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Wenjing Jia

Publications and source records attributed to Wenjing Jia.

2 recordsLinked to original sources

Description of the cardiac movement using hexagonal image structures.

The most notable characteristic of the heart is its movement. Detection of dynamic information describing cardiac movement such as amplitude, speed and acceleration facilitates interpretation of normal and abnormal function. In recent years, the Omni-directional M-mode Echocardiography System (OMES) has been developed as a process that builds moving information from a sequence of echocardiography image frames. OMES detects cardiac movement through construction and analysis of Position-Time Grey Waveform (PTGW) images on some feature points of the boundaries of the ventricles. Image edge detection plays an important role in determining the feature boundary points and their moving directions as the basis for extraction of PTGW images--Spiral Architecture (SA) has proved efficient for image edge detection. SA is a hexagonal image structure in which an image is represented as a collection of hexagonal pixels. There are two operations called spiral addition and spiral multiplication defined on SA. They correspond to image translation and rotation, respectively. In this paper, we perform ventricle boundary detection based on SA using various defined chain codes. The gradient direction of each boundary point is determined at the same time. PTGW images at each boundary point are obtained through a series of spiral additions according to the directions of boundary points. Unlike the OMES system, our new approach is no longer affected by the translation movement of the heart. As its result, three curves representing the amplitude, speed and acceleration of cardiac movement can be easily drawn from the PTGW images obtained. Our approach is more efficient and accurate than OMES, and our results contain a more robust and complete description of cardiac motion.

Algorithms↗

Role of the Escherichia coli nitrate transport protein, NarU, in survival during severe nutrient starvation and slow growth.

Escherichia coli K-12 strains expressing either NarU or NarK as the only nitrate transport protein are both able to support nitrate-dependent anaerobic growth. The narK gene is highly expressed during anaerobic growth in the presence of nitrate, consistent with a role for NarK in nitrate transport coupled to nitrate reduction by the most active nitrate reductase encoded by the adjacent narGHJI operon. The physiological role of NarU is unknown. Reverse transcriptase PCR experiments established that, unlike the monocistronic narK gene, narU is co-transcribed with narZ as the first gene of a five-gene narUZYWV operon. The narK and narU genes were fused in-frame to a myc tag: the encoded fusion proteins complemented the nitrate-dependent growth defect of chromosomal narK and narU mutations. A commercial anti-Myc antibody was used to detect NarK and NarU in membrane fractions. During anaerobic growth in the presence of nitrate, the quantity of NarU-Myc accumulated during exponential growth was far less than that of NarK-Myc, but NarU was more abundant than NarK in stationary-phase cultures in the absence of nitrate. Although the concentration of NarU-Myc increased considerably during the post-exponential phase of growth, NarK-Myc was still more abundant than NarU-Myc in stationary-phase bacteria in the presence of nitrate. In chemostat competition experiments, a strain expressing only narU had a selective advantage relative to a strain expressing only narK during nutrient starvation or very slow growth, but NarK(+) bacteria had a much greater selective advantage during rapid growth. The data suggest that NarU confers a selective advantage during severe nutrient starvation or slow growth, conditions similar to those encountered in vivo.

Anion Transport Proteins↗