anti-Trefoil Factor 2 (TFF2) Antikörper

Human Trefoil Factor 2 (TFF2) Interaktionspartner

1. The urine TFF1 (zeige TFF1 Antikörper) and TFF3 (zeige TFF3 Antikörper) levels significantly increased with the progression of chronic kidney disease stages, but not the urine TFF2 levels.

2. Data show that trefoil factor 2 (TFF2( urine levels continuously decreased with disease progression, TFF2 serum concentrations progressively increased from the early to later chronic kidney disease (CKD) stages, indicating changes in renal function and offering the potential to examine the course of CKD.

3. this work reveals that TFF2 has tumor-suppressor activity, which may, in part, be regulated by SMAD4 (zeige SMAD4 Antikörper).

4. Data indicate that the antitumor activity of trefoil factor 2 (TFF2) is mediated by an interaction with the transcription factor Sp3 (Sp3) in gastric cancer cells.

5. Data show the important functions of TFF2 in the gastric mucus barrier, mucus epithelia, immune system, central nervous system, and during fertilization. It has been shown to interact with the gastric mucin MUC6 (zeige MUC6 Antikörper). [Review]

6. These findings suggest that the rs184432 and rs225359 polymorphisms in TFF1 (zeige TFF1 Antikörper) have protective effects for GC and contribute to the development of GC in Korean individuals.

7. We reproducibly associate higher expression of the ligand-receptor axis of TFF2 and CXCR4 (zeige CXCR4 Antikörper) with BRAF (zeige BRAF Antikörper) V600E-mutant colon cancer

8. protease-activated receptor 4 (zeige F2RL3 Antikörper) and Trefoil factor 2 are expressed in human colorectal cancer

9. The structural features of the N-linked N,N'-di-N-acetyllactosediamine-inducing determinant on human TFF2 are discussed.

10. Human TTF2 (zeige FOXE1 Antikörper) is a lectin that binds alpha-GlcNAc-capped mucin 6 (zeige MUC6 Antikörper) g with antibiotic activity against Helicobacter pylori.

Pig (Porcine) Trefoil Factor 2 (TFF2) Interaktionspartner

1. Low intestinal TFF2 expression was measured at early maturation stages. Weaning, however, was associated with a distinct response of increased TFF2 expression, indicating an important role in enhancing mucosal integrity.

Mouse (Murine) Trefoil Factor 2 (TFF2) Interaktionspartner

1. the Tg(Tff1 (zeige TFF1 Antikörper)-CreERT2;Tff2-rtTA;Tff3 (zeige TFF3 Antikörper)-Luc) strain can confer intermittent transgene expression to gastric epithelial cells that have undergone previous gene modification, and may be suitable to genetically model therapeutic intervention during development, tumorigenesis, and other genetically tractable diseases

2. Splenic TFF2 is released by vagally modulated memory T cells to suppress expansion of myeloid-derived suppressor cells (MDSC) through CXCR4 (zeige CXCR4 Antikörper). TFF2 is important to the anti-inflammatory reflex arc (zeige NOL3 Antikörper) and has an essential role in arresting MDSC proliferation.

3. hnRNP A1 (zeige HNRNPA1 Antikörper) improves intestinal injury in anti-CD3 (zeige CD3E Antikörper) antibody-induced enteritis mice through the upregulation of TFF2, which regulates apoptosis and enhances epithelial restoration

4. Overexpressing Tff2 in cultured cells reduced doubling time in vitro and rapidly increased xenograft tumor size in vivo

5. Epithelial TFF2 is an important endogenous regulator of gut (zeige GUSB Antikörper) mucosal homeostasis that can modulate immune and epithelial compartments.

6. The Tff2 gene is expressed in the hypothalamus and is regulated by food intake. Knockout mice are leaner (zeige CACNA1A Antikörper) and have reduced fat mass compared to wild-type.

7. The increased expression of endogenous TFF2 in response to chronic allergic inflammation is insufficient to prevent the progression of airway inflammation and remodeling in a model of chronic allergic airways disease.

8. TFF2 functions as a regulator of intestinal homeostasis that suppresses Toxoplasma gondii-driven type 1 inflammation.

9. TFF2 (trefoil factor 2), an epithelial cell-derived repair molecule, is needed for the control of lung injury caused by the hookworm parasite Nippostrongylus brasiliensis and for type 2 immunity after infection.

10. results suggest that during retinal cell death periods, requiring a tightly regulated balance between cell survival and cell death, TFF2 acts pro-proliferative and pro-apoptotic at least in developing mouse retinae cultured in vivo