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Micromachined Angular Rate Sensors for Automotive Applications

IEEE sensors journal, 2007-02, Vol.7 (2), p.302-309

2007

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Micromachined gyros for automotive applications

IEEE Sensors, 2005, 2005, p.4 pp.

2005

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A modeling approach to include mechanical microsystem components into the system simulation

Proceedings Design, Automation and Test in Europe, 1998, p.510-517

1998

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New surface micromachined angular rate sensor for vehicle stabilizing systems in automotive applications

The 13th International Conference on Solid-State Sensors, Actuators and Microsystems, 2005. Digest of Technical Papers. TRANSDUCERS '05, 2005, Vol.1, p.184-187 Vol. 1

2005

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System Level Modeling of the Relevant Physical Effects of Inertial Sensors Using Order Reduction Methods

Analog integrated circuits and signal processing, 2005-08, Vol.44 (2), p.129-135

2005

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A surface micromachined silicon gyroscope using a thick polysilicon layer

Technical Digest. IEEE International MEMS 99 Conference. Twelfth IEEE International Conference on Micro Electro Mechanical Systems (Cat. No.99CH36291), 1999, p.57-60

1999

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Towards a tool independent standard simulation library - A pragmatic approach to model exchange and simplification

1999 European Control Conference (ECC), 1999, p.2701-2706

1999

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A modeling approach to include mechanical microsystem components into the system simulation

Design, Automation, and Test in Europe: Proceedings of the conference on Design, automation and test in Europe; 23-26 Feb. 1998, 1998, p.510-517

1998

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Detection of neurophysiological features in female R255X MeCP2 mutation mice

Neurobiology of disease, 2020-11, Vol.145, p.105083-105083, Article 105083

2020

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Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome

Clinical genetics, 2019-05, Vol.95 (5), p.575-581

2019

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Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes

Nature (London), 2010-11, Vol.468 (7321), p.263-269

2010

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Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndrome

Human molecular genetics, 2020-08, Vol.29 (15), p.2461-2470

2020

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Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome

Human molecular genetics, 2016-08, Vol.25 (15), p.3284-3302

2016

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The spatial dynamics of commercial burglary during the COVID-19 lockdown in San Francisco

Journal of experimental criminology, 2024-03, Vol.20 (1), p.187-205

2024

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Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors

Pediatric neurology, 2017-05, Vol.70, p.20-25

2017

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Vicinal Difunctionalization of Alkenes: Chlorotrifluoromethylation with CF3SO2Cl by Photoredox Catalysis

Organic letters, 2014-03, Vol.16 (5), p.1310-1313

2014

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Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndrome

Genes, brain and behavior, 2022-01, Vol.21 (1), p.e12739-n/a

2022

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Preclinical research in Rett syndrome: setting the foundation for translational success

Disease models & mechanisms, 2012-11, Vol.5 (6), p.733-745

2012

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Progressive Changes in a Distributed Neural Circuit Underlie Breathing Abnormalities in Mice Lacking MeCP2

The Journal of neuroscience, 2016-05, Vol.36 (20), p.5572-5586

2016

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Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome

PloS one, 2016-11, Vol.11 (11), p.e0165550-e0165550

2016

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A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome

Human molecular genetics, 2008-06, Vol.17 (12), p.1718-1727

2008

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How to model and simulate microgyroscope systems

IEEE spectrum, 1998-07, Vol.35 (7), p.66-75

1998

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Insulinotropic treatments exacerbate metabolic syndrome in mice lacking MeCP2 function

Human molecular genetics, 2013-07, Vol.22 (13), p.2626-2633

2013

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Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors

Pediatric neurology, 2016-05, Vol.58, p.67-74

2016

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Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome

PLoS genetics, 2014-03, Vol.10 (3), p.e1004258-e1004258

2014

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