Examples of using Variable expression in English and their translations into Portuguese
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Variable Expression.
CD11b and CD16 show variable expression.
Variable expression of CD11b, CD56, and CD57 are observed.
It has an autosomal recessive transmission with variable expression.
Variable expression is one of the most striking features of NF1.
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Values can also be used in integer and decimal variable expressions.
Variable expression is seen in follicular dendritic cells and endothelial cells.
Definición Inglés: Rare autosomal recessive disease with variable expressions.
Brothers with albinism can show variable expression in the visual function and clinical phenotype, suggesting that other genes can modify the phenotypic ocular findings.
Aniridia is inherited in an autosomal dominant manner with high penetrance and variable expression.
Then a new XPath can be chosen by entering a new value for Variable expression then clicking the Set expression button.
The disease is inherited by autosomal dominant transmission with complete penetrance but variable expression.
Hereditary pancreatitis(hp) is an autosomal dominant disorder with variable expression and incomplete penetrance estimated at 80.
Tuberous sclerosis is a congenital autosomal dominant disorder with high penetration and variable expression.
Although the majority of Dercum's disease cases occurs sporadically,there are reports suggesting an autosomal dominant inheritance, with variable expression.
It usually passes on in an autosomal dominant manner with variable expression and incomplete penetrance.
Like other sarcomas, pleomorphic liposarcoma expresses vimentin, while protein S100, smooth-muscle actin, cytokeratins AE1/AE3 and CAM5.2have variable expression.
Variable expressions of enzymes involved in pro-drugs biotransformation may lead to differences in conversion rates and active metabolite plasma concentration in interindividual and interethnic way.
Genetic counseling Transmission is autosomal dominant with almost complete penetrance but variable expression in severity within and between families.
Variable expressions of enzymes involved in the biotransformation of prodrugs may lead to differences in conversion rates and plasma concentration of the active metabolite in an inter-individual and interethnical manner.
NF1 is considered the most common"new" spontaneous, dominant, genetic mutation in human beings, with complete penetrance,despite having variable expression.
In this framework, a recent genetic study is worth noting. The study demonstrated variable expression of matrix metalloproteinase genes of the aorta that greatly influence physiological vascular remodeling during pregnancy.
Recent immunohistochemical studies on the gct demonstrate the presence of various proteins and metalloproteinases with variable expression in the tumor cell surface.
Several studies have been conducted in order to expand knowledge of the etiology of isolated OC. The knowledge of etiologic factors,prevalence, and variable expression of this phenotype and its associated malformations can help in clinical management and patient approach, as well as contribute to a better understanding of its etiology and pathogenesis.
In spite of the fact that its molecular base is unclear,Bart's syndrome is considered an autosomal dominant inheritance with complete penetration but variable expression.
Classically, it affects adolescent males andits presentation is variable. Although an autosomal dominant model of inheritance with incomplete penetrance and variable expression has been confirmed, both the autosomal-recessive inheritance and x-linked inheritance forms have been suggested. The pathogenesis of this condition also remains to be clarified; however, it is believed to be triggered by abnormal amounts of some substance in the plasma of affected individuals.
Sphingosine kinase-1(sphk1) mrna levels were increased in bc in both tissue and whole blood, buts1p-receptors showed variable expression, which was dependent on cell type of patients.
The wide variability spectrum reported by diverse authors is probably given by multiple factors such as the size of the samples, the methodology used andthe ancestral biologic features that determine the variable expression of these structures in the evaluated populations.
Bicuspid aortic valve is recognized as a multifaceted congenital heart disease,since it is an autosomal dominant condition with incomplete penetrance and variable expression, therefore the family members should be investigated.