2006
DOI: 10.3168/jds.s0022-0302(06)72219-6
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Endoscopic Examination and Tissue Sampling of the Bovine Teat and Udder Cistern

Abstract: The aim of this study was to evaluate the application of an endoscopic technique to investigate the teat and udder cisterns of the bovine mammary gland, and to biopsy tissues within the cisterns. An anesthetic protocol for application in standing animals was designed, using a combination of general and local anesthesia. Individual quarter milk production (QMP), quarter somatic cell count (SCC), and occurrence of new intramammary infection were assessed after application of the technique, and possible applicati… Show more

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Cited by 7 publications
(2 citation statements)
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“…In addition, they do not provide opportunities for multiple sampling, to perform longitudinal studies and follow-up on local epithelial changes at the early stages of infection. An alternative is to use endoscopic techniques for the collection of fresh MG biopsies (Vangroenweghe et al, 2006;VanKlompenberg et al, 2012). However, with such techniques, it is difficult to collect biopsy samples from the alveolar tissue in the upper part of the MG Validation of RNA isolated from milk fat globules to profile mammary epithelial cell expression during lactation and transcriptional response to a bacterial infection P. Brenaut ,* R. Bangera , † C. Bevilacqua ,* ‡ E. Rebours ,* ‡ C. Cebo ,* and P. Martin * ‡ 1 6131 rich in secretory parenchyma.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, they do not provide opportunities for multiple sampling, to perform longitudinal studies and follow-up on local epithelial changes at the early stages of infection. An alternative is to use endoscopic techniques for the collection of fresh MG biopsies (Vangroenweghe et al, 2006;VanKlompenberg et al, 2012). However, with such techniques, it is difficult to collect biopsy samples from the alveolar tissue in the upper part of the MG Validation of RNA isolated from milk fat globules to profile mammary epithelial cell expression during lactation and transcriptional response to a bacterial infection P. Brenaut ,* R. Bangera , † C. Bevilacqua ,* ‡ E. Rebours ,* ‡ C. Cebo ,* and P. Martin * ‡ 1 6131 rich in secretory parenchyma.…”
Section: Introductionmentioning
confidence: 99%
“…By using conventional PCR, it is possible to identify genes in small samples (Vangroenweghe et al, 2006), but by using real-time PCR, it is possible to quantify genes in small quantities of tissue or in a limited number of cells. Real-time PCR also has the potential to quantify rare transcripts (Bustin, 2000;Goossens et al, 2005).…”
mentioning
confidence: 99%