Cookies on VetMed Resource

Like most websites we use cookies. This is to ensure that we give you the best experience possible.

 

Continuing to use www.cabi.org  means you agree to our use of cookies. If you would like to, you can learn more about the cookies we use.

VetMed Resource

Veterinary information to support practice, based on evidence and continuing education

Sign up to receive our Veterinary & Animal Sciences e-newsletter, book alerts and offers direct to your inbox.

Results per page:

Search results

Abstract

Canine progressive rod-cone degeneration (PRCD) is a middle- to late-onset, autosomal recessive, inherited retinal disorder caused by a substitution (c.5 G > A) in the canine PRCD gene that has been identified in 29 or more purebred dogs. In the present study, a TaqMan probe-based real-time PCR...

Author(s)
Kohyama, M.; Tada, N.; Mitsui, H.; Tomioka, H.; Tsutsui, T.; Yabuki, A.; Rahman, M. M.; Kushida, K.; Mizukami, K.; Yamato, O.
Publisher
Japanese Society of Veterinary Science, Tokyo, Japan
Citation
Journal of Veterinary Medical Science, 2016, 78, 3, pp 481-484
Abstract

The effective elastic modulus, yield strength, yield strain, ultimate strength, ultimate strain, strain energy density at yield and strain energy density at ultimate failure of femoral diaphyseal cortical bone were investigated on canine femurs. Four femurs representative of the canine population...

Author(s)
Autefage, A.; Palierne, S.; Charron, C.; Swider, P.
Publisher
Elsevier Ltd, Oxford, UK
Citation
Veterinary Journal, 2012, 194, 2, pp 202-209
Abstract

In a genetically heterogenous French breed, 181 individuals (105 females, 76 males; 146 miniature poodles, 32 standards, 2 toy and 1 giant), aged from 0.5 to 14 years, underwent an ophthalmological examination to look for cataract lesions. Electroretinography (ERG) has been performed to identify...

Author(s)
Chaudieu, G.
Publisher
Elsevier Masson, Issy-les Moulineaux Cedex, France
Citation
Revue Vétérinaire Clinique, 2019, 54, 2, pp 69-77
Abstract

GM2 gangliosidosis variant 0 (Sandhoff disease, SD) is a fatal, progressive neurodegenerative lysosomal storage disease caused by mutations of the HEXB gene. In canine SD, a pathogenic mutation (c.283delG) of the canine HEXB gene has been identified in toy poodles. In the present study, a TaqMan...

Author(s)
Rahman, M. M.; Yabuki, A.; Kohyama, M.; Mitani, S.; Mizukami, K.; Uddin, M. M.; Chang HyeSook; Kushida, K.; Kishimoto, M.; Yamabe, R.; Yamato, O.
Publisher
Japanese Society of Veterinary Science, Tokyo, Japan
Citation
Journal of Veterinary Medical Science, 2014, 76, 2, pp 295-299
Abstract

The intestinal microbiota was revealed with the recent advances in molecular techniques, such as high-throughput sequencing analysis. As a result, the microbial changes are thought to influence the health of humans and animals and such changes are affected by several factors including diet,...

Author(s)
Omatsu, T.; Omura, M.; Katayama, Y.; Kimura, T.; Okumura, M.; Okumura, A.; Murata, Y.; Mizutani, T.
Publisher
Japanese Society of Veterinary Science, Tokyo, Japan
Citation
Journal of Veterinary Medical Science, 2018, 80, 5, pp 749-754
Abstract

GM2 gangliosidosis variant 0 (Sandhoff disease, SD) is a fatal, progressive neurodegenerative lysosomal storage disease caused by mutations in the HEXB gene. Toy poodles recently were reported as the second breed of dog with SD. The present paper describes the molecular defect of this canine SD as...

Author(s)
Rahman, M. M.; Chang HyeSook; Mizukami, K.; Hossain, M. A.; Yabuki, A.; Tamura, S.; Kitagawa, M.; Mitani, S.; Higo, T.; Uddin, M. M.; Uchida, K.; Yamato, O.
Publisher
Elsevier Ltd, Oxford, UK
Citation
Veterinary Journal, 2012, 194, 3, pp 412-416
Abstract

Differences in the distribution of single nucleotide polymorphisms (SNPs) and haplotypes in the estrogen receptor α gene (ESR1) were examined in Miniature Dachshunds (n=48), Chihuahuas (n=20) and Toy Poodles (n=18). Five DNA fragments located in the 40-kb region at the 3′ end of ESR1 were amplified ...

Author(s)
Pathirana, I. N.; Tanaka, K.; Kawate, N.; Tsuji, M.; Hatoya, S.; Inaba, T.; Tamada, H.
Publisher
Wiley-Blackwell, Melbourne, Australia
Citation
Animal Science Journal, 2011, 82, 3, pp 390-395
Abstract

Much of the research on pedigree dog breeding has been directed towards understanding the implications of reduced genetic diversity and the prevalence of inherited disorders. An example is the potential role of the popular sire effect in perpetuating genetic defects. If male dogs are more likely...

Author(s)
Wilson, B. J.; Kasbarian, A. J.; Dhand, N.; McGreevy, P. D.
Publisher
MDPI AG, Basel, Switzerland
Citation
Animals, 2018, 8, 12, pp 240
Abstract

Canine primary hypoplasia of the portal vein (PHPV) is a microscopic malformation of the hepatic vasculature. The prevalence, clinical signs, and clinicopathological findings of PHPV in dogs are unclear, because there are few reports concerning PHPV in the veterinary literature. This retrospective...

Author(s)
Akiyoshi, M.; Hisasue, M.; Akiyoshi, M.
Publisher
Frontiers Media S.A., Lausanne, Switzerland
Citation
Frontiers in Veterinary Science, 2017, 4, December, pp 224
Abstract

Patellar luxation (PL) is one of the most common orthopedic disorders in dogs and a genetic factor is considered to play an important role in the development of PL. Genomic analysis has attempted to identify the genetic markers associated with the development of PL but only suggestive markers have...

Author(s)
Maeda, K.; Inoue, M.; Tanaka, M.; Momozawa, Y.
Publisher
Japanese Society of Veterinary Science, Tokyo, Japan
Citation
Journal of Veterinary Medical Science, 2019, 81, 4, pp 532-537

Refine Results

Sort Order
Author
Geographical Location
Item Type
Language
Organisms
Subject Topics