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Abstract

Author(s)
Gough, A.
Publisher
Veterinary Business Development Ltd, Peterborough, UK
Citation
Veterinary Times, 2017, 47, 21, pp 23
Abstract

Background: Molecular genetics has made significant advances in the analysis of hereditary dermatoses during the last several years. Objectives: To provide an update on currently available genetic tests for skin diseases of dogs, cats and horses, and to aid the veterinary clinician in the...

Author(s)
Leeb, T.; Müller, E. J.; Roosje, P.; Welle, M.
Publisher
Wiley, Oxford, UK
Citation
Veterinary Dermatology, 2017, 28, 1, pp e1
Abstract

Background: Spinocerebellar ataxia also referred to as hereditary ataxia comprises different forms of progressive neurodegenerative diseases. A complex mode of inheritance was most likely in Parson Russell Terriers (PRT) and in Jack Russell Terriers (JRT). Recently, the missense mutation ...

Author(s)
Gast, A. C.; Metzger, J.; Tipold, A.; Distl, O.
Publisher
BioMed Central Ltd, London, UK
Citation
BMC Veterinary Research, 2016, 12, 225, pp (10 October 2016)
Abstract

Background: Cerebellar cortical degeneration (CCD) is an increasingly recognised neurodegenerative disease process affecting many dog breeds. Typical presentation consists of a progressive cerebellar ataxia, with a variable age at onset and rate of progression between different breeds. Cerebellar...

Author(s)
Fenn, J.; Boursnell, M.; Hitti, R. J.; Jenkins, C. A.; Terry, R. L.; Priestnall, S. L.; Kenny, P. J.; Mellersh, C. S.; Forman, O. P.
Publisher
BioMed Central Ltd, London, UK
Citation
BMC Genetics, 2016, 17, 123, pp (26 August 2016)
Abstract

This study aimed to investigate the association between cystine uroliths and gene mutations in 24 English Bulldogs in Italy with or without clinical signs of urinary tract diseases [date not given]. The DNA test showed an association between mutations in the SLC3A1 and SLC7A9 genes and the presence ...

Author(s)
Ruggerone, B.; Marelli, S. P.; Scarpa, P.; Polli, M.
Publisher
BMJ Publishing Group, London, UK
Citation
Veterinary Record, 2016, 179, 7, pp 174
Abstract

Background: Neuronal ceroid lipofuscinosis (NCL), a fatal neurodegenerative disease, has been diagnosed in young adult Australian Cattle Dogs. Objective: Characterize the Australian Cattle Dog form of NCL and determine its molecular genetic cause. Animals: Tissues from 4 Australian Cattle Dogs with ...

Author(s)
Kolicheski, A.; Johnson, G. S.; O'Brien, D. P.; Mhlanga-Mutangadura, T.; Gilliam, D.; Guo, J.; Anderson-Sieg, T. D.; Schnabel, R. D.; Taylor, J. F.; Lebowitz, A.; Swanson, B.; Hicks, D.; Niman, Z. E.; Wininger, F. A.; Carpentier, M. C.; Katz, M. L.
Publisher
Wiley-Blackwell, Boston, USA
Citation
Journal of Veterinary Internal Medicine, 2016, 30, 4, pp 1149-1158
Abstract

Identification of genetic mutations causing disease is helpful in breeding programmes aimed at enhancing the qualities of a breed. The ceský fousek (CF), also known as the Bohemian wirehaired pointing griffon, is a versatile hunting dog that dates back to the 14th century. Because no genetic...

Author(s)
Shaffer, L. G.; Ramirez, C. J.; Sundin, K.; Connell, L. B.; Ballif, B. C.
Publisher
BMJ Publishing Group, London, UK
Citation
Veterinary Record Case Reports, 2016, 4, 2, pp e000346
Abstract

Background: A variety of presumed hereditary, neurologic diseases have been reported in young Rottweilers. Overlapping ages of onset and clinical signs have made antemortem diagnosis difficult. One of these diseases, neuronal vacuolation and spinocerebellar degeneration (NVSD) shares clinical and...

Author(s)
Mhlanga-Mutangadura, T.; Johnson, G. S.; Ashwini, A.; Shelton, G. D.; Wennogle, S. A.; Johnson, G. C.; Kuroki, K.; O'Brien, D. P.
Publisher
Wiley-Blackwell, Boston, USA
Citation
Journal of Veterinary Internal Medicine, 2016, 30, 3, pp 813-818
Abstract

Objective: The purpose of this study was to investigate the inheritance and phenotype of retinal dysplasia (RD) in the American pit bull terrier. Animals Studied: A breeding colony established from a single female pure-bred American pit bull terrier dog with RD. Procedures: A female pure-bred...

Author(s)
Rodarte-Almeida, A. C. V.; Petersen-Jones, S.; Langohr, I. M.; Occelli, L.; Dornbusch, P. T.; Shiokawa, N.; Montiani-Ferreira, F.
Publisher
Wiley-Blackwell, Oxford, UK
Citation
Veterinary Ophthalmology, 2016, 19, 1, pp 11-21
Abstract

Although deafness can be acquired throughout an animal's life from a variety of causes, hereditary deafness, especially congenital hereditary deafness, is a significant problem in several species. Extensive reviews exist of the genetics of deafness in humans and mice, but not for deafness in...

Author(s)
Strain, G. M.
Publisher
Frontiers Media S.A., Lausanne, Switzerland
Citation
Frontiers in Veterinary Science, 2015, 2, September, pp 29

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