Zobrazeno 1 - 10
of 32
pro vyhledávání: '"M. C. Patterson"'
Autor:
Alex R. Paciorkowski, H. B. Clark, Christopher M. Gomez, M. B. Tennison, Y. Shafrir, M. C. Patterson, J. Hrivnak
Publikováno v:
Neurology. 77:1055-1060
Objective: To provide clinical data on a cohort of 6 patients with massive expansion (>200 CAG repeats) of spinocerebellar ataxia type 2 (SCA2) and investigate possible pathways of pathogenesis using bioinformatics analysis of ATXN2 networks. Methods
Autor:
M. C. Patterson, David L. Dunkelberger
Publikováno v:
Journal of Vinyl and Additive Technology. 1:21-25
Accurate molecular weight characterization of PVC is necessary before attempting to modify the properties of the polymer using additives and/or process the compound in some fashion. Commercial PVC resins are characterized by many different dilute sol
Autor:
Jerome F. Strauss, Roscoe O. Brady, Mark Garfield, Anna Maria Hibbs, Calvin F. Roff, Ehud Goldin, Peter G. Pentchev, George C. Agritellis, M. C. Patterson, Howard Jaffe
Publikováno v:
Endocrinology. 133:2913-2923
We have determined the effects of the Niemann-Pick type C (NPC) lesion, which impairs transport of cholesterol from lysosomes, on the androgenic status of male NPC mice. The mice have low serum testosterone levels resulting from decreased testosteron
Autor:
M. C. Patterson
Publikováno v:
International Journal of Production Research. 31:845-849
The issue of setup time has received a great deal of research effort during the past decade. Most of the related literature has focused on attempts to reduce the setup time, also referred to as quick changeover. First, rather than analysing setup tim
Autor:
M H Polymeropoulos, Sevilla D. Detera-Wadleigh, M T Vanier, Colette C. Parker, E D Carstea, Richard E. Straub, Hua Xiao, M. C. Patterson, Ehud Goldin, Raymond R. O'Neill
Publikováno v:
Proceedings of the National Academy of Sciences. 90:2002-2004
We analyzed the involvement of chromosome 18 in Niemann-Pick disease type C (NPC), an autosomal recessive cholesterol-processing disorder. Within affected offspring, the chromosome 18 parental contributions were identified by using allele-specific mi
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 15(3)
A variety of cerebral insults can result in static encephalopathy with developmental delays and relatively fixed motor and cognitive deficits. We describe two boys with static encephalopathy who experienced recurrent episodes of generalized, violent
Publikováno v:
American journal of medical genetics. 79(5)
Autosomal dominant cerebellar ataxias are a heterogeneous group of neurodegenerative disorders that generally present in adulthood. Spinocerebellar ataxia type 2 typically presents with progressive cerebellar symptoms, slow ocular saccades, and perip
Publikováno v:
Veterinary microbiology. 56(3-4)
The development of immunity to Rhodococcus equi, particularly to a virulence-associated protein (VapA) based antigen preparation, was examined in CD1 and BALB/c mice after intraperitoneal vaccination. Immunization with VapA based antigen without adju
Publikováno v:
American journal of medical genetics. 70(3)
Hajdu-Cheney syndrome is an autosomal dominant disorder of acroosteolysis, skull deformities, characteristic facial abnormalities, osteoporosis, joint laxity, early loss of teeth, hearing loss, and a hoarse voice. We report on an 8 1/2-year-old boy w
Autor:
J F, Prescott, V M, Nicholson, M C, Patterson, M C, Zandona Meleiro, A, Caterino de Araujo, J A, Yager, M A, Holmes
Publikováno v:
American journal of veterinary research. 58(4)
To evaluate use of the virulence-associated protein of Rhodococcus equi in immunizing foals against R equi pneumonia.Eight (experimental group) and 6 (controls) mares with their foals.Virulence-associated protein extracted from R equi was used to pre