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Exceptional phenotypes

Fig. 5. Illustrations of modified pigment types and distributions given by one state of as a consequence of removal of Spm by meiotic segregation. Upper part of an ear of a plant that was a Sht/Ci sht in constitution and had one fully active Spm element, not linked with these markers. The ear was produced by a cross with a plant that was homozygous for Oi and shi and had no active Spm element. All the nonshrunken kernels received Oi" from the ear parent. The kernels with many deeply pigmented spots also received the Spm element. All the other nonshrunken kernels lack this element. Note the differences in pigment distribution and intensity among the kernels not receiving Spm. These kernels have the exceptional phenotypes referred to in the text. Fig. 5. Illustrations of modified pigment types and distributions given by one state of as a consequence of removal of Spm by meiotic segregation. Upper part of an ear of a plant that was a Sht/Ci sht in constitution and had one fully active Spm element, not linked with these markers. The ear was produced by a cross with a plant that was homozygous for Oi and shi and had no active Spm element. All the nonshrunken kernels received Oi" from the ear parent. The kernels with many deeply pigmented spots also received the Spm element. All the other nonshrunken kernels lack this element. Note the differences in pigment distribution and intensity among the kernels not receiving Spm. These kernels have the exceptional phenotypes referred to in the text.
Fig. 6. Illustration of the frequent erasure of the exceptional phenotypes in a succeeding generation. Upper part of an ear of a plant grown from a darkly pigmented, nonshrunken kernel lacking an Spm element. The pollen parent had the same constitution as indicated in Fig. 5. Only two kernels on this ear are like the ear-parent kernel. The capacity of Ui" to continue to produce the exceptional phenotype had been lost in all other kernels. Fig. 6. Illustration of the frequent erasure of the exceptional phenotypes in a succeeding generation. Upper part of an ear of a plant grown from a darkly pigmented, nonshrunken kernel lacking an Spm element. The pollen parent had the same constitution as indicated in Fig. 5. Only two kernels on this ear are like the ear-parent kernel. The capacity of Ui" to continue to produce the exceptional phenotype had been lost in all other kernels.
A newer prognostic index uses similar risk factors except that poor performance status is replaced with low hemoglobin (less than 12 g/dL). Current research is focused on the prognostic importance of phenotypic and molecular characteristics of NHL. [Pg.721]

Ethylene is the major feminizing hormone in most cucurbits showing a wide range of sex phenotypes with some exception of watermelon in which a steady increase in ACS isozymes transcript level in male flowers compared with female flowers has been reported. ... [Pg.113]

An alternative way to validate the critical function eliciting the disease-relevant phenotype is the use of tool modulators these can be small molecules, peptides, or antibodies that may not have the properties to be considered a drug, but may display sufficient potency and selectivity to be used to interrogate the specific protein function in the relevant system. Such tools, however, are rarely available with the required characteristics to allow for a robust interpretation of the experiment. The exception is represented by the... [Pg.10]

In order to eliminate parameters that are correlated to each other, we calculate their Pearson correlation coefficients (25). Linearly uncorrelated parameters have Pearson correlation coefficients close to zero and likely describe different aspects of the phenotype under study (exception for non-linearly correlated parameters which cannot be scored using Pearson s coefficient). We have developed an R template in KNIME to calculate Pearson correlation coefficients between parameters. Redundant parameters that yield Pearson correlation coefficients above 0.4 are eliminated. It is important to visually inspect the structure of the data using scatter matrices. A Scatter Plot and a Scatter Matrix node from KNIME exist that allow color-coding the controls for ease of viewing. [Pg.117]

Some fetal activity by 16 weeks gestation. Poor activity between birth and 2 months of age. Adult phenotype distribution reached by 4-6 months with adult activity reached by 1-3 years. Fetal levels approximately 30% of adult values. In newborns, activity is approximately 50% higher than adults with phenotype distribution which approximates adults. Exception is Korean children where adult activity is seen by 7-9 years of age. [Pg.186]


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Exceptions

Phenotype

Phenotype/phenotyping

Phenotypic

Phenotyping

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