Aperçu des produits pour anti-MUC1 (MUC1) Anticorps

Human Mucin 1, Cell Surface Associated (MUC1) interaction partners

1. MUC1 was intensely positive in 46% and negative in 37.9% of colorectal tumors. Loss of MUC1 expression was more frequent in cases with disease recurrence or death, as compared with patients with stable disease, in whom intense positivity was more frequently seen. These findings disagree with the majority of previous studies.

2. upregulation of MUC1 in involved psoriatic lesion compared to uninvolved and normal skin may suggest MUC1 role in pathogenesis of psoriasis especially early stages; MUC1 may be responsible for less severity of psoriasis in old aged patients

3. The potential prognostic relevance of EP3 expression for OS in TA-MUC1 negative patients might reflect an interplay between the COX and the MUC1 pathway, as it has been shown that MUC1 could induce COX2 expression.

4. the level of serum KL-6 in the silicosis group was significantly decreased compared with the control group, while the level of KL-6 in the serum of the silica dust-exposed group was significantly increased

5. This study demonstrates that precise positioning of the causative mutation(s) and identification of other coding and noncoding sequence variants in autosomal dominant tubulointerstitial kidney -MUC1 is feasible. SMRT sequencing could provide a powerful tool to uncover potential factors encoded within the VNTR that associate with intra- and interfamilial phenotype variability of MUC1 related kidney disease.

6. The main genetic cause of autosomal dominant tubulointerstitial kidney disease in a Spanish cohort is a MUC1 pathogenic mutation.

7. A colon score derived from serum CEA, CA19-9, CK1 and MUC1 is a potential valuable non-invasive index that could be used for detection and screening early stage colon cancer patients

8. The suprachoroidal region of the eye comprises vascular channels, melanocytes, and thin fibroblasts with elongated cytoplasm that are positioned directly adjacent to the densely collagenous sclera. Granular, diffuse, and cytoplasmic EMA expression was seen in suprachoroidal fibroblasts, but this was not contiguous with the similar pattern of EMA expression in adjacent perineurium and arachnoid.

9. Calgranulin B and KL-6 in BAL proved to be reliable biomarkers of diopathic pulmonary fibrosis (IPF) and non-specific interstitial pneumonia (NSIP) and to have prognostic meaning, discriminating severe and advanced patients. The combination of the two biomarkers can facilitate the stratification of severity.

10. MUC1 is related to the occurrence and development of salivary gland acinic cell carcinoma

11. Baseline elevated serum KL-6 may predict deterioration of lung function of systemic sclerosis-interstitial lung disease patients with mild lung injury.

12. MUC1 expression is involved in accelerated growth of EMM1 cells.

13. These results suggest that certain proteins, such as MUC1, are selectively enriched in the exosome compartment. The mechanisms for their preferential localization and their biological roles remain to be studied

14. Through IL-11-STAT3/ERK signaling by upregulating MUC1.

15. this study shows that changes in serum KL-6 levels are associated with the development of chronic lung allograft dysfunction in lung transplant recipients

16. Interstitial lung disease patients with clubbing had lower oxygen levels, higher serum KL-6 levels, and lower pulmonary function than those without clubbing.

17. Mutated MUC1 (insC) affects vesicular transport in renal epithelial cells. It changes gene expression of vesicular transport-associated proteins, for example VTA1.

18. MUC1-C thereby contributes to the integration of PRC2 and PRC1-mediated repression of tumor suppressor genes, such as CDH1, CDKN2A, PTEN and BRCA1. Like PRC2 and PRC1, MUC1-C is associated with the epithelial-mesenchymal transition (EMT) program, cancer stem cell (CSC) state, and acquisition of anticancer drug resistance. [review]

19. MUC-1, CK7, and c-p27 immunostaining can be used as the predictive markers for esophageal cancer progression from Barrett's esophagus.

20. The CA 15-3 assay using 115D8-DF3 antibody pair is more suitable for monitoring therapy in pregnancy-associated breast cancer

Pig (Porcine) Mucin 1, Cell Surface Associated (MUC1) interaction partners

1. The results indicate that Muc1 gene is significantly associated with litter size in pigs.

2. Adhesion between Lactococcus lactis, the model for lactic acid bacteria (LAB) and mucins, is reported.

3. The epiblast expressed epithelial markers, MUC1 and E-CADHERIN, and the pluripotency markers, DNMT3B and CRIPTO.

Cow (Bovine) Mucin 1, Cell Surface Associated (MUC1) interaction partners

1. Endometrial expressions of MUC1 and cytokine genes differed among normal, fertile versus diseased, and subfertile dairy cows.

2. Bovine Muc1 prevents binding of bacteria to human intestinal cells and may have a role in preventing the binding of common enteropathogenic bacteria to human intestinal epithelial surfaces.

3. concluded that bovine Muc1 protein is probably an inducible innate immune effector and an important component of the first line of defense against bacterial invasion of epithelial surfaces

Mouse (Murine) Mucin 1, Cell Surface Associated (MUC1) interaction partners

1. Pseudomonas aeruginosa flagellin provokes NEU1-mediated airway shedding of MUC1-ectodomain, which functions as a decoy receptor protecting against lethal Pa lung infection.

2. The results showed that co-administration of an adjuvant plasmid and a DNA vaccine stimulated the production of higher titers of specific antibodies and a T cell response and suppressed the growth of subcutaneous tumors expressing MUC1.

3. these data showed that sustained abnormal MUC1 induction accompanies failing epithelial repair, chronic inflammation and kidney fibrosis. In conclusion, MUC1 exerts opposite effects during kidney response to IR: first protective and then harmful

4. MUC1 plays an important role in protection against severe pneumococcal disease, potentially mediated by facilitating macrophage phagocytosis.

5. this study implicates the MUC1 as a critical and dynamic component of the innate host response that limits the severity of influenza and provides the foundation for exploration of MUC1 in resolving inflammatory disease

6. Tumor growth delays observed by tumor irradiation combined with MVA-MUC1-IL-2 vaccine were significantly more prolonged than those observed by vaccine, radiation, or radiation with MVA empty vector.

7. Muc1 has anti-fibrotic properties in the mouse lung.

8. our data suggest a novel molecular mechanism by which tMUC1 may modulate NRP1-dependent VEGFR signaling in PDA cells.

9. Low expression of MUC1 is associated with lung carcinogenesis.

10. Using an extensive collection of novel murine cell lines we have identified distinct roles for Kras and Pten on MUC1 and EMT in vivo and in vitro. The data has implications for future design of combination therapies targeting Kras mutations, Pten deletions and MUC1 vaccines.

11. Gp91phox NADPH oxidase modulates litter size by up-regulating mucin1 expression in the uterus of mice.

12. In summary, we have demonstrated that MUC1 on immune cells is a novel regulator of the NLRP3 inflammasome, and propose this is mediated by an interaction with signalling components at the cytoplasmic domains of TLRs that involves inhibition of IRAK4 activation.

13. MUC1 regulates IL-1beta secretion induced by the NLRP3-activating bacteria Haemophilus influenzae but not bacteria that activate other inflammasomes.

14. Muc1 protection during acute kidney injury proceeds by enhancing both the HIF-1 and beta-catenin protective pathways.

15. MAMs MUC1 and MUC16 contribute to the maintenance of immune homeostasis at the ocular surface by limiting TLR-mediated innate immune responses.

16. the present study provides evidence that Muc1 is a direct target of let-7a and let-7b in mouse uteri during embryo implantation.

17. Anatomical site-specific Cre-loxP recombination throughout the genital tract of MUC1KrasPten mice leads to MUC1 positive genital tract tumors, and the development of these tumors is influenced by the anatomical environment

18. Muc1 clearly plays a significant role in enhancing the hypoxia-inducible transcription factors protective pathway during ischemic insult and recovery in kidney epithelia

19. Epithelial Muc1 is important for gastric mucosa healing by enhancing cell migration and proliferation.

20. the present study provides evidence that MUC1 is a direct target of miRNA-199a during embryo implantation.