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EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Microcephaly
Pancreatic ?-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes.
causal interaction
ongoing research
unassigned
4
2
0
Microcephaly
Mutations in the tRNA methyltransferase 1 gene TRMT1 cause congenital microcephaly, isolated inferior vermian hypoplasia and cystic leukomalacia in addition to intellectual disability.
unassigned
0
Microcephaly
tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly.
causal interaction
ongoing research
unassigned
4
1
0
Microcephaly
TRMT10A mutation in a child with diabetes, short stature, microcephaly and hypoplastic kidneys.
causal interaction
unassigned
3
0
Microcephaly
Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases.
causal interaction
unassigned
4
0
Neoplasms
Methyl-accepting RNA in 13762 mammary adenocarcinoma correlated with low adenine methyltransferase levels.
causal interaction
unassigned
2
0
Neoplasms
A human tRNA methyltransferase 9-like protein prevents tumour growth by regulating LIN9 and HIF1-?.
diagnostic usage
ongoing research
therapeutic application
unassigned
3
1
1
0
Neoplasms
A system of RNA modifications and biased codon use controls cellular stress response at the level of translation.
unassigned
0
Neoplasms
Somatic cancer mutations in the DNMT2 tRNA methyltransferase alter its catalytic properties.
causal interaction
diagnostic usage
ongoing research
unassigned
4
1
4
0
Neoplasms
tRNA Methyltransferase Defects and Intellectual Disability.
diagnostic usage
ongoing research
therapeutic application
unassigned
2
1
1
0
<< < Results 21 - 30 of 36 > >>