Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Nancy N. Huang"'
Autor:
Nancy N. Huang, Craig P. Hunter
Publikováno v:
Gene. 554:160-173
The RNA binding protein MEX-3 is required to restrict translation of pal-1, the Caenorhabditis elegans caudal homolog, to the posterior of the early embryo. MEX-3 is present uniformly throughout the newly fertilized embryo, but becomes depleted in th
Publikováno v:
Annals of the New York Academy of Sciences. 76:289-307
MEX-3 interacting proteins link cell polarity to asymmetric gene expression inCaenorhabditis elegans
Publikováno v:
Development. 129:747-759
The KH domain protein MEX-3 is central to the temporal and spatial control of PAL-1 expression in the C. elegans early embryo. PAL-1 is a Caudal-like homeodomain protein that is required to specify the fate of posterior blastomeres. While pal-1 mRNA
Autor:
Palmer, Judy, Dillon-Baker, Cindy, Tecklin, Jan S., Wolfson, Barbara, Rosenberg, Beth, Burroughs, Barbara, Holsclaw Jr., Douglas S., Scanlin, Thomas F., Nancy N. Huang, Sewell, Edward M., Palmer, J, Dillon-Baker, C, Tecklin, J S, Wolfson, B, Rosenberg, B, Burroughs, B, Holsclaw, D S Jr, Scanlin, T F, Huang, N N, Sewell, E M
Publikováno v:
Annals of Internal Medicine; Nov83, Vol. 99 Issue 5, p596-600, 5p, 5 Charts
Autor:
Carolyn R. Denning, Nancy N. Huang, L. R. Cuasay, Harry Shwachman, Paul Tocci, Warren J. Warwick, Lewis E. Gibson
Publikováno v:
Pediatrics. 66:752-757
Directors of cystic fibrosis centers in the United States have noted an increasing number of patients with histories of either false-positive or false-negative sweat tests. These inaccuracies were attributed to the use of rapid test methods which avo
Autor:
Nancy N. Huang, Harold W. Lischner
Publikováno v:
Pediatric Annals. 6:51-68
The primary hypogammaglobulinemias, with onset of acute and recurrent bacterial infections in infancy and early childhood, consist of a heterogeneous group of largely genetically determined antibody deficiency states including that congenital sex-lin
Publikováno v:
The Journal of Pediatrics. 89:23-26
The majority (86.6%) of patients with cystic fibrosis were found to be carriers of Pseudomonas aeruginosa. None of them, however, carried P. aeruginosa in their nares. In contrast, none of the non-CF family members of the patients with CF were carrie
Publikováno v:
Infection. 4:S465-S471
Sisomicin was administered to 24 patients with cystic fibrosis who were experiencing acute exacerbation of their pulmonary infections. Five patients were given 3 mg/kg/day i.v. in three divided doses (Group I), five patients were given 5 mg/kg/day i.
Autor:
Dale S. Huff, Adamadia Deforest, Nancy N. Huang, Lourdes R. Laraya-Cuasay, Harold W. Lischner
Publikováno v:
American Review of Respiratory Disease. 116:617-625
In 3 male patients, chronic pulmonary sequelae followed influenza virus infection at 5, 24, and 42 months of age. Varying degrees of interstitial fibrosis, bronchial and bronchiolar erosions and metaplasia, obliterative bronchiolitis, and interstitia
Autor:
Nancy N. Huang
Publikováno v:
Pediatric Annals. 6:27-50