基于Image Quilting算法的纹理合成

基于样图的纹理合成方法是继纹理映射、过程纹理合成方法后发展起来的纹理拼接技术,用于解决传统方法中出现的缝隙、扭曲、变形和参数调整等问题.Image Quilting算法是简单易行的接缝消除方法,采用Image Quilting算法合成纹理并生成Wang Tile集,继而拼接大图像.实验表明,Image Quilting算法能够较好地保持纹理特征的连续性,但在接缝处可能破坏纹元特征.     

A New Way of the Skeletal Metals Synthesis

1 Results Strongly disordered metals with the high chemical and catalytic activity are often called as skeletal metals.Usually for their preparation the metallides of d-metal (which afterwards will be left in the “skeleton“) and chemically active component(s) are firstly synthesized.Then the last one(s) is (are) removed by the leaching with aqueous solutions of alkalis or carbonates.However,this method sometime fails,first of all,for the reactions,which should be realized in non-aqueous conditions.In th...     

Structural Changes of Water Molecules Upon the Reduction of Quinones in The Reaction Center from Rhodobactery Sphaeroides

1 Results The photosynthetic bacterial reaction center (RC) is a membrane protein complex.The RC is composed of three protein subunits and redox components such as bacteriochlorophylls, bacteriopheophytins,and quinones.The RC performs the photochemical electron transfer from the bacteriochlorophyll dimer through a series of electron donor and acceptor molecules to a secondary quinone,QB.QB accepts electrons from a primary quinone,QA,in two sequential electron transfer reactions.The second electron trans...     

混凝土早龄期热膨胀系数试验研究

通过设计开发新的早龄期混凝土热膨胀系数测量装置,测量了不同配合比的混凝土从初凝后开始的热膨胀系数,总结了在早龄期混凝土热膨胀系数随龄期的发展规律,并给出了其拟合公式。     

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

Protein-protein interaction analyses have uncovered a ciliary and basal body protein network that, when disrupted, can result in nephronophthisis (NPHP), Leber congenital amaurosis, Senior-L?ken syndrome (SLSN) or Joubert syndrome (JBTS). However, details of the molecular mechanisms underlying these disorders remain poorly understood. RPGRIP1-like protein (RPGRIP1L) is a homolog of RPGRIP1 (RPGR-interacting protein 1), a ciliary protein defective in Leber congenital amaurosis. We show that RPGRIP1L interacts with nephrocystin-4 and that mutations in the gene encoding nephrocystin-4 (NPHP4) that are known to cause SLSN disrupt this interaction. RPGRIP1L is ubiquitously expressed, and its protein product localizes to basal bodies. Therefore, we analyzed RPGRIP1L as a candidate gene for JBTS and identified loss-of-function mutations in three families with typical JBTS, including the characteristic mid-hindbrain malformation. This work identifies RPGRIP1L as a gene responsible for JBTS and establishes a central role for cilia and basal bodies in the pathophysiology of this disorder.     

织物设计中的色彩搭配

本文以色彩构成理论为依据，找出小配色模纹和较大配色模纹的不同配色所产生外观效应的规律，应用色彩构成规律使织物组织的设计尽可能符合美学观点。     

关于严格循环权位移的一个问题

给出了一个内射单侧权位移,其权序列空间H~2(β)≠H~∞(β),但对任意φ(z)属于H~∝(β),其部分和序列按算子范数收敛于φ(z).从而否定回答了Shields在文献[1]中的第12问题.     

Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger protein

We describe an Israeli Jewish Moroccan family presenting with autosomal dominant seborrhea-like dermatosis with psoriasiform elements, including enhanced keratinocyte proliferation, parakeratosis, follicular plugging, Pityrosporum ovale overgrowth and dermal CD4 lymphocyte infiltrate. We mapped the disease gene to a 0.5-cM region overlapping the PSORS2 locus (17q25) and identified a frameshift mutation in ZNF750, which encodes a putative C2H2 zinc finger protein. ZNF750 is normally expressed in keratinocytes but not in fibroblasts and is barely detectable in CD4 lymphocytes.     

一类优美有向图的充要条件

研究了由恰有一个公共顶点的有向回路→／Ｃｍ和→／Ｃｎ（ｍ，ｎ≥３）组成的有向图→／Ｗｍ，ｎ的优美性，给出了→／Ｗｍ，ｎ是优美有向图的充要条件。