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1
Precisely Ordered Phosphorylation Reactions in the p38 Mitogen-activated Protein (MAP) Kinase Cascade
Precisely Ordered Phosphorylation Reactions in the p38 Mitogen-activated Protein (MAP) Kinase Cascade
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Precisely Ordered Phosphorylation Reactions in the p38 Mitogen-activated Protein (MAP) Kinase Cascade

The Journal of biological chemistry, 2013-08, Vol.288 (32), p.23322-23330 [Peer Reviewed Journal]

2013 © 2013 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology. ;2013 by The American Society for Biochemistry and Molecular Biology, Inc. 2013 ;ISSN: 0021-9258 ;EISSN: 1083-351X ;DOI: 10.1074/jbc.M113.462101 ;PMID: 23744074

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2
The protein kinase MAP3K19 phosphorylates MAP2Ks and thereby activates ERK and JNK kinases and increases viability of KRAS-mutant lung cancer cells
The protein kinase MAP3K19 phosphorylates MAP2Ks and thereby activates ERK and JNK kinases and increases viability of KRAS-mutant lung cancer cells
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The protein kinase MAP3K19 phosphorylates MAP2Ks and thereby activates ERK and JNK kinases and increases viability of KRAS-mutant lung cancer cells

The Journal of biological chemistry, 2020-06, Vol.295 (25), p.8470-8479 [Peer Reviewed Journal]

2020 ;ISSN: 0021-9258 ;EISSN: 1083-351X ;DOI: 10.1074/jbc.RA119.012365 ;PMID: 32358059

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3
Structure, Function and Regulation of the Hsp90 Machinery
Structure, Function and Regulation of the Hsp90 Machinery
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Structure, Function and Regulation of the Hsp90 Machinery

Biomedical Journal, 2013-05, Vol.36 (3), p.106-117 [Peer Reviewed Journal]

COPYRIGHT 2013 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt Ltd May-Jun 2013 ;ISSN: 2319-4170 ;EISSN: 2320-2890 ;DOI: 10.4103/2319-4170.113230 ;PMID: 23806880

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4
The Global Phosphorylation Landscape of SARS-CoV-2 Infection
The Global Phosphorylation Landscape of SARS-CoV-2 Infection
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The Global Phosphorylation Landscape of SARS-CoV-2 Infection

Cell, 2020-08, Vol.182 (3), p.685-712.e19 [Peer Reviewed Journal]

2020 Elsevier Inc. ;Copyright © 2020 Elsevier Inc. All rights reserved. ;2020. Not withstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://www.elsevier.com/legal/elsevier-website-terms-and-conditions ;Attribution - NonCommercial ;2020 Elsevier Inc. 2020 Elsevier Inc. ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2020.06.034 ;PMID: 32645325

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5
Structural Insights Support Targeting ASK1 Kinase for Therapeutic Interventions
Structural Insights Support Targeting ASK1 Kinase for Therapeutic Interventions
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Structural Insights Support Targeting ASK1 Kinase for Therapeutic Interventions

International journal of molecular sciences, 2021-12, Vol.22 (24), p.13395 [Peer Reviewed Journal]

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms222413395 ;PMID: 34948191

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6
RUNX3 regulates cell cycle-dependent chromatin dynamics by functioning as a pioneer factor of the restriction-point
RUNX3 regulates cell cycle-dependent chromatin dynamics by functioning as a pioneer factor of the restriction-point
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RUNX3 regulates cell cycle-dependent chromatin dynamics by functioning as a pioneer factor of the restriction-point

Nature communications, 2019-04, Vol.10 (1), p.1897-17, Article 1897 [Peer Reviewed Journal]

The Author(s) 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-09810-w ;PMID: 31015486

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7
PAK signalling drives acquired drug resistance to MAPK inhibitors in BRAF-mutant melanomas
PAK signalling drives acquired drug resistance to MAPK inhibitors in BRAF-mutant melanomas
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PAK signalling drives acquired drug resistance to MAPK inhibitors in BRAF-mutant melanomas

Nature (London), 2017-10, Vol.550 (7674), p.133-136 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Oct 5, 2017 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature24040 ;PMID: 28953887

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8
Structural basis for the action of the drug trametinib at KSR-bound MEK
Structural basis for the action of the drug trametinib at KSR-bound MEK
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Structural basis for the action of the drug trametinib at KSR-bound MEK

Nature (London), 2020-12, Vol.588 (7838), p.509-514 [Peer Reviewed Journal]

Copyright Nature Publishing Group Dec 17, 2020 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-020-2760-4 ;PMID: 32927473

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9
MEKK1/MEKK4 are responsible for TRAIL-induced JNK/p38 phosphorylation
MEKK1/MEKK4 are responsible for TRAIL-induced JNK/p38 phosphorylation
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MEKK1/MEKK4 are responsible for TRAIL-induced JNK/p38 phosphorylation

Oncology reports, 2011-02, Vol.25 (2), p.537-544

2015 INIST-CNRS ;ISSN: 1021-335X ;EISSN: 1791-2431 ;DOI: 10.3892/or.2010.1079 ;PMID: 21152872

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10
Integrative Genomic and Proteomic Analyses Identify Targets for Lkb1-Deficient Metastatic Lung Tumors
Integrative Genomic and Proteomic Analyses Identify Targets for Lkb1-Deficient Metastatic Lung Tumors
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Integrative Genomic and Proteomic Analyses Identify Targets for Lkb1-Deficient Metastatic Lung Tumors

Cancer cell, 2010-06, Vol.17 (6), p.547-559 [Peer Reviewed Journal]

2010 Elsevier Inc. ;Copyright 2010 Elsevier Inc. All rights reserved. ;2010 Elsevier Inc. All rights reserved. 2010 ;ISSN: 1535-6108 ;EISSN: 1878-3686 ;DOI: 10.1016/j.ccr.2010.04.026 ;PMID: 20541700

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11
Dysregulation of Wnt/β‐catenin signaling by protein kinases in hepatocellular carcinoma and its therapeutic application
Dysregulation of Wnt/β‐catenin signaling by protein kinases in hepatocellular carcinoma and its therapeutic application
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Dysregulation of Wnt/β‐catenin signaling by protein kinases in hepatocellular carcinoma and its therapeutic application

Cancer science, 2021-05, Vol.112 (5), p.1695-1706 [Peer Reviewed Journal]

2021 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1347-9032 ;EISSN: 1349-7006 ;DOI: 10.1111/cas.14861 ;PMID: 33605517

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12
Droplet-based screening of phosphate transfer catalysis reveals how epistasis shapes MAP kinase interactions with substrates
Droplet-based screening of phosphate transfer catalysis reveals how epistasis shapes MAP kinase interactions with substrates
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Droplet-based screening of phosphate transfer catalysis reveals how epistasis shapes MAP kinase interactions with substrates

Nature communications, 2022-02, Vol.13 (1), p.844-844, Article 844 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-022-28396-4 ;PMID: 35149678

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13
The redox‐active site of thioredoxin is directly involved in apoptosis signal‐regulating kinase 1 binding that is modulated by oxidative stress
The redox‐active site of thioredoxin is directly involved in apoptosis signal‐regulating kinase 1 binding that is modulated by oxidative stress
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The redox‐active site of thioredoxin is directly involved in apoptosis signal‐regulating kinase 1 binding that is modulated by oxidative stress

The FEBS journal, 2020-04, Vol.287 (8), p.1626-1644 [Peer Reviewed Journal]

2019 Federation of European Biochemical Societies ;2019 Federation of European Biochemical Societies. ;Copyright © 2020 Federation of European Biochemical Societies ;ISSN: 1742-464X ;EISSN: 1742-4658 ;DOI: 10.1111/febs.15101 ;PMID: 31623019

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14
The Aspergillus nidulans MAPK module AnSte11-Ste50-Ste7-Fus3 controls development and secondary metabolism
The Aspergillus nidulans MAPK module AnSte11-Ste50-Ste7-Fus3 controls development and secondary metabolism
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The Aspergillus nidulans MAPK module AnSte11-Ste50-Ste7-Fus3 controls development and secondary metabolism

PLoS genetics, 2012-07, Vol.8 (7), p.e1002816-e1002816 [Peer Reviewed Journal]

COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;2012 Bayram et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Bayram Ö, Bayram ÖS, Ahmed YL, Maruyama J-i, Valerius O, et al. (2012) The Aspergillus nidulans MAPK Module AnSte11-Ste50-Ste7-Fus3 Controls Development and Secondary Metabolism. PLoS Genet 8(7): e1002816. doi:10.1371/journal.pgen.1002816 ;Bayram et al. 2012 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002816 ;PMID: 22829779

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15
Kir2.1 Interaction with Stk38 Promotes Invasion and Metastasis of Human Gastric Cancer by Enhancing MEKK2-MEK1/2-ERK1/2 Signaling
Kir2.1 Interaction with Stk38 Promotes Invasion and Metastasis of Human Gastric Cancer by Enhancing MEKK2-MEK1/2-ERK1/2 Signaling
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Kir2.1 Interaction with Stk38 Promotes Invasion and Metastasis of Human Gastric Cancer by Enhancing MEKK2-MEK1/2-ERK1/2 Signaling

Cancer research (Chicago, Ill.), 2018-06, Vol.78 (11), p.3041-3053 [Peer Reviewed Journal]

2018 American Association for Cancer Research. ;Copyright American Association for Cancer Research, Inc. Jun 1, 2018 ;ISSN: 0008-5472 ;EISSN: 1538-7445 ;DOI: 10.1158/0008-5472.CAN-17-3776 ;PMID: 29549164

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16
Inhibition of p70 S6 kinase activity by A77 1726 induces autophagy and enhances the degradation of superoxide dismutase 1 (SOD1) protein aggregates
Inhibition of p70 S6 kinase activity by A77 1726 induces autophagy and enhances the degradation of superoxide dismutase 1 (SOD1) protein aggregates
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Inhibition of p70 S6 kinase activity by A77 1726 induces autophagy and enhances the degradation of superoxide dismutase 1 (SOD1) protein aggregates

Cell death & disease, 2018-03, Vol.9 (3), p.407-16, Article 407 [Peer Reviewed Journal]

2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2041-4889 ;EISSN: 2041-4889 ;DOI: 10.1038/s41419-018-0441-0 ;PMID: 29540819

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17
TGFβ-activated Kinase 1 (TAK1) Inhibition by 5Z-7-Oxozeaenol Attenuates Early Brain Injury after Experimental Subarachnoid Hemorrhage
TGFβ-activated Kinase 1 (TAK1) Inhibition by 5Z-7-Oxozeaenol Attenuates Early Brain Injury after Experimental Subarachnoid Hemorrhage
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TGFβ-activated Kinase 1 (TAK1) Inhibition by 5Z-7-Oxozeaenol Attenuates Early Brain Injury after Experimental Subarachnoid Hemorrhage

The Journal of biological chemistry, 2015-08, Vol.290 (32), p.19900-19909 [Peer Reviewed Journal]

2015 © 2015 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology. ;2015 by The American Society for Biochemistry and Molecular Biology, Inc. ;2015 by The American Society for Biochemistry and Molecular Biology, Inc. 2015 ;ISSN: 0021-9258 ;EISSN: 1083-351X ;DOI: 10.1074/jbc.M115.636795 ;PMID: 26100626

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18
MEK drives BRAF activation through allosteric control of KSR proteins
MEK drives BRAF activation through allosteric control of KSR proteins
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MEK drives BRAF activation through allosteric control of KSR proteins

Nature (London), 2018-02, Vol.554 (7693), p.549-553 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Feb 22, 2018 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature25478 ;PMID: 29433126

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19
Choosing Kinase Inhibitors for Androgen Deprivation Therapy-Resistant Prostate Cancer
Choosing Kinase Inhibitors for Androgen Deprivation Therapy-Resistant Prostate Cancer
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Choosing Kinase Inhibitors for Androgen Deprivation Therapy-Resistant Prostate Cancer

Pharmaceutics, 2022-02, Vol.14 (3), p.498 [Peer Reviewed Journal]

2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 1999-4923 ;EISSN: 1999-4923 ;DOI: 10.3390/pharmaceutics14030498 ;PMID: 35335873

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20
Identification of Host Kinase Genes Required for Influenza Virus Replication and the Regulatory Role of MicroRNAs
Identification of Host Kinase Genes Required for Influenza Virus Replication and the Regulatory Role of MicroRNAs
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Identification of Host Kinase Genes Required for Influenza Virus Replication and the Regulatory Role of MicroRNAs

PloS one, 2013-06, Vol.8 (6), p.e66796-e66796 [Peer Reviewed Journal]

COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Bakre et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2013 Bakre et al 2013 Bakre et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0066796 ;PMID: 23805279

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