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871.
通过一系列实验分析了温度和pH值对羊毛纤维的膨胀和羊毛织物尺寸变化的影响.在pH2.1的溶液中,羊毛织物的尺寸随温度的升高而下降,变化的幅度取决于织物组织和织物的定型率.在羊毛等电点pH4.8时,纤维的膨胀达到最小值,而织物的尺寸则随着溶液酸性的增加而减小.  相似文献   
872.
Pigmentary glaucoma is a significant cause of human blindness. Abnormally liberated iris pigment and cell debris enter the ocular drainage structures, leading to increased intraocular pressure (IOP) and glaucoma. DBA/2J (D2) mice develop a form of pigmentary glaucoma involving iris pigment dispersion (IPD) and iris stromal atrophy (ISA). Using high-resolution mapping techniques, sequencing and functional genetic tests, we show that IPD and ISA result from mutations in related genes encoding melanosomal proteins. IPD is caused by a premature stop codon mutation in the Gpnmb (GpnmbR150X) gene, as proved by the occurrence of IPD only in D2 mice that are homozygous with respect to GpnmbR150X; otherwise, similar D2 mice that are not homozygous for GpnmbR150X do not develop IPD. ISA is caused by the recessive Tyrp1b mutant allele and rescued by the transgenic introduction of wildtype Tyrp1. We hypothesize that IPD and ISA alter melanosomes, allowing toxic intermediates of pigment production to leak from melanosomes, causing iris disease and subsequent pigmentary glaucoma. This is supported by the rescue of IPD and ISA in D2 eyes with substantially decreased pigment production. These data indicate that pigment production and mutant melanosomal protein genes may contribute to human pigmentary glaucoma. The fact that hypopigmentation profoundly alleviates the D2 disease indicates that therapeutic strategies designed to decrease pigment production may be beneficial in human pigmentary glaucoma.  相似文献   
873.
以对苯半醌负离子自由基为模型 ,利用ESR技术研究黄酮类化合物清除自由基的作用 ,初步获得一些构效关系。  相似文献   
874.
目的是将用于测量片状试样的热扩散率的激光闪光法推广至测量薄膜试样。应用 1 5纳秒脉冲 Nd:YAG激光及响应时间 0 .9微秒的 (Hg,Cd) Te红外探测器等建立了闪光法热扩散率测量系统 ,并应用此系统对微米量级厚度的不锈钢薄膜进行了测量。同时针对将激光闪光法应用于薄膜时所出现的问题 ,如激光的有限脉冲时间及有限吸收厚度效应 ,测量系统的滞后效应 ,以及增强红外吸收及辐射用表面黑化膜的影响进行了分析并提出了解决方法  相似文献   
875.
Comprehensive field investigations and laboratory analyses show that palaeolakes, including fresh- mesohaline water Megalake Tengger and other semi-con- nected, isolated water bodies, during late Pleistocene covered an area of more than 20000 km2, which is more than half of the Tengger Desert in NW China. Stratigraphic correlation and chronological evidence indicate that before ca. 42000 aBP the area was more arid. The palaeolakes started to develop around 40000 uncal. 14C aBP but until 37000 14C aBP their scope was limited. High water levels established from 35000 14C aBP lasted until 22000 14CaBP. Lake levels regressed between 22000 and 20000 14C aBP but transgressed from 20000 to 18600 14C aBP. Subsequently, water level declined further and the Megalake Tengger finally desiccated at around 18000 14C aBP. Megalake Tengger possessed a fresh-mesohaline water property, implying that the regional precipitation increased significantly. During the period of Megalake Tengger, the climate was warmer-humid than present. The annual rainfall was 250 to 350 mm more than that of today and the temperature was 1.5 to 3.0℃ higher.  相似文献   
876.
:(U-Th)/He ages of 13 samples from Yuexi-Luotian core and its flanks in Dabieshan orogen fall in the range of 155~85 Ma. He ages for samples from the core range between 85~107 Ma, while those from the flanks range between 114~155 Ma. The result shows that the Yuexi-Luotian core was a thermal dome in Cretaceous with core temperature being much higher than those of the flanks. The thermal extension which resulted in the formation of Dabie core complex lasted until ca. 85 Ma. The magnitude of exhumation in the core is approximately 1528.8 m more than that in the flanks.  相似文献   
877.
提出了一种由样品辨识、模糊推理和控制处理 3个子网模块构成的基于知识的多层神经网络 .这种网络由各子网分别构成并按照最初的模糊控制结构适当连接而建立 ,具有明确区分各组成子网功能及其知识流结构 .由于综合了模糊逻辑的推理过程及神经网络的学习能力 ,使它能够在其结构中以模糊规则的形式引入语言知识并通过网络的训练及自学习对这些知识进行加工 ,从而实现了真正意义上的自适应模糊控制器 .最后还讨论了这种 NFN网络在动态过程控制中的应用  相似文献   
878.
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880.
Retinitis pigmentosa (RP) comprises a clinically and genetically heterogeneous group of diseases that afflicts approximately 1.5 million people worldwide. Affected individuals suffer from a progressive degeneration of the photoreceptors, eventually resulting in severe visual impairment. To isolate candidate genes for chorioretinal diseases, we cloned cDNAs specifically or preferentially expressed in the human retina and the retinal pigment epithelium (RPE) through a novel suppression subtractive hybridization (SSH) method. One of these cDNAs (RET3C11) mapped to chromosome 1q31-q32.1, a region harbouring a gene involved in a severe form of autosomal recessive RP characterized by a typical preservation of the para-arteriolar RPE (RP12; ref. 3). The full-length cDNA encodes an extracellular protein with 19 EGF-like domains, 3 laminin A G-like domains and a C-type lectin domain. This protein is homologous to the Drosophila melanogaster protein crumbs (CRB), and denoted CRB1 (crumbs homologue 1). In ten unrelated RP patients with preserved para-arteriolar RPE, we identified a homozygous AluY insertion disrupting the ORF, five homozygous missense mutations and four compound heterozygous mutations in CRB1. The similarity to CRB suggests a role for CRB1 in cell-cell interaction and possibly in the maintenance of cell polarity in the retina. The distinct RPE abnormalities observed in RP12 patients suggest that CRB1 mutations trigger a novel mechanism of photoreceptor degeneration.  相似文献   
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