELISA Kits) function and downstream signaling in a cellular model of human squamous cell carcinoma.

5. Downregulation of PINCH1 is associated with metastatic breast cancer.

6. changes in CSF (zeige CSF2 ELISA Kits) levels of PINCH appear to correlate with changes in blood CD4 (zeige CD4 ELISA Kits) count and with changes in CSF (zeige CSF2 ELISA Kits) hyperphosphorylated Tau levels

7. two novel genes, galectin 9 (zeige LGALS9 ELISA Kits) and PINCH, were expressed at much higher levels in cancerous lesions than in normal tissues in all the patients with clear-cell carcinoma who were examined

8. PINCH predicts survival in rectal cancer patients with RT, but not in patients without RT. The expression of PINCH may be regulated by radiation and by environmental factors surrounding the cells.

9. PINCH is increased and binds to hp-Tau. These studies address a new mechanism by which AD and HIV may intersect and identify PINCH as a contributing factor to the accumulation of hyperphosphorylated Tau.

10. Pinch-1 mRNA and protein were significantly up-regulated in acute lymphoblastic leukemia and acute myeloid leukemia (zeige BCL11A ELISA Kits) bone marrow stromal cells compared to normal bone marrow stromal cells (p<0.01).

Mouse (Murine) LIM and Senescent Cell Antigen-Like Domains 1 (LIMS1) Interaktionspartner

1. findings suggest that PINCH-1 regulates integrin-mediated adhesion of keratinocytes through the interactions with ILK as well as EPLIN.

2. Rsu-1 (zeige RSU1 ELISA Kits) expression is dramatically decreased in PINCH double knockout mouse livers.

3. PINCH is increased and binds to hp-Tau. These studies address a new mechanism by which AD and HIV may intersect and identify PINCH as a contributing factor to the accumulation of hyperphosphorylated Tau.

4. PINCH-1 inhibits JNK (zeige MAPK8 ELISA Kits)-mediated apoptosis by stabilising the PINCH-1 binding protein RSU-1 (zeige RSU1 ELISA Kits) and promotes Bcl-2 (zeige BCL2 ELISA Kits)-dependent pro-survival signalling downstream of integrins.

5. Data suggest that the adapter protein (zeige GRB10 ELISA Kits) PINCH1 critically participates in the regulation of the cellular radiosensitivity of normal and malignant cells similarly under adhesion and suspension conditions.

6. PINCH1 plays an essential role in early murine embryonic development but is dispensable in ventricular cardiomyocytes.

7. These results provide important evidence for a crucial role of the PINCH-1-ILK-alpha-parvin complex in the control of podocyte adhesion, morphology, and survival.

8. LIM (zeige PDLIM5 ELISA Kits) 5 domain of PINCH1 interacts with Rsu-1 (zeige RSU1 ELISA Kits) in mammalian cells and functions, in part, by altering cell adhesion.

9. The PINCH1 is composed of 5 LIM domains, binds ILK and locates to integrin-mediated adhesion sites, and PINCH1 is for integrin function, actin organization, cell-cell adhesion and endodermal cell survival during the implanting of mouse embryos.

10. PICH1, Ilk and alpha-parvin form a complex to costameres in neonatal mouse ventricular myocytes. This complex is stimulated by fibronectins and phenylephrine, and by both by drug synergism, to regulate cardiac myocyte hypertrophy.