Results 71 to 80 of about 52,415 (197)
Microtubule-dependent nuclear-cytoplasmic shuttling of Runx2
RUNX/AML transcription factors are critical regulators of cell growth and differentiation in multiple lineages and have been linked to human cancers including acute myelogenous leukemia (RUNX1), as well as breast (RUNX2) and gastric cancers (RUNX3). RUNX
Lian, Jane B. +11 more
core +1 more source
Cleidocranial dysplasia (CCD; MIM 119600) is an autosomal dominant hereditary disorder of skeletal features whose characteristic clinical symptoms are caused by mutations in the RUNX2 gene. Varying degrees of clavicular hypoplasia and dental abnormalities are the most prominent features of this disorder.
L Z, Wu +5 more
openaire +2 more sources
Background/Aims: Esophageal carcinoma is a frequently occurring cancer at upper gastrointestinal tract. We aimed to evaluate the roles and possible mechanism of Runt Related Transcription Factor 2 (RUNX2) in the development of esophageal cancer. Methods:
Huibin Lu +6 more
doaj +1 more source
Background The Runt-related transcription factor Runx2 is essential for bone development but is also implicated in progression of several cancers of breast, prostate and bone, where it activates cancer-related genes and promotes invasive properties.
Tandon Manish +6 more
doaj +1 more source
RUNX2 promueve la progresión tumor en osteosarcoma [PDF]
Magíster en ciencias médicas, mención biología celularEl Osteosarcoma (OS) es el tumor sólido maligno más frecuente en la infancia y la adolescencia, corresponde al 20% de todos los tumores óseos y al 5% de los cánceres pediátricos.
Vega Villa, Óscar Andrés
core
Analysis of RUNX2 expression in SKOV3 cells.
A. Semi-quantitative duplex RT-PCR analysis of RUNX2 mRNA expression levels in the shRNA-RUNX2 clones 3 and 6, compared to the mock-transfected control clone. Displayed are images of representative results following sqRT-PCR analysis.
Stephane Gobeil (108928) +10 more
core +1 more source
Pin1-mediated Runx2 modification is critical for skeletal development
Runx2 is the master transcription factor for bone formation. Haploinsufficiency of RUNX2 is the genetic cause of cleidocranial dysplasia (CCD) that is characterized by hypoplastic clavicles and open fontanels.
Islam, Rabia +13 more
core +2 more sources
DNA methylation of the RUNX2 P1 promoter mediates MMP13 transcription in chondrocytes
The Runt-related transcription factor 2 (RUNX2) is critical for bone formation as well as chondrocyte maturation. Matrix metalloproteinase (MMP)-13 is a major contributor to cartilage degradation in osteoarthritis (OA).
Atsushi Takahashi +6 more
doaj +1 more source
Primary extraskeletal osteosarcoma of the omentum in a young dog
Extraskeletal osteosarcoma (EOSA) is a rare and aggressive mesenchymal neoplasm in dogs, primarily affecting older animals, with the spleen being the most common site of involvement.
João Pedro Sanches de Ávila +6 more
doaj +1 more source
BMP2 signaling and RUNX2 regulatory pathways converge for transcriptional control of bone formation in vivo. SMAD proteins are recruited to RUNX2 regulatory complexes via an overlapping nuclear matrix targeting signal/Smad interacting domain sequence ...
Pratap, Jitesh +19 more
core +1 more source

