Korn shell programming by example

por O'Brien, Dennis, Pitts, David
Publicado 2001

Cardiac safety of afatinib: a review of data from clinical trials

por Ewer, Michael S., Patel, Kalpesh, O’Brien, Dennis, Lorence, Robert M.
Publicado 2015

Case report: MELAS and concomitant presumed antiphospholipid antibody syndrome in an adult woman

por Nouduri, Sirisha, Padmanabhan, Rajiv, Hicks, Richard, Abbott, Mary-Alice, O'Brien, Dennis, Schlaug, Gottfried
Publicado 2022

A L2HGDH initiator methionine codon mutation in a Yorkshire terrier with L-2-hydroxyglutaric aciduria

por Farias, Fabiana HG, Zeng, Rong, Johnson, Gary S, Shelton, G D, Paquette, Dominique, O’Brien, Dennis P
Publicado 2012

A Missense Mutation in Canine CLN6 in an Australian Shepherd with Neuronal Ceroid Lipofuscinosis

por Katz, Martin L., Farias, Fabiana H., Sanders, Douglas N., Zeng, Rong, Khan, Shahnawaz, Johnson, Gary S., O'Brien, Dennis P.
Publicado 2011

A KCNJ10 mutation previously identified in the Russell group of terriers also occurs in Smooth-Haired Fox Terriers with hereditary ataxia and in related breeds

por Rohdin, Cecilia, Gilliam, Douglas, O’Leary, Caroline A., O’Brien, Dennis P., Coates, Joan R., Johnson, Gary S., Jäderlund, Karin Hultin
Publicado 2015

Neuronal Ceroid Lipofuscinosis in a Domestic Cat Associated with a DNA Sequence Variant That Creates a Premature Stop Codon in CLN6

por Katz, Martin L., Buckley, Reuben M., Biegen, Vanessa, O’Brien, Dennis P., Johnson, Gayle C., Warren, Wesley C., Lyons, Leslie A.
Publicado 2020

International veterinary canine dyskinesia task force ECVN consensus statement: Terminology and classification

por Cerda‐Gonzalez, Sofia, Packer, Rebecca A., Garosi, Laurent, Lowrie, Mark, Mandigers, Paul J. J., O'Brien, Dennis P., Volk, Holger A.
Publicado 2021

A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia

por Kolicheski, Ana L., Johnson, Gary S., Mhlanga-Mutangadura, Tendai, Taylor, Jeremy F., Schnabel, Robert D., Kinoshita, Taroh, Murakami, Yoshiko, O’Brien, Dennis P.
Publicado 2016

A rare homozygous MFSD8 single-base-pair deletion and frameshift in the whole genome sequence of a Chinese Crested dog with neuronal ceroid lipofuscinosis

por Guo, Juyuan, O’Brien, Dennis P, Mhlanga-Mutangadura, Tendai, Olby, Natasha J, Taylor, Jeremy F, Schnabel, Robert D, Katz, Martin L, Johnson, Gary S
Publicado 2015

A Novel Mutation in CLCN1 Associated with Feline Myotonia Congenita

por Gandolfi, Barbara, Daniel, Rob J., O'Brien, Dennis P., Guo, Ling T., Youngs, Melanie D., Leach, Stacey B., Jones, Boyd R., Shelton, G. Diane, Lyons, Leslie A.
Publicado 2014

An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed

por Forman, Oliver P., Hitti, Rebekkah J., Pettitt, Louise, Jenkins, Christopher A., O’Brien, Dennis P., Shelton, G. Diane, De Risio, Luisa, Quintana, Rodrigo Gutierrez, Beltran, Elsa, Mellersh, Cathryn
Publicado 2016

Novel Homozygous ADAMTS2 Variants and Associated Disease Phenotypes in Dogs with Dermatosparactic Ehlers–Danlos Syndrome

por Jaffey, Jared A., Bullock, Garrett, Guo, Juyuan, Mhlanga-Mutangadura, Tendai, O’Brien, Dennis P., Coates, Joan R., Morrissey, Rochelle, Hutchison, Robert, Donnelly, Kevin S., Cohn, Leah A., Katz, Martin L., Johnson, Gary S.
Publicado 2022

An ADAMTSL2 Founder Mutation Causes Musladin-Lueke Syndrome, a Heritable Disorder of Beagle Dogs, Featuring Stiff Skin and Joint Contractures

por Bader, Hannah L., Ruhe, Alison L., Wang, Lauren W., Wong, Aaron K., Walsh, Kari F., Packer, Rebecca A., Mitelman, Jonathan, Robertson, Kathryn R., O'Brien, Dennis P., Broman, Karl W., Shelton, G. Diane, Apte, Suneel S., Neff, Mark W.
Publicado 2010

Global Regulatory Landscape for Aggregate Safety Assessments: Recent Developments and Future Directions

por Ball, Greg, Kurek, Raffael, Hendrickson, Barbara A., Buchanan, James, Wang, William W., Duke, Susan P., Bhattacharyya, Amit, Li, Mengchun, O’Brien, Dennis, Weigel, Judith, Wang, Wenquan, Jiang, Qi, Ahmad, Faiz, Seltzer, Jonathan H., Herrero-Martinez, Esteban, Tremmel, Lothar
Publicado 2020

Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24

por Agler, Caryline, Nielsen, Dahlia M., Urkasemsin, Ganokon, Singleton, Andrew, Tonomura, Noriko, Sigurdsson, Snaevar, Tang, Ruqi, Linder, Keith, Arepalli, Sampath, Hernandez, Dena, Lindblad-Toh, Kerstin, van de Leemput, Joyce, Motsinger-Reif, Alison, O'Brien, Dennis P., Bell, Jerold, Harris, Tonya, Steinberg, Steven, Olby, Natasha J.
Publicado 2014

A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog

por Vernau, Karen M., Struys, Eduard, Letko, Anna, Woolard, Kevin D., Aguilar, Miriam, Brown, Emily A., Cissell, Derek D., Dickinson, Peter J., Shelton, G. Diane, Broome, Michael R., Gibson, K. Michael, Pearl, Phillip L., König, Florian, Van Winkle, Thomas J., O’Brien, Dennis, Roos, B., Matiasek, Kaspar, Jagannathan, Vidhya, Drögemüller, Cord, Mansour, Tamer A., Brown, C. Titus, Bannasch, Danika L.
Publicado 2020

A One Health overview, facilitating advances in comparative medicine and translational research

por Stroud, Cheryl, Dmitriev, Igor, Kashentseva, Elena, Bryan, Jeffrey N., Curiel, David T., Rindt, Hans, Reinero, Carol, Henry, Carolyn J., Bergman, Philip J., Mason, Nicola J., Gnanandarajah, Josephine S., Engiles, Julie B., Gray, Falon, Laughlin, Danielle, Gaurnier-Hausser, Anita, Wallecha, Anu, Huebner, Margie, Paterson, Yvonne, O’Connor, Daniel, Treml, Laura S., Stannard, James P., Cook, James L., Jacobs, Marc, Wyckoff, Gerald J., Likins, Lee, Sabbagh, Ubadah, Skaff, Andrew, Guloy, Amado S., Hays, Harlen D., LeBlanc, Amy K., Coates, Joan R., Katz, Martin L., Lyons, Leslie A., Johnson, Gayle C., Johnson, Gary S., O’Brien, Dennis P., Duan, Dongsheng, Calvet, James P., Gandolfi, Barbara, Baron, David A., Weiss, Mark L., Webster, Debra A., Karanu, Francis N., Robb, Edward J., Harman, Robert J.
Publicado 2016