According to the fact that the abnormalities of visual pigment genes were always involved in the changing of the exon 5, two oligonucleotide primers were designed to amplify the exon 5 of red pigment gene and green pi...According to the fact that the abnormalities of visual pigment genes were always involved in the changing of the exon 5, two oligonucleotide primers were designed to amplify the exon 5 of red pigment gene and green pigment gene. After electrophoresis of the PCR products digested with Rsal or Sau3A, the DNA fragments from the exon 5 of red pigment gene (RPG) and green pigment gene (GPG) were separated since there are different restriction endonuclease sites. On the other hand, we analyzed the exon 5 rela...展开更多
Purpose : To investigate correlation of variation in the exon 5 of red and green pigment genes with color vision defects.Methods : Exon 5 of the red and green pigment genes in 11 protans, 19 deutans and 38 normal cont...Purpose : To investigate correlation of variation in the exon 5 of red and green pigment genes with color vision defects.Methods : Exon 5 of the red and green pigment genes in 11 protans, 19 deutans and 38 normal controls were analyzed by heteroduplux-SSCP analysis.Results : In all 11 protans and 8 of the 19 deutans, defects of the red or green pigment gene could be identified. The C polymorphism (A/C at codon 283) in green pigment gene was present in 8 of 44 trichromats and 5 of 24 dichromats. Specific electrophoretic bands were found in 2 normal controls and a deutan.Conclusions: Variation in the exon 5 of the red and green pigment genes is the most common cause for color vision defects. Heteroduplex-SSCP analysis is a suitable way in screening specific variation in visual pigment genes. Eye Science 1998; 14 : 130 - 133.展开更多
AIM: To evaluate the effects of chronic smoking on color vision in young subjects.METHODS: This study included 91 smokers and 88non-smokers(a total of 179 volunteers) without any ophthalmologic and systemical disorder...AIM: To evaluate the effects of chronic smoking on color vision in young subjects.METHODS: This study included 91 smokers and 88non-smokers(a total of 179 volunteers) without any ophthalmologic and systemical disorders. The subjects were between 18-40 years of age with a best corrected visual acuity(BCVA) of 20/20, normal anterior and posterior segment examinations and normal intraocular pressure. The color vision of the subjects were evaluated with Farnsworth-Munsell 100 Hue test(FMHT). The total error scores and axis calculation were performed for each subject and the results correlated.RESULTS: Mean age and the standard deviation was28±5y in the smokers group, and 26.7±5.5y in the control group(P =0.101). Sex distribution was similar in the two groups(P =0.365). There was no significant correlation between age and FMHT total error scores(P =0.069).Median of FMHT total error scores of smokers and non-smokers were 65 and 50.50, respectively. FMHT total error scores was found significantly higher in smokers than non-smokers(P =0.004). There was no statisticaly significant difference between smoker and non-smoker groups with respect to axis ratio calculation(P =0.611).There was no significant correlation with FMHT total error scores with neither smoking duration nor number of cigarettes smoked per day(P =0.405, P =0.454,respectively).· CONCLUSION: This study suggested that chronic smoking affects the color vision of young smokers but this may not be sector selective.展开更多
For the typical color detects of polysilicon wafers, i.e., edge discoloration, color inaccuracy and color non-uniformity, a new integrated machine vision detection method is proposed based on an HSV color model. By tr...For the typical color detects of polysilicon wafers, i.e., edge discoloration, color inaccuracy and color non-uniformity, a new integrated machine vision detection method is proposed based on an HSV color model. By transforming RGB image into three-channel HSV images, the HSV model can efficiently reduce the disturbances of complex wafer textures. A fuzzy color clustering method is used to detect edge discoloration by defining membership function for each channel image. The mean-value classi- fying method and region growing method are used to identify the other two defects, respectively. A vision detection system is developed and applied in the produc- tion of polysilicon wafers.展开更多
Purpose: To disclose the structure of visual pigment gene for a protanopia with specific variation.Methods: Exon 5 fragments of the red andgreen visual pigment genes from the protanopia with specific varnation as well...Purpose: To disclose the structure of visual pigment gene for a protanopia with specific variation.Methods: Exon 5 fragments of the red andgreen visual pigment genes from the protanopia with specific varnation as well as controls were amplified by poly-merase chain reaction (PCR). The PCR products were put through heteroduplex-SSCP analysis and PCR-RFLP (restriction fragement length polymorphism) analysis to clarify the specific variation. The specific variation of the exon 5 DNA fragment from the protanopia was identified by sequencing.Results: A novel 5’green-3’red hybrid gene fragment without the normal red and green visual pigment gene was discovered in the protanopia. He should only have a single visual pigment gene, 5’green-3’red hybrid gene, on his X chromosome. The fusion point is between codon 285 and codon 296 in exon 5. Conclusion : Unequal intragenic recombination may occur in exon 5 as well as its upstream. A 5’green-3’red hybrid gene may present independently on the X chromosome without展开更多
文摘According to the fact that the abnormalities of visual pigment genes were always involved in the changing of the exon 5, two oligonucleotide primers were designed to amplify the exon 5 of red pigment gene and green pigment gene. After electrophoresis of the PCR products digested with Rsal or Sau3A, the DNA fragments from the exon 5 of red pigment gene (RPG) and green pigment gene (GPG) were separated since there are different restriction endonuclease sites. On the other hand, we analyzed the exon 5 rela...
基金This work was supported by the National Natural Science Foundation of China (39670776 Qingjiong Zhang) and the Returnee Startup Foundation of National Educational Committee of China (Qingjiong Zhang)
文摘Purpose : To investigate correlation of variation in the exon 5 of red and green pigment genes with color vision defects.Methods : Exon 5 of the red and green pigment genes in 11 protans, 19 deutans and 38 normal controls were analyzed by heteroduplux-SSCP analysis.Results : In all 11 protans and 8 of the 19 deutans, defects of the red or green pigment gene could be identified. The C polymorphism (A/C at codon 283) in green pigment gene was present in 8 of 44 trichromats and 5 of 24 dichromats. Specific electrophoretic bands were found in 2 normal controls and a deutan.Conclusions: Variation in the exon 5 of the red and green pigment genes is the most common cause for color vision defects. Heteroduplex-SSCP analysis is a suitable way in screening specific variation in visual pigment genes. Eye Science 1998; 14 : 130 - 133.
文摘AIM: To evaluate the effects of chronic smoking on color vision in young subjects.METHODS: This study included 91 smokers and 88non-smokers(a total of 179 volunteers) without any ophthalmologic and systemical disorders. The subjects were between 18-40 years of age with a best corrected visual acuity(BCVA) of 20/20, normal anterior and posterior segment examinations and normal intraocular pressure. The color vision of the subjects were evaluated with Farnsworth-Munsell 100 Hue test(FMHT). The total error scores and axis calculation were performed for each subject and the results correlated.RESULTS: Mean age and the standard deviation was28±5y in the smokers group, and 26.7±5.5y in the control group(P =0.101). Sex distribution was similar in the two groups(P =0.365). There was no significant correlation between age and FMHT total error scores(P =0.069).Median of FMHT total error scores of smokers and non-smokers were 65 and 50.50, respectively. FMHT total error scores was found significantly higher in smokers than non-smokers(P =0.004). There was no statisticaly significant difference between smoker and non-smoker groups with respect to axis ratio calculation(P =0.611).There was no significant correlation with FMHT total error scores with neither smoking duration nor number of cigarettes smoked per day(P =0.405, P =0.454,respectively).· CONCLUSION: This study suggested that chronic smoking affects the color vision of young smokers but this may not be sector selective.
基金supported by the National Natural Science Foundation of China(Grant Nos.51205242,and 51075261)the Shanghai Science and Technology Innovation Action Plan,China(Grant No.13111102900)
文摘For the typical color detects of polysilicon wafers, i.e., edge discoloration, color inaccuracy and color non-uniformity, a new integrated machine vision detection method is proposed based on an HSV color model. By transforming RGB image into three-channel HSV images, the HSV model can efficiently reduce the disturbances of complex wafer textures. A fuzzy color clustering method is used to detect edge discoloration by defining membership function for each channel image. The mean-value classi- fying method and region growing method are used to identify the other two defects, respectively. A vision detection system is developed and applied in the produc- tion of polysilicon wafers.
文摘Purpose: To disclose the structure of visual pigment gene for a protanopia with specific variation.Methods: Exon 5 fragments of the red andgreen visual pigment genes from the protanopia with specific varnation as well as controls were amplified by poly-merase chain reaction (PCR). The PCR products were put through heteroduplex-SSCP analysis and PCR-RFLP (restriction fragement length polymorphism) analysis to clarify the specific variation. The specific variation of the exon 5 DNA fragment from the protanopia was identified by sequencing.Results: A novel 5’green-3’red hybrid gene fragment without the normal red and green visual pigment gene was discovered in the protanopia. He should only have a single visual pigment gene, 5’green-3’red hybrid gene, on his X chromosome. The fusion point is between codon 285 and codon 296 in exon 5. Conclusion : Unequal intragenic recombination may occur in exon 5 as well as its upstream. A 5’green-3’red hybrid gene may present independently on the X chromosome without
