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1.
Guang Pu Xue Yu Guang Pu Fen Xi ; 32(9): 2322-6, 2012 Sep.
Artigo em Chinês | MEDLINE | ID: mdl-23240388

RESUMO

Tunable diode laser absorption spectroscopy technology (TDLAS), with its advantages of high selectivity and accuracy, provides a reliable approach to the on-line detection of escaping ammonia. Firstly, the present paper introduces the TDLAS principle, experimental system and the analyses of system noise. Then with the concentration of 90 x 10(-6) and 30 x 10(-6) NH3 for example, we used TDLAS system to collect their second harmonic original spectrum with all kinds of noise interference. To improve the signal spectrum, five types of digital filtering methods were respectively used to filter the original spectrum. Finally we did the NH3 experiments of concentration gradient and the long time monitoring: NH3 experiment of 20 x 10(-6). The analysis indicated that the averaging-wavelet filtering is validated to be more accurate than the other filtering methods in the noise reduction, which can improve the precision of the monitoring system from 10 x 10(-6) to 1.25 x 10(-6) and the SNR also increases by 14 times. It provides an effective pretreatment during the monitoring of escaping ammonia of extremely low concentration.

2.
Arch Dermatol Res ; 298(2): 58-63, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16552539

RESUMO

Darier's disease (DD) is an autosomal dominantly inherited skin disorder characterized by loss of adhesion between epidermal cells (acantholysis) and abnormal keratinization. To date, at least 140 mutations in the ATP2A2 gene have been identified as the genetic basis of DD. Here we reported three familial and two sporadic Chinese DD patients totally with four missense mutations (N767D, M494I, M494L, C318F) and one splice-site mutation (1288-6A-->G) in ATP2A2 gene, and presented a literature review of DD cases reported in China since 1989. Our data add new variants to the repertoire of ATP2A2 gene in DD and confirms that most mutations in the ATP2A2 gene are private and missense type. Likewise, the literature review indicates that DD is not uncommon in China and presents more information about genotype-phenotype correlations.


Assuntos
Doença de Darier/enzimologia , Doença de Darier/genética , Mutação , ATPases Transportadoras de Cálcio do Retículo Sarcoplasmático/genética , Povo Asiático/genética , Sequência de Bases , China , DNA/genética , Análise Mutacional de DNA , Doença de Darier/patologia , Feminino , Genes Dominantes , Humanos , Masculino
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