Publications by authors named "Alphan Altinok"

Cancer biomarker research has become a data-intensive discipline requiring innovative approaches for data analysis that can combine traditional and data-driven methods. Significant leveraging can be done transferring methodologies and capabilities across scientific disciplines, such as planetary science and astronomy, each of which are grappling with and developing similar solutions for the analysis of massive scientific data.

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In plants mechanical signals pattern morphogenesis through the polar transport of the hormone auxin and through regulation of interphase microtubule (MT) orientation. To date, the mechanisms by which such signals induce changes in cell polarity remain unknown. Through a combination of time-lapse imaging, and chemical and mechanical perturbations, we show that mechanical stimulation of the SAM causes transient changes in cytoplasmic calcium ion concentration (Ca) and that transient Ca response is required for downstream changes in PIN-FORMED 1 (PIN1) polarity.

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Article Synopsis
  • Cell populations, like embryonic stem cells (ESCs), are diverse and can exhibit random fluctuations in gene expression, posing a challenge to decipher this variability.
  • Researchers utilized single-molecule RNA-FISH and time-lapse imaging to analyze individual ESCs, revealing that gene expression can switch between stable states and also show bursts of activity.
  • Inhibition of the "2i" signaling pathway affects these variations, and DNA methylation is crucial for maintaining the balance of gene expression states, highlighting the interplay between noise, coherent states, and epigenetic factors in ESC dynamics.
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Protein gradients and gene expression patterns are major determinants in the differentiation and fate map of the developing embryo. Here we discuss computational methods to quantitatively measure the positions of gene expression domains and the gradients of protein expression along the dorsal-ventral axis in the Drosophila embryo. Our methodology involves three layers of data.

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Quantitative studies in plant developmental biology require monitoring and measuring the changes in cells and tissues as growth gives rise to intricate patterns. The success of these studies has been amplified by the combined strengths of two complementary techniques, namely live imaging and computational image analysis. Live imaging records time-lapse images showing the spatial-temporal progress of tissue growth with cells dividing and changing shape under controlled laboratory experiments.

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Quantitative single-cell time-lapse microscopy is a powerful method for analyzing gene circuit dynamics and heterogeneous cell behavior. We describe the application of this method to imaging bacteria by using an automated microscopy system. This protocol has been used to analyze sporulation and competence differentiation in Bacillus subtilis, and to quantify gene regulation and its fluctuations in individual Escherichia coli cells.

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Tau is a multiply phosphorylated protein that is essential for the development and maintenance of the nervous system. Errors in Tau action are associated with Alzheimer disease and related dementias. A huge literature has led to the widely held notion that aberrant Tau hyperphosphorylation is central to these disorders.

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This paper focuses on contour tracking, an important problem in computer vision, and specifically on open contours that often directly represent a curvilinear object. Compelling applications are found in the field of bioimage analysis where blood vessels, dendrites, and various other biological structures are tracked over time. General open contour tracking, and biological images in particular, pose major challenges including scene clutter with similar structures (e.

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Background: The dynamic growing and shortening behaviors of microtubules are central to the fundamental roles played by microtubules in essentially all eukaryotic cells. Traditionally, microtubule behavior is quantified by manually tracking individual microtubules in time-lapse images under various experimental conditions. Manual analysis is laborious, approximate, and often offers limited analytical capability in extracting potentially valuable information from the data.

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