A5101442871- Genomic variations and chromosomal abnormalities
- Congenital heart defects research
- Cancer-related molecular mechanisms research
- Congenital Ear and Nasal Anomalies
- Circular RNAs in diseases
- Cellular transport and secretion
- Ocular Disorders and Treatments
- Hippo pathway signaling and YAP/TAZ
- RNA Research and Splicing
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Jining First People's Hospital
2018
Central South University
2012-2015
Second Xiangya Hospital of Central South University
2013-2015
Abstract SNHG20 is a novel lncRNA which has been showed to be overexpressed and functions as oncogenic in several types of human cancer. The role osteosarcoma still unknown. purpose our study was identify the clinical value biological function osteosarcoma. Our results indicated tissues cell lines compared with paired non‐tumor normal osteoblast line, respectively. Moreover, we observed high‐expression obviously associated Enneking stage, distant metastasis, histological grade. expression...
Chromosome region 10q22.3–q23.3 contains several low copy repeats (LCRs) and is prone to recombination. Deletions with breakpoints within LCR3 LCR4 have been described be associated intellectual disability dysmorphic features, while the reciprocal duplications are rarely reported. We present an additional case multiple congenital anomalies that include microcephaly, cardiac defect, mild disability, in which a de novo interstitial 8.2‐Mb duplication of 10q22.3–q23.3, including BMPR1A NGR3 ,...