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0D/1D Heterojunction Implant with Electro‐Mechanobiological Coupling Cues Promotes Osteogenesis
0D/1D Heterojunction Implant with Electro‐Mechanobiological Coupling Cues Promotes Osteogenesis
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0D/1D Heterojunction Implant with Electro‐Mechanobiological Coupling Cues Promotes Osteogenesis

Huang, Xiao ; Xing, Jun ; Wang, Zhengao ; Han, Jin ; Wang, Renxian ; Li, Changhao ; Xiao, Cairong ; Lu, Fang ; Zhai, Jinxia ; Zhou, Zhengnan ; Li, Yangfan ; Zhou, Lei ; Song, Zhiguo ; Chen, Dafu ; Yu, Peng ; Ning, Chengyun ; Jiang, Xieyuan

Advanced functional materials, 2021-12, Vol.31 (50), p.n/a [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc

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1,2‐Diaza‐1,3‐diene‐Based Multicomponent Reactions in Sequential Protocols to Synthesize Arylamino‐5‐hydrazonothiophene‐3‐carboxylates
1,2‐Diaza‐1,3‐diene‐Based Multicomponent Reactions in Sequential Protocols to Synthesize Arylamino‐5‐hydrazonothiophene‐3‐carboxylates
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1,2‐Diaza‐1,3‐diene‐Based Multicomponent Reactions in Sequential Protocols to Synthesize Arylamino‐5‐hydrazonothiophene‐3‐carboxylates

Mari, Giacomo ; De Crescentini, Lucia ; Favi, Gianfranco ; Santeusanio, Stefania ; Mantellini, Fabio

European journal of organic chemistry, 2018-12, Vol.2018 (46), p.6548-6556 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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3
1,2,4‐Triazole and benzimidazole fused dihydropyrimidine derivatives: Design, green synthesis, antibacterial, antitubercular, and antimalarial activities
1,2,4‐Triazole and benzimidazole fused dihydropyrimidine derivatives: Design, green synthesis, antibacterial, antitubercular, and antimalarial activities
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1,2,4‐Triazole and benzimidazole fused dihydropyrimidine derivatives: Design, green synthesis, antibacterial, antitubercular, and antimalarial activities

Mokariya, Jaydeep A. ; Rajani, Dhanji P. ; Patel, Manish P.

Archiv der Pharmazie (Weinheim), 2023-04, Vol.356 (4), p.e2200545-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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4
1,2,4-Triazole-based N-heterocyclic carbene complexes of gold(I): synthesis, characterization and biological activity
1,2,4-Triazole-based N-heterocyclic carbene complexes of gold(I): synthesis, characterization and biological activity
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1,2,4-Triazole-based N-heterocyclic carbene complexes of gold(I): synthesis, characterization and biological activity

Turek, Jan ; Růžičková, Zdeňka ; Tloušťová, Eva ; Mertlíková-Kaiserová, Helena ; Günterová, Jana ; Rulíšek, Lubomír ; Růžička, Aleš

Applied organometallic chemistry, 2016-05, Vol.30 (5), p.318-322 [Periódico revisado por pares]

Blackwell Publishing Ltd

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5
1,2,4,5-Tetraoxane derivatives/hybrids as potent antimalarial endoperoxides: Chronological advancements, structure-activity relationship (SAR) studies and future perspectives
1,2,4,5-Tetraoxane derivatives/hybrids as potent antimalarial endoperoxides: Chronological advancements, structure-activity relationship (SAR) studies and future perspectives
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1,2,4,5-Tetraoxane derivatives/hybrids as potent antimalarial endoperoxides: Chronological advancements, structure-activity relationship (SAR) studies and future perspectives

T A, Abdul Rahaman ; Rajendra, Thakar Neha ; Suhas, Kshirsagar Prasad ; Ippagunta, Sirish K ; Chaudhary, Sandeep

Medicinal research reviews, 2024-04 [Periódico revisado por pares]

United States

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6
1,25‐dihydroxyvitamin D3‐induced dendritic cells suppress experimental autoimmune encephalomyelitis by increasing proportions of the regulatory lymphocytes and reducing T helper type 1 and type 17 cells
1,25‐dihydroxyvitamin D3‐induced dendritic cells suppress experimental autoimmune encephalomyelitis by increasing proportions of the regulatory lymphocytes and reducing T helper type 1 and type 17 cells
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1,25‐dihydroxyvitamin D3‐induced dendritic cells suppress experimental autoimmune encephalomyelitis by increasing proportions of the regulatory lymphocytes and reducing T helper type 1 and type 17 cells

Xie, Zhongxiang ; Chen, Jingtao ; Zheng, Chao ; Wu, Jing ; Cheng, Yun ; Zhu, Shan ; Lin, Chenhong ; Cao, Qingqing ; Zhu, Jie ; Jin, Tao

Immunology, 2017-11, Vol.152 (3), p.414-424 [Periódico revisado por pares]

Oxford: Wiley Subscription Services, Inc

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7
(1,3-Benzodioxol-5-ylmethyl)ammonium 2-methoxy-5-[(1 E )-3-oxo-3-phenylprop-1-en-1-yl]bezenesulfonate monohydrate
(1,3-Benzodioxol-5-ylmethyl)ammonium 2-methoxy-5-[(1 E )-3-oxo-3-phenylprop-1-en-1-yl]bezenesulfonate monohydrate
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(1,3-Benzodioxol-5-ylmethyl)ammonium 2-methoxy-5-[(1 E )-3-oxo-3-phenylprop-1-en-1-yl]bezenesulfonate monohydrate

Silva, Luiz Everson da ; Andrighetti-Fröhner, Carla Regina ; Nunes, Ricardo José ; Simões, Cláudia Maria Oliveira ; Foro, Sabine

Acta crystallographica. Section E, Structure reports online, 2006-07, Vol.62 (7), p.o2785-o2787

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8
1,3‐Dipolar Cycloaddition between Dehydroalanines and C,N‐Cyclic Azomethine Imines: Application to Late‐Stage Peptide Modification
1,3‐Dipolar Cycloaddition between Dehydroalanines and C,N‐Cyclic Azomethine Imines: Application to Late‐Stage Peptide Modification
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1,3‐Dipolar Cycloaddition between Dehydroalanines and C,N‐Cyclic Azomethine Imines: Application to Late‐Stage Peptide Modification

Bao, Guangjun ; Wang, Peng ; Li, Guofeng ; Yu, Changjun ; Li, Yiping ; Liu, Yuyang ; He, Zeyuan ; Zhao, Tiantian ; Rao, Jing ; Xie, Junqiu ; Hong, Liang ; Sun, Wangsheng ; Wang, Rui

Angewandte Chemie, 2021-03, Vol.133 (10), p.5391-5398 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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9
1,3‐Dipolar Cycloaddition between Dehydroalanines and C,N‐Cyclic Azomethine Imines: Application to Late‐Stage Peptide Modification
1,3‐Dipolar Cycloaddition between Dehydroalanines and C,N‐Cyclic Azomethine Imines: Application to Late‐Stage Peptide Modification
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1,3‐Dipolar Cycloaddition between Dehydroalanines and C,N‐Cyclic Azomethine Imines: Application to Late‐Stage Peptide Modification

Bao, Guangjun ; Wang, Peng ; Li, Guofeng ; Yu, Changjun ; Li, Yiping ; Liu, Yuyang ; He, Zeyuan ; Zhao, Tiantian ; Rao, Jing ; Xie, Junqiu ; Hong, Liang ; Sun, Wangsheng ; Wang, Rui

Angewandte Chemie (International ed.), 2021-03, Vol.60 (10), p.5331-5338 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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10
1,3-Disubstituted-4-Aminopyrazolo [3, 4-d] Pyrimidines, a New Class of Potent Inhibitors for Phospholipase D
1,3-Disubstituted-4-Aminopyrazolo [3, 4-d] Pyrimidines, a New Class of Potent Inhibitors for Phospholipase D
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1,3-Disubstituted-4-Aminopyrazolo [3, 4-d] Pyrimidines, a New Class of Potent Inhibitors for Phospholipase D

Kulkarni, Aditya ; Quang, Phong ; Curry, Victoriana ; Keyes, Renee ; Zhou, Weihong ; Cho, Hyejin ; Baffoe, Jonathan ; Török, Béla ; Stieglitz, Kimberly

Chemical biology & drug design, 2014-09, Vol.84 (3), p.270-281 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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