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Stochastic Inversion Transduction Grammars and Bilingual Parsing of Parallel Corpora

by Dekai Wu , 1997
"... ..."
Abstract - Cited by 562 (33 self) - Add to MetaCart
Abstract not found

J.Otsuki1,2,6, A.Okada3, K.Morimoto4, Y.Nagai1 and H.Kubo5

by unknown authors
"... endoplasmic reticulum clusters in MII human oocytes ..."
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endoplasmic reticulum clusters in MII human oocytes

3-D Sound for Virtual Reality and Multimedia

by Durand Begault , 2000
"... This paper gives HRTF magnitude data in numerical form for 43 frequencies between 0.2---12 kHz, the average of 12 studies representing 100 different subjects. However, no phase data is included in the tables; group delay simulation would need to be included in order to account for ITD. In 3-D sound ..."
Abstract - Cited by 282 (5 self) - Add to MetaCart
This paper gives HRTF magnitude data in numerical form for 43 frequencies between 0.2---12 kHz, the average of 12 studies representing 100 different subjects. However, no phase data is included in the tables; group delay simulation would need to be included in order to account for ITD. In 3-D sound

The Counting Board Algebra and its Applications

by unknown authors
"... (Mitsuo MORIMOTO) ..."
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(Mitsuo MORIMOTO)

Health Organization

by States (nis Who, Independent States , 1997
"... WHO monographs on medicinal plants ..."
Abstract - Cited by 233 (0 self) - Add to MetaCart
WHO monographs on medicinal plants

The reliability of a dialogue structure coding scheme

by Jean Carletta, Amy Isard, Jacqueline C. Kowtko - Computational Linguistics , 1997
"... This paper describes the reliability of a dialogue structure coding scheme which is based on utterance function, game structure, and higher level transaction structure, and which has been applied to a corpus of spontaneous task-oriented spoken dialogues. 1. ..."
Abstract - Cited by 222 (16 self) - Add to MetaCart
This paper describes the reliability of a dialogue structure coding scheme which is based on utterance function, game structure, and higher level transaction structure, and which has been applied to a corpus of spontaneous task-oriented spoken dialogues. 1.

Morimoto’s Conjecture for M-Small Knots

by TSUYOSHI KOBAYASHI , YO’AV RIECK , 2002
"... Let X be the exterior of connected sum of knots and Xi the exteriors of the individual knots. In [10] Morimoto conjectured (originally for n = 2) that g(X) < Σ n i=1 g(Xi) if and only if there exists a so-called primitive meridian in the exterior of the connected sum of a proper subset of the kno ..."
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Let X be the exterior of connected sum of knots and Xi the exteriors of the individual knots. In [10] Morimoto conjectured (originally for n = 2) that g(X) < Σ n i=1 g(Xi) if and only if there exists a so-called primitive meridian in the exterior of the connected sum of a proper subset

Knots with g(E(K)) = 2 and g(E(K#K#K)) = 6 and Morimoto’s Conjecture

by TSUYOSHI KOBAYASHI , YO’AV RIECK , 2008
"... We show that there exist knotsK ⊂ S 3 with g(E(K)) = 2 and g(E(K#K#K)) = 6. Together with [5, Theorem 1.5], this proves existence of counterexamples to Morimoto’s Conjecture [10]. This is a special case of [6]. ..."
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We show that there exist knotsK ⊂ S 3 with g(E(K)) = 2 and g(E(K#K#K)) = 6. Together with [5, Theorem 1.5], this proves existence of counterexamples to Morimoto’s Conjecture [10]. This is a special case of [6].

Knot exteriors with additive Heegaard genus and Morimoto’s Conjecture

by Tsuyoshi Kobayashi, Yo’av Rieck , 2007
"... Given integers {gi ≥ 2} n i=1 we prove that there exists infinitely may knots Ki ⊂ S3 so that g(E(Ki)) = gi and g(E( # n i=1Ki) = Σn i=1g(E(Ki)). (Here, E(·) denotes the exterior and g(·) the Heegaard genus.) Together with [8, Theorem 1.5], this proves the existence of counterexamples to Morimot ..."
Abstract - Cited by 11 (0 self) - Add to MetaCart
to Morimoto’s Conjecture [14].

Analysis Transcriptional control of human p53-regulated genes

by Todd Riley, Eduardo Sontag, Patricia Chen, Arnold Levine , 2008
"... The p53 protein regulates the transcription of many different genes in response to a wide variety of stress signals. Following DNA damage, p53 regulates key processes, including DNA repair, cell-cycle arrest, senescence and apoptosis, in order to suppress cancer. This Analysis article provides an ..."
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The p53 protein regulates the transcription of many different genes in response to a wide variety of stress signals. Following DNA damage, p53 regulates key processes, including DNA repair, cell-cycle arrest, senescence and apoptosis, in order to suppress cancer. This Analysis article provides an overview of the current knowledge of p53-regulated genes in these pathways and others, and the mechanisms of their regulation. In addition, we present the most comprehensive list so far of human p53-regulated genes and their experimentally validated, functional binding sites that confer p53 regulation.
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