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W. G. Clark

Clark-MXR (United States)

Publishes on Neuropeptides and Animal Physiology, Neuroscience and Neuropharmacology Research, Receptor Mechanisms and Signaling. 169 papers and 5.7k citations.

169Publications
5.7kTotal Citations

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Top publicationsby citations

Self-Similar Evolution of Parabolic Pulses in a Laser
F. Ömer İlday, J. R. Buckley, W. G. Clark et al.|Physical Review Letters|2004
Cited by 874Open Access

Self-similar propagation of ultrashort, parabolic pulses in a laser resonator is observed theoretically and experimentally. This constitutes a new type of pulse shaping in mode-locked lasers: in contrast to the well-known static (solitonlike) and breathing (dispersion-managed soliton) pulse evolutions, asymptotic solutions to the nonlinear wave equation that governs pulse propagation in most of the laser cavity are observed. Stable self-similar pulses exist with energies much greater than can be tolerated in solitonlike pulse shaping, and this has implications for practical lasers.

Alignment of genetic and restriction maps of the photosynthesis region of the Rhodopseudomonas capsulata chromosome by a conjugation-mediated marker rescue technique
Dean P. Taylor, Stanley N. Cohen, W. G. Clark et al.|Journal of Bacteriology|1983
Cited by 262Open Access

The restriction map of a 46-kilobase fragment of the Rhodopseudomonas capsulata chromosome was aligned with the genetic map of the photosynthesis region of that chromosome by a marker rescue technique. Marker rescue was effected by mobilization of vectors bearing fragments of R. capsulata DNA from Escherichia coli to a set of R. capsulata mutants. Plasmids pDPT51 and pDPT55 were constructed to mediate the intergeneric mobilization of pBR322 derivatives, and a mutant of R. capsulata with improved intergeneric recipient activity was isolated. Four previously unmapped genes affecting bacteriochlorophyll synthesis and two genes affecting photochemical reaction center synthesis have been located by marker rescue. Some of the fragments of R. capsulata DNA are capable of vector-independent complementation, implying that promoters are located on these fragments. Other fragments complement only in one orientation of insertion in the vector, implying transcription from promotors on the vectors and thereby fixing the direction of transcription for those fragments. Still other fragments of DNA show rescue only via recombination between homologous plasmid-borne DNA fragments and chromosomal mutations. The physical dimensions of the genetic map are 3.0 megadaltons per map unit, which agrees with previous estimates based on the size of the R. capsulata gene transfer agent.