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101.
102.
M. F. Humphrey S. A. Dunlop A. Shimada L. D. Beazley 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》1992,90(3):630-634
Summary In this study, we crushed one optic nerve in the frog Litoria (Hyla) moorei and at intervals thereafter anterogradely labelled optic axons with horseradish peroxidase (HRP). For one series, HRP was applied between the eye and the crush site and in a second series between the crush site and the chiasm. A tectal projection of regenerating axons was seen in both series but, in addition, up to 12 weeks post-crush, the second series displayed an additional projection. Its appearance matched that of the disconnected, but persisting, optic axon terminals which are found after enucleation or optic nerve ligation. We conclude that, in the frog, many disconnected optic axons persist throughout the period of optic nerve regeneration and of restoration of an orderly retino-tectal map.Abbreviation HRP
horseradish peroxidase 相似文献
103.
104.
Toshio Shimada Norimasa Okui Thoru Kawai 《Macromolecular chemistry and physics.》1980,181(12):2643-2654
The discontinuous change of the lamellar thickness with crystallization temperature was studied for low molecular weight fractions of OH-terminated poly(ethylene oxide) (PEO). IR analyses demonstrated that almost all of the molecular chain ends were associated in the molten state, whereas a large part of their ends were free in dilute solution. Discontinuous changes were observed for low molecular weight PEO fractions crystallized from the melt, whereas continuous changes were found both for PEO's crystallized from dilute solution and those with phenylated end groups crystallized from the melt. Accordingly, it was pointed out that the association of the end groups could play an important role in the crystallization mechanism and the conformation of the resultant PEO crystals. 相似文献
105.
Comparison of inhibition of the action of C1 on C4 by two synthetic substrates of C1 esterase, TAMe and ATEe
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Two synthetic substrates, TAMe and ATEe, were tested for their abilities to inhibit the formation of SAC14 and SAC142 and found to act as inhibitors in different ways. In addition to inhibition of the formation of SAC142 from SAC14 and C2, TAMe inhibited the formation of SAC14 from SAC1 and C4 and the inactivation of C4 by C1 and EAC1. ATEe inhibited the formation of SAC14, but only slightly inhibited the inactivation of C4 by C1 and EAC1 and further did not interfere with the formation of SAC142. ATEe could be entirely replaced by acetyl-L-tyrosine in these effects on the action of C1 on C4. The possible mechanism of inhibitions by these compounds was discussed. 相似文献
106.
A common mutation in methylenetetrahydrofolate reductase gene among the Japanese population 总被引:7,自引:0,他引:7
Hisahide Nishio Myeong Jin Lee Motoko Fujii Kazuomi Kario Kazunori Kayaba Kazuyuki Shimada Masafumi Matsuo Kimiaki Sumino 《Journal of human genetics》1996,41(2):247-251
Summary Hyperhomocysteinemia has been reported as an independent risk factor for atherosclerotic cerebrovascular and coronary heart diseases. 5,10-Methylenetetrahydrofolate reductase (MTHFR) is one of the enzymes responsible for hyperhomocysteinemia. The C to T transition of the MTHFR gene at nucleotide position 677 results in decreasing the enzymatic activity and increasing the plasma homocysteine level. We studied the distribution of the MTHFR gene mutation among the Japanese population. The subjects were 129 Japanese males (aged 40–59 years). The allele frequency of the mutation was 0.38. The frequencies of the three genotypes were as follows: +/+, 11%; +/–, 54%; –/–, 35% (+ and – indicate the presence and absence of the mutation, respectively). We also studied the frequency of the MTHFR gene mutation in the middle-aged Japanese males with hypertension to investigate the possibility that this mutation is related to essential hypertension. The normotensive and hypertensive subjects were identical in the distribution of the mutated allele and the frequencies of the three genotypes. Furthermore, the prevalence of hypertension in each genotype group was same, although the mean diastolic pressure of the group with homozygous mutation was significantly higher than that of other groups (p<0.05). 相似文献
107.
108.
Yamamoto T Minami R Ohbayashi C Inaba M 《Archives of pathology & laboratory medicine》2002,126(4):468-470
Epithelioid leiomyosarcoma in the external deep soft tissue is extremely rare. Most epithelioid leiomyosarcomas occur in the uterus. We present a case of epithelioid leiomyosarcoma occurring in the muscle of the thigh of a 78-year-old man. Histologically, the tumor predominantly consisted of round or polygonal cells arranged in sheets with a focal spindle cell component. Immunohistochemical analysis revealed that the tumor cells expressed vimentin, alpha-smooth muscle actin, and alpha-sarcomeric actin. The tumor was negative for desmin, S100 protein, glial fibrillary acidic protein, pan-keratin, epithelial membrane antigen, CAM 5.2, HMB-45, leukocyte common antigen, factor VIII-associated antigen, and CD34. Electron microscopically, some tumor cells contained abundant actin-type filaments in their cytoplasm. 相似文献
109.
110.
Masanori Taira Jun Kudoh Shinsei Minoshima Taizo Iizasa Hideaki Shimada Yoshiko Shimizu Masamiti Tatibana Nobuyoshi Shimizu 《Somatic Cell and Molecular Genetics》1989,15(1):29-37
Complementary DNA clones for phosphoribosylpyrophosphate synthetase subunits I and II (PRS I and PRS II) were used to determine the chromosomal localization of the corresponding human genes. Southern blot analysis of genomic DNAs isolated from human placenta and a panel of humanmouse somatic cell hybrids revealed that the rat PRS I cDNA probe detected at least five human specific DNA segments (23, 20, 14.5, 6.7, and 4.3 kb) in BamHI digests. The 23-, 14.5-, and 6.7-kb DNA segments were detected only if the hybrids contained human chromosome X or translocation chromosome 7p
+ (7qter>7p22::Xq21>Xqter), indicating the location of these segments to Xq21-qter (PRPS1). The 20- and 4.3-kb DNA segments did not cosegregate with the other three segments, and spot blot hybridization analysis using flow-sorted human chromosomes indicated that these are the PRPS1-related genes (PRPS1L1 and PRPS1L2) and could be assigned to chromosomes 7 and 9, respectively. The human-specific PRS II cDNA probe revealed a BamHI DNA segment (17 kb), which segregated condordantly with the X chromosome but not with the PRPS1 gene. We surmise that the gene for PRS II (PRPS2) is located at a different region of the X chromosome, namely Xpter-q21.Preliminary report of this research was presented at Ninth International Workshop on Human Gene Mapping, Abstract supplement p. 5 (1987). 相似文献