Search
Filter Results
- Resource Type
- Book2
- Article1
- Book Digital1
- Book Print1
- Result From
- Lane Catalog1
- PubMed1
- SearchWorks (biomedical subset) 1
-
Year
- Journal Title
- Biochim Biophys Acta1
Search Results
Sort by
- BookRobert W. Baloh, MD, Professor of Neurology and Head and Neck Surgery, David Geffen School of Medicine at UCLA, Director of Neurotology Clinic and Laboratory, Ronald Regan Medical Center, Los Angeles, CA.Contents:
Ménière recognizes that vertigo can originate from the inner ear
Ménière, a man of many interests
Breuer discovers how the balance portion of the inner ear works
Breuer, the Renaissance man
Breuer's experiments on the semicircular canals and otolith organs
Breuer's contributions to psychiatry and philosophy
Politzer's otology clinic and the discovery of the caloric test
Bárány's formative years and the conflict in Politzer's clinic
The war years and Bárány's decision to leave Vienna
Bárány's test battery and the first description of BPPV
Bárány's life in Uppsala and his work with Lorente de Nó
Hallpike and the pathology of Ménière's disease
Hallpike's formative years
Hallpike's caloric test
Hallpike defines the syndrome of BPPV
Schuknecht and his breakthrough on BPPV
Schuknecht's temporal bone bank in Boston
Schuknecht's crusade against myths in otology
Semont and Epley maneuvers
Evolution of treatment maneuvers for BPPV
Summary and future directions.Digital Access Oxford 2017 - Bookby Doreen Duchesne = Le déclin du travail familial non rémunéré au Canada / par Doreen Duchesne.Print c1989
- ArticleFukumaki Y, Shimada K, Takagi Y.Biochim Biophys Acta. 1977 Sep 06;478(1):90-8.Regulation of expression of a bacterial guaA gene inserted into colicin E1 DNA by an in vitro recombination was studied under various growth conditions. In Escherichia coli K-12 cells that carried this hybrid ColEl plasmid the level of guaA enzyme activity was not regulated by the concentration of guanine in the medium, but by the number of plasmid DNA copies. The optimal conditions for amplifying the guaA gene product by chloramphenicol treatment were determined. The level of guaA enzyme activity found under the optimal conditions was about 37 times that in extracts of wild-type E. coli cultured in guanine-free medium. The properties of the promoter for the guaA gene and applicability of this hybrid ColEl plasmid for amplification of various gene products were discussed.