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A novel functional polymorphism of GSTM 3 reduces clear cell renal cell carcinoma risk through enhancing its expression by interfering miR‐556 binding

Journal of Cellular and Molecular Medicine (Online), Jun 2018, Vol.22(6), pp.3005-3015 [Peer Reviewed Journal]

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Facile Synthesis of 4-Arylidene-1H-imidazol-5(4H)-ones by an Ugi-Aza-Wittig Sequence
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Facile Synthesis of 4-Arylidene-1H-imidazol-5(4H)-ones by an Ugi-Aza-Wittig Sequence

Synthesis-Stuttgart, 2014 Feb, Vol.46(3), pp.336-342 [Peer Reviewed Journal]

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Locking Interconversion of Aromatic Oligoamide Foldamers by Intramolecular Side-chain Crosslinking: toward Absolute Control of Helicity in Synthetic Aromatic Foldamers
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Locking Interconversion of Aromatic Oligoamide Foldamers by Intramolecular Side-chain Crosslinking: toward Absolute Control of Helicity in Synthetic Aromatic Foldamers

Chemistry-A European Journal, 2017 Apr 19, Vol.23(22), pp.5361-5367 [Peer Reviewed Journal]

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Synthesis and c-Met kinase inhibition of 3,5-disubstituted and 3,5,7-trisubstituted quinolines: identification of 3-(4-acetylpiperazin-1-yl)-5-(3-nitrobenzylamino)-7- (trifluoromethyl)quinoline as a novel anticancer agent.

Journal of medicinal chemistry, April 14, 2011, Vol.54(7), pp.2127-2142 [Peer Reviewed Journal]

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Analyses of CIA5, the master regulator of the carbon-concentrating mechanism in Chlamydomonas reinhardtii, and its control of gene expression

Canadian Journal of Botany/Revue Canadienne de Botanique, July 2005, Vol.83(7), pp.765-779 [Peer Reviewed Journal]

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Green synthesis of peptide-templated gold nanoclusters as novel fluorescence probes for detecting protein kinase activity

Chemical communications (Cambridge, England), 21 June 2015, Vol.51(49), pp.10006-9 [Peer Reviewed Journal]

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Discovery of 3H-imidazo[4,5-b]pyridines as potent c-Met kinase inhibitors: design, synthesis, and biological evaluation.

ChemMedChem, June 2012, Vol.7(6), pp.1057-1070 [Peer Reviewed Journal]

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SAR of amino pyrrolidines as potent and novel protein-protein interaction inhibitors of the PRC2 complex through EED binding.

Bioorganic & medicinal chemistry letters, April 1, 2017, Vol.27(7), pp.1576-1583 [Peer Reviewed Journal]

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Synthesis and biological evaluation of 2-amino-5-aryl-3-benzylthiopyridine scaffold based potent c-Met inhibitors.

Bioorganic & medicinal chemistry, November 1, 2013, Vol.21(21), pp.6804-6820 [Peer Reviewed Journal]

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O-linked triazolotriazines: potent and selective c-Met inhibitors.

ChemMedChem, July 2012, Vol.7(7), pp.1276-1285 [Peer Reviewed Journal]

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