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Dissertations / Theses on the topic 'Genetic diseases of dogs'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

Swenson, Lennart. "Population studies on genetic diseases in the dog /." Uppsala : Swedish Univ. of Agricultural Sciences (Sveriges lantbruksuniv.), 2001. http://epsilon.slu.se/avh/2001/91-576-5822-6.pdf.

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2

Boag, Alisdair Matthew. "An immunological and genetic investigation of canine hypoadrenocorticism (Addison's Disease)." Thesis, Royal Veterinary College (University of London), 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618317.

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3

Bianchi, Matteo. "Genetic Studies of Immunological Diseases in Dogs and Humans." Doctoral thesis, Uppsala universitet, Institutionen för medicinsk biokemi och mikrobiologi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-319962.

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This thesis presents genetic studies aiming at enlarging our knowledge regarding the genetic factors underlying two immune-mediated diseases, hypothyroidism and autoimmune Addison’s disease (AAD), in dogs and humans, respectively. Genetic and environmental factors are indicated to contribute to canine hypothyroidism, which can be considered a model for human Hashimoto’s thyroiditis (HT). In Paper I we performed the first genome-wide association (GWA) study of this disease in three high-risk dog breeds (Gordon Setter, Hovawart and Rhodesian Ridgeback). Using an integrated GWA and meta-analysis

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4

Melville, Scott Andrew Biotechnology &amp Biomolecular Sciences Faculty of Science UNSW. "Disease gene mapping in border collie dogs." Awarded by:University of New South Wales. School of Biotechnology and Biomolecular Sciences, 2006. http://handle.unsw.edu.au/1959.4/25511.

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Pedigree dog breeds are genetically isolated and inbred populations with characteristics specific to each breed. Some breeds carry genetic diseases which affect the health of the animals, but may also serve as a valuable model to identify genes involved in human disease. In the Border Collie breed in Australia, the identification of two disease genes would enable breeders to DNA test their animals and prevent future cases. Over 530 samples were collected to identify the genes responsible for these diseases through linkage mapping and candidate gene approaches. Collie Eye Anomaly (CEA) defines

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5

Woma, Timothy Yusufu. "The isolation and genetic characterization of canine distemper viruses from domestic dogs (Canis familiaris) in South Africa." Diss., University of Pretoria, 2008. http://hdl.handle.net/2263/26280.

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Studies comparing canine distemper virus (CDV) strains from Africa with that of previously described lineages have been hampered due to a lack of field strains for in vitro experiments. There are no reports of CDV isolations in southern Africa, and although CDV is said to have geographically distinct lineages, molecular information of African strains has not yet been documented. Clinical specimens consisting of whole blood, spleen, lungs, brain and cerebrospinal fluid from dogs with clinical signs suggestive of distemper were obtained from private veterinary practices and diagnostic laboratori

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6

Kathrani, Aarti Ashok. "An investigation into the role of pattern recognition receptors in canine inflammatory bowel disease." Thesis, Royal Veterinary College (University of London), 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559061.

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7

Salmon, Hillbertz Nicolette. "The origin of the ridge and associated anomalies in Rhodesian Ridgebacks /." Uppsala : Dept. of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, 2007. http://epsilon.slu.se/2007133.pdf.

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8

Chen, Yi-wen. "Molecular genetic investigation of Shar-Pei fever : a disease similar to human Familial Mediterranean fever /." free to MU campus, to others for purchase, 1998. http://wwwlib.umi.com/cr/mo/fullcit?p9924873.

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9

Hultin, Jäderlund Karin. "Mitochondrially inherited sensory ataxic neuropathy in golden retriever dogs : phenotype, clinical course and genotype of a novel neurological syndrome /." Uppsala : Dept of Clinical Sciences, Swedish University of Agricultural Sciences, 2009. http://epsilon.slu.se/200973.pdf.

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10

Harnevik, Lotta. "Molecular genetic studies on cystinuria." Doctoral thesis, Linköping : Univ, 2007. http://www.bibl.liu.se/liupubl/disp/disp2007/med1034s.pdf.

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11

Orsatti, Cláudio Lera [UNESP]. "Avaliação do polimorfismo genético da lecitina ligante de manose (MBL2) e da expressão gênica dos receptores Toll-Like (TLR) como bio-marcadores do risco cardiovascular em mulheres na pós-menopausa." Universidade Estadual Paulista (UNESP), 2014. http://hdl.handle.net/11449/123279.

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Made available in DSpace on 2015-05-14T16:53:16Z (GMT). No. of bitstreams: 0 Previous issue date: 2014-01-24Bitstream added on 2015-05-14T16:59:06Z : No. of bitstreams: 1 000828949.pdf: 463776 bytes, checksum: bd97d483f32c7167f14a3385ab44d9f0 (MD5)<br>Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)<br>FAPESP: 2009/14884-9

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12

Bedin, Márcia Regina. "Associação dos polimorfismos -318C/T, CT60 e A49G do gene CTLA4, R620W do gene PTPN22 e A946T do gene IFIH1 em pacientes pediátricos com doença autoimune tireoidiana e diabetes mellitus tipo 1." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/5/5141/tde-27092013-123929/.

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As doenças autoimunes da tireoide (DAIT) representadas, principalmente pela doença de Graves (DG) e tireoidite de Hashimoto (TH), apresentam causas multifatoriais, incluindo fatores genéticos e ambientais. Diversos genes estão envolvidos, entre eles CTLA4, PTPN22 e mais recentemente IFIH1, principalmente quando associados a diabetes mellitus tipo 1 (DM1). OBJETIVOS: Determinar a frequência alélica e genotípica dos polimorfismos: -318C/T, A49G e CT60 do CTLA4, R620W do PTPN22 e A946T do IFIH1 em pacientes pediátricos portadores de DG, TH e DM1 associado a TH e em uma população controle normal,

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13

Perini, Ana Priscila. "Diversidade genética dos Vírus Parainfluenza 1, 2 e 3, identificados em amostras colhidas no Hospital Universitário da Universidade de São Paulo, durante os anos de 1995 a 2005." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-26112012-082543/.

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Introdução: Os vírus parainfluenza são importante causa de infecções respiratórias. Na população pediátrica a doença característica associada com HPIV-1 e 2 é a laringotraqueobronquite, enquanto que o HPIV-3 está associado com a pneumonia e bronquiolite. Objetivos: Realizar a análise molecular do fragmento do gene da HN. Métodos: Foram analisados aspirados nasofaríngeos coletados entre 1995 a 2005, de crianças com doença respiratória aguda. A detecção dos HPIV 1, 2 e 3 foi realizada por multiplex RT-PCR. Posteriormente, o fragmento de gene HN foi amplificado, sequenciado e, a análise molecula

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14

Orsatti, Cláudio Lera. "Avaliação do polimorfismo genético da lecitina ligante de manose (MBL2) e da expressão gênica dos receptores Toll-Like (TLR) como bio-marcadores do risco cardiovascular em mulheres na pós-menopausa /." Botucatu, 2014. http://hdl.handle.net/11449/123279.

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Orientador: Eliana Aguiar Petri Nahas<br>Coorientador: Steven Witkins<br>Banca: Maria Terezinha Serrão Peraçoli<br>Banca: Cesar E. Fernandes<br>Banca: Aarão Mendes Pinto<br>Banca: Renata D. Jouiliano<br>Resumo: Não disponível<br>Abstract: Not available<br>Doutor

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15

Rowell, Jennie Lynn. "GENETIC VARIATION IN THE DOMESTICATED DOG AS A MODEL OF HUMAN DISEASE." The Ohio State University, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=osu1338237356.

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16

Júnior, Edgar Borges de Oliveira. "Uma nova abordagem para o estudo dos defeitos genético-moleculares da doença granulomatosa crônica e análise de suas relações genótipo-fenótipo." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/42/42133/tde-16122010-101612/.

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A Doença Granulomatosa Crônica é uma imunodeficiência grave e rara, na qual os quadros infecciosos por bactérias e fungos, ocorrem predominantemente nas barreiras naturais do organismo. O defeito reside em mutações em um dos componentes do sistema NADPH oxidase. O dHPLC mostrou-se mais sensível que o SSCP, sendo eficaz na detecção de alterações em 100% dos casos. Identificamos sete mutações diferentes no gene CYBB, sendo quatro delas inéditas. São elas R226X; R290X; e C537R. Dentre as mutações inéditas identificamos: T302fsX46; c.141 +5 G> T; C185R; e H222L. Identificamos a mutação V25fsX51 no

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17

Matthewman, Linda A. "Ehrlichiosis : the disease in dogs and cats in Zimbabwe." Thesis, Royal Veterinary College (University of London), 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558976.

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18

Tivers, Michael Samuel. "The role of hepatic regeneration and angiogenesis in the response to surgical attenuation of congenital portosystemic shunts in dogs." Thesis, Royal Veterinary College (University of London), 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618310.

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19

Correard, Solenne. "Analyses génétiques et génomiques de maladies neurologiques chez le chien comme modèle de maladies rares humaines." Thesis, Rennes 1, 2018. http://www.theses.fr/2018REN1B028/document.

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L’identification des mutations génétiques impliquées dans les maladies rares est un prérequis pour mieux les comprendre, les traiter et accompagner les patients. Pour se faire, des modèles animaux présentant des maladies spontanées homologues aux maladies humaines sont très prometteurs. Le chien développe spontanément des maladies génétiques, rares chez l’Homme, mais fréquentes dans certaines races de chiens, ce qui simplifie les analyses génétiques. Ma thèse a porté sur deux maladies neurologiques : l’épilepsie et la neuropathie. Pour l’épilepsie, l’objectif était d’identifier des variants gé

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20

Kristensen, Signe Frost. "Are mixed-breed dogs healthier than purebred dogs? A review of the current data on diseases and longevity in dogs." Thesis, Linnéuniversitetet, Institutionen för biologi och miljö (BOM), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-96779.

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In today’s world, more than 400 different dog breeds have been registered and the number continues to increase, as people come up with new ways of breeding dogs. Purebred dogs are prone to many inherited disorders, inbreeding depression and a decreasing gene pool. Mixed-breed dogs, on the other hand, are said to be less prone to these problems, as they have a higher genetic variation. This review combined knowledge from the last 25 years of research in the field of mixed-breed dogs and purebred dogs to see what we know and what we still need to examine further. The literature all in all agrees

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21

Hansson, Kerstin. "Diagnostic imaging of cardiopulmonary structures in normal dogs and dogs with mitral regurgitation /." Uppsala : Dept. of Biomedicine and Veterinary Public Health, Division of Diagnostic Imaging and Clinical Pathology, Swedish Univ. of Agricultural Sciences, 2004. http://epsilon.slu.se/v167.pdf.

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22

Trevisan, Flavio. "Transformação genética de maracujazeiro (Passiflora edulis f. flavicarpa) para resistência ao vírus do endurecimento dos frutos." Universidade de São Paulo, 2005. http://www.teses.usp.br/teses/disponiveis/11/11144/tde-29092005-134710/.

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O objetivo do trabalho foi estudar uma forma alternativa para o controle do endurecimento dos frutos do maracujazeiro, pela produção de plantas transgênicas contendo o gene da proteína capsidial do Passionfruit woodness virus - PWV. O vetor de expressão foi construído utilizando-se os plasmídeos pCambia 2300 e pCambia 2301, que contêm o gene de seleção nptII, para resistência ao antibiótico canamicina. O plasmídeo pCambia 2301 contém também o gene repórter uidA (GUS). Os plasmídeos foram introduzidos em Agrobacterium tumefaciens, estirpes EHA 105 e LBA 4404, pelo método do choque térmico. Os

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23

Rak, Simone Gerlinde. "Molecular genetic analysis of congenital deafness in Dalmatian dogs." [S.l.] : [s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=981462391.

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24

Hodges, Elizabeth. "Genetic analysis of lymphoproliferative diseases." Thesis, University of Portsmouth, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294061.

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25

Hejmanowski, Ashley Quintin. "Allelic and genetic heterogeneity of two common genetic diseases." Connect to this title online, 2004. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1095309751.

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Thesis (Ph. D.)--Ohio State University, 2004.<br>Title from first page of PDF file. Document formatted into pages; contains xvi, 137 p.; also includes graphics (some col.). Includes bibliographical references (p. 127-137).

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26

Hejmanowski, Ashley Q. "Allelic and genetic heterogeneity of two common genetic diseases." The Ohio State University, 2004. http://rave.ohiolink.edu/etdc/view?acc_num=osu1095309751.

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27

Chowdhury, Budhaditya. "Behavioral Genetic Characterization of Hunting in Domestic Dogs, Canis Familiaris." Bowling Green State University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1320084128.

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28

Kolicheski, Ana Leticia. "Discovering Disease Causing Variants in Dogs Through Whole Genome Sequencing." Thesis, University of Missouri - Columbia, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=13877152.

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<p> This dissertation focuses on the use of whole genome sequencing (WGS) for the identification of disease causing variants in canine genomes. A brief review on the historical milestones of genetics, the creation and popularization of the fast throughput DNA sequencing technologies and their advantages and potential problems and biases, the importance of the study of canine genetics and the current state of the canine genome assembly is presented. Our lab sequenced ~100 dogs in the attempt to discover disease-causing variants. So far 20 such variants have been identified. This dissertation co

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29

Lopez-Alvarez, Jordi. "Evaluation of early indicators of disease progression in dogs with degenerative mitral valve disease." Thesis, Royal Veterinary College (University of London), 2015. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669194.

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30

Einarsdottir, Elisabet. "Mapping genetic diseases in northern Sweden." Doctoral thesis, Umeå universitet, Medicinsk biovetenskap, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-499.

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The population of northern Sweden has previously been shown to be well suited for the mapping of monogenic diseases. In this thesis we have tested the hypothesis that this population could also be used for efficient identification of risk genes for common diseases. In Paper I we have hypothesised that despite the admixture of Swedish, Finnish and Sami, the northern Swedish population consists of sub-populations geographically restricted by the main river valleys running through the region. This geographic isolation, in combination with founder effects and genetic drift, could represent a uniqu

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31

Einarsdóttir, Elísabet. "Mapping genetic diseases in northern Sweden." Umeå : Department of Medical Biosciences, Umeå University, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-499.

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32

Weersma, Rinse Karel. "Genetic susceptibility for inflammatory bowel diseases." [S.l. : Groningen : s.n. ; University Library Groningen] [Host], 2007. http://irs.ub.rug.nl/ppn/304870935.

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33

Shah, Paresh Rameshchandra. "Complex genetic approaches to neurodegenerative diseases." Thesis, University College London (University of London), 2007. http://discovery.ucl.ac.uk/1445084/.

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Neurodegenerative diseases are fatal disorders in which disease pathogenesis results in the progressive degeneration of the central and/or the peripheral nervous systems. These diseases currently affect -2% of the population but are expected to increase in prevalence as average life expectancy increases. The majority of these diseases have a complex genetic basis. The work presented in this thesis aimed to investigate the genetic basis of two neurodegenerative diseases, amyotrophic lateral sclerosis (ALS) and the human prion diseases kuru and sporadic Creutzfeldt-Jakob disease (sCJD), using no

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34

Lau, Kin-chong, and 劉健莊. "Microarray-based investigations of genetic diseases." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B45894760.

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35

Pennington, Catherine Margaret. "Genetic aspects of human prion diseases." Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/24216.

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Introduction: Human prion diseases are progressive, fatal neurological conditions linked to conformational changes in the structure of the prion protein. Prion diseases may be sporadic (sporadic Creutzfeldt-Jakob disease or sCJD, Sporadic Fatal Insomnia), acquired (variant CJD, iatrogenic CJD, kuru) or genetic (genetic prion disease, gPD). gPD is due to a disease-specific point or octapeptide repeat insertion (OPRI) mutation in the prion protein gene (PRNP). Numerous different PRNP mutations have been described. In some cases of gPD the phenotype may closely resemble that of sCJD, and it can b

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36

Wong, Hei Sunny. "Genetic susceptibility to common mycobacterial diseases." Thesis, University of Oxford, 2010. http://ora.ox.ac.uk/objects/uuid:cb4dd818-4693-4168-ad8a-cdeb59e2d5f3.

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Common mycobacterial diseases, including tuberculosis and leprosy, contribute to major mortality and morbidity worldwide. Despite evidence of an important role of host genetic factors in susceptibility to these infections, few compelling genetic associations have been identified with previous candidate gene and linkage approaches. This thesis investigates the genetic factors of human immunity to these mycobacterial diseases using a high-throughput approach of association testing. To assess genetic susceptibility to tuberculosis, I have conducted a genome-wide association study in the Gambian p

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37

Mieskes, Katharina. "Molecular genetic analysis of canine congenital sensorineural deafness in Dalmatian dogs." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=980847508.

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38

Choi, Hwa-Soon. "Mechanical properties of canine pericardium." Diss., Georgia Institute of Technology, 1989. http://hdl.handle.net/1853/15492.

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39

Spotswood, Timothy C. "Echocardiographic changes of left ventricular size and function in a canine normovolaemic anaemia model." Diss., University of Pretoria, 2006. http://hdl.handle.net/2263/23732.

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The objective of this study was to non-invasively document the changes in echocardiographic variables of left ventricular size and function during acute normovolaemic anaemia. This model was developed as a pilot study with the purpose of providing baseline information to investigate the pathophysiology, and more specifically the effect on the heart, of canine babesiosis-induced anaemia. The study group comprised of 11 mature healthy Beagle dogs that weighed between 9 and 15 kg. Severe normovolaemic anaemia was induced over a 3-4 day period by serial bleeding while maintaining normovolaemia by

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40

Upstill-Goddard, Rosanna. "Genetic dissection of early-onset breast cancer and other genetic diseases." Thesis, University of Southampton, 2015. https://eprints.soton.ac.uk/386938/.

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Genetic variation in the genome of an individual plays a key role in susceptibility to many human diseases. Analysis of the genetic variants harboured by individuals presenting with disease phenotypes is crucial for unravelling the genetic landscape of human disease. The methods that are now available for the characterisation of genetic variants, including single nucleotide polymorphism (SNP) microarrays and next generation sequencing, make it possible to explore all genetic variants harboured within an individual with a specific disease phenotype, allowing for tailoring of treatments. This th

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41

Mao, Weidong. "Prediction of Genetic Susceptibility to Complex Diseases." Digital Archive @ GSU, 2006. http://digitalarchive.gsu.edu/cs_diss/6.

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The accessibility of high-throughput biology data brought a great deal of attention to disease association studies. High density maps of single nucleotide polymorphism (SNP's) as well as massive genotype data with large number of individuals and number of SNP's become publicly available. By now most analysis of the new data is undertaken by the statistics community. In this dissertation, we pursue a different line of attack on genetic susceptibility to complex disease that adheres to the computer science community with an emphasis on design rather than analytical methodology. The main goal

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42

Spataro, Nino 1984. "Human genetic disorders: Mendelian and complex diseases." Doctoral thesis, Universitat Pompeu Fabra, 2016. http://hdl.handle.net/10803/482220.

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From Darwin’s “On the Origin of Species”, many years elapsed before human diseases were considered in an evolutionary framework. Besides theoretical and empirical advances, we are far from the complete understanding of disease aetiology. Highly penetrant disorders with Mendelian inheritance are mostly explained by the mutation-selection balance model, which is insufficient to describe the selective pressures acting on the full set of alleles related to diseases. We show in the first two papers that Next Generation Sequencing (NGS) technologies provide a unique opportunity to investigate variat

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43

Guo, Youling, and 郭友玲. "Genetic and genomic mapping of common diseases." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B50533861.

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Genome-wide mapping of susceptibility genes was conducted in two complex disorders of hypertension and epilepsy, allowing the dissection of the genetic architecture of these common diseases and related quantitative traits. The study performed comprehensive genetic analyses in a genome-wide scale, using different structure of data – sib-pairs and case-control samples. To identify genes influencing hypertension and blood pressure, a combined linkage and association study was conducted using over half a million SNPs genotyped in 328 siblings. Regions of significant linkage were identified fo

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44

Hennig, Branwen Johanna Wanda. "Genetic polymorphisms and early-onset periodontal diseases." Thesis, University of Newcastle Upon Tyne, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311107.

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45

Rajab, Anna. "The impact of genetic diseases in Oman." Thesis, St George's, University of London, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286157.

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46

Schmitz, Silke. "Investigations into the efficacy of probiotics in canine inflammatory bowel disease." Thesis, Royal Veterinary College (University of London), 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618324.

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47

Childers, Martin K. "Contraction-induced muscle damage in dogs with golden retriever muscular dystrophy." free to MU campus, others may purchase free online, 2002. http://wwwlib.umi.com/cr/mo/preview?3074385.

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48

Gould, D. J. "Molecular genetic investigations into inherited progressive retinal degenerations of dogs and cats." Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.599550.

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Generalized Progressive Retinal Atrophy (gPRA) represents an inherited group of retinal degenerations affecting pedigree dogs and cats. The disease is genetically heterogeneous between breeds, and with the exception of rod-cone dysplasia 1 (<I>red1</I>) in the Irish setter, the genetic causes remain unknown. The disease closely resembles retinitis pigmentosa, the commonest cause of inherited blindness in man. I have used a candidate gene approach in an attempt to identify mutations causing gPRA in dogs and cats. Rom-1, a structural gene of the rod photoreceptor of the retina, was cloned, seque

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49

House, Arthur Kingsley. "An immunological and genetic investigation of anal furunculosis in German Shepherd dogs." Thesis, Royal Veterinary College (University of London), 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.479141.

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50

Rüfenacht, Silvia. "A behaviour test in German shepherd dogs : genetic parameters for seven traits /." [S.l.] : [s.n.], 2002. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.

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