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625 results on '"Sun, Li-Ying"'

8. Anesthesia and Critical Care for the Prediction and Prevention for Small-for-size Syndrome: Guidelines from the ILTS-iLDLT-LTSI Consensus Conference

Author

Chadha, Ryan, Sakai, Tetsuro, Rajakumar, Akila, Shingina, Alexandra, Yoon, Uzung, Patel, Dhupal, Spiro, Michael, Bhangui, Pooja, Sun, Li-Ying, Humar, Abhinav, Bezinover, Dmitri, Findlay, James, Saigal, Sanjiv, Singh, Shweta, Yi, Nam-Joon, Rodriguez-Davalos, Manuel, Kumar, Lakshmi, Kumaran, Vinay, Agarwal, Shaleen, Berlakovich, Gabriela, Egawa, Hiroto, Lerut, Jan, Clemens Broering, Dieter, Berenguer, Marina, Cattral, Mark, Clavien, Pierre-Alain, Chen, Chao-Long, Shah, Samir, Zhu, Zhi-Jun, Ascher, Nancy, Bhangui, Prashant, Rammohan, Ashwin, Emond, Jean, and Rela, Mohamed

Published
2023
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11. An international, multicenter, survey-based analysis of practice and management of acute liver failure

Author

Gurakar, Ahmet, primary, Conde Amiel, Isabel, additional, Ozturk, N. Begum, additional, Artru, Florent, additional, Selzner, Nazia, additional, Psoter, Kevin J., additional, Dionne, Joanna C., additional, Karvellas, Constantine, additional, Rajakumar, Akila, additional, Saner, Fuat, additional, Subramanian, Ram M., additional, Sun, Li-Ying, additional, Dhawan, Anil, additional, and Coilly, Audrey, additional

Published
2024
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33. Crystal structure of poly[(5-bimethylamino-1-naphthalenesulfonato-κO)-(μ3-hexamethylenetetramino-κ3N:N′:N′′)silver(I)] dihydrate, C36H52Ag2N10O8S2

Author

Jiang Jin-Ke, Yang Gang, Sun Li-Ying, Wang Chun-Yan, and Wang Feng

Subjects
1985662, Physics, QC1-999, Crystallography, QD901-999
Abstract

C36H52Ag2N10O8S2, orthorhombic, Pna21 (no. 33), a = 11.7911(16) Å, b = 31.310(5) Å, c = 10.6883(11) Å, V = 3945.9(9) Å3, Z = 4, Rgt(F) = 0.0353, wRref(F2) = 0.0784, T = 293(2) K.

Published
2020
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34. Epithelial Tight Junction Anomalies in Nasal Inverted Papilloma.

Author

Huang, Zhi‐Qun, Zhou, Xiang‐Min, Yuan, Tian, Liu, Jing, Ong, Hsiao H., Sun, Li‐Ying, Tu, Jun‐Hao, Li, Meng‐Yue, Thong, Kim T. M., Ye, Jing, Shi, Li, Wang, De‐Yun, and Xu, Yu

Abstract

Objectives: As a critical component of the epithelial barrier, tight junctions (TJs) are essential in nasal mucosa against pathogen invasion. However, the function of TJs has rarely been reported in nasal inverted papilloma (NIP). This study aims to investigate the potential factors of TJs' abnormality in NIP. Methods: We assessed the expression of ZO‐1, occludin, claudin‐1, claudin‐3, and claudin‐7 in healthy controls and NIP by real‐time quantitative polymerase chain reaction and immunofluorescent staining. The correlation between TJs expression and neutrophil count, TH1/TH2/TH17 and regulatory T cell biomarkers, and the proportion of nasal epithelial cells was investigated. Results: Upregulation of ZO‐1, occludin, claudin‐1, and claudin‐7, along with downregulation of claudin‐3, was found in NIP compared to control (all p < 0.05). An abnormal proportion with a lower number of ciliated cells (control vs. NIP: 37.60 vs. 8.67) and goblet cells (12.52 vs. 0.33) together with a higher number of basal cells (45.58 vs. 124.00) in NIP. Meanwhile, claudin‐3 was positively correlated with ciliated and goblet cells (all p < 0.01). Additionally, neutrophils were excessively infiltrated in NIP, negatively correlated with ZO‐1, but positively with claudin‐3 (all p < 0.05). Furthermore, FOXP3, IL‐10, TGF‐β1, IL‐5, IL‐13, and IL‐22 levels were induced in NIP (all p < 0.01). Occludin level was negatively correlated with IL‐10, IL‐5, IL‐13, and IL‐22, whereas ZO‐1 was positively with TGF‐β1 (all p < 0.05). Conclusion: Nasal epithelial barrier dysfunction with TJs anomalies is commonly associated with abnormal proliferation and differentiation of epithelial cells and imbalance of immune and inflammatory patterns in NIP. Level of Evidence: NA Laryngoscope, 134:552–561, 2024 [ABSTRACT FROM AUTHOR]

Published
2024
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37. Impact of immunosuppression level on liver allograft fibrosis after pediatric liver transplantation: a retrospective cohort study

Author

Jiang, Yi-Zhou, primary, Zhao, Xin-Yan, additional, Zhou, Guang-Peng, additional, Wei, Lin, additional, Qu, Wei, additional, Zeng, Zhi-Gui, additional, Wu, Shan-Shan, additional, Zhang, Hai-Ming, additional, Liu, Ying, additional, Tan, Yu-Le, additional, Wang, Jun, additional, Zhu, Zhi-Jun, additional, and Sun, Li-Ying, additional

Published
2023
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47. Unravelling the Roles of Solvophobic Effects and π⋅⋅⋅π Stacking Interactions in the Formation of [2]Catenanes Featuring Di‐(N‐Heterocyclic Carbene) Building Blocks.

Author

Zhang, Ya‐Wen, Lu, Ye, Sun, Li‐Ying, Dutschke, Patrick D., Gan, Ming‐Ming, Zhang, Le, Hepp, Alexander, Han, Ying‐Feng, and Hahn, F. Ekkehardt

Subjects
STACKING interactions, CATENANES, CARBENE synthesis, SUPRAMOLECULAR chemistry, BIPYRIDINE, PYRENE
Abstract

A series of [2]catenanes has been prepared from di‐NHC building blocks by utilizing solvophobic effects and/or π⋅⋅⋅π stacking interactions. The dinickel naphthobiscarbene complex syn‐[1] and the kinked biphenyl‐bridged bipyridyl ligand L2 yield the [2]catenane [2‐IL](OTf)4 by self‐assembly. Solvophobic effects are pivotal for the formation of the interlocked species. Substitution of the biphenyl‐linker in L2 for a pyromellitic diimide group gave ligand L3, which yielded in combination with syn‐[1] the [2]catenane [3‐IL](OTf)4. This assembly exhibits enhanced stability in diluted solution, aided by additional π⋅⋅⋅π stacking interactions. The π⋅⋅⋅π stacking was augmented by the introduction of a pyrene bridge between two NHC donors in ligand L4. Di‐NHC precursor H2‐L4(PF6)2 reacts with Ag2O to give the [Ag2L42]2 [2]catenane [4‐IL](PF6)4, which shows strong π⋅⋅⋅π stacking interactions between the pyrene groups. This assembly was readily converted into the [Au2L42]2 gold species [5‐IL](PF6)4, which exhibits exceptional stability based on the strong π⋅⋅⋅π stacking interactions and the enhanced stability of the Au‐CNHC bonds. [ABSTRACT FROM AUTHOR]

Published
2023
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48. The effect of liver transplantation for argininemia—the largest experiences in a single center

Author

Cui, Bin, Wei, Lin, Sun, Li-Ying, Qu, Wei, Zeng, Zhi-Gui, Liu, Ying, and Zhu, Zhi-Jun

Subjects
Pediatrics, Perinatology and Child Health, Original Article
Abstract

BACKGROUND: Argininemia, a rare urea cycle disorder resulting from an arginase-1 deficiency, is characterized by a progressive spastic paraplegia. While advances in diagnosis and treatment have increased the management of this condition, not all symptoms are resolved in response to traditional therapies. Interestingly, there exist some rare reports on the use of liver transplantation (LT) for the treatment of argininemia. METHODS: We conducted a retrospective study of eleven patients with argininemia receiving a LT as performed at our center over the period from January 2015 to November 2019. These patients were included due to their poor responses to protein restriction diets and alternative therapies of nitrogen scavengers. Detailed information on coagulation, liver function, histopathological and morphological examination of liver samples, and other clinical presentations were extracted from these patients. A grading scale was used for evaluating the neurological status, classification of physical growth and quality of life of these patients in response to the LT. RESULTS: Prior to LT, high levels of arginine were detected in all of argininemia patients and liver enzymes were elevated in nine of those patients. Nine patients presented with coagulation dysfunction without bleeding symptoms. Spastic paraplegia, irritability, intellectual developmental disability, and growth deficits were hallmarks of these nine patients, while four patients showed repeated, generalized tonic-clonic seizures before the operation. Seven novel mutations were found in these patients. The indication for LT in this series of patients was a presentation of progressive neurological impairments. After LT, the coagulation index and plasma arginine levels returned to normal and episodes of seizure were controlled in four patients. To date, all patients have survived and their LT has resulted a restoration of arginine metabolism and liver function, along with preventing further neurological deterioration, all of which provided an opportunity for future recuperation. Overall, the neurological status, growth deficits and quality of life were all significantly improved after LT with no evidence of severe complications. CONCLUSIONS: LT can serve as an effective treatment for argininemia in patients who respond poorly to traditional therapy. An early intervention of LT should be conducted in these patients to prevent neurological damage and improve their quality of life.

Published
2022

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