PT/P(VDF-TrFE) hydrophone array

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A poling study of lead zirconate titanate/polyurethane 0–3 composites

Author name used in this publication: S. T. LauAuthor name used in this publication: K. W. KwokAuthor name used in this publication: F. G. ShinAuthor name used in this publication: S. Kopf2007-2008 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe

PZT/P(VDF-TrFE) nanocomposite hydrophones for ultrasonic measurements

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Resting-state abnormalities in amnestic mild cognitive impairment: a meta-analysis

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Quality of life (QoL) in southern Chinese with systemic lupus erythematosus (SLE)

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Macro-approach of cell formation problem with consideration of machining sequence

Cellular Manufacturing System (CMS) which is based on the concept of Group Technology (GT) has been recognized as an efficient and effective way to improve the productivity in the factory. In recent years, there has been much effort done for continuing to improve CMS. Most researches concentrated on distinguishing the part families and machine cells either simultaneously or individually by considering of minimizing intercellular and intracellular part movements. However, fewer researches have studied the impact of the sequencing of machine cells. In light of this, the main aim of this present work is to study the impact of the sequencing of allocating the machine cells in minimizing intercellular part movement. The problem scope, which is also called as machine-part grouping problem (MPGP) together with the background of cell layout problem (CLP), has been identified. A mathematical model is formulated and part incidence matrix with operational sequence is often used. Since MPGP has been proved as an NP complete, genetic algorithm (GA) is employed as cell formation algorithms in solving this problem. © 2004 IEEE.published_or_final_versio

Cumulative disease damage in southern Chinese patients with systemic lupus erythematosus (SLE)

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Identification of five novel WASP mutations in Chinese families with Wiskott-Aldrich syndrome.

The Wiskott-Aldrich Syndrome (WAS) is an X-linked recessive immunodeficiency caused by mutation in the gene encoding WAS protein (WASP). The disease is characterized by eczema, thrombocytopenia and severe immunodeificency and is associated with extensive clinical heterogeneity. Mutation studies indicated that the mutated genotypes are also highly variable. In this study, we performed PCR-direct sequencing analysis of the WAS gene in six unrelated Chinese families. Five novel mutations identified, included two nonsense mutations (506C-->T, 1388-->T), a small insertion (685-686insCGCA) and two single-base deletions (384delT, 984delC). All of the mutations are predicted to lead to premature translational termination of WASP. Copyright 2002 Wiley-Liss, Inc.postprin