نتایج جستجو برای: micronano rod
تعداد نتایج: 23244 فیلتر نتایج به سال:
A dominant form of human congenital nightblindness is caused by a gly90-->asp (G90D) mutation in rhodopsin. G90D has been shown to activate the phototransduction cascade in the absence of light in vitro. Such constitutive activity of G90D rhodopsin in vivo would desensitize rod photoreceptors and lead to nightblindness. In contrast, other rhodopsin mutations typically give rise to nightblindnes...
Introduction & Objective: Before using multi hook segmental fixation in schuerman kyphosis (SK) surgery, instrumentation by harington rod (H.R) was common. Materials & Methods: In this study we evaluated the complication and pre and post surgical kyphosis in 26 SK patients who had anterior release and anterior fusion and then halofemoral traction and finally posterior fusion and instrument...
A method combined the self-consistent field theory (SCFT) for the rigid rod with the Helfrich curvature elasticity theory for the vesicle has been developed for studying the shape of vesicles anchored by rigid rod. Both the deformation of the vesicle and the density distribution of rod segments can be obtained. Because of the vesicle's impenetrability for the rod segments and the decrease of th...
The organization of the rod spherule and of the horizontal cell axon terminals within the invagination of the rod spherule in the human retina was examined in serial sections by electron microscopy. Twenty-one rod spherules were reconstructed in this study. Axon terminal processes of type I horizontal cells consistently make one or two small punctate synapses onto each rod spherule within the i...
PURPOSE To investigate the slow and fast rod signals of the scotopic 15-Hz flicker ERG in patients with molecularly confirmed Stargardt disease type I (STGD1). There is evidence that these slow and the fast rod ERG signals can be attributed to the rod bipolar-AII cell pathway and the rod-cone coupling pathway, respectively. METHODS Twenty-seven patients with STGD1 with mutations in both allel...
Mutations in rod opsin-the light-sensitive protein of rod cells-cause retinitis pigmentosa. Many rod opsin mutations lead to protein misfolding, and therefore it is important to understand the role of molecular chaperones in rod opsin biogenesis. We show that BiP (HSPA5) prevents the aggregation of rod opsin. Cleavage of BiP with the subtilase cytotoxin SubAB results in endoplasmic reticulum (E...
RNA was analyzed in the whole rod cell and in the rod cell nucleus of the rabbit retina. The analysis was performed on rod cells or rod cell nuclei after they were isolated by microdissection and collected. The nuclei were denuded by selectively lysing inner and outer segments chemically. The rod cell contained an average of 0.65 micromicrog RNA. About 60% of the total RNA was nuclear. RNA conc...
Ameloglyphics is the study of enamel rod end patterns on a tooth surface. Our aim was to study the in vivo analysis of enamel rod end patterns on tooth surfaces for personal identification. In this study, the maxillary left canine and 1st premolar of 30 men and 30 women were included. The cellulose acetate peel technique was used to record enamel rod endings on tooth surfaces. Photomicrographs ...
Specification of retinal rod photoreceptors is determined by several different transcription factors that activate expression of rod-specific genes and repress expression of cone photoreceptor-specific genes. The mechanism by which this dual regulation occurs is unclear. We have found that Pias3, a transcriptional coregulator and E3 SUMO ligase that is selectively expressed in developing photor...
in this paper, a connecting rod was modeled and analyzed by finite element method. byusing genetic algorithm (ga) and modified cuckoo optimization algorithm (mcoa), the materialproperties and some geometrical specifications were optimized. cost function was a combination ofweight and stress. the connecting rod was under a load of 21.8 kn which obtained 360o crank angleat 5700 rev/min. the reduc...
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