Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Polly Foureman"'
Publikováno v:
Anim Genet
Mucopolysaccharidosis (MPS) VI is a lysosomal storage disease caused by a deficiency of N-acetylgalactosamine-4-sulfatase, also called arylsulfatase B (ARSB, EC 3.1.6.12). Dogs with MPS VI show progressive predominantly oculoskeletal signs homologous
Autor:
G. Inal Gultekin, Karthik Raj, S. Lehman, Polly Foureman, Urs Giger, Osheiza Abdulmalik, K. Manhart
Publikováno v:
Journal of Veterinary Internal Medicine. 26:935-944
Background Erythrocytic pyruvate kinase (PK) deficiency, first documented in Basenjis, is the most common inherited erythroenzymopathy in dogs. Objectives To report 3 new breed-specific PK-LR gene mutations and a retrospective survey of PK mutations
Publikováno v:
Journal of Veterinary Internal Medicine. 19:373-376
Autor:
Sharon A. Center, Karen L. Warner, Jennifer McCabe, Polly Foureman, Walter E. Hoffmann, Hollis N. Erb
Publikováno v:
American Journal of Veterinary Research. 66:330-341
Objective—To evaluate the influence of a 1,4- butanedisulfonate stable salt of S-adenosylmethionine (SAMe) administered orally on clinicopathologic and hepatic effects induced by long-term administration of prednisolone in dogs. Animals—12 health
Publikováno v:
Journal of Veterinary Internal Medicine. 16:518-523
Canine leukocyte adhesion deficiency (CLAD) is a primary immunodeficiency disease characterized by recurrent bacterial infections in the presence of marked leukocytosis. The disease was 1st described in the mid-1980s in a cross-breed Irish Setter Dog
Publikováno v:
Gene. 218:121-128
Double minute chromosomes (DMs) are the principal genetic vehicles for amplifying oncogenes in human tumors and drug resistance genes in cultured mouse cells. Mouse EMT-6 cells resistant to methotrexate (MTX) generally contain circular DMs, approxima
Autor:
Carol Margolis, Ping Wang, Polly Foureman, Gloria Lin, Lisa Berman, Karthik Raj, Urs Giger, Adrian Sewell, Rachel Han
Publikováno v:
Molecular Genetics and Metabolism. 120:S137
Autor:
Brigitte Rigat, Henry J. Baker, Polly Foureman, Misako Hwang, Don J. Mahuran, Barbara K. Krum, Bruce F. Smith, John W. Callahan, G.S. Varadarajan, Douglas R. Martin
Publikováno v:
Molecular genetics and metabolism. 94(2)
G(M1) gangliosidosis is an inherited, fatal neurodegenerative disease caused by deficiency of lysosomal beta-d-galactosidase (EC 3.2.1.23) and consequent storage of undegraded G(M1) ganglioside. To characterize the genetic mutation responsible for fe
Publikováno v:
Journal of veterinary internal medicine. 16(5)
Canine leukocyte adhesion deficiency (CLAD) is a primary immunodeficiency disease characterized by recurrent bacterial infections in the presence of marked leukocytosis. The disease was 1st described in the mid-1980s in a cross-breed Irish Setter Dog
Publikováno v:
Journal of Veterinary Internal Medicine. 19:373
A6-year-old 5.5-kg female spayed domestic short-haired cat from Tucson, AZ, presented with an ˜5-day history of progressive pelvic limb weakness. The owners had returned from a weekend away to find the cat unable to use her left pelvic limb. Approxi