Displaying results 21 - 30 of 30 items found.

21. Identifying Genes Regulating Addison's Disease in the Portuguese Water Dog (PWD)

(Web Page; Wed Aug 21 09:05:00 CDT 2019)

None at this time.


Addison's disease, or primary adrenocortical insufficiency, is characterized by destruction of the adrenal cortex, resulting in the inability to produce cortisone when stimulated with the hormone ACTH. In Portuguese Water Dogs (PWDs), this disease occurs with a frequency of 1-2 percent, and is a heritable autoimmune disease of low penetrance, caused by several interacting genes. Using both new and existing data, we propose to identify regions of the PWD genome that contain genes regulating the frequency of Addison's disease. Within those large regions we propose to identify the specific DNA sequence variants that are associated with Addison's. To date we have obtained DNA from about 90 Addisonian PWDs, as well as a number of unaffected PWDs, for which no family history of Addison's is reported. We have already identified two genomic regions, on canine chromosomes 12 and 37, that appear to be associated with the disease. To identify candidate genes, we will make selections using the newly available canine genome sequence, as well as the more detailed human genome sequence. Once affected gene disease frequency is identified, our long term hope is that prognostic tests can be developed that will aid breeders in selecting the most genetically compatible dogs for future breeding.

22. Identification and Inheritance of DNA Markers for Addison's Disease

(Web Page; Fri Aug 16 10:21:00 CDT 2019)

Famula, T. R., Belanger, J. M., & Oberbauer, A. M. (2003). Heritability and complex segregation analysis of hypoadrenocorticism in the Standard Poodle. Journal of Small Animal Practice, 44(1), 8–12. https://doi.org/10.1111/j.17...


The study found that Addison's Disease (AD), the late-onset failure of adrenal gland function, is clearly inherited and appears to be regulated by a single gene that is inherited as an autosomal recessive. Researchers collected DNA samples and pedigrees from 390 Bearded Collies, 533 Standard Poodles and 167 Leonbergers. The samples were from both affected and non-affected dogs. Not enough affected Leonbergers were found, so research could not be completed for this breed. Researchers found that AD equally affects males and females; contrary to the bias in the literature, which stated that females were primarily affected. They also found that the coat color of the dog was not relevant. This study has provided the basis for an important next step: scientists will start screening DNA for a genetic marker. Once that marker is found, a DNA test to determine carriers for the disease can be developed.

23. Examining Hypoadrenocorticism in Nova Scotia Duck Tolling Retrievers Utilizing Whole Genome SNP Association

(Web Page; Fri Aug 16 10:21:00 CDT 2019)

Hughes, A. M., Bannasch, D. L., Kellett, K., & Oberbauer, A. M. (2011). Examination of candidate genes for hypoadrenocorticism in Nova Scotia Duck Tolling Retrievers. The Veterinary Journal, 187(2), 212–216. https://doi.org/10....


Background: Canine Addison's disease is a dog's inability to produce one or two hormones due to a deficiency of corticosteriods and mineralocorticoids produced by the adrenal glands. In Nova Scotia Duck Tolling Retrievers (NSDTRs) this disorder is much more common than in the general dog population and is inherited. While genetic studies of NSDTRs with Addison's disease have excluded many candidate genes, researchers are still in search of the causative mutations. Objective: This study is extensively examining the entire canine genome utilizing state-of-the-art technologies in search of areas that are associated with this disease in NSDTRs.

24. 2007 Annual Report

(File; Thu Oct 28 10:17:00 CDT 2010)

2007 Annual Reporttableof contentsLetter from the President2Board of Directors3Mission & Goals4Alliances5American Kennel ClubNestlé Purina PetCare CompanyResearch6-9Education, Communications & Club Relations10-11Development12-13L...

Description: The AKC Canine Health Foundation 2007 Annual Report contains audited financials for 2006 and 2007 and the Foundation's accomplishments for the year 2007.

25. 2008 Annual Report

(File; Thu Oct 28 12:16:00 CDT 2010)

2008 Annual ReportWWW.AKCCHF.ORG • 888.682.9696CHF continues to lead the world in caninehealth research. In 2008 CHF approved $1.46million for a wide variety of studies.AKC CANINE HEALTH FOUNDATIONTable of ContentsLetter from the Chairma...

Description: The AKC Canine Health Foundation 2008 Annual Report contains audited financials for 2007 and 2008 and the Foundation's accomplishments for the year 2008.

26. 2000 Annual Report

(File; Thu Oct 28 09:24:00 CDT 2010)

AKC CANINE HEALTH FOUNDATION ANNUAL REPORT2000WORKING TOGETHER FOR THE HEALTH OF OUR DOGS… AND DOGS EVERYWHEREMISSIONThe mission of the AKC Canine HealthFoundation is to develop significant resourcesfor basic and applied health programs ...

Description: The AKC Canine Health Foundation 2000 Annual Report contains audited financials for 1999 and 2000 and the Foundation's accomplishments for the year 2000.

27. Genome Wide Association Mapping to Identify Genes Associated with Hypoadrenocorticism in the Bearded Collie

(Web Page; Wed Aug 21 09:05:00 CDT 2019)

None at this time.


Background: Canine Addison's disease is a late onset disorder caused by deterioration of the adrenal gland cortex and insufficient production of glucocorticoids and mineralocorticoids normally produced by that tissue. These hormones are involved in pathways important to normal body function including energy production, blood pressure, and stress response. Treatment is available but is expensive and life-long. Furthermore, delay in diagnosis and treatment can be fatal. Although hypoadrenocorticism occurs in the general canine population, some breeds show a greater prevalence particularly the Bearded Collie. We have demonstrated that hypoadrenocorticism is highly heritable in this breed and likely reflects the presence of a very small number of susceptibility genes. Objective: The researchers are using the canine single nucleotide polymorphism (SNP) test to perform an extensive genome scan of the DNA from Bearded Collies with the goal of identifying genomic regions associated with hypoadrenocorticism. Identifying probable locations that harbor mutations will allow the characterization of the gene(s) that cause this disease.

28. Hypothyroidism and AutoImmune Susceptibility Genes in the Bearded Collie

(Web Page; Tue Aug 27 09:40:00 CDT 2019)

Gershony, L. C., Belanger, J. M., Short, A. D., Le, M., Hytönen, M. K., Lohi, H., … Oberbauer, A. M. (2019). DLA class II risk haplotypes for autoimmune diseases in the Bearded Collie offer insight to autoimmunity signatures ...


Background: Autoimmune disorders, for which hypothyroidism is one, have been cited by dog breeders as a concern. Reports suggest that higher inbreeding is correlated with autoimmune disease expression. A diagnosis of hypothyroidism often accompanies other immune mediated diseases and many breeds are afflicted with several autoimmune disorders. This evidence suggests different autoimmune diseases actually reflect a common set of susceptibility genes that express differentially depending upon additional genetic mutations carried by an individual dog. Objective: The researchers are extensively examining the entire canine genome utilizing state-of-the-art technologies to search for chromosomal regions associated with hypothyroidism. They will then explore the genetic relationship between hypothyroidism and another immune mediated disease present in the Bearded Collie population, Addison's disease. Common genomic regions associated with both diseases would suggest a single set of susceptibility genes underlying endocrine immune mediated disorders.

29. Study of PLE/PLN (Protein-losing Enteropathy/Nephropathy) in Soft-coated Wheaten Terriers

(Web Page; Fri Aug 16 11:20:00 CDT 2019)

Littman, M. P., Wiley, C. A., Raducha, M. G., & Henthorn, P. S. (2013). Glomerulopathy and mutations in NPHS1 and KIRREL2 in soft-coated Wheaten Terrier dogs. Mammalian Genome, 24(3–4), 119–126. https://doi.org/10.1007/s0...


In 1997 the Soft-coated Wheaten Terrier (SCWT) Club of America helped us start an Open Registry which lists dogs affected with familial diseases common to this breed such as inflammatory bowel disease (IBD), protein-losing enteropathy (PLE), protein-losing nephropathy (PLN), combination PLE/PLN, Addison's disease (AD), and juvenile renal disease/renal dysplasia (JRD). The 2009 update lists almost 1000 affected dogs, with the vast majority affected with PLN, PLE, or PLE/PLN, in that order. These protein-losing diseases have had a devastating impact on the SCWT breed because: 1) there are no predictive tests, just annual screening tests, 2) there is no age limit, so dogs might be used for breeding before they show illness, and 3) the mode of inheritance is unknown and appears complex. The PennVet SCWT DNA Bank contains more than 500 blood or tissue samples from affected dogs as well as geriatric (14 years or older) non-affected Wheatens. Most affected samples are from confirmed PLE and/or PLN cases, with diagnosis documented by blood, urine, and histopathology test results. The proposed study will utilize SNP chip and genome-wide association analysis to identify chromosomal regions that are associated with these serious diseases. Further testing (fine-mapping) of regions of interest may then reveal specific mutations, deletions, or insertions, which could be used to identify carriers of disease-predisposing alleles. We also hope to learn more about the pathogenesis of these diseases (immune-dysregulation vs. structural/functional abnormalities) which may help Wheatens, other breeds of dogs, and humans with these diseases.

30. Major Histocompatibility Complex and Autoimmune Disease in Dogs

(Web Page; Wed Nov 10 20:16:00 CST 2010)

The Major Histocompatibility Complex (MHC) can best be described as the “factory floor” of the immune system. The MHC is an area of the human, and canine genome, which has been identified to code for the creation of proteins ...

Description: The Major Histocompatibility Complex (MHC) can best be described as the factory floor of the immune system. An autoimmune disease is basically a condition where something “goes haywire” with the codes produced by the MHC, and the body basically turns on itself.

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