ADAM Metallopeptidase with thrombospondin Type 1 Motif, 18 (ADAMTS18) ELISA Kits

Mouse (Murine) ADAM Metallopeptidase with thrombospondin Type 1 Motif, 18 (ADAMTS18) interaction partners

1. The underlying molecular mechanisms could be attributed in part to the abnormal vascular remodeling, including deficiency of carotid body (glomus) and aberrant carotid basal lamina. These results indicate a novel function of ADAMTS18 in vascular remodeling and associated thrombus formation.

2. Adamts18 deficiency enhances tumorigenesis and intestinal inflammation through elevated Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) and p38MAPK (show MAPK14 ELISA Kits)/ERK1/2 (show MAPK1/3 ELISA Kits) signaling and promotes colon cancer in a mouse model.

3. these data demonstrate a thrombin (show F2 ELISA Kits) cleavage site and confirm a short form of ADAMTS-18 presents in vivo.

4. Adamts18 is expressed in the lens and retina in the developing murine eye.

Human ADAM Metallopeptidase with thrombospondin Type 1 Motif, 18 (ADAMTS18) interaction partners

1. In summary, we demonstrate that ADAMTS18 silencing in breast cancer is significantly correlated with promoter CpG methylation. ADAMTS18 acts as an antagonist of AKT (show AKT1 ELISA Kits) and NF-kappaB (show NFKB1 ELISA Kits) signaling, further suppressing EMT (show ITK ELISA Kits) and metastasis of breast cancer cells.

2. This study showed that ADAMTS1 (show ADAMTS1 ELISA Kits), 8, and 18 are highly expressed in GC and its nodal metastases, suggesting important roles of these proteases in carcinogenesis and lymphatic metastasis. The findings from the present study indicate that these proteases may be promising candidates for novel and alternative treatments in GC (gastric cancer)

3. Studies suggest that ADAM metallopeptidase (show ECEL1 ELISA Kits) with thrombospondin type 1 motif, 18 protein (ADAMTS-18) as a promising diagnostic and therapeutic target.

4. Novel homozygous mutations in ADAMTS18 were identified, consisting of c.1067T>A [p.L356*] in the first proband, c.2159G>C [p.C720S] in the 2 affected brothers

5. Results suggest that ADAMTS18 plays an essential role in early eye development and that mutations therein cause a distinct eye phenotype that is mainly characterized by microcornea and myopia.

6. study reveals that mutations in the ADAMTS18 gene can cause a broad phenotypic spectrum of eye disorders and contribute to shed further light on the complexity of retinal diseases

7. the study identified ADAMTS18 as the only gene carrying a homozygous protein altering mutation.

8. ADAMTS18 mutations promote growth, migration, and metastasis in melanoma

9. ADAMTS18 gene methylation in 3 types of cancers was significantly higher than normal tissues. No significant association was found between methylation status & TNM staging. Epigenetic regulation of ADAMTS18 was associated with carcinogenesis.

10. comparison of the effects of C-terminal truncation on the GAG-binding properties and aggrecanase (show ADAMTS4 ELISA Kits) activity of ADAMTS-5 (show ADAMTS5 ELISA Kits) relative to three other ADAMTS (show ADAMTS13 ELISA Kits) family members, ADAMTS-9 (show ADAMTS9 ELISA Kits), ADAMTS-16 (show ADAMTS16 ELISA Kits) and ADAMTS-18