Any feedback?
Please rate this page
(search_result.php)
(0/150)

BRENDA support

Refine search

Search Disease/ Diagnostics

show results
Refine your search

Search term:

Results 1 - 10 of 36 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Bacterial Infections 22509481 Crystal structure of peptidyl-tRNA hydrolase from mycobacterium smegmatis reveals novel features related to enzyme dynamics. unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Carcinoma 29328466 Knockdown of immature colon carcinoma transcript 1 induces suppression of proliferation, S-phase arrest and apoptosis in leukemia cells. unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Colonic Neoplasms 31257922 High ANKZF1 expression is associated with poor overall survival and recurrence-free survival in colon cancer. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
4
2
1
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Colorectal Neoplasms 31257922 High ANKZF1 expression is associated with poor overall survival and recurrence-free survival in colon cancer. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
4
2
1
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Infections 16849786 Peptidyl-tRNA hydrolase and its critical role in protein biosynthesis. unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Intellectual Disability 27753167 PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Intellectual Disability 29143421 PTRHD1 and possibly ADORA1 mutations contribute to Parkinsonism with intellectual disability. unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Intellectual Disability 30398675 PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disability. causal interaction
unassigned
1
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Intellectual Disability 33004232 Lack of PTRHD1 mutation in patients with young-onset and familial Parkinson's disease in a Taiwanese population. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.1.29Lyme Disease 8635758 Microbial genes homologous to the peptidyl-tRNA hydrolase-encoding gene of Escherichia coli. unassigned 0
Results 1 - 10 of 36 > >>