EC Number   |
Disease   |
PubMed ID   |
Title of Publication   |
Category |
Confidence Level |
|---|
  2.4.1.25 | 4-alpha-glucanotransferase deficiency |
10444083 |
Biochemical characterization of the chlamydomonas reinhardtii alpha-1,4 glucanotransferase supports a direct function in amylopectin biosynthesis |
unassigned |
0 |
  2.4.1.25 | Anemia, Hypochromic |
19946617 |
Blocking the metabolism of starch breakdown products in Arabidopsis leaves triggers chloroplast degradation. |
causal interaction |
1 |
  2.4.1.25 | Anemia, Hypochromic |
19946617 |
Blocking the metabolism of starch breakdown products in Arabidopsis leaves triggers chloroplast degradation. |
therapeutic application |
1 |
  2.4.1.25 | Anemia, Hypochromic |
19946617 |
Blocking the metabolism of starch breakdown products in Arabidopsis leaves triggers chloroplast degradation. |
unassigned |
0 |
  2.4.1.25 | Carcinoma |
16612594 |
Co-expression of alpha(1,3)galactosyltransferase and Bacillus thuringiensis PIPLC enhances hyperacute rejection of tumor cells. |
therapeutic application |
1 |
  2.4.1.25 | Carcinoma |
16612594 |
Co-expression of alpha(1,3)galactosyltransferase and Bacillus thuringiensis PIPLC enhances hyperacute rejection of tumor cells. |
ongoing research |
4 |
  2.4.1.25 | Carcinoma |
16612594 |
Co-expression of alpha(1,3)galactosyltransferase and Bacillus thuringiensis PIPLC enhances hyperacute rejection of tumor cells. |
unassigned |
0 |
  2.4.1.25 | Glycogen Storage Disease |
11977176 |
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean area. |
causal interaction |
3 |
  2.4.1.25 | Glycogen Storage Disease |
12442284 |
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGL. |
causal interaction |
3 |
  2.4.1.25 | Glycogen Storage Disease |
24257475 |
A mutation analysis of the AGL gene in Korean patients with glycogen storage disease type III. |
causal interaction |
3 |