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1.
Anat Sci Educ ; 10(2): 144-151, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-27533319

RESUMEN

Ultrasonography is increasingly used in medical education, but its impact on learning outcomes is unclear. Adding ultrasound may facilitate learning, but may also potentially overwhelm novice learners. Based upon the framework of cognitive load theory, this study seeks to evaluate the relationship between cognitive load associated with using ultrasound and learning outcomes. The use of ultrasound was hypothesized to facilitate learning in anatomy for 161 novice first-year medical students. Using linear regression analyses, the relationship between reported cognitive load on using ultrasound and learning outcomes as measured by anatomy laboratory examination scores four weeks after ultrasound-guided anatomy training was evaluated in consenting students. Second anatomy examination scores of students who were taught anatomy with ultrasound were compared with historical controls (those not taught with ultrasound). Ultrasound's perceived utility for learning was measured on a five-point scale. Cognitive load on using ultrasound was measured on a nine-point scale. Primary outcome was the laboratory examination score (60 questions). Learners found ultrasound useful for learning. Weighted factor score on "image interpretation" was negatively, but insignificantly, associated with examination scores [F (1,135) = 0.28, beta = -0.22; P = 0.61]. Weighted factor score on "basic knobology" was positively and insignificantly associated with scores; [F (1,138) = 0.27, beta = 0.42; P = 0.60]. Cohorts exposed to ultrasound had significantly higher scores than historical controls (82.4% ± SD 8.6% vs. 78.8% ± 8.5%, Cohen's d = 0.41, P < 0.001). Using ultrasound to teach anatomy does not negatively impact learning and may improve learning outcomes. Anat Sci Educ 10: 144-151. © 2016 American Association of Anatomists.


Asunto(s)
Anatomía/educación , Cognición , Educación de Pregrado en Medicina/métodos , Aprendizaje , Estudiantes de Medicina/psicología , Enseñanza , Ultrasonografía , Alberta , Comprensión , Gráficos por Computador , Instrucción por Computador , Curriculum , Evaluación Educacional/métodos , Escolaridad , Humanos , Modelos Lineales , Análisis de Componente Principal , Facultades de Medicina , Encuestas y Cuestionarios , Carga de Trabajo
2.
Protein Sci ; 19(8): 1490-9, 2010 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-20521333

RESUMEN

Circularly permuted fluorescent proteins (FPs) have a growing number of uses in live cell fluorescence biosensing applications. Most notably, they enable the construction of single fluorescent protein-based biosensors for Ca(2+) and other analytes of interest. Circularly permuted FPs are also of great utility in the optimization of fluorescence resonance energy transfer (FRET)-based biosensors by providing a means for varying the critical dipole-dipole orientation. We have previously reported on our efforts to create circularly permuted variants of a monomeric red FP (RFP) known as mCherry. In our previous work, we had identified six distinct locations within mCherry that tolerated the insertion of a short peptide sequence. Creation of circularly permuted variants with new termini at the locations corresponding to the sites of insertion led to the discovery of three permuted variants that retained no more than 18% of the brightness of mCherry. We now report the extensive directed evolution of the variant with new termini at position 193 of the protein sequence for improved fluorescent brightness. The resulting variant, known as cp193g7, has 61% of the intrinsic brightness of mCherry and was found to be highly tolerant of circular permutation at other locations within the sequence. We have exploited this property to engineer an expanded series of circularly permuted variants with new termini located along the length of the 10th beta-strand of mCherry. These new variants may ultimately prove useful for the creation of single FP-based Ca(2+) biosensors.


Asunto(s)
Colorantes Fluorescentes/química , Proteínas Luminiscentes/química , Isoformas de Proteínas/química , Estructura Secundaria de Proteína , Estructura Terciaria de Proteína , Secuencia de Aminoácidos , Técnicas Biosensibles , Calcio/química , Evolución Molecular Dirigida , Proteínas Luminiscentes/genética , Modelos Moleculares , Datos de Secuencia Molecular , Pliegue de Proteína , Isoformas de Proteínas/genética , Alineación de Secuencia , Proteína Fluorescente Roja
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