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Institution

University of New Mexico

EducationAlbuquerque, New Mexico, United States
About: University of New Mexico is a education organization based out in Albuquerque, New Mexico, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 28870 authors who have published 64767 publications receiving 2578371 citations. The organization is also known as: UNM & Universitatis Novus Mexico.


Papers
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Journal ArticleDOI
01 May 1991-Nature
TL;DR: In this paper, a new detector for atom interferometers, constructed with the aid of modern quantum optics, provides a way around the obstacle of position-momentum uncertainty relation and allows the investigation of other mechanisms that enforce complementarity.
Abstract: Simultaneous observation of wave and particle behaviour is prohibited, usually by the position–momentum uncertainty relation New detectors, constructed with the aid of modern quantum optics, provide a way around this obstacle in atom interferometers, and allow the investigation of other mechanisms that enforce complementarity

763 citations

Journal Article
TL;DR: The geomeffy, bond valences, and polymerization of hexavalent uranium polyhedra from 105 well-refined structures are analyzed in this article, where a series of coordiaation polyhedr4 from square bipyramidal polyhedras with uranyl ions to holosymmehic octahedral geometry are discussed.
Abstract: The geomeffy, bond valences, and polymerization ofhexavalent uranium polyhedra from 105 well-refined structures are analyzed. The Utu cation is almost always present in crystal stnrctures as part of a nearly linear (UOr)z* uranyl ion that is coordinated by four, five or six equatorial anions in an approximately planar arangement perpendicular to the uranyl ion, giving square, pentagonal and hexagonal bipyramids, respectively. The Utu-O7\" bond length (Oy,: uranyl-ion O atom) is independent of the equatorial anions of the polyhedra;-averages of all polyhedra tlat contain uranyl ions ffs; I6lIJ6f-Or. = 1.79(3), mg0.-.9 a,= 1.79(4), and t8lu6+-Our = 1.78(3) A. Not a[ r6lu6+ polyhedra contain uranyl ions; there is a continuous series of coordiaation polyhedr4 from square bipyramidal polyhedra with uranyl ions to holosymmehic octahedral geometry. The mUo* and t8lu6+ polyhedra invariably contaitl a uranyl ion. The equatorial U6.-0 (0: O,-, OH-) bond-lengths of uranyl polyhedra depend upon coordhation number; averages for all polyhedra are t6lu6+-dq = 2,28(5), rlUot-$* = 2.37(9), afi t8tlJ6+-$q2.47 (12) A. Cunently available bond-valence parameters for U& are unsatisfactory for determining bond-valence sums. Coordination-specific bond-valence paxameters have been derived for U6|, together with parameters applicable to all coordination geometries. The parameters give bond-valence sums for Ue of -6 vlr and reasonable bond-valences for Uc,-Ou, bonds. The bond-valence paraneters facilitate the recognition of Ua, U5+ and U6| catiotrs in refined crystal structures. The crystal-chemical consfraints ofpolyhedral polymerization in uranyl phases are discussed.

762 citations

Journal ArticleDOI
04 Nov 2016-Science
TL;DR: The results are consistent with the proposition that smoking increases cancer risk by increasing the somatic mutation load, although direct evidence for this mechanism is lacking in some smoking-related cancer types.
Abstract: Tobacco smoking increases the risk of at least 17 classes of human cancer. We analyzed somatic mutations and DNA methylation in 5243 cancers of types for which tobacco smoking confers an elevated risk. Smoking is associated with increased mutation burdens of multiple distinct mutational signatures, which contribute to different extents in different cancers. One of these signatures, mainly found in cancers derived from tissues directly exposed to tobacco smoke, is attributable to misreplication of DNA damage caused by tobacco carcinogens. Others likely reflect indirect activation of DNA editing by APOBEC cytidine deaminases and of an endogenous clocklike mutational process. Smoking is associated with limited differences in methylation. The results are consistent with the proposition that smoking increases cancer risk by increasing the somatic mutation load, although direct evidence for this mechanism is lacking in some smoking-related cancer types.

762 citations

Book
01 Jan 2001

761 citations

Journal ArticleDOI
TL;DR: Methodological quality of studies was significantly but modestly correlated with the reporting of a specific effect of treatment, and strongest evidence of efficacy was found for brief interventions, social skills training, the community reinforcement approach, behavior contracting, behavioral marital therapy and case management.
Abstract: Aim A 3-year update with 59 new controlled trials is provided for the ongoing Mesa Grande project reviewing clinical trials of treatments for alcohol use disorders. The project summarizes the current evidence for various treatment approaches, weighting findings differentially according to the methodological strength of each study. Design The review includes 361 controlled studies that (1) evaluated at least one treatment for alcohol use disorders, (2) compared it with an alternative condition (such as a control group, a placebo, a brief intervention or an alternative treatment), (3) used a procedure designed to create equivalent groups before treatment and (4) reported at least one outcome measure of drinking or alcohol-related consequences. Studies were rated by two reviewers on 12 methodological criteria, and outcome logic was analyzed for the specific treatment modalities tested. Findings Methodological quality of studies was significantly but modestly correlated with the reporting of a specific effect of treatment. Among psychosocial treatments, strongest evidence of efficacy was found for brief interventions, social skills training, the community reinforcement approach, behavior contracting, behavioral marital therapy and case management. For the first time, two pharmacotherapies also appeared among the most strongly supported approaches: opiate antagonists (naltrexone, nalmefene) and acamprosate. Least supported were methods designed to educate, confront, shock or foster insight regarding the nature and causes of alcoholism. Conclusions Treatment methods differ substantially in apparent efficacy. It would be sensible to consider these differences in designing and funding treatment programs.

759 citations


Authors

Showing all 29120 results

NameH-indexPapersCitations
Bruce S. McEwen2151163200638
David Miller2032573204840
Jing Wang1844046202769
Paul M. Thompson1832271146736
David A. Weitz1781038114182
David R. Williams1782034138789
John A. Rogers1771341127390
George F. Koob171935112521
John D. Minna169951106363
Carlos Bustamante161770106053
Lewis L. Lanier15955486677
Joseph Wang158128298799
John E. Morley154137797021
Fabian Walter14699983016
Michael F. Holick145767107937
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202390
2022595
20213,060
20203,049
20192,779
20182,729