Explore your search results using the filter checkboxes, or amend your search or start a new search.
| Attachment | Size |
|---|---|
| Genetic diversity of vector_borne pathogens in spotted and brown hyenas.pdf | 1.93 MB |
| Attachment | Size |
|---|---|
| Communication hubs of an asocial cat are the source of a human_carnivore conflict and key to its solution.pdf | 460 KB |
| Attachment | Size |
|---|---|
| Species_specific differences in Toxoplasma gondii_Neospora caninum and Besnoitia besnoiti seroprevalence in Namibian wildlife.pdf | 416.2 KB |
| Attachment | Size |
|---|---|
| Differences in Toxoplasma gondii_Neospora caninum and Besnoitia besnoiti seroprevalence in Namibian wildlife.pdf | 1.59 MB |
| Attachment | Size |
|---|---|
| Long_term data reveal two distinct male spatial tactics at different life_history stages in Namibian cheetahs.pdf | 529.53 KB |
| Attachment | Size |
|---|---|
| Feliform carnivores have a distinguished constitutive innate immune response.pdf | 597.59 KB |
| Attachment | Size |
|---|---|
| Benign Pigmented Dermal Basal Cell Tumor in a Namibian Cheetah.pdf | 501.98 KB |
| Attachment | Size |
|---|---|
| Cheetahs have a stronger constitutive innate immunity than leopards.pdf | 1.02 MB |
| Attachment | Size |
|---|---|
| Comparative Serum Fatty Acid Profiles of Captive and Free_Ranging Cheetahs.pdf | 197.38 KB |