These animals have been shown to develop normally; the expressed antibody repertoire largely mirrors that in humans.
Apparently it is made from rapeseed, which is supposedly highly toxic and has been shown to develop cancer in rats.
ES cell-derived neural precursors have been shown to develop into morphologically mature neurons and glia when grafted into brain and spinal cord.
Cytochromes c3 are polyheme c-type cytochromes characterized by low redox potentials, that have been shown to develop metal-reductase activity.
While large doses of the chemical, are known to cause nerve damage in people, acrylamide is deemed "a probable" human carcinogen by the Environmental Protection Agency because only rodents have been shown to develop tumors from exposure to it.
However, IFNs are species-specific and antibodies have been shown to develop in response to the high rHuIFN-α doses necessary for an effective therapy.
"Animal-Animal" chimeric embryos have been shown to develop into a target organ by using blastocyst complementation (Kobayashi et al. 2010; Matsunari et al. 2013).
In addition, up to 41% of EVAR patients have been shown to develop post-procedural complications, with 20% subsequently requiring fluoroscopically based radiological re-intervention [1].
Similarly, children with IL-12 receptor β1 (IL-12Rβ1) deficiency have been shown to develop the severe form of TB, frequently [13].
While orthopedic trauma patients have been shown to develop greater rates of adverse events, no study has examined septic complications in isolation from other less serious conditions.
Animal models of serum sickness, a circulating immune complex disease, have been shown to develop cellular infiltrates in the uvea [7].
