共查询到20条相似文献,搜索用时 15 毫秒
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The Curious Mr Catesby,edited for the Catesby Commemorative Trust by E. Charles Nelson and David J. Elliott. Athens,Georgia: University of Georgia Press, 2015, 425 pp. Hardcover. £35.21; $49.95. ISBN 978‐0‐8203‐4726‐4.
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Mary Morris 《Biological journal of the Linnean Society. Linnean Society of London》2016,117(2):402-402
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Hypomethylating Agent 5‐Aza‐2′‐deoxycytidine (DAC) Ameliorates Multiple Sclerosis in Mouse Models
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Katia Mangano Paolo Fagone Klaus Bendtzen Pier Luigi Meroni Cinzia Quattrocchi Santa Mammana Michelino Di Rosa Lucia Malaguarnera Marinella Coco Gaetano Magro Roberto Di Marco Ferdinando Nicoletti 《Journal of cellular physiology》2014,229(12):1918-1925
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Albert K.B. Chiu Mukund K. Gurjar Leslie Hough Lee V. Sincharoenkul Anthony C. Richardson 《Carbohydrate research》1982,100(1):247-261
1′-O-Mesyl-6,6′-di-O-tritylsucrose and the corresponding 1′-O-tosyl derivative were prepared from 6,6′-di-O-tritylsucrose by selective sulphonylation. Both sulphonates underwent intramolecular cyclisation reactions, to give 2,1′-anhydrosucrose in high yields rather than the isomeric 1′,4′-anhydride. Sequential benzoylation, detritylation, and mesylation of the 2,1′-anhydride afforded 2,1′-anhydro-6,6′-di-O-mesylsucrose tetrabenzoate which, in the presence of base, gave 2,1′:3,6:3′,6′-trianhydrosucrose that was not identical with the product previously claimed to have this structure. Several derivatives of 2,1′-anhydrosucrose were prepared possessing different functional groups at either the 6,6′- or 4,6′-positions. Dimolar mesitylene-sulphonylation of 3,3′,4′6′-tetra-O-acetylsucrose gave the 6,1′-disulphonate, which, in the presence of alkali, gave 2,1′:3,6-dianhydrosucrose, which was transformed into the 2,1′:3,6:3′,6′-trianhydride by sequential bromination at C-6′ (carbon tetrabromide-triphenylphosphine) and base-catalysed cyclisation. Treatment of 3,3′,4′,6′-tetra-O-benzoylsucrose with sulphuryl chloride furnished the 4,6,1′-trichloro derivative, which, on alkaline hydrolysis, was converted into 2,1′:3,6-dianhydro-4-chloro-4-deoxy-galacto-sucrose. 相似文献
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《Cell cycle (Georgetown, Tex.)》2013,12(19):3848-3850
Georgia is situated in the Caucasus region where Eastern Europe and Western Asia meet. The country covers a territory of 69,700 km² and its population is 4.385 million people. Formerly a part of the Soviet Union, Georgia restored its independence in 1991. Since then the country has struggled to renovate its economical and political structure, while saving the best from the past and exploring new opportunities. Bioscience is an essential part of this process. We have interviewed several leading Georgian scientists and asked them to describe the problems and accomplishments in their areas of bioscience. 相似文献
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RANGAPRASAD SARANGARAJAN YANG ZHAO GEORGE BABCOCK JAMES CORNELIUS M. LYNN LAMOREUX RAYMOND E. BOISSY 《Pigment cell & melanoma research》2000,13(5):337-344
Tyrosinase related protein‐1 (TRP‐1) is a melanocyte‐specific gene product involved in eumelanin synthesis. Mutation in the Tyrp1 gene is associated with brown pelage in mouse and oculocutaneous albinism Type 3 in humans (OCA3). It has been demonstrated that TRP‐1 expresses DHICA oxidase activity in the murine system. However, its actual function in the human system is still unclear. The study was designed to determine the effects of mutation at two Typr1 alleles, namely the Tyrp1b (brown) and Tyrp1b‐cj (cordovan) compared with wild type Tyrp1B (black) on melanocyte function and melanin biosynthesis. The most significant finding was that both of the Tyrp1 mutations (i.e. brown expressing a point mutation and cordovan expressing decreased amount of TRP‐1 protein) resulted in attenuation of cell proliferation rates. Neither necrosis nor apoptosis was responsible for the observed decrease in cell proliferation rates of the brown and cordovan melanocytes. Ultrastructural evaluation by electron microscopic analysis revealed that both mutations in Tyrp1 affected melanosome maturation without affecting its structure. These observations demonstrate that mutation in Tyrp1 compromised tyrosinase activity within the organelle. DOPA histochemistry revealed differences in melanosomal stages between black and brown melanocytes but not between black and cordovan melanocytes. There were no significant differences in tyrosine hydroxylase activities of tyrosinase and TRP‐1 in wild type black, brown and cordovan melanocyte cell lysates. We conclude that mutations in Tyrp1 compromise cell proliferation and melanosomal maturation in mouse melanocyte cultures. 相似文献
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Hiroshi Karasawa Kiyosumi Takaishi Yoshihiro Kumagae 《Obesity (Silver Spring, Md.)》2011,19(3):514-521
An obesity‐induced diabetes model using genetically normal mouse strains would be invaluable but remains to be established. One reason is that several normal mouse strains are resistant to high‐fat diet‐induced obesity. In the present study, we show the effectiveness of gold thioglucose (GTG) in inducing hyperphagia and severe obesity in mice, and demonstrate the development of obesity‐induced diabetes in genetically normal mouse strains. GTG treated DBA/2, C57BLKs, and BDF1 mice gained weight rapidly and exhibited significant increases in nonfasting plasma glucose levels 8–12 weeks after GTG treatment. These mice showed significantly impaired insulin secretion, particularly in the early phase after glucose load, and reduced insulin content in pancreatic islets. Interestingly, GTG treated C57BL/6 mice did not become diabetic and retained normal early insulin secretion and islet insulin content despite being as severely obese and insulin resistant as the other mice. These results suggest that the pathogenesis of obesity‐induced diabetes in GTG‐treated mice is attributable to the inability of their pancreatic β‐cells to secrete enough insulin to compensate for insulin resistance. Mice developing obesity‐induced diabetes after GTG treatment might be a valuable tool for investigating obesity‐induced diabetes. Furthermore, comparing the genetic backgrounds of mice with different susceptibilities to diabetes may lead to the identification of novel genetic factors influencing the ability of pancreatic β‐cells to secrete insulin. 相似文献
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