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1
Diverse mechanisms activate the PI 3-kinase/mTOR pathway in melanomas: implications for the use of PI 3-kinase inhibitors to overcome resistance to inhibitors of BRAF and MEK
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Diverse mechanisms activate the PI 3-kinase/mTOR pathway in melanomas: implications for the use of PI 3-kinase inhibitors to overcome resistance to inhibitors of BRAF and MEK

Tran, Khanh B ; Kolekar, Sharada ; Jabed, Anower ; Jaynes, Patrick ; Shih, Jen-Hsing ; Wang, Qian ; Flanagan, Jack U ; Rewcastle, Gordon W ; Baguley, Bruce C ; Shepherd, Peter R

BMC cancer, 2021-02, Vol.21 (1), p.136-136, Article 136 [Peer Reviewed Journal]

England: BioMed Central Ltd

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2
Inhibitors of Discoidin Domain Receptor (DDR) Kinases for Cancer and Inflammation
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Inhibitors of Discoidin Domain Receptor (DDR) Kinases for Cancer and Inflammation

Denny, William A ; Flanagan, Jack U

Biomolecules (Basel, Switzerland), 2021-11, Vol.11 (11), p.1671 [Peer Reviewed Journal]

Switzerland: MDPI AG

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3
Evaluation of Novel Inhibitors of Tryptophan Dioxygenases for Enzyme and Species Selectivity Using Engineered Tumour Cell Lines Expressing Either Murine or Human IDO1 or TDO2
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Evaluation of Novel Inhibitors of Tryptophan Dioxygenases for Enzyme and Species Selectivity Using Engineered Tumour Cell Lines Expressing Either Murine or Human IDO1 or TDO2

Tijono, Sofian M ; Palmer, Brian D ; Tomek, Petr ; Flanagan, Jack U ; Henare, Kimiora ; Gamage, Swarna ; Braun, Lukas ; Ching, Lai-Ming

Pharmaceuticals (Basel, Switzerland), 2022-08, Vol.15 (9), p.1090 [Peer Reviewed Journal]

Basel: MDPI AG

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4
Crystal structures of three classes of non-steroidal anti-inflammatory drugs in complex with aldo-keto reductase 1C3
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Article
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Crystal structures of three classes of non-steroidal anti-inflammatory drugs in complex with aldo-keto reductase 1C3

Flanagan, Jack U ; Yosaatmadja, Yuliana ; Teague, Rebecca M ; Chai, Matilda Z L ; Turnbull, Andrew P ; Squire, Christopher J Pastore, Annalisa

PloS one, 2012-08, Vol.7 (8), p.e43965-e43965 [Peer Reviewed Journal]

United States: Public Library of Science

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5
Evidence That GRIN2A Mutations in Melanoma Correlate with Decreased Survival
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Article
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Evidence That GRIN2A Mutations in Melanoma Correlate with Decreased Survival

D'mello, Stacey Ann N ; Flanagan, Jack U ; Green, Taryn N ; Leung, Euphemia Y ; Askarian-Amiri, Marjan E ; Joseph, Wayne R ; McCrystal, Michael R ; Isaacs, Richard J ; Shaw, James H F ; Furneaux, Christopher E ; During, Matthew J ; Finlay, Graeme J ; Baguley, Bruce C ; Kalev-Zylinska, Maggie L

Frontiers in oncology, 2014-01, Vol.3, p.333-333 [Peer Reviewed Journal]

Switzerland: Frontiers Media S.A

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6
Residues Glutamate 216 and Aspartate 301 Are Key Determinants of Substrate Specificity and Product Regioselectivity in Cytochrome P450 2D6
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Residues Glutamate 216 and Aspartate 301 Are Key Determinants of Substrate Specificity and Product Regioselectivity in Cytochrome P450 2D6

Paine, Mark J.I. ; McLaughlin, Lesley A. ; Flanagan, Jack U. ; Kemp, Carol A. ; Sutcliffe, Michael J. ; Roberts, Gordon C.K. ; Wolf, C. Roland

The Journal of biological chemistry, 2003-02, Vol.278 (6), p.4021-4027 [Peer Reviewed Journal]

United States: Elsevier Inc

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7
A single discrete Rab5-binding site in phosphoinositide 3-kinase β is required for tumor cell invasion
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A single discrete Rab5-binding site in phosphoinositide 3-kinase β is required for tumor cell invasion

Heitz, Samantha D. ; Hamelin, David J. ; Hoffmann, Reece M. ; Greenberg, Nili ; Salloum, Gilbert ; Erami, Zahra ; Khalil, Bassem D. ; Shymanets, Aliaksei ; Steidle, Elizabeth A. ; Gong, Grace Q. ; Nürnberg, Bernd ; Burke, John E. ; Flanagan, Jack U. ; Bresnick, Anne R. ; Backer, Jonathan M.

The Journal of biological chemistry, 2019-03, Vol.294 (12), p.4621-4633 [Peer Reviewed Journal]

United States: Elsevier Inc

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8
Identification of a non-purple tartrate-resistant acid phosphatase: an evolutionary link to Ser/Thr protein phosphatases?
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Article
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Identification of a non-purple tartrate-resistant acid phosphatase: an evolutionary link to Ser/Thr protein phosphatases?

Hadler, Kieran S ; Huber, Thomas ; Cassady, A Ian ; Weber, Jane ; Robinson, Jodie ; Burrows, Allan ; Kelly, Gregory ; Guddat, Luke W ; Hume, David A ; Schenk, Gerhard ; Flanagan, Jack U

BMC research notes, 2008-09, Vol.1 (1), p.78-78 [Peer Reviewed Journal]

England: BioMed Central Ltd

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9
Why is quinidine an inhibitor of cytochrome P450 2D6? The role of key active-site residues in quinidine binding
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Article
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Why is quinidine an inhibitor of cytochrome P450 2D6? The role of key active-site residues in quinidine binding

McLaughlin, Lesley A ; Paine, Mark J I ; Kemp, Carol A ; Maréchal, Jean-Didier ; Flanagan, Jack U ; Ward, Clive J ; Sutcliffe, Michael J ; Roberts, Gordon C K ; Wolf, C Roland

The Journal of biological chemistry, 2005-11, Vol.280 (46), p.38617 [Peer Reviewed Journal]

United States

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10
Why Is Quinidine an Inhibitor of Cytochrome P450 2D6?
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Article
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Why Is Quinidine an Inhibitor of Cytochrome P450 2D6?

McLaughlin, Lesley A. ; Paine, Mark J.I. ; Kemp, Carol A. ; Maréchal, Jean-Didier ; Flanagan, Jack U. ; Ward, Clive J. ; Sutcliffe, Michael J. ; Roberts, Gordon C.K. ; Wolf, C. Roland

The Journal of biological chemistry, 2005-11, Vol.280 (46), p.38617-38624 [Peer Reviewed Journal]

Elsevier Inc

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