16 research outputs found

    SDLFormer: A Sparse and Dense Locality-enhanced Transformer for Accelerated MR Image Reconstruction

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    Transformers have emerged as viable alternatives to convolutional neural networks owing to their ability to learn non-local region relationships in the spatial domain. The self-attention mechanism of the transformer enables transformers to capture long-range dependencies in the images, which might be desirable for accelerated MRI image reconstruction as the effect of undersampling is non-local in the image domain. Despite its computational efficiency, the window-based transformers suffer from restricted receptive fields as the dependencies are limited to within the scope of the image windows. We propose a window-based transformer network that integrates dilated attention mechanism and convolution for accelerated MRI image reconstruction. The proposed network consists of dilated and dense neighborhood attention transformers to enhance the distant neighborhood pixel relationship and introduce depth-wise convolutions within the transformer module to learn low-level translation invariant features for accelerated MRI image reconstruction. The proposed model is trained in a self-supervised manner. We perform extensive experiments for multi-coil MRI acceleration for coronal PD, coronal PDFS and axial T2 contrasts with 4x and 5x under-sampling in self-supervised learning based on k-space splitting. We compare our method against other reconstruction architectures and the parallel domain self-supervised learning baseline. Results show that the proposed model exhibits improvement margins of (i) around 1.40 dB in PSNR and around 0.028 in SSIM on average over other architectures (ii) around 1.44 dB in PSNR and around 0.029 in SSIM over parallel domain self-supervised learning. The code is available at https://github.com/rahul-gs-16/sdlformer.gitComment: Accepted at MICCAI workshop MILLanD 2023 Medical Image Learning with noisy and Limited Dat

    Exogenous MAL Reroutes Selected Hepatic Apical Proteins into the Direct Pathway in WIF-B Cells

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    Unlike simple epithelial cells that directly target newly synthesized glycophosphatidylinositol (GPI)-anchored and single transmembrane domain (TMD) proteins from the trans-Golgi network to the apical membrane, hepatocytes use an indirect pathway: proteins are delivered to the basolateral domain and then selectively internalized and transcytosed to the apical plasma membrane. Myelin and lymphocyte protein (MAL) and MAL2 have been identified as regulators of direct and indirect apical delivery, respectively. Hepatocytes lack endogenous MAL consistent with the absence of direct apical targeting. Does MAL expression reroute hepatic apical residents into the direct pathway? We found that MAL expression in WIF-B cells induced the formation of cholesterol and glycosphingolipid-enriched Golgi domains that contained GPI-anchored and single TMD apical proteins; polymeric IgA receptor (pIgA-R), polytopic apical, and basolateral resident distributions were excluded. Basolateral delivery of newly synthesized apical residents was decreased in MAL-expressing cells concomitant with increased apical delivery; pIgA-R and basolateral resident delivery was unchanged. These data suggest that MAL rerouted selected hepatic apical proteins into the direct pathway
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