排序方式: 共有28条查询结果,搜索用时 0 毫秒
1.
Genetic polymorphisms and intrauterine development. Evidence of decreased heterozygosity in light-for-dates human newborn babies 总被引:2,自引:0,他引:2
E. Bottini F. Gloria-Bottini P. Lucarelli A. Polzonetti F. Santoro A. Varveri 《Cellular and molecular life sciences : CMLS》1979,35(12):1565-1567
Summary In 2 independent samples of low-birth-weight infants the proportion of females and homozygotes for a series of polymorphic systems was higher in light-for-dates than in preterm babies. The observation seems to give support to the hypothesis that homozygosity for normal polymorphisms may decrease in general intrauterine growth rate. Since it is known that survival rate is strongly related to birth weight, a correlation between growth retardation and homozygosity may have a major role in the maintenance of such polimorphisms.We thank Prof. L. Ginzburg for helpful comments. 相似文献
2.
新疆少数民族中学"体育与健康"课程教学现状的调查与研究 总被引:1,自引:0,他引:1
本对新疆南、北疆、东疆地区和乌鲁木齐市的101所民族中学进行实地的调查研究,通过对各民族中学体育教学中大纲、教材、场地器材、汉语授课、男女生分班情况、教师培训、教学计划以及对课程改革的认识等方面的分析.进一步了解新疆各地区民族中学学校体育状况,特别是“体育与健康”课程实施后,各地区民族中学学校体育教学现状以及所面临的问题,旨在加快新疆少数民族中学的体育教学改革和《体育与健康》课程教学研究。为新疆教育主管部门制定实施“体育与健康”课程教学提供决策依据。 相似文献
3.
Riassunto Gli Autori dimostrano che lo spettro di diffrazione a basso angolo del tessuto osseo è determinato da micelle elissoidali (elissoidi di rivoluzione) delle dimensioni di 200 × 70 Å, pertinenti all'osseina e accolte in incavi delimitati dalla frazione inorganica. 相似文献
4.
Summary It is reported that Ca2+-induced discharge of in situ nematocytes of acontia ofCalliactis parasitica can occur by cell-to-cell transmission along the acontial filament at a speed that averages 9.8·10–3 cm–1. The discharge is preceded by protrusion of nematocytes that proceeds along the acontium at a slightly higher speed. 相似文献
5.
Molecular mechanism of cAMP modulation of HCN pacemaker channels. 总被引:26,自引:0,他引:26
Hyperpolarization-activated cation channels of the HCN gene family contribute to spontaneous rhythmic activity in both heart and brain. All four family members contain both a core transmembrane segment domain, homologous to the S1-S6 regions of voltage-gated K+ channels, and a carboxy-terminal 120 amino-acid cyclic nucleotide-binding domain (CNBD) motif. Homologous CNBDs are responsible for the direct activation of cyclic nucleotide-gated channels and for modulation of the HERG voltage-gated K+ channel--important for visual and olfactory signalling and for cardiac repolarization, respectively. The direct binding of cyclic AMP to the cytoplasmic site on HCN channels permits the channels to open more rapidly and completely after repolarization of the action potential, thereby accelerating rhythmogenesis. However, the mechanism by which cAMP binding modulates HCN channel gating and the basis for functional differences between HCN isoforms remain unknown. Here we demonstrate by constructing truncation mutants that the CNBD inhibits activation of the core transmembrane domain. cAMP binding relieves this inhibition. Differences in activation gating and extent of cAMP modulation between the HCN1 and HCN2 isoforms result largely from differences in the efficacy of CNBD inhibition. 相似文献
6.
7.
8.
Cornea regeneration in the Pacific giant octopus,Octopus dofleini,and the common octopus,O. vulgaris
Summary Cornea regeneration in a Pacific giant octopus,Octopus dofleini, occurred within 10 days after the injury was observed. Surgical removal of the cornea in 2 common octopi,O. vulgaris experimentally duplicated this cornea regeneration within a 10-day period. It is, therefore, concluded that besides sucking discs, arms, and nerve fibres, octopi can also regenerated corneal tissue.The authors would like to thank U. E. Friese, B. Borowski, P. Burn, J.W. Atz, G.J. Nelson, H. Feinberg, P. Fenimore, C. Roper, M. Nixon, M. Segalla, G. Clark, D.O. Calligaro, J.M. Anderson and R.J. Koestler for assistance and advice. Illustrations were drawn by G.D. This work was supported by the New York Aquarium of the New York Zoological Society, while G.D. was at the New York Aquarium. 相似文献
9.
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria. 总被引:22,自引:0,他引:22
J N Spelbrink F Y Li V Tiranti K Nikali Q P Yuan M Tariq S Wanrooij N Garrido G Comi L Morandi L Santoro A Toscano G M Fabrizi H Somer R Croxen D Beeson J Poulton A Suomalainen H T Jacobs M Zeviani C Larsson 《Nature genetics》2001,28(3):223-231
The gene products involved in mammalian mitochondrial DNA (mtDNA) maintenance and organization remain largely unknown. We report here a novel mitochondrial protein, Twinkle, with structural similarity to phage T7 gene 4 primase/helicase and other hexameric ring helicases. Twinkle colocalizes with mtDNA in mitochondrial nucleoids. Screening of the gene encoding Twinkle in individuals with autosomal dominant progressive external ophthalmoplegia (adPEO), associated with multiple mtDNA deletions, identified 11 different coding-region mutations co-segregating with the disorder in 12 adPEO pedigrees of various ethnic origins. The mutations cluster in a region of the protein proposed to be involved in subunit interactions. The function of Twinkle is inferred to be critical for lifetime maintenance of human mtDNA integrity. 相似文献
10.