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At least 289 records · Page 16Linked to original sources
PubMed2000

Is skin color a marker for racial discrimination? Explaining the skin color-hypertension relationship.

It is widely assumed that dark-skinned Blacks have higher rates of hypertension than their lighter-skinned cohorts because the former experience greater racial discrimination. However, there is no empirical evidence linking skin color to discrimination. This study tested the extent to which skin color is associated with differential exposure to discrimination for a sample of 300 Black adults. Results revealed that dark-skinned Blacks were 11 times more likely to experience frequent racial discrimination than their light-skinned counterparts; 67% of subjects reporting high discrimination were dark-skinned and only 8.5% were light-skinned. These preliminary findings suggest that skin color indeed may be a marker for racial discrimination and highlight the need to assess discrimination in studies of the skin color-hypertension relationship.

Adolescent↗
PubMed2006

Performance comparison of one-color and two-color platforms within the MicroArray Quality Control (MAQC) project.

Microarray-based expression profiling experiments typically use either a one-color or a two-color design to measure mRNA abundance. The validity of each approach has been amply demonstrated. Here we provide a simultaneous comparison of results from one- and two-color labeling designs, using two independent RNA samples from the Microarray Quality Control (MAQC) project, tested on each of three different microarray platforms. The data were evaluated in terms of reproducibility, specificity, sensitivity and accuracy to determine if the two approaches provide comparable results. For each of the three microarray platforms tested, the results show good agreement with high correlation coefficients and high concordance of differentially expressed gene lists within each platform. Cumulatively, these comparisons indicate that data quality is essentially equivalent between the one- and two-color approaches and strongly suggest that this variable need not be a primary factor in decisions regarding experimental microarray design.

Equipment Design↗
PubMed1997

Color pattern formation on the wing of the butterfly Pieris rapae. 1. Cautery induced alteration of scale color and delay of arrangement formation.

Experimental approaches to color pattern formation of lepidopteran insects have been made exclusively by analyzing pattern alterations in adult wings induced by operations. We microcauterized the presumptive black region of the dorsal forewing of the butterfly Pieris rapae and analyzed not only the resultant color pattern in the adult wing but also the cell behavior in the pupal wing epidermis around the injury. Cautery induced color alterations were as follows: (i) cautery up to 49.5 h after pupation resulted in white regions appearing within the black region while later cauteries induced larger white regions; (ii) cautery between 50 and 59.5 h resulted in the white regions induced by the cauteries being dramatically decreased; (iii) cautery after 60 h resulted in white regions that had almost disappeared. The examination of the cell behavior in the pupal wing epidermis after cauteries showed that the row formation of scale precursor cells was delayed. This delayed area varied with the time of cautery, in the same manner as that in the induced white area in the adult wing ((i)-(iii) above). The relationship between scale color alteration and the developmental delay of the scale row formation is discussed.

Animals↗
PubMed1997

Color pattern formation on the wing of a butterfly Pieris rapae. 2. Color determination and scale development.

It has been shown that microcautery on the prospective apical black region of the early pupal forewing of a butterfly, Pieris rapae, causes alteration of the scale color on the adult wing and a delay in histogenesis of the pupal wing. From these results, it has been assumed that the developmental delay of scale cells in the pupal wing alters their developmental fate and the hypothesis that different color fates of scales are determined by differences in the developmental timetables between scale cells is proposed. In this study, we attempted to find the developmental timetables of individual scales expressing specific color to test this hypothesis. It was found that the holes on the upper surface of a scale become larger as they develop and the hole sizes of scales in the white region are always larger than in the black region on the same wings either during pupal period or after eclosion. This suggests that the scale hole size is a good index that reflects developmental rate of the scale and a difference in the hole size between adult scales is attributed to a difference in the developmental timetables when their ancestral scale precursor cells were in the pupal period. A comparison of the hole sizes between adult scales in different color regions suggested that normal white scales were in a more advanced state than were the black ones but white scales induced by microcautery were in a less advanced state than black ones on the same wing. This supports our hypothesis.

Animals↗
PubMed2004

Improvement of chromatic aberration of a plastic rod lens array. 1. Combination-color lens arrays consisting of several kinds of rod lenses with different gradient constants and different color filter functions.

We propose a new type of rod lens array with improved chromatic aberration. The new rod lens array consists of several kinds of rod lenses with different gradient constants and different color filter functions. The gradient constant of each lens was prepared such that the total conjugate length was identical to the specific wavelength of the lens with a constant lens length. We call our new type of rod lens array a combination-color lens array. The characteristics of this color-type lens array are as follows: high angular aperture, short focal length, and ease of production with established procedures. The optical resolution of the rod lens array is 300 dpi in a wide wavelength range that is high enough to be applied to color scanners.

Journal Article↗
PubMed1999

Measuring muscle color on beef carcasses using the L*a*b* color space.

Because beef muscle color affects consumers' purchasing decisions, is a factor in determining USDA grades, and has been shown to be useful in sorting carcasses according to palatability, this study was conducted to determine the effects of measurement conditions on L*, a*, and b* values, to determine the relationships among USDA quality grading factors, muscle pH, electrical impedance, and colorimeter readings, and to develop a classification system that could be used to sort beef carcasses with respect to muscle color. Data were collected over 2 d from 145 beef carcasses in a commercial packing plant. The exposed longissimus muscle at the 12th/13th rib was used for all muscle pH, electrical impedance, and colorimeter measurements. A Minolta Chroma Meter CR-310 was used to obtain L*, a*, and b* readings. Bloom time, from 0 to 93 min, had a greater effect on a* and b* readings than on L* readings. The L* values stabilized after approximately 30 min bloom time, and a* and b* values stabilized after 78 min bloom time, but relative differences among carcasses in L*, a*, and b* values did not change after 3 to 12 min bloom time. Days postmortem, cut surface (anterior versus posterior), and within-muscle location (medial vs lateral) did not affect L*, a*, and b* readings (P > .05). Blotting the surface moisture from the longissimus muscle resulted in lower a* readings (P < .05), but did not affect L* and b* readings (P > .05). The L*, a*, and b* values were correlated with lean maturity scores (-.67, -.30, and -.40, respectively), dark cutter discount (-.60, -.76, and -.73, respectively), muscle pH (-.57, -.79, and -.78, respectively), and electrical impedance (-.27, -.21, and -.25, respectively). Two muscle color classification systems, nine classes each, are proposed, one system based on L* and one system based on b*. The main advantage of the L* categorization system over the b* system is that the L* value was less sensitive to bloom time, and the main advantage of the b* categorization system over the L* system is that the b* system was slightly more precise at segregating carcasses based upon corresponding differences in muscle pH. This research provides procedural guidelines for measuring beef muscle color and shows that a colorimeter can effectively aid researchers and graders in assessing beef carcass quality.

Animal Husbandry↗
PubMed2006

[Genetic analysis of feather color and shank color traits based on F-2 resource population in Tibetan chicken].

Tibetan chickens were crossed reciprocally with White Leghorn and Shou-Guang chicken respectively, and inter se matings in F1 were carried out to generate the F2 population. Feather color and shank color appearance and segregation ratio in F1 and F2 were observed. Results indicate that white feather of White Leghorn chicken and black feather of Shou-Guang chicken exhibit complete dominant heredity to hemp feather of Tibetan chicken. Hemp feather is determined by two or more alleles. Only when these two or more alleles are concurrently present, will hemp feather then be displayed. The Id/id allele that determines shank color demonstrates sex-linked inheritance, and the recessive id is expressed gradually in the homozygotes. We confirm that genotype of shank color in White Leghorn rooster used in this study is the dominant homozygote.

Animal Structures↗
PubMed1977

[Contribution to the problem of color reproduction in photomicrography with color films (author's transl)].

In order to define clearly the possibilities and conformities in reproducing stained microscopic specimens we need an exact system of formal co-ordination and conception. Therefore, an assay was made to find practical criterions allowing the choice of the most suited color films for the photomicrography of stained preparations. This was done by splitting up the transfer of information by adequate reproducible colors of the slides with the color space. Examples are given for Eosin bluish, for the mixture of Light green and Xylidin Ponceau and for the colors of Fujichrome R 100.

Histological Techniques↗
PubMed1994

Ball color, eye color, and a reactive motor skill.

Researchers investigating performance differences between light- and dark-eyed individuals have indicated that dark-eyed individuals perform better on reactive activities than light-eyed individuals. College students (61 men, 64 women) performed a forehand rally with different colored racquetballs. Eye color, sex, and total hits were recorded for each subject. Men scored significantly better with balls of each color than did women. Dark-eyed men performed better than other subjects and performance was better with blue balls than yellow or green balls.

Adolescent↗
PubMedDate not supplied

Using a computer color-matching system in color reproduction of porcelain restorations. Part 3: A newly developed spectrophotometer designed for clinical application.

This paper reports the development of a newly modified, noncontact spectrophotometer for clinical use. The instrument is capable of accurately measuring the color within small areas (1 x 2 mm) of a tooth. This spectrophotometer used a 45 degree/0 degree geometry, a 150W halogen lamp, and fiberoptics to focus the light, together with a lens having a focal point distance of 85 mm. A movable platform was added to the apparatus to automatically scan and measure the color of specific areas. Short-term repeatability indicated the color difference delta E to be approximately 0.15.

Color↗
PubMed2000

Three-color versus four-color multiparameter cell cycle analyses of primary acute myeloid leukemia samples.

Checkpoint alterations that impact cell cycle and apoptosis responses to therapeutic treatments may produce drug resistance in acute myeloid leukemia (AML). To study these, we have developed flow cytometry assays of checkpoint function that also allow quantitation of key molecular regulators of apoptosis and cell cycle. We have used three-color (3C) assays, with FITC-labeled anti-BCL-2 and PE-labeled anti-proliferating cell nuclear antigen (PCNA) antibodies, and the DNA dye 7-aminoactinomycin, to characterize primary leukemia cells identified in DNA x side light scatter (SSC) histograms. We showed that 3C assays are accurate and reproducible in analyses of leukemia cell lines and of primary AML and normal bone marrow samples (Banker et al.: Blood 89: 243-255, 1997; Banker et al.: Leukemia Res 22: 221-239, 1998; Banker et al.: Clin Cancer Res 4: 3051-3062, 1998). To further confirm the validity of our SSC leukemia cell gating and to address whether immunophenotypic AML subsets might have different biologic properties, we have now designed four-color (4C) flow assays to characterize checkpoint status in leukemic blasts specifically identified by surface immunostaining. In modeling this assay strategy, PE/Cy5-labeled anti-CD34 antibody was used to detect blasts, with FITC-labeled anti-BCL-2, PE-labeled anti-PCNA antibodies, and Hoechst 33342 (H33342) DNA dye. Four-color CD34-gated data was concordant with 3C, SSC-gated data for leukemia cell lines and for most primary AML samples with high and intermediate blast counts. BCL-2 and PCNA immunopositivity and sub-G1 apoptosis determinations were different in the CD34-gated versus SSC-gated blasts in particular samples with smaller CD34(+) subsets, suggesting that leukemia samples can contain blast subsets with different biologic properties. On the other hand, PCNA-gated cell-cycle distributions in untreated cells and G1 versus S phase cell-cycle arrests after cytosine arabinoside treatments were completely concordant in 4C and 3C assays. We conclude that both 3C and 4C assays can be used to characterize protein expression and cell-cycle drug response patterns in leukemia blasts, but that 4C assays may additionally allow discrimination of these properties in immunophenotypic leukemia subsets.

Antibodies↗
PubMed1997

The sensitivity of new color systems in blood-flow diagnosis. The maximum entropy method and angio-color-comparative in vitro flow measurements to determine sensitivity.

BACKGROUND: Two new blood-flow-diagnosis techniques have recently been developed as supplements to the established color techniques: the MEM (maximum entropy method) technique and color flow amplitude (power Doppler). These are capable of representing blood flow in distinctly more slowly flowing areas than is possible with the conventional Doppler technique. METHODS: Both methods make use of the Doppler technique in part, yet analyze the reflected signal in a different manner, in so doing optimizing the relation between the noise and the signal. Measurements were obtained on two anatomic flow models to test the sensitivity of both techniques under slow flow conditions. RESULTS: The slowest flow the MEM technique was capable of recording was 0.5 mm/s, albeit utilizing a 5-MHz transducer for the MEM technique and a 10-MHz transducer for the angio technique. One may thus assume that the MEM technique would be still more sensitive when utilizing a 10-MHz transducer. The advantage of the MEM technique is its real-time flow representation: The angio technique requires a few seconds of acquisition time. This could have serious consequences during clinical utilization. Doppler sonography was merely capable of detecting a minimum flow velocity of 15 mm/s. The angio technique is less dependent on the angle during flow representation than the MEM technique. CONCLUSIONS: The distinctly higher sensitivity of these two new color techniques offers new possibilities in the clinical sector as far as the perfusion diagnosis of organs and tumors is concerned.

Angiography↗
PubMed1991

Effect of background color and low temperature on skin color and circulating alpha-MSH in two species of leopard frog.

Circulating levels of alpha-melanocyte stimulating hormone (alpha-MSH) in two species of leopard frog, Rana pipiens and R. chiricahuensis, were measured by radioimmunoassay to reveal the correlation between skin color change induced by background color and by low temperature. High levels of alpha-MSH were found in both species of frog on a black background, but R. chiricahuensis had eight times higher levels than R. pipiens, R. chiricahuensis also exhibited the ability to darken its ventral surface, whereas the ventral surface of R. pipiens remained white. Neither skin color nor plasma alpha-MSH of R. pipiens was affected by cold. Low temperature did, however, darken dorsal and ventral skin of R. chiricahuensis in vivo, which corresponded to increased levels of plasma alpha-MSH. Dorsal and ventral skin of R. chiricahuensis, in vitro, darken in a dose-dependent manner to alpha-MSH, but not to cold.

Adaptation, Physiological↗
PubMed1983

Cellular mechanisms for color-coding in holostean retinas and the evolution of color vision.

Electrophysiological recording and microspectrophotometry were used to analyze retinal function in representatives of the two surviving genera of holostean grade fish--the bowfin (Amia calva) and gars (Lepisosteus sp.). The properties of the cone photopigments, horizontal cells and ganglion cells show that these holostean retinas have cellular mechanisms for color vision which are fundamentally similar to those previously described for teleosts, turtle and mammals. These findings suggest that trichromatic receptor systems and opponent color-coding mechanisms may have evolved in primitive Neopterygii or more ancient fish, before the advent of teleosts. In conjunction with other recent data on living representatives of primitive fishes, these findings also add renewed plausibility for the view that vertebrate color vision could have taken a common origin some 400 million years ago from an ancestral aquatic jawed vertebrate.

Action Potentials↗
PubMed1987

Early color deprivation and subsequent color vision in a dichromatic monkey.

A squirrel monkey (Saimiri sciureus) was reared for the first 4 months of life in a dim, colorless environment. Following an additional 10 months of normal visual experience, tests of color vision and spectral sensitivity were run on this animal and a control subject. The results suggest that the adult expression of dichromatic color vision does not depend on color experience during the first 4 months of life.

Animals↗
PubMed2000

Color-specific depth mechanisms revealed by a color-contingent depth aftereffect.

Models of stereoscopic depth perception for both natural and random-dot images have focused mainly on the matching of achromatic features of binocular images. Recently, a growing body of research has investigated whether chromatic features can also contribute to the construction of stereoscopic depth. Here we present experiments yielding color-contingent depth aftereffects comparable in magnitude to those measured after adaptation to achromatic stimuli as evidence of neural mechanisms tuned to both color and depth. Furthermore, we report that the locus of the combined processing of color and depth is likely to lie beyond the site of binocular matching.

Adaptation, Physiological↗