EC Number   |
Disease |
PubMed ID  |
Title of Publication |
Category |
Confidence Level |
|---|
    1.3.1.70 | Liver Cirrhosis, Biliary |
2167346 |
Identification and characterization of autoantibodies against the nuclear envelope lamin B receptor from patients with primary biliary cirrhosis. |
ongoing research
unassigned |
4
0 |
| 1.3.1.70 | Liver Cirrhosis, Biliary |
8550049 |
Autoantibodies from patients with primary biliary cirrhosis recognize a region within the nucleoplasmic domain of inner nuclear membrane protein LBR. |
ongoing research
unassigned |
2
0 |
| 1.3.1.70 | Herpes Simplex |
11507226 |
Fate of the inner nuclear membrane protein lamin B receptor and nuclear lamins in herpes simplex virus type 1 infection. |
unassigned |
0 |
| 1.3.1.70 | Infections |
11507226 |
Fate of the inner nuclear membrane protein lamin B receptor and nuclear lamins in herpes simplex virus type 1 infection. |
unassigned |
0 |
| 1.3.1.70 | Chondrodysplasia Punctata |
11592808 |
Genetic disorders of cholesterol biosynthesis in mice and humans. |
unassigned |
0 |
| 1.3.1.70 | Metabolism, Inborn Errors |
11592808 |
Genetic disorders of cholesterol biosynthesis in mice and humans. |
unassigned |
0 |
| 1.3.1.70 | Mevalonate Kinase Deficiency |
11592808 |
Genetic disorders of cholesterol biosynthesis in mice and humans. |
unassigned |
0 |
| 1.3.1.70 | Herpes Simplex |
11866460 |
A three-residue signal confers localization of a reporter protein in the inner nuclear membrane. |
ongoing research
unassigned |
2
0 |
| 1.3.1.70 | Ichthyosis |
12490533 |
Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly. |
unassigned |
0 |
| 1.3.1.70 | Pelger-Huet Anomaly |
12490533 |
Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly. |
unassigned |
0 |
