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pro vyhledávání: '"John Neely"'
Autor:
John Neely
Publikováno v:
Academia Letters.
Publikováno v:
Journal of drugs in dermatology : JDD. 16(11)
pAtopic dermatitis and prurigo nodularis result from complex interactions between the skin, the immune system, and the external environment. The pruritus associated with these conditions greatly impacts patients' quality of life and lacks uniformly e
Autor:
Robert A. Wirtz, Joseph Nigro, Penny Masuoka, Phillip Lawyer, Richard G. Andre, Charles E. Cannon, John Neely, George Schultz, Leon L. Robert, Donald R. Roberts, David Goodfriend, David N. Gaines, Denise Pettit, Patricia D. Santos-Ciminera, Carol W. Garvey
Publikováno v:
Journal of the American Mosquito Control Association. 21:187-193
Two recent outbreaks of locally acquired, mosquito-transmitted malaria in Virginia in 1998 and 2002 demonstrate the continued risk of endemic mosquito-transmitted malaria in heavily populated areas of the eastern United States. Increasing immigration
Publikováno v:
Journal of Biological Chemistry. 277:40697-40702
Proteasome-mediated processing of the nfkappab2 gene product p100 is a regulated event that generates the NF-kappaB subunit p52. This event can be induced through p100 phosphorylation by a signaling pathway involving the nuclear factor-kappaB-inducin
Autor:
Kennedy, John Neely
Publikováno v:
Ellis County Press. 5/9/2024, Vol. 33 Issue 7, p3-3. 1/3p.
Autor:
Jerry D. Kerce, Ray Noblet, Elmer W. Gray, Bruce A. Harrison, C. John Neely, Michael L. Womack
Publikováno v:
Journal of the American Mosquito Control Association. 21:144-146
Although the 1st published record of Ochlerotatus japonicus japonicus in Georgia (Rabun County) occurred in 2004, we report here a 2002 collection and identification in Fulton County, Georgia (metro Atlanta). The finding of Oc. j. japonicus in Fulton
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 13(10)
Hunter syndrome, or mucopolysaccharidosis type II, is an X-linked recessive disorder resulting from iduronate sulfatase deficiency. Typical manifestations include short stature, mental retardation, hydrocephalus, macroglossia and cardiac valvulopathy
Akademický článek
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