Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Y W, Kan"'
Publikováno v:
Pediatric dentistry. 32(2)
The purpose of this study was to investigate the rate of dental development in children with nonsyndromic hypodontia and nonsyndromic hyperdontia compared to age- and gender-matched controls.Dental age assessment was performed using orthopantomograms
Publikováno v:
Pediatric dentistry. 32(2)
The aim of the present investigation was to compare the prevalence of taurodontism in the permanent mandibular first molars of nonsyndromic children with hypodontia and supernumerary teeth with age- and gender-matched controls.The crown-body root rat
Autor:
Y. W. Kan
Publikováno v:
JAMA: The Journal of the American Medical Association. 267:1532-1536
Publikováno v:
The Journal of biological chemistry. 274(52)
Nrf1 is a member of the CNC-basic leucine zipper (CNC-bZIP) family of transcription factors. CNC bZIP factors, together with small Maf proteins, bind as heterodimers to the NF-E2/AP-1 element. Similarity between the NF-E2/AP-1 element and the antioxi
Publikováno v:
Blood. 92(8)
The mechanisms by which pharmacologic agents stimulate gamma-globin gene expression in beta-globin disorders has not been fully established at the molecular level. In studies described here, nucleated erythroblasts were isolated from patients with be
Publikováno v:
Blood. 88(5)
We have disrupted the 5' locus of the duplicated adult alpha-globin genes by gene targeting in the mouse embryonic stem cells and created mice with alpha-thalassemia syndromes. The heterozygous knockout mice (.alpha/alpha alpha) are asymptomatic like
Publikováno v:
The Journal of biological chemistry. 271(24)
To characterize the protein-DNA interactions important for the developmental control of the human beta-globin locus, we analyzed by in vivo dimethyl sulfate footprinting erythroid cells expressing either the fetal or the adult globin developmental pr
Publikováno v:
Blood. 81(1)
The molecular lesions causing beta-thalassemia in Sicily can be subdivided into two groups. One that occurs at a 71% frequency and consists of the beta 39, IVS 1,110 and IVS 1,6 mutations and the other group at a 20% frequency comprising the -87, bet
Autor:
K M, Shannon, J, Watterson, P, Johnson, P, O'Connell, B, Lange, N, Shah, P, Steinherz, Y W, Kan, J R, Priest
Publikováno v:
Blood. 79(5)
Loss of constitutional heterozygosity is a common molecular feature of cancers in which inactivation of one or more tumor suppressor genes is thought to contribute to tumorigenesis. Recent evidence suggests that the gene responsible for neurofibromat
Publikováno v:
Methods in enzymology. 216