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11.
禄丰古猿地点的猪尾鼠类化石 总被引:5,自引:3,他引:2
本文记述亚洲首次发现的猪尾鼠类化石。材料系1983年于云南禄丰古猿地点最晚中新世石灰坝组采集到的,计有代表两属三种——Platacanthomys dianensis sp.nov.,Typhlomysprimitivus sp.nov.和T.hipparionum sp.nov.的百余枚牙齿。文中除对新种的形态作了描述和对比外,还对猪尾鼠类的分类位置及系统发育作了探讨。 相似文献
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X Qiu K P Padmanabhan V E Carperos A Tulinsky T Kline J M Maraganore J W Fenton 《Biochemistry》1992,31(47):11689-11697
The X-ray crystallographic structure of the human alpha-thrombin complex with hirulog 3 (a potent, noncleavable hirudin-based peptide of the "hirulog" class containing a beta-homoarginine at the scissile bond), which is isomorphous with that of the hirugen-thrombin crystal structure, was solved at 2.3-A resolution by starting with a model for thrombin derived from the hirugen-thrombin complex and was refined by restrained least squares methods (R = 0.132). Residues of hirulog 3 were well-defined in the electron density, which included most of the pentaglycine linker and the C-terminal helical turn that was disordered in a related structure of thrombin with hirulog 1. The interactions of D-Phe1'-Pro2'-beta-homoArg3' with the active site of thrombin were essentially identical to those of related structures of PPACK- (D-Phe-Pro-Arg chloromethyl ketone) and hirulog 1-thrombin, with the guanidinium function of the arginyl P1 residue forming a hydrogen-bonding ion pair with Asp189 of the S1 site. A noticeable shift in the CA atom of beta-homoArg3' due to the methylene insertion displaces the scissile bond from attack by Ser195, thus imparting proteolytic stability to the beta-homoArg hirulog derivative. Resolution of the pentaglycine spacer, linking N- and C-terminal functional domains into a single oligopeptide bivalent inhibitor, permitted delineation of corresponding S' subsites of thrombin. The position of Gly4' (P1') is stabilized by three hydrogen bonds with His57, Lys60F, and Ser195, while the conformational angles maintained in a strained, nonallowed configuration for non-glycyl amino acids.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
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通过对杉木、台湾杉、香杉22个种源的叶长、叶宽、叶厚、维管束的宽与厚、栅栏组织厚、机械组织厚、表皮厚和气孔数等9个叶性状进行逐步判别分析,选取栅栏组织厚(X_6)、叶长(X_1)和叶厚(X_3)三个重要因子,建立优化判别方程:F_1(台湾杉)=-235.8714+17.3104X_6+26.3587X_1+5.9046X_3F_2(杉木)=-564.9259+78.4254X_6+93.1923X_1+0.6295X_3F_3(香杉)=-349.4205+64.1926X_6+62.6479X_1+0.8969X_3定量地区分这三个树种,旨在对逐步判别分析法在树种分类上的应用进行探讨。 相似文献
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Expression and characterization of virus-like particles containing rubella virus structural proteins. 总被引:7,自引:1,他引:6 下载免费PDF全文
Rubella virus (RV) virions contain two envelope glycoproteins (E1 and E2) and a capsid protein (C). Noninfectious RV-like particles (VLPs) containing three structural proteins were expressed in a BHK cell line (BHK-24S) by using an inducible promoter. These VLPs were found to resemble RV virons in terms of their size, their morphology, and some biological activities. In immunoblotting studies, VLPs were found to bind similarly to native RV virions with 10 of a panel of 12 RV-specific murine monoclonal antibodies. Immunization of mice with VLPs induced specific antibody responses against RV structural proteins as well as virus-neutralizing and hemagglutination-inhibiting antibodies. After immunization of mice with VLPs, in vitro challenge of isolated lymphocytes with inactivated RV and individual RV structural proteins stimulated proliferation. Our data suggest the possibility of using VLPs as immunogens for serodiagnostic assays and RV vaccines. 相似文献
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观察了hFPIL6/2对6.5Gyγ线照射NIH小鼠第10天造血功能恢复的影响。结果表明:照射小鼠连续4d给予hFPIL6/2250μg·kg-1·d-1,其脾重、CFU-8、骨髓有核细胞数及CM-CFU分别比对照组增加59.0%、278.5%、57.9%和138.2%,统计学处理均有显著差异;对此四项指标的改善也明显优于25μg组。另外,250μg剂量组小鼠外周血象30d的动态观察结果表明,hFPIL6/2不但能明显提高红细胞和血红蛋白的最低值,而且能使血小板的恢复提前。提示hFPIL6/2在促进血小板生成和促进红系造血方面可能具有良好的应用前景。 相似文献
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Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD) 总被引:4,自引:0,他引:4 下载免费PDF全文
J. R. Gilbert J. M. Stajich S. Wall S. C. Carter H. Qiu J. M. Vance C. S. Stewart M. C. Speer J. Pufky L. H. Yamaoka M. Rozear F. Samson M. Fardeau A. D. Roses M. A. Pericak-Vance 《American journal of human genetics》1993,53(2):401-408
Facioscapulohumeral muscular dystrophy (FSHD) is a slowly progressive primary disease of muscle which is usually inherited as an autosomal dominant disorder. FSHD has been localized to the long arm of chromosome 4, specifically to the 4q3.5-qter region. Initially published linkage studies showed no evidence for heterogeneity in FSHD. In the present study we have examined individuals in seven FSHD families. Two-point lod scores show significant evidence for linkage for D4S163 (lod score 3.04 at recombination fraction .21) and D4S139 (lod score 3.84 at recombination fraction .20). D4S171 also gave a positive score (lod score 2.56 at recombination fraction .24). Significant evidence for heterogeneity was found for each of the three markers. Multipoint linkage analysis in this region resulted in a peak multipoint lod score of 6.47. The multipoint analysis supported the two-point studies with odds of 20:1 showing linkage and heterogeneity over linkage and homogeneity. Five of the seven families gave a posterior probability of >95% of being of the linked type, while two families appeared unlinked to this region of 4q (P < .01%). Individuals in the two unlinked families met the clinical criteria for the diagnosis of FSHD, including facial weakness, clavicular flattening, scapula winging, proximal muscle weakness, and myopathic changes on muscle biopsies without inflammatory or mitochondrial pathology. This study demonstrates genetic heterogeneity in FSHD and has important implications for both genetic counseling and the elucidation of the etiology of FSHD. 相似文献