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The Complete Atomic Structure of the Large Ribosomal Subunit at 2.4 Å Resolution
 Science
, 2000
"... ation, and termination phases of protein synthesis. Because the structures of several DNA and RNA polymerases have been determined at atomic resolution, the mechanisms of DNA and RNA synthesis are both well understood. Determination of the structure of the ribosome, however, has proven a daunting t ..."
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Cited by 529 (13 self)
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mystery. Electron microscopy has contributed to our understanding of ribosome structure ever since the ribosome was discovered. In the last few years, threedimensional (3D) electron microscopic images of the ribosome have been produced at resolutions sufficiently high to visualize many of the proteins
Singularity Detection And Processing With Wavelets
 IEEE Transactions on Information Theory
, 1992
"... Most of a signal information is often found in irregular structures and transient phenomena. We review the mathematical characterization of singularities with Lipschitz exponents. The main theorems that estimate local Lipschitz exponents of functions, from the evolution across scales of their wavele ..."
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Cited by 590 (13 self)
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Most of a signal information is often found in irregular structures and transient phenomena. We review the mathematical characterization of singularities with Lipschitz exponents. The main theorems that estimate local Lipschitz exponents of functions, from the evolution across scales
An almost ideal demand system
 American Economic Review
, 1980
"... prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, noncommercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtai ..."
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Cited by 600 (0 self)
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prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, noncommercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at
Superconformal field theory on threebranes at a CalabiYau singularity
 Nucl. Phys. B
, 1998
"... Just as parallel threebranes on a smooth manifold are related to string theory on AdS5 × S 5, parallel threebranes near a conical singularity are related to string theory on AdS5 × X5, for a suitable X5. For the example of the conifold singularity, for which X5 = (SU(2) × SU(2))/U(1), we argue that ..."
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Cited by 690 (37 self)
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Just as parallel threebranes on a smooth manifold are related to string theory on AdS5 × S 5, parallel threebranes near a conical singularity are related to string theory on AdS5 × X5, for a suitable X5. For the example of the conifold singularity, for which X5 = (SU(2) × SU(2))/U(1), we argue
A multilinear singular value decomposition
 SIAM J. Matrix Anal. Appl
, 2000
"... Abstract. We discuss a multilinear generalization of the singular value decomposition. There is a strong analogy between several properties of the matrix and the higherorder tensor decomposition; uniqueness, link with the matrix eigenvalue decomposition, firstorder perturbation effects, etc., are ..."
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Cited by 467 (20 self)
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Abstract. We discuss a multilinear generalization of the singular value decomposition. There is a strong analogy between several properties of the matrix and the higherorder tensor decomposition; uniqueness, link with the matrix eigenvalue decomposition, firstorder perturbation effects, etc
KodairaSpencer theory of gravity and exact results for quantum string amplitudes
 Commun. Math. Phys
, 1994
"... We develop techniques to compute higher loop string amplitudes for twisted N = 2 theories with ĉ = 3 (i.e. the critical case). An important ingredient is the discovery of an anomaly at every genus in decoupling of BRST trivial states, captured to all orders by a master anomaly equation. In a particu ..."
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Cited by 545 (60 self)
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We develop techniques to compute higher loop string amplitudes for twisted N = 2 theories with ĉ = 3 (i.e. the critical case). An important ingredient is the discovery of an anomaly at every genus in decoupling of BRST trivial states, captured to all orders by a master anomaly equation. In a
Partial Functions
"... this article we prove some auxiliary theorems and schemes related to the articles: [1] and [2]. MML Identifier: PARTFUN1. WWW: http://mizar.org/JFM/Vol1/partfun1.html The articles [4], [6], [3], [5], [7], [8], and [1] provide the notation and terminology for this paper. We adopt the following rules ..."
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Cited by 494 (10 self)
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this article we prove some auxiliary theorems and schemes related to the articles: [1] and [2]. MML Identifier: PARTFUN1. WWW: http://mizar.org/JFM/Vol1/partfun1.html The articles [4], [6], [3], [5], [7], [8], and [1] provide the notation and terminology for this paper. We adopt the following
Measuring individual differences in implicit cognition: The implicit association test
 J PERSONALITY SOCIAL PSYCHOL 74:1464–1480
, 1998
"... An implicit association test (IAT) measures differential association of 2 target concepts with an attribute. The 2 concepts appear in a 2choice task (e.g., flower vs. insect names), and the attribute in a 2nd task (e.g., pleasant vs. unpleasant words for an evaluation attribute). When instructions ..."
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Cited by 937 (63 self)
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oblige highly associated categories (e.g., flower + pleasant) to share a response key, performance is faster than when less associated categories (e.g., insect + pleasant) share a key. This performance difference implicitly measures differential association of the 2 concepts with the attribute. In 3
The irreducibility of the space of curves of given genus
 Publ. Math. IHES
, 1969
"... Fix an algebraically closed field k. Let Mg be the moduli space of curves of genus g over k. The main result of this note is that Mg is irreducible for every k. Of course, whether or not M s is irreducible depends only on the characteristic of k. When the characteristic s o, we can assume that k ~ ..."
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Cited by 512 (2 self)
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~ (1, and then the result is classical. A simple proof appears in EnriquesChisini [E, vol. 3, chap. 3], based on analyzing the totality of coverings of p1 of degree n, with a fixed number d of ordinary branch points. This method has been extended to char. p by William Fulton [F], using specializations
Rho GTPases and the actin cytoskeleton
 Science
, 1998
"... The actin cytoskeleton mediates a variety of essential biological functions in all eukaryotic cells. In addition to providing a structural framework around which cell shape and polarity are defined, its dynamic properties provide the driving force for cells to move and to divide. Understanding the b ..."
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Cited by 589 (4 self)
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), leading to the assembly of a meshwork of actin filaments at the cell periphery to produce lamellipodia and membrane ruffles (Fig. 1E) (2). More recently, activation of Cdc42, a third member of the Rho subfamily, was shown to induce actinrich surface protrusions called filopodia (Fig. 1G) (3, 4
Results 1  10
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3,688,593