scholarly journals Identification of Novel "Pathologs" (Human Disease-Related Gene Candidates) From the RIKEN Full-Length Mouse cDNA Data Set

2003 ◽  
Vol 13 (6) ◽  
pp. 1559-1559
Author(s):  
D. G. Silva
2019 ◽  
Vol 119 ◽  
pp. S10
Author(s):  
A.C. Bretz ◽  
G. Streubel ◽  
U. Parnitzke ◽  
M. Borgmann ◽  
S. Hamm

iScience ◽  
2021 ◽  
Vol 24 (4) ◽  
pp. 102357
Author(s):  
Brenda Morsey ◽  
Meng Niu ◽  
Shetty Ravi Dyavar ◽  
Courtney V. Fletcher ◽  
Benjamin G. Lamberty ◽  
...  

2011 ◽  
pp. OR30-3-OR30-3 ◽  
Author(s):  
Emi Ishida ◽  
Koshi Hashimoto ◽  
Atsushi Ozawa ◽  
Nobuyuki Shibusawa ◽  
Tetsurou Satoh ◽  
...  

2021 ◽  
Vol 11 ◽  
Author(s):  
Yan Qiu ◽  
Min Pan ◽  
Xuemei Chen

ObjectiveThe aim of the present study was to construct and test a liquid-liquid phase separation (LLPS)-related gene signature as a prognostic tool for epithelial ovarian cancer (EOC).Materials and MethodsThe data set GSE26712 was used to screen the differentially expressed LLPS-related genes. Functional enrichment analysis was performed to reveal the potential biological functions. GSE17260 and GSE32062 were combined as the discovery to construct an LLPS-related gene signature through a three-step analysis (univariate Cox, least absolute shrinkage and selection operator, and multivariate Cox analyses). The EOC data set from The Cancer Genome Atlas as the test set was used to test the LLPS-related gene signature.ResultsThe differentially expressed LLPS-related genes involved in several cancer-related pathways, such as MAPK signaling pathway, cell cycle, and DNA replication. Eleven genes were selected to construct the LLPS-related gene signature risk index as prognostic biomarker for EOC. The risk index could successfully divide patients with EOC into high- and low-risk groups. The patients in high-risk group had significantly shorter overall survival than those with in low-risk group. The LLPS-related gene signature was validated in the test set and may be an independent prognostic factor compared to routine clinical features.ConclusionWe constructed and validated an LLPS-related gene signature as a prognosis tool in EOC through integrated analysis of multiple data sets.


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