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Institution

Agilent Technologies

CompanySanta Clara, California, United States
About: Agilent Technologies is a company organization based out in Santa Clara, California, United States. It is known for research contribution in the topics: Signal & Mass spectrometry. The organization has 7398 authors who have published 11518 publications receiving 262410 citations. The organization is also known as: Agilent Technologies, Inc..


Papers
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Patent
22 Jul 1998
TL;DR: In this article, the authors propose a method and apparatus for accurately distributing traceable time values to a set of nodes in a system, where each node includes a slave clock that synchronizes a slave time value using a synchronization protocol.
Abstract: A method and apparatus for accurately distributing traceable time values to a set of nodes in a system. Each node includes a slave clock that synchronizes a slave time value using a synchronization protocol. The system includes a traceable time source that generates a traceable time value and a master node having a master clock that synchronizes a master time value to the traceable time value and that distributes the master time value to the slave clocks via the communication link. The nodes may be distributed nodes or cards connected to a backplane.

72 citations

Journal ArticleDOI
TL;DR: Ten novel LCB-Ps were discovered and characterized in tissues from human and mouse, as well in D. melanogaster and S. cerevisiae, and have immediate relevance for the understanding of sphingosine-1-phosphate biosynthesis, signaling, and degradation.
Abstract: Current mass spectrometry-based lipidomics aims to comprehensively cover wide ranges of lipid classes. We introduce a strategy to capture phospho-monoester lipids and improve the detection of long-chain base phosphates (LCB-Ps, e.g., sphingosine-1-phosphate). Ten novel LCB-Ps (d18:2, t20:1, odd carbon forms) were discovered and characterized in tissues from human and mouse, as well in D. melanogaster and S. cerevisiae. These findings have immediate relevance for our understanding of sphingosine-1-phosphate biosynthesis, signaling, and degradation.

71 citations

Journal ArticleDOI
TL;DR: The details of monitoring optical signal parameters and link impairments are the focus of this paper and two distinct techniques are presented: one based on Stokes space analysis, and the other on Kalman filtering.
Abstract: Modern spectrally efficient optical communication systems utilize polarization-multiplexed coherent transmission in complex modulation format. Coherent receivers used in these systems measure the amplitude and phase of the optical signals for both orthogonally polarized components carrying information. Knowledge of the amplitude and phase of the optical field, in combination with digital signal processing, gives the receiver an inherent metrology and performance monitoring capability. As the optical signal propagates from the transmitter over optical fiber to the receiver, a signal transformation and degradation is expected. The receiver observes the properties of the transmitted optical signal as degraded by the impairments of the transmission medium. The details of monitoring optical signal parameters and link impairments are the focus of this paper. The optical signal parameters include polarization state and residual carrier phase; optical link impairments include chromatic dispersion and polarization mode dispersion. Two distinct techniques are presented: one based on Stokes space analysis, and the other on Kalman filtering. The Stokes space techniques are modulation-format independent and do not require demodulation. The Kalman filtering provides optimal estimation of the physical quantities that describe the optical signal and the optical medium.

71 citations

Journal ArticleDOI
TL;DR: Observations indicate that dysregulated coronary vasculogenesis plays a pivotal role in formation of the infundibular pouches and suggests an essential role for Cx43alpha1 gap junctions in coronary Vasculogenesis and vascular remodeling.

71 citations

Patent
19 Apr 1995
TL;DR: In this paper, the authors presented a modified pyrococcus furiosus DNA polymerase that migrates on a nondenaturing polyacrylamide gel faster than phosphorylase B and Taq polymerase and more slowly than bovine serum albumin.
Abstract: Purified thermostable Pyrococcus furiosus DNA polymerase that migrates on a non-denaturing polyacrylamide gel faster than phosphorylase B and Taq polymerase and more slowly than bovine serum albumin and has an estimated molecular weight of 90,000-93,000 daltons when compared with a Taq polymerase standard assigned a molecular weight of 94,000 daltons.

71 citations


Authors

Showing all 7402 results

NameH-indexPapersCitations
Hongjie Dai197570182579
Zhuang Liu14953587662
Jie Liu131153168891
Thomas Quertermous10340552437
John E. Bowers102176749290
Roy G. Gordon8944931058
Masaru Tomita7667740415
Stuart Lindsay7434722224
Ron Shamir7431923670
W. Richard McCombie7114464155
Tomoyoshi Soga7139221209
Michael R. Krames6532118448
Shabaz Mohammed6418817254
Geert Leus6260919492
Giuseppe Gigli6154115159
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20231
20228
2021142
2020157
2019168
2018164