L.‐C. Tsui

Peak atrial longitudinal strain as an independent predictor of composite endpoint in patients received aortic valve replacement for severe aortic stenosis: a prospective cohort study

L.‐C. Tsui, Yi-Kei Tse, S Y Yu, H L Li et autres

Abstract Objective Severe aortic stenosis (AS) is the primary valvular heart disease, treatable only by aortic valve replacement (AVR). The prognostic value of pre-operative left atrial (LA) function on post-AVR clinical outcomes is uncertain. The study aims to evaluate the prognostic value …

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Prognostic value of pre-operative left atrial strain on composite endpoint in patients received aortic valve replacement for severe aortic stenosis: a retrospective cohort study

L.‐C. Tsui, Kai Hang Yiu, Hung‐Fat Tse, L Y Lam et autres

Abstract Funding Acknowledgements Type of funding sources: None. Objective Severe aortic stenosis (AS) is the most common primary valvular heart disease, treatable only by aortic valve replacement (AVR). Current literatures have shown that severe AS may precede atrial dysfunction which predicts adverse …

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Arrhythmia and sudden death associated with elevated cardiac chloride channel activity

L. Ye, Wei Zhu, Peter H. Backx, Miguel A. Cortez et autres

The identification and analysis of several cationic ion channels and their associated genes have greatly improved our understanding of the molecular and cellular mechanisms of cardiac arrhythmia. Our objective in this study was to examine the involvement of anionic ion channels in …

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Localization of the human gene encoding the 13.3-kDa subunit of mitochondrial complex III (UQCRB) to 8q22 by in situ hybridization

Suzann Malaney, Henry H. Heng, L.‐C. Tsui, X.-M. Shi et autres

We have localized the human gene encoding the 13.3-kDa subunit of mitochondrial complex III (UQCRB) to chromosome 8 using both radioactive in situ hybridization and fluorescence in situ hybridization. The additional peak obtained with the former method is attributed to the higher …

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Author Index, Vol. 73, 1996

Nigel K. Spurr, Susan L. Naylor, О. В. Зацепина, Christian Schöfer et autres

Refined localization of the asparagine synthetase gene (ASNS) to chromosome 7, region q21.3, and characterization of the somatic cell hybrid line 4AF/106/K015

Henry H. Heng, X-M. Shi, Stephen W. Scherer, Irene L. Andrulis et autres

We have mapped the asparagine synthetase gene (ASNS) to 7q21.3 by fluorescence in situ hybridization. While this study refined the localization of the gene, it also revealed a rearrangement in a somatic cell hybrid line which was used in previous ASNS mapping. …

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Fluorescence in situ hybridization mapping of the cystic fibrosis transmembrane conductance regulator (CFTR) gene to 7q31.3

Henry H. Heng, X.-M. Shi, L.‐C. Tsui

We have used the fluorescence in situ hybridization (FISH) technique to refine the localization of the cystic fibrosis transmembrane conductance regulator (CFTR) gene on human chromosome 7. The result shows that the gene is most likely located within band q31.3.

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In situ hybridization of two cloned chromosome 7 sequences tightly linked to the cystic fibrosis locus

Alessandra M.V. Duncan, Manuel Buchwald, L.‐C. Tsui

Two DNA sequences closely linked to the cystic fibrosis locus have been sublocalized to 7q31.3----q32 by in situ hybridization. These findings are consistent with previously published maps of that region of human chromosome 7. The cystic fibrosis locus therefore maps to the …

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Linkage of cystic fibrosis to the proα 2(I) collagen gene, COL1A2, on chromosome 7

Manuel Buchwald, M. Zsiga, D. Markiewicz, N. Plavsic et autres

A linkage has been detected between the locus for cystic fibrosis (CF) and the pro alpha 2(I) collagen gene (COL1A2) which is located in the region q21.3----q22.1 of chromosome 7. Based on the combined linkage data derived from 50 informative two-generation nuclear …

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12* Modulatory effect of MBL2 on the onset of Pseudomonas aeruginosa infection is influenced by the TGFβ1 variants in pediatric CF patients

Ruslan Dorfman, Andrew J. Sandford, C. Taylor, Bi Huang et autres

Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X

Isabel Aznarez, Julian Zielenski, Johanna M. Rommens, Benjamin J. Blencowe et autres

Nonsense mutations that occur more than 50 bases upstream of terminal spliced junctions are generally thought to lead to degradation of the corresponding transcripts by the process of nonsense-mediated mRNA decay. It has also been proposed that some nonsense mutations may affect …

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Novel mutation in the gene encoding c‐Abl‐binding protein SH3BP2 causes cherubism

Bernard Lo, Muhammad Faiyaz‐Ul‐Haque, Shelley Kennedy, Richard I. Aviv et autres

Cherubism is a rare autosomal dominant inherited condition caused by mutations in the c-Abl-binding protein SH3BP2. It is characterized by multiple cystic giant cell lesions of the jaw appearing in early childhood with stabilization and remission after puberty. In the present study, …

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