Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Shishi Lin"'
Autor:
Ke Li, Qiaolin Zhu, Jianzhang Wu, Juntao Ding, Bo Liu, Xixi Zhu, Shishi Lin, Wentao Yan, Wulan Li
Publikováno v:
Mathematical Biosciences and Engineering, Vol 21, Iss 1, Pp 1110-1124 (2024)
Retinal tears (RTs) are usually detected by B-scan ultrasound images, particularly for individuals with complex eye conditions. However, traditional manual techniques for reading ultrasound images have the potential to overlook or inaccurately diagno
Externí odkaz:
https://doaj.org/article/d27e6d174d8d462fbdfdba5b75340cc3
Autor:
Colm McAlinden, Qinmei Wang, Konrad Pesudovs, Xin Yang, Fangjun Bao, Ayong Yu, Shishi Lin, Yifan Feng, Jinhai Huang
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128929 (2015)
To evaluate axial length (AL) measurement failure rate with the IOLMaster (Carl Zeiss AG, Germany) and Lenstar LS 900 (Haag-Streit AG, Switzerland) in eyes with cataract.Two hundred and ninety-six eyes of 170 patients with cataract were enrolled. Cat
Externí odkaz:
https://doaj.org/article/793b07f82a83463e8f1062961fe413d9
Autor:
Liling Lin, Jianwei Lin, Junxiong Qiu, Ning Liufu, Shishi Lin, Feng Wei, Qingping Liu, Jingxian Zeng, Mingzhi Zhang, Minghui Cao
Publikováno v:
British Journal of Anaesthesia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e156f61ebe7216ef20278a6eb5630fbd
https://doi.org/10.1016/j.bja.2023.04.020
https://doi.org/10.1016/j.bja.2023.04.020
Publikováno v:
Reaction Chemistry & Engineering. 7:354-360
Enhanced reactivity of decarboxylative cross-coupling using a new parallel photoreactor.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16020e6c46d5b6657646423d7bef5aa7
https://doi.org/10.1039/d1re00317h
https://doi.org/10.1039/d1re00317h
Autor:
Si-Jie Chen, Cyndi Qixin He, May Kong, Jun Wang, Shishi Lin, Shane W. Krska, Shannon S. Stahl
Pharmaceutical and agrochemical discovery efforts rely on robust methods for chemical synthesis that rapidly access diverse molecules. Cross-coupling reactions are the most widely used synthetic methods, but these methods typically form bonds to C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::624117bcc1b44e54a878e5911d649f92
https://doi.org/10.26434/chemrxiv-2022-p98xq
https://doi.org/10.26434/chemrxiv-2022-p98xq
Publikováno v:
Chemical Science
C(sp3)–H functionalization methods provide an ideal synthetic platform for medicinal chemistry; however, such methods are often constrained by practical limitations. The present study outlines a C(sp3)–H isocyanation protocol that enables the syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::753db7eb4ba588e7310a4c63a169a24e
http://europepmc.org/articles/PMC8336431
http://europepmc.org/articles/PMC8336431
Autor:
Mitchell H. Keylor, Anmol Gulati, Solomon D. Kattar, Rebecca E. Johnson, Ryan W. Chau, Kaila A. Margrey, Michael J. Ardolino, Cayetana Zarate, Kelsey E. Poremba, Vladimir Simov, Gregori J. Morriello, John J. Acton, Barbara Pio, Xin Yan, Rachel L. Palte, Spencer E. McMinn, Lisa Nogle, Charles A. Lesburg, Donovon Adpressa, Shishi Lin, Santhosh Neelamkavil, Ping Liu, Jing Su, Laxminarayan G. Hegde, Janice D. Woodhouse, Robert Faltus, Tina Xiong, Paul J. Ciaccio, Jennifer Piesvaux, Karin M. Otte, Harold B. Wood, Matthew E. Kennedy, David Jonathan Bennett, Erin F. DiMauro, Matthew J. Fell, Peter H. Fuller
Publikováno v:
Journal of medicinal chemistry. 65(1)
The leucine-rich repeat kinase 2 (LRRK2) protein has been genetically and functionally linked to Parkinson's disease (PD), a disabling and progressive neurodegenerative disorder whose current therapies are limited in scope and efficacy. In this repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6720c280fccf3e18653a864a196348ad
https://pubmed.ncbi.nlm.nih.gov/34967623
https://pubmed.ncbi.nlm.nih.gov/34967623
Publikováno v:
Science. 360:186-190
A guide for catalyst choice in the forest Chemists often discover reactions by applying catalysts to a series of simple compounds. Tweaking those reactions to tolerate more structural complexity in pharmaceutical research is time-consuming. Ahneman e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c32cdb75279e8c9fac1d2f9dbca56ad
https://doi.org/10.1126/science.aar5169
https://doi.org/10.1126/science.aar5169
Autor:
Keylor, Mitchell H., Gulati, Anmol, Kattar, Solomon D., Johnson, Rebecca E., Chau, Ryan W., Margrey, Kaila A., Ardolino, Michael J., Zarate, Cayetana, Poremba, Kelsey E., Simov, Vladimir, Morriello, Gregori J., Acton, John J., Pio, Barbara, Xin Yan, Palte, Rachel L., McMinn, Spencer E., Nogle, Lisa, Lesburg, Charles A., Adpressa, Donovon, Shishi Lin
Publikováno v:
Journal of Medicinal Chemistry; 1/13/2022, Vol. 65 Issue 1, p838-856, 19p