25 research outputs found
Understanding Expressivity of GNN in Rule Learning
Rule learning is critical to improving knowledge graph (KG) reasoning due to
their ability to provide logical and interpretable explanations. Recently,
Graph Neural Networks (GNNs) with tail entity scoring achieve the
state-of-the-art performance on KG reasoning. However, the theoretical
understandings for these GNNs are either lacking or focusing on
single-relational graphs, leaving what the kind of rules these GNNs can learn
an open problem. We propose to fill the above gap in this paper. Specifically,
GNNs with tail entity scoring are unified into a common framework. Then, we
analyze their expressivity by formally describing the rule structures they can
learn and theoretically demonstrating their superiority. These results further
inspire us to propose a novel labeling strategy to learn more rules in KG
reasoning. Experimental results are consistent with our theoretical findings
and verify the effectiveness of our proposed method. The code is publicly
available at https://github.com/LARS-research/Rule-learning-expressivity.Comment: 24 pages, 6 figure
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Comparison of macular structural and vascular changes in neuromyelitis optica spectrum disorder and primary open angle glaucoma: a cross-sectional study.
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Comparison of macular structural and vascular changes in neuromyelitis optica spectrum disorder and primary open angle glaucoma: a cross-sectional study.
AIMS: To compare macular structure and vasculature between neuromyelitis optica spectrum disorder (NMOSD) and primary open angle glaucoma (POAG) using optical coherence tomography angiography. METHODS: NMOSD patients (n=124) with/without a history of optic neuritis (ON) (NMO+ON: 113 eyes; NMO-ON: 95 eyes), glaucomatous patients (n=102) with early/advanced glaucoma (G-E: 74 eyes; G-A: 50 eyes) and healthy controls (n=62; 90 eyes) were imaged. The main outcome measures were macular ganglion cell-inner plexiform layer (GC-IPL) thickness, vessel density (VD) and perfusion density (PD) in the superficial capillary plexus, and diagnostic capabilities of the parameters as calculated by area under the curve (AUC). RESULTS: Significant losses in GC-IPL, VD and PD were detected in both patients with NMOSD and POAG. With matched losses in the peripapillary retinal nerve fibre layer, NMOSD group showed significant thinning of GC-IPL in the nasal-superior quadrant, whereas in POAG group, significant thinning was observed in the inferior and temporal-inferior quadrants. GC-IPL thinning was more prominent in the superior, nasal-superior and nasal-inferior quadrants in NMO+ON eyes. In G-A eyes, significant GC-IPL thinning was seen in the temporal-inferior quadrant. The specific structural parameters combining VD and foveal avascular zone (FAZ) indices showed the best diagnostic accuracies. The FAZ area in eyes with NMOSD was significantly smaller than the eyes of healthy controls and POAG. CONCLUSION: NMOSD and POAG have specific patterns of macular structural and vascular changes associated with pathophysiology. Our results indicate that FAZ could be a sensitive biomarker of macular changes in NMOSD
Whole exome sequencing identifies frequent somatic mutations in cell-cell adhesion genes in chinese patients with lung squamous cell carcinoma
Lung squamous cell carcinoma (SQCC) accounts for about 30% of all lung cancer cases. Understanding of mutational landscape for this subtype of lung cancer in Chinese patients is currently limited. We performed whole exome sequencing in samples from 100 patients with lung SQCCs to search for somatic mutations and the subsequent target capture sequencing in another 98 samples for validation. We identified 20 significantly mutated genes, including TP53, CDH10, NFE2L2 and PTEN. Pathways with frequently mutated genes included those of cell-cell adhesion/Wnt/Hippo in 76%, oxidative stress response in 21%, and phosphatidylinositol-3-OH kinase in 36% of the tested tumor samples. Mutations of Chromatin regulatory factor genes were identified at a lower frequency. In functional assays, we observed that knockdown of CDH10 promoted cell proliferation, soft-agar colony formation, cell migration and cell invasion, and overexpression of CDH10 inhibited cell proliferation. This mutational landscape of lung SQCC in Chinese patients improves our current understanding of lung carcinogenesis, early diagnosis and personalized therapy
The complete chloroplast genome sequence of Pennisetum flaccidum (Poaceae)
Pennisetum flaccidum Grisebach is a typical high-quality forage and adrought-tolerant grass. In this study, we firstly reported the complete chloroplast (cp) genome of P. flaccidum, which was 138,336 bp in length, including a pair of inverted repeats (IR: 22,293 bp), a large single copy (LSC: 81,329 bp), and a small single copy (SSC: 12,421 bp) region. A total of 131 genes were annotated, containing seven rRNA genes, 38 tRNA genes, and 86 protein-coding genes. The GC content of the cp genome was 38.63%. The maximum-likelihood (ML) phylogenetic tree indicated that P. flaccidum was closely related to P. cetaceum in Poaceae
RESEARCH ON BIOMECHANICS PROPERTIES AND HEMODYNAMICS PERFORMANCE OF THE CONVERTIBLE VENA CAVA FILTER
Implementation of Photosensitive, Injectable, Interpenetrating, and Kartogenin-Modified GELMA/PEDGA Biomimetic Scaffolds to Restore Cartilage Integrity in a Full-Thickness Osteochondral Defect Model
Cartilage defects caused by mechanical tear and wear
are challenging
clinical problems. Articular cartilage has unique load-bearing properties
and limited self-repair ability. The current treatment methods, such
as microfractures and autogenous cartilage transplantation to repair
full-thickness cartilage defects, have apparent limitations. Tissue
engineering technology has the potential to repair cartilage defects
and directs current research development. To enhance the regenerative
capacities of cartilage in weight-bearing areas, we attempted to develop
a biomimetic scaffold loaded with a chondroprotective factor that
can recreate structure, restore mechanical properties, and facilitate
anabolic metabolism in larger joint defects. For enhanced spatial
control over both bone and cartilage layers, it is envisioned that
biomaterials that meet the needs of both tissue components are required
for successful osteochondral repair. We used gelatin methacrylate
(GELMA) and polyethylene glycol diacrylate (PEGDA) light-cured dual-network
cross-linking modes that can significantly increase the mechanical
properties of scaffolds and are capable of restoring function and
prolonging the degradation time. Once the hydrogel complex was injected
into the osteochondral defect, in situ UV light curing
was applied to seamlessly connect the defect repair tissue with the
surrounding normal cartilage tissue. The small molecule active substance
kartogenin (KGN) can promote cartilage repair. We encapsulated KGN
in biomimetic scaffolds so that, as the scaffold degrades, scaffold-loaded
KGN was slowly released to induce endogenous mesenchymal stem cells
to home and differentiate into chondrocytes to repair defective cartilage
tissue. Our experiments have proven that, compared with the control
group, GELMA/PEGDA + KGN repaired cartilage defects and restored cartilage
to hyaline cartilage. Our study suggests that implementing photosensitive,
injectable, interpenetrating, and kartogenin-modified GELMA/PEDGA
biomimetic scaffolds may be a novel approach to restore cartilage
integrity in full-thickness osteochondral defects
Patient is a 16 year-old female with neuromuscular scoliosis.
<p>A and B, Standing preoperative anteroposterior and lateral radiographs. C and D, Standing anteroposterior and lateral radiographs 4 days after operation showing pedicle screw loosening. E and F, Standing anteroposterior and lateral radiographs 5 days after reoperation.</p