Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Hon-For Tsui"'
Autor:
Yik Wa Law, Rita Hui Ting Lok, Byron Chiang, Carmen Chui Shan Lai, Sik Hon Matthew Tsui, Pui Yin Joseph Chung, Siu Chung Leung
Publikováno v:
JMIR Formative Research, Vol 7, p e43526 (2023)
BackgroundFor patients with self-harm behaviors, the urge to hurt themselves persists after hospital discharge, leading to costly readmissions and even death. Hence, postdischarge intervention programs that reduce self-harm behavior among patients sh
Externí odkaz:
https://doaj.org/article/e3c0089f182c473083acc2b212b355c6
Publikováno v:
Journal of Orthopaedics, Trauma and Rehabilitation, Vol 26 (2019)
Introduction: Partial knee replacement (PKR) is one of the treatment options in middle-aged patients with less extensive knee osteoarthritis, with unicompartmental knee replacement (UKR) most commonly done for medial osteoarthritis. There are numerou
Externí odkaz:
https://doaj.org/article/e4d12c44f43248a09949b7dbf93161d0
Publikováno v:
Anesthesia & Analgesia. 130:498-504
BACKGROUND Hip fracture is a challenging geriatric problem for the health care professionals, especially in patients with multiple comorbidities. In patients with inoperable hip fracture secondary to severe comorbid conditions, the pain can lead to s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1986d09770581ca4f800605e3579122
https://doi.org/10.1213/ane.0000000000004172
https://doi.org/10.1213/ane.0000000000004172
Publikováno v:
Journal of Orthopaedics, Trauma and Rehabilitation, Vol 26 (2019)
Introduction: Partial knee replacement (PKR) is one of the treatment options in middle-aged patients with less extensive knee osteoarthritis, with unicompartmental knee replacement (UKR) most commonly done for medial osteoarthritis. There are numerou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90ad5d0d6a89edf444366491024f2221
https://doaj.org/article/e4d12c44f43248a09949b7dbf93161d0
https://doaj.org/article/e4d12c44f43248a09949b7dbf93161d0
Autor:
Christopher Sondey, Theirry Fischmann, Kristine Devito, Haiquin Tang, W. Michael Seganish, Rui Zhang, Jennifer Hanisak, Hon-Chung Tsui, Deen Tulshian, Daniel Lundell, Charles G. Garlisi, William T. McElroy, Xiaoda Niu, James Fossetta, James R. Tata
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 26:4250-4255
IRAK4 has been identified as potential therapeutic target for inflammatory and autoimmune diseases. Herein we report the identification and initial SAR studies of a new class of pyrazole containing IRAK4 inhibitors designed to expand chemical diversi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f36bde751943a6860892af80d72d0b9
https://doi.org/10.1016/j.bmcl.2016.07.048
https://doi.org/10.1016/j.bmcl.2016.07.048
Autor:
Liang Zhu, Weihong Jin, Xin Yao, Hong Mei, Abdul Basit Alhassan, William T. Windsor, Donna Carr, Li Xiao, Sunil Paliwal, Neng-Yang Shih, Sun Robert, Gerald W. Shipps, Sobhana Babu Boga, Yang Nan, Joseph Kelly, Alexei V. Buevich, Brian Long, Paul Kirschmeier, Bradley Sherborne, Kiran Muppalla, Stuart Black, Hon-Chung Tsui, Doll Ronald J, Hugh Y. Zhu, Stacey A. Taylor, Subrahmanyam Gudipati, Gongjie Liu, Alan B. Cooper, Li-Kang Zhang, Kathleen Cox, Robert Bishop, David Hesk, Yongqi Deng, Alan Hruza, Mehul D. Patel, Xiaolei Gao, Priya Dayananth, Tong Wang, Desai Jagdish A, Wang James J-S, Ahmed A. Samatar
[Image: see text] The emergence and evolution of new immunological cancer therapies has sparked a rapidly growing interest in discovering novel pathways to treat cancer. Toward this aim, a novel series of pyrrolidine derivatives (compound 5) were ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab2250ac0d2e55d7a37e61d512ca2156
https://europepmc.org/articles/PMC6047169/
https://europepmc.org/articles/PMC6047169/
Publikováno v:
Tetrahedron Letters. 54:6199-6203
Piperidines are ubiquitous in pharmaceuticals and bioactive natural products. Understanding the structural and functional properties of piperidines plays a key role in drug design and development. This Letter reported studies of conformation of a set
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb48bc49a2cc24a35bc22cdfe75c76dc
https://doi.org/10.1016/j.tetlet.2013.08.131
https://doi.org/10.1016/j.tetlet.2013.08.131
Autor:
Mehul D. Patel, Alexei V. Buevich, Ahmed A. Samatar, Kelly Joseph M, Kiran Muppalla, Sobhana Babu Boga, Li Xiao, Alan B. Cooper, Robert Bishop, William T. Windsor, Hon-Chung Tsui, Sunil Paliwal, Liang Zhu, Sun Robert, David Hesk, Yongqi Deng, Alan Hruza, Subrahmanyam Gudipati, James Wang, Gerald W. Shipps, Tong Wang, Hugh Y. Zhu, Yang Nan, Paul Kirschmeier, Brian Long, Doll Ronald J, Xiaolei Gao, Jagdish Desai, Donna Carr, Stuart Black, Priya Dayananth, Abdul-Basit Alhassan, Bradley Sherborne, Neng-Yang Shih
Publikováno v:
Acta Crystallographica Section A Foundations and Advances. 74:a197-a197
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22d0bce201ee6e795d079d3a554847cd
https://doi.org/10.1107/s0108767318098021
https://doi.org/10.1107/s0108767318098021
Publikováno v:
The Journal of Arthroplasty. 20:275-281
One hundred and twelve hips in 101 Chinese patients received primary cemented Exeter total hip arthroplasty (Howmedica, Hong Kong). The implant had a collarless, double-tapered and polished stem. Seventy-five hips in 67 patients were available for as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b9a6efbfe43cc9279929956acbee92a
https://doi.org/10.1016/j.arth.2004.01.014
https://doi.org/10.1016/j.arth.2004.01.014
Autor:
Gregory A Reichard, Cheng Wang, Ruth A. Duffy, Robert G. Aslanian, Fei Liu, Cynthia A. Morgan, Sunil Paliwal, Hon-Chung Tsui, Dong Xiao, Amin A. Nomeir, Anandan Palani, Neng-Yang Shih, Geoffrey B. Varty, Jean E. Lachowicz
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:6313-6315
Modification of prototype NK(1) antagonist 2 resulted in the synthesis of a series of simple amides 6 and retroamides 9. These compounds were shown to be potent and orally active NK(1) antagonists.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24bf3f62168db7c74f87f35dfdee7fdb
https://doi.org/10.1016/j.bmcl.2010.08.059
https://doi.org/10.1016/j.bmcl.2010.08.059