Results 71 to 80 of about 69,808 (343)
Chromatin accessibility is critical for tumor development, whose mechanisms remain unclear. As a crucial regulator for chromatin remodeling, BRD4 promotes tumor progression by regulating multiple genes.
Si-Qi Zhou +15 more
semanticscholar +1 more source
Clear cell renal cell carcinoma (ccRCC) is one of the most common malignancies with rapid growth and high metastasis, but lacks effective therapeutic targets. Here, using public sequencing data analyses, quantitative real-time PCR assay, western blotting,
Chen-Yan Wu +5 more
semanticscholar +1 more source
Runx2/Sp7 double transgenic mice.
(A) X-ray analysis of lower limb bones from a wild-type mouse (wt), Runx2 transgenic mouse (Runx2), Sp7 transgenic mouse (Sp7), and Runx2/Sp7 double transgenic mouse (Runx2/Sp7) at 6 weeks of age.
Hiroshi Kawaguchi (33997) +15 more
core +1 more source
Antagonistic Functions of USAG-1 and RUNX2 during Tooth Development [PDF]
Supernumerary teeth and tooth agenesis are common morphological anomalies in humans. We previously obtained evidence that supernumerary maxillary incisors form as a result of the successive development of the rudimentary maxillary incisor tooth germ in ...
Mary MacDougall +38 more
core +2 more sources
RUNX2-modifying enzymes: therapeutic targets for bone diseases
RUNX2 is a master transcription factor of osteoblast differentiation. RUNX2 expression in the bone and osteogenic front of a suture is crucial for cranial suture closure and membranous bone morphogenesis.
Woo-Jin Kim +4 more
semanticscholar +1 more source
The phenotypes of Usag-1+/+/Runx2+/+, Usag-1+/+/Runx2-/-, Usag-1-/-/Runx2+/+ and Usag-1-/-/Runx2-/- mice at E15 and P0.
Kazuyuki Saito (506650) +12 more
core +1 more source
The role of miR‐335‐5p in the redifferentiation of BRAF p.V600E thyroid cancers
The BRAF p.V600E mutation promotes thyroid cancer dedifferentiation and radioiodine resistance. Using a network approach, we identified miR‐335‐5p as a key regulator of BRAF‐mutated thyroid tumors. Restoring miR‐335‐5p increased thyroid‐specific gene expression and iodine uptake in cells and organoids.
Valeria Pecce +11 more
wiley +1 more source
La displasia cleidocraneal (OMIM #119600) es una osteocondrodisplasia de herencia autosómica dominante debida a una mutación en heterocigosis en el gen RUNX2. Su prevalencia es 1 en 1.000.000 individuos.
Nolis Camacho-Camargo +4 more
doaj +1 more source
Identification of the hub genes RUNX2 and FN1 in gastric cancer
This study identified key genes in gastric cancer (GC) based on the mRNA microarray GSE19826 from the Gene Expression Omnibus (GEO) database and preliminarily explored the relationships among the key genes.
Han Chao +5 more
doaj +1 more source
Inducible regulation of Runx2-stimulated osteogenesis [PDF]
Ex vivo gene therapy is a promising approach to orthopedic regenerative medicine. These strategies typically focus on the constitutive overexpression of osteogenic factors to induce osteoblastic differentiation and matrix mineralization. However, the unregulated production of osteoinductive molecules has also resulted in abnormal bone formation and ...
C A, Gersbach +3 more
openaire +2 more sources

