نتائج البحث

Development, Molecular Docking, and in Silico ADME Evaluation of Selective ALR2 Inhibitors for the Treatment of Diabetic Complications via Suppression of the Polyol Pathway

• Authors : Imran, Aqeel; Shehzad, Muhammad Tariq; Shah, Syed Jawad Ali

• Source: Imran , A , Shehzad , M T , Shah , S J A , Laws , M , Al-Adhami , T , Rahman , K M , Khan , I A , Shafiq , Z & Iqbal , J 2022 , ' Development, Molecular

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Development, Molecular Docking, and in Silico ADME Evaluation of Selective ALR2 Inhibitors for the Treatment of Diabetic Complications via Suppression of the Polyol Pathway

• Authors : Imran, Aqeel; Shehzad, Muhammad Tariq; Shah, Syed Jawad Ali

• Source: Imran , A , Shehzad , M T , Shah , S J A , Laws , M , Al-Adhami , T , Rahman , K M , Khan , I A , Shafiq , Z & Iqbal , J 2022 , ' Development, Molecular

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Interaction of amisulpride with GLUT1 at the blood-brain barrier. Relevance to Alzheimer's disease

• Authors : Boyanova, Sevda T; Lloyd-Morris, Ethlyn; Corpe, Christopher

Subjects: Humans; Mice; Animals

• Source: Boyanova , S T , Lloyd-Morris , E , Corpe , C , Rahman , K M , Farag , D B , Page , L K , Wang , H , Fleckney , A L , Gatt , A , Troakes , C , Vizcay-Barrena , G , Fleck , R , Reeves , S J & Thomas ,

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Novel drug-target interactions via link prediction and network embedding

• Authors : Amiri Souri, E; Laddach, R; Karagiannis, S N

Subjects: Algorithms; Drug Interactions; Drug Repositioning

• Source: Amiri Souri , E , Laddach , R , Karagiannis , S N , Papageorgiou , L G & Tsoka , S 2022 , ' Novel drug-target interactions via link prediction and network embedding ' , BMC Bioinformatics , vol. 23 ,

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Novel drug-target interactions via link prediction and network embedding

• Authors : Amiri Souri, E; Laddach, R; Karagiannis, S N

Subjects: Algorithms; Drug Interactions; Drug Repositioning

• Source: Amiri Souri , E , Laddach , R , Karagiannis , S N , Papageorgiou , L G & Tsoka , S 2022 , ' Novel drug-target interactions via link prediction and network embedding ' , BMC Bioinformatics , vol. 23 ,

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Stimulation of platelet P2Y 1 receptors by different endogenous nucleotides leads to functional selectivity via biased signalling

• Authors : Arkless, Kate L.; Pan, Dingxin; Shankar‐Hari, Manu

• Source: Arkless , K L , Pan , D , Shankar‐Hari , M , Amison , R T , Page , C P , Rahman , K M & Pitchford , S C 2024 , ' Stimulation of platelet P2Y 1 receptors by different endogenous nucleotides leads to

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Stimulation of platelet P2Y 1 receptors by different endogenous nucleotides leads to functional selectivity via biased signalling

• Authors : Arkless, Kate L.; Pan, Dingxin; Shankar‐Hari, Manu

• Source: Arkless , K L , Pan , D , Shankar‐Hari , M , Amison , R T , Page , C P , Rahman , K M & Pitchford , S C 2023 , ' Stimulation of platelet P2Y 1 receptors by different endogenous nucleotides leads to

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Diverse signaling of the platelet P2Y1 receptor leads to a dichotomy in platelet function

• Authors : Amison, Richard T.; Jamshidi, Shirin; Rahman, Khondaker M.

Subjects: Platelets; P2Y1 receptor; PLC

• Source: Amison , R T , Jamshidi , S , Rahman , K M , Page , C P & Pitchford , S C 2018 , ' Diverse signaling of the platelet P2Y1 receptor leads to a dichotomy in platelet function ' , European Journal of

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Repositioning of Anti-Inflammatory Drugs for the Treatment of Cervical Cancer Sub-Types

• Authors : Kori, Medi; Arga, Kazim Yalcin; Mardinoglu, Adil

Subjects: anti-inflammatory drugs; cervical cancer; drug repurposing

• Source: Kori , M , Arga , K Y , Mardinoglu , A & Turanli , B 2022 , ' Repositioning of Anti-Inflammatory Drugs for the Treatment of Cervical Cancer Sub-Types ' , Frontiers in Pharmacology , vol. 13 , 884548 .

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Development and exploration of novel substituted thiosemicarbazones as inhibitors of aldose reductase via in vitro analysis and computational study

• Authors : Imran, Aqeel; Shehzad, Muhammad Tariq; Shah, Syed Jawad Ali

• Source: Imran , A , Shehzad , M T , Shah , S J A , al Adhami , T , Laws , M , Rahman , K M , Alharthy , R D , Khan , I A , Shafiq , Z & Iqbal , J 2022 , ' Development and exploration of novel substituted

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