10644717 |
Characterization of a novel human serine protease that has extensive homology to bacterial heat shock endoprotease HtrA and is regulated by kidney ischemia. |
10873535 |
Expression, purification, and functional analysis of the human serine protease HtrA2. |
10971580 |
Characterization of human HtrA2, a novel serine protease involved in the mammalian cellular stress response. |
10995577 |
Tissue-specific splicing of Omi stress-regulated endoprotease leads to an inactive protease with a modified PDZ motif. |
11583623 |
A serine protease, HtrA2, is released from the mitochondria and interacts with XIAP, inducing cell death. |
11967569 |
Structural insights into the pro-apoptotic function of mitochondrial serine protease HtrA2/Omi. |
15200957 |
Dual role of BRUCE as an antiapoptotic IAP and a chimeric E2/E3 ubiquitin ligase. |
15489334 |
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |
15815621 |
Generation and annotation of the DNA sequences of human chromosomes 2 and 4. |
15961413 |
Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease. |
18364387 |
Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls. |
18401856 |
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease. |
19502560 |
THAP5 is a human cardiac-specific inhibitor of cell cycle that is cleaved by the proapoptotic Omi/HtrA2 protease during cell death. |
21269460 |
Initial characterization of the human central proteome. |
24275569 |
An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome. |
25422467 |
Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease. |
25944712 |
N-terminome analysis of the human mitochondrial proteome. |
27208207 |
Deficiency of HTRA2/Omi is associated with infantile neurodegeneration and 3-methylglutaconic aciduria. |
27535533 |
Analysis of protein-coding genetic variation in 60,706 humans. |
27696117 |
Pathogenic variants in HTRA2 cause an early-onset mitochondrial syndrome associated with 3-methylglutaconic aciduria. |