Search Results - "Grahn, Robert A."

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    Extent of linkage disequilibrium in the domestic cat, Felis silvestris catus, and its breeds by Alhaddad, Hasan, Khan, Razib, Grahn, Robert A, Gandolfi, Barbara, Mullikin, James C, Cole, Shelley A, Gruffydd-Jones, Timothy J, Häggström, Jens, Lohi, Hannes, Longeri, Maria, Lyons, Leslie A

    Published in PloS one (07-01-2013)
    “…Domestic cats have a unique breeding history and can be used as models for human hereditary and infectious diseases. In the current era of genome-wide…”
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    Genetic heterogeneity and diversity of North American golden retrievers using a low density STR marker panel by Ontiveros, Eric S, Hughes, Shayne, Penedo, Maria Cecilia T, Grahn, Robert A, Stern, Joshua A

    Published in PloS one (27-02-2019)
    “…Thirty-three autosomal short tandem repeat (STR) markers were used to evaluate genetic heterogeneity and diversity in 525 golden retrievers (GRs). This breed…”
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    A Novel Variant in CMAH Is Associated with Blood Type AB in Ragdoll Cats by Gandolfi, Barbara, Grahn, Robert A, Gustafson, Nicholas A, Proverbio, Daniela, Spada, Eva, Adhikari, Badri, Cheng, Janling, Andrews, Gordon, Lyons, Leslie A, Helps, Chris R

    Published in PloS one (12-05-2016)
    “…The enzyme cytidine monophospho-N-acetylneuraminic acid hydroxylase is associated with the production of sialic acids on cat red blood cells. The cat has one…”
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    naked truth: Sphynx and Devon Rex cat breed mutations in KRT71 by Gandolfi, Barbara, Outerbridge, Catherine A, Beresford, Leslie G, Myers, Jeffrey A, Pimentel, Monica, Alhaddad, Hasan, Grahn, Jennifer C, Grahn, Robert A, Lyons, Leslie A

    Published in Mammalian genome (01-10-2010)
    “…Hair is a unique structure, characteristic of mammals, controlling body homeostasis, as well as cell and tissue integration. Previous studies in dog, mouse,…”
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    A Third MLPH Variant Causing Coat Color Dilution in Dogs by Van Buren, Samantha L, Minor, Katie M, Grahn, Robert A, Mickelson, James R, Grahn, Jennifer C, Malvick, Julia, Colangelo, Jennifer R, Mueller, Elisabeth, Kuehnlein, Petra, Kehl, Alexandra

    Published in Genes (10-06-2020)
    “…Altered melanosome transport in melanocytes, resulting from variants in the melanophilin ( ) gene, are associated with inherited forms of coat color dilution…”
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    Feline polycystic kidney disease mutation identified in PKD1 by LYONS, Leslie A, BILLER, David S, ERDMAN, Carolyn A, LIPINSKI, Monika J, YOUNG, Amy E, ROE, Bruce A, BAIFANG QIN, GRAHN, Robert A

    “…Autosomal dominant polycystic kidney disease (ADPKD) is a commonly inherited disorder in humans that causes the formation of fluid-filled renal cysts, often…”
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    Erythrocyte pyruvate kinase deficiency mutation identified in multiple breeds of domestic cats by Grahn, Robert A, Grahn, Jennifer C, Penedo, Maria Ct, Helps, Chris R, Lyons, Leslie A

    Published in BMC veterinary research (30-10-2012)
    “…Erythrocyte pyruvate kinase deficiency (PK deficiency) is an inherited hemolytic anemia that has been documented in the Abyssinian and Somali breeds as well as…”
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    A study on methods for preimplantation genetic testing (PGT) on in vivo- and in vitro-produced equine embryos, with emphasis on embryonic sex determination by Ramírez-Agámez, Luisa, Castaneda, Caitlin, Hernández-Avilés, Camilo, Grahn, Robert A., Raudsepp, Terje, Love, Charles C.

    Published in Theriogenology (01-10-2024)
    “…Two methods for preimplantation genetic testing (PGT) have been described for equine embryos: trophoblast cell biopsy (TCB) or blastocoele fluid aspiration…”
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    Prevalence of Genetic Mutations in Horses With Muscle Disease From a Neuromuscular Disease Laboratory by Aleman, Monica, Scalco, Rebeca, Malvick, Julia, Grahn, Robert A., True, Alexander, Bellone, Rebecca R.

    Published in Journal of equine veterinary science (01-11-2022)
    “…•Genetic variants impacting skeletal muscle are an important cause of disease in horses as reflected by one third of a horse population having known genetic…”
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    A novel noninvasive genetic survey technique for small mammals by Aylward, Cody M., Grahn, Robert A., Barthman-Thompson, Laureen M., Kelt, Douglas A., Sacks, Benjamin N., Statham, Mark J.

    Published in Journal of mammalogy (31-12-2022)
    “…Noninvasive genetic surveys, often conducted by collecting fecal samples, have become a popular tool for surveying wildlife, but have primarily been applied to…”
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    Aristaless-Like Homeobox protein 1 (ALX1) variant associated with craniofacial structure and frontonasal dysplasia in Burmese cats by Lyons, Leslie A., Erdman, Carolyn A., Grahn, Robert A., Hamilton, Michael J., Carter, Michael J., Helps, Christopher R., Alhaddad, Hasan, Gandolfi, Barbara

    Published in Developmental biology (15-01-2016)
    “…Frontonasal dysplasia (FND) can have severe presentations that are medically and socially debilitating. Several genes are implicated in FND conditions,…”
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    Whole genome sequencing in cats, identifies new models for blindness in AIPL1 and somite segmentation in HES7 by Lyons, Leslie A, Creighton, Erica K, Alhaddad, Hasan, Beale, Holly C, Grahn, Robert A, Rah, HyungChul, Maggs, David J, Helps, Christopher R, Gandolfi, Barbara

    Published in BMC genomics (31-03-2016)
    “…The reduced cost and improved efficiency of whole genome sequencing (WGS) is drastically improving the development of cats as biomedical models. Persian cats…”
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    Studies of trichomonad protozoa in free ranging songbirds: Prevalence of Trichomonas gallinae in house finches ( Carpodacus mexicanus) and corvids and a novel trichomonad in mockingbirds ( Mimus polyglottos) by Anderson, Nancy L., Grahn, Robert A., Van Hoosear, Karen, BonDurant, Robert H.

    Published in Veterinary parasitology (12-05-2009)
    “…This study refutes the accepted dogma that significant pathogenic effects of Trichomonas gallinae are limited to columbiformes and raptors in free ranging bird…”
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    SNP Miniplexes for Individual Identification of Random-Bred Domestic Cats by Brooks, Ashley, Creighton, Erica K., Gandolfi, Barbara, Khan, Razib, Grahn, Robert A., Lyons, Leslie A.

    Published in Journal of forensic sciences (01-05-2016)
    “…Phenotypic and genotypic characteristics of the cat can be obtained from single nucleotide polymorphisms (SNPs) analyses of fur. This study developed…”
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    COLQ variant associated with Devon Rex and Sphynx feline hereditary myopathy by Gandolfi, Barbara, Grahn, Robert A, Creighton, Erica K, Williams, D. Colette, Dickinson, Peter J, Sturges, Beverly K, Guo, Ling T, Shelton, G. Diane, Leegwater, Peter A. J, Longeri, Maria, Malik, Richard, Lyons, Leslie A

    Published in Animal genetics (01-12-2015)
    “…Some Devon Rex and Sphynx cats have a variably progressive myopathy characterized by appendicular and axial muscle weakness, megaesophagus, pharyngeal weakness…”
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