Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Douglas P. Kalinowski"'
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 331:149-159
Frameshift mutations occur by a number of mechanisms. To better understand the nature of these mechanisms, we determined the DNA sequence changes of 232 independent, spontaneous frameshift mutations in the HIS4 gene of REV1 and rev1-1 strains of Sacc
Publikováno v:
Nucleic Acids Research. 20:3485-3494
The polymerase chain reaction (PCR) represents an alternative to the current methods for investigating DNA damage and repair in specific genomic segments. In theory, any DNA lesion which blocks Taq polymerase can be measured by this assay. We used qu
Autor:
Michael S. Brogan, Laura E. Edsberg, Robert A. Hewson, Douglas P. Kalinowski, Robert H. Johnson
Publikováno v:
Journal of the American Podiatric Medical Association. 94(6)
Onychomycosis, most commonly caused by two species of dermatophyte fungi—Trichophyton rubrum and Trichophyton mentagrophytes—is primarily treated with regimens of topical and systemic antifungal medications. This study was undertaken to evaluate
Publikováno v:
Physical therapy. 76(12)
Background and Purpose. Electrical stimulation (ES) is used in wound management. Concerns, however, have been raised about the possible role ES might play in promoting or exacerbating wound infections, especially bacterial infections. The purpose of
Publikováno v:
Environmental and molecular mutagenesis. 20(2)
A mutation spectrum was constructed from a series of randomly isolated spontaneous His+ revertants of the frameshift mutant his4-38 in Saccharomyces cerevisiae. For each true revertant, a 438 bp region encompassing his4-38 on chromosome III was recov
Publikováno v:
Physical Therapy; Dec1996, Vol. 76 Issue 12, p1340, 8p, 4 Charts
Autor:
Douglas P Kalinowski, Navnit S Mitter, Karen J Sanders, Michael H Rattier, Lawrence P. Gordon, David A Clark, Lytt I Gardner
Publikováno v:
Pediatric Research. 19:247A-247A
This 3 mos old boy was found to have a karyotype of 46,XY,-18, +t(11;18)(q23;q23). His mother had a balanced reciprocal trans-location 46,XX,t(11;18)(23;23). He had dysmorphic, low-set ears, asymmetrical facies, epicanthus and high-arched palate. Lip
Publikováno v:
Pediatric Research. 18:225A-225A
A two year old girl with several dysmorphic features was found to have an isochromosome for the long arm of number 9: 46,XX,−9,+i(9q). We could find no previous report of this chromosome abnormality. Furthermore, the mother reported that she "drank