| Models Name |
Cat.No. |
Animal Type |
Disease Area |
|
Congenital adrenal hyperplasia, Cyp21a1 knockout/xenograft (Fibroblasts (CYP21A-overexpressing)), in mouse
|
AB227627 |
mouse |
Congenital adrenal hyperplasia |
|
Congenital muscular dystrophy, Lama2 knockout, in mouse
|
AB227628 |
mouse |
Congenital muscular dystrophy |
|
Congenital myasthenic syndrome, Colq knockout, in mouse
|
AB227629 |
mouse |
Congenital myasthenic syndrome |
|
Congenital myasthenic syndrome, transgenic (CHRNB1), in mouse
|
AB227630 |
mouse |
Congenital myasthenic syndrome |
|
Congenital stationary night blindness, Cacna1f mutated, in mouse
|
AB227631 |
mouse |
Congenital stationary night blindness |
|
Conjunctival disorders, allograft (T-lymphocytes (CD4+) (spleen), mouse)/conjunctival dissection-induced, in SCID mouse
|
AB227632 |
mouse |
Conjunctival and scleral disorders |
|
Conjunctival disorders, allograft (T-lymphocytes (spleen), mouse (CD8a+))/conjunctival dissection-induced, in SCID mouse
|
AB227633 |
mouse |
Conjunctival and scleral disorders |
|
Constipation, high-fat diet-induced, in mouse
|
AB227634 |
mouse |
Constipation |
|
Constipation, low-fiber diet-induced, in mouse
|
AB227635 |
mouse |
Constipation |
|
Craniosynostosis, Prrx1 knockout, in mouse
|
AB227636 |
mouse |
Craniosynostosis |