UPSpace Home
→
University of Pretoria: Research Output
→
Research Articles (University of Pretoria)
→
Browsing Research Articles (University of Pretoria) by Author

Browsing Research Articles (University of Pretoria) by Author "Labuschagne, Christiaan"

Now showing items 1-4 of 4

Characterisation of staphylococci isolated from milk samples of a water buffalo herd

Labuschagne, Christiaan; Karzis, Joanne; Britz, Hans; Petzer, Inge-Marie (MDPI, 2022-11-12)

Water buffalo produce a tenth of milk for global human consumption. Non-aureus staphylococci (NAS) are among the most commonly isolated bacteria from mastitis in water buffalo and dairy cows. These results described the ...
A premature stop codon in the CYP2C19 gene may explain the unexpected sensitivity of vultures to diclofenac toxicity

Adawaren, Emmanuel Oluwasegun; Labuschagne, Christiaan; Abera, Aron B.; Naidoo, Vinny (Elsevier, 2024-01)

The unintended environmental exposure of vultures to diclofenac has resulted in the deaths of millions of old-world vultures on the Asian subcontinent. While toxicity has been since associated with a long half-life of ...
Species identification and cow risks of non-aureus staphylococci from South African dairy herds

Petzer, Inge-Marie; Labuschagne, Christiaan; Phophi, Lufuno; Karzis, Joanne (AOSIS OpenJournals, 2022-07-27)

Detailed information on specific species of non-aureus staphylococci (NAS) has become a necessity for effective udder health control programs in South Africa. The main objective of this preliminary study was to identify ...
Spectrum of MYO7A mutations in an indigenous South African population further elucidates the nonsyndromic autosomal recessive phenotype of DFNB2 to include both homozygous and compound heterozygous mutations

Kabahuma, Rosemary Ida; Schubert, Wolf-Dieter; Labuschagne, Christiaan; Yan, Denise; Blanton, Susan Halloran; Pepper, Michael Sean; Liu, Xue Zhong (MDPI, 2021-02-15)

MYO7A gene encodes unconventional myosin VIIA, which, when mutated, causes a phenotypic spectrum ranging from recessive hearing loss DFNB2 to deaf-blindness, Usher Type 1B (USH1B). MYO7A mutations are reported in nine DFNB2 ...

Now showing items 1-4 of 4

Search UPSpace

Advanced Search

Browse

All of UPSpace
This Collection
- Issue Date
- Authors
- Titles
- Subjects
- Supervisor
- UP Author
- UP Postgraduate
- Type

Browsing Research Articles (University of Pretoria) by Author "Labuschagne, Christiaan"

Browsing Research Articles (University of Pretoria) by Author "Labuschagne, Christiaan"

Search UPSpace

Browse

All of UPSpace

This Collection

My Account

UPSpace Workspace