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共有 2670 条符合本次的查询结果, 用时 2.6692009 秒

2221. The generation of diversity and pattern in animal development.

作者: J B Gurdon.
来源: Cell. 1992年68卷2期185-99页

2222. Cap recap: the involvement of eIF-4F in regulating gene expression.

作者: R E Thach.
来源: Cell. 1992年68卷2期177-180页

2223. Making a difference: the role of cell-cell interactions in establishing separate identities for equivalent cells.

作者: I Greenwald.;G M Rubin.
来源: Cell. 1992年68卷2期271-81页

2224. Homeobox genes and axial patterning.

作者: W McGinnis.;R Krumlauf.
来源: Cell. 1992年68卷2期283-302页

2225. Boundaries and fields in early embryos.

作者: P W Ingham.;A Martinez Arias.
来源: Cell. 1992年68卷2期221-35页

2226. The molecular and cellular basis of affinity maturation in the antibody response.

作者: G J Nossal.
来源: Cell. 1992年68卷1期1-2页

2227. MAP kinase by any other name smells just as sweet.

作者: G Thomas.
来源: Cell. 1992年68卷1期3-6页

2228. Leukocyte-endothelial cell recognition: three (or more) steps to specificity and diversity.

作者: E C Butcher.
来源: Cell. 1991年67卷6期1033-6页

2229. Clearing up glycoprotein hormones.

作者: K Drickamer.
来源: Cell. 1991年67卷6期1029-32页

2230. Sensory transduction: entering the mainstream of membrane signaling.

作者: G M Shepherd.
来源: Cell. 1991年67卷5期845-51页

2231. Autoantibodies in pathology and cell biology.

作者: E M Tan.
来源: Cell. 1991年67卷5期841-2页

2232. Irresistible force meets immovable object: transcription and the nucleosome.

作者: R D Kornberg.;Y Lorch.
来源: Cell. 1991年67卷5期833-6页

2233. Redox redux: the control of oxidative stress responses.

作者: B Demple.;C F Amábile-Cuevas.
来源: Cell. 1991年67卷5期837-9页

2234. Molecular cross talk between epithelial cells and pathogenic microorganisms.

作者: M J Wick.;J L Madara.;B N Fields.;S J Normark.
来源: Cell. 1991年67卷4期651-9页
The conference brought together epithelial cell biologists and molecular microbiologists and emphasized that these seemingly diverse disciplines are intricately intertwined. The model systems discussed throughout the meeting emphasized the novel approaches available to address key issues and begin to understand the molecular details of responses triggered at the microbial-epithelial interface. For example, co-crystallization of native ligand-receptor complexes as well as biologically or chemically altered forms of these complexes will allow fine details of receptor-ligand interactions to be determined. This approach is critical in development of new generation antimicrobial agents. Furthermore, transfection techniques that allow receptor expression in model epithelia, development of representative animal model systems, and development of transgenic mouse strains will aid in dissecting microbial-epithelial interactions and will provide further advances in studies on pathogenesis and tissue and host tropism. We are only beginning to uncover the nature of the bidirectional regulatory signals that occur between microbes and hosts. We know little about how these signals relate to the disease state, to microbial virulence, or to immune function. Clearly the cross talk between cell biologists and microbiologists is an important step in unraveling the events occurring between microbes and eukaryotic cells.

2235. Chromosome first aid.

作者: C W Greider.
来源: Cell. 1991年67卷4期645-7页

2236. Translocations, master genes, and differences between the origins of acute and chronic leukemias.

作者: T H Rabbitts.
来源: Cell. 1991年67卷4期641-4页

2237. Multiple targets for brefeldin A.

作者: H R Pelham.
来源: Cell. 1991年67卷3期449-51页

2238. Slow axonal transport models come full circle: evidence that microtubule sliding mediates axon elongation and tubulin transport.

作者: D W Cleveland.;P N Hoffman.
来源: Cell. 1991年67卷3期453-6页

2239. Something old, some things new: the steroid receptor superfamily in Drosophila.

作者: W A Segraves.
来源: Cell. 1991年67卷2期225-8页

2240. A dual receptor system is required for basic fibroblast growth factor activity.

作者: M Klagsbrun.;A Baird.
来源: Cell. 1991年67卷2期229-31页
共有 2670 条符合本次的查询结果, 用时 2.6692009 秒