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Index by author

November 01, 2015; Volume 88,Issue 5

A

  1. Albillos, Almudena

    1. α-Conotoxins Identify the α3β4* Subtype as the Predominant Nicotinic Acetylcholine Receptor Expressed in Human Adrenal Chromaffin Cells
      Arik J. Hone, J. Michael McIntosh, Layla Azam, Jon Lindstrom, Linda Lucero, Paul Whiteaker, Juan Passas, Jesús Blázquez and Almudena Albillos
      Molecular Pharmacology November 2015, 88 (5) 881-893; DOI: https://doi.org/10.1124/mol.115.100982

  2. Albrecht, Hugo

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  3. Alexander, Shawn T.

    1. Critical Cysteine Residues in Both the Calcium-Sensing Receptor and the Allosteric Activator AMG 416 Underlie the Mechanism of Action
      Shawn T. Alexander, Thomas Hunter, Sarah Walter, Jin Dong, Derek Maclean, Amos Baruch, Raju Subramanian and James E. Tomlinson
      Molecular Pharmacology November 2015, 88 (5) 853-865; DOI: https://doi.org/10.1124/mol.115.098392

  4. Alves, Carlos Roberto

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

  5. Azam, Layla

    1. α-Conotoxins Identify the α3β4* Subtype as the Predominant Nicotinic Acetylcholine Receptor Expressed in Human Adrenal Chromaffin Cells
      Arik J. Hone, J. Michael McIntosh, Layla Azam, Jon Lindstrom, Linda Lucero, Paul Whiteaker, Juan Passas, Jesús Blázquez and Almudena Albillos
      Molecular Pharmacology November 2015, 88 (5) 881-893; DOI: https://doi.org/10.1124/mol.115.100982

B

  1. Baruch, Amos

    1. Critical Cysteine Residues in Both the Calcium-Sensing Receptor and the Allosteric Activator AMG 416 Underlie the Mechanism of Action
      Shawn T. Alexander, Thomas Hunter, Sarah Walter, Jin Dong, Derek Maclean, Amos Baruch, Raju Subramanian and James E. Tomlinson
      Molecular Pharmacology November 2015, 88 (5) 853-865; DOI: https://doi.org/10.1124/mol.115.098392

  2. Basnet, Sunita K.C.

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  3. Batista, Paulo Ricardo

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

  4. Bhayana, Brijesh

    1. Breathing Stimulant Compounds Inhibit TASK-3 Potassium Channel Function Likely by Binding at a Common Site in the Channel Pore
      Rikki H. Chokshi, Aaron T. Larsen, Brijesh Bhayana and Joseph F. Cotten
      Molecular Pharmacology November 2015, 88 (5) 926-934; DOI: https://doi.org/10.1124/mol.115.100107

  5. Blázquez, Jesús

    1. α-Conotoxins Identify the α3β4* Subtype as the Predominant Nicotinic Acetylcholine Receptor Expressed in Human Adrenal Chromaffin Cells
      Arik J. Hone, J. Michael McIntosh, Layla Azam, Jon Lindstrom, Linda Lucero, Paul Whiteaker, Juan Passas, Jesús Blázquez and Almudena Albillos
      Molecular Pharmacology November 2015, 88 (5) 881-893; DOI: https://doi.org/10.1124/mol.115.100982

  6. Bonaventure, Pascal

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  7. Borges, Perla Villani

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

C

  1. Caffarena, Ernesto Raúl

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

  2. Carruthers, Nicholas

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  3. Cervenka, Rene

    1. Mechanism of Modification, by Lidocaine, of Fast and Slow Recovery from Inactivation of Voltage-Gated Na+ Channels
      Vaibhavkumar S. Gawali, Peter Lukacs, Rene Cervenka, Xaver Koenig, Lena Rubi, Karlheinz Hilber, Walter Sandtner and Hannes Todt
      Molecular Pharmacology November 2015, 88 (5) 866-879; DOI: https://doi.org/10.1124/mol.115.099580

  4. Chokshi, Rikki H.

    1. Breathing Stimulant Compounds Inhibit TASK-3 Potassium Channel Function Likely by Binding at a Common Site in the Channel Pore
      Rikki H. Chokshi, Aaron T. Larsen, Brijesh Bhayana and Joseph F. Cotten
      Molecular Pharmacology November 2015, 88 (5) 926-934; DOI: https://doi.org/10.1124/mol.115.100107

  5. Coate, Heather

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  6. Corsino, Patrick E.

    1. Cyclin-Dependent Kinase Inhibitors as Anticancer Therapeutics
      Mary E. Law, Patrick E. Corsino, Satya Narayan and Brian K. Law
      Molecular Pharmacology November 2015, 88 (5) 846-852; DOI: https://doi.org/10.1124/mol.115.099325

  7. Cotten, Joseph F.

    1. Breathing Stimulant Compounds Inhibit TASK-3 Potassium Channel Function Likely by Binding at a Common Site in the Channel Pore
      Rikki H. Chokshi, Aaron T. Larsen, Brijesh Bhayana and Joseph F. Cotten
      Molecular Pharmacology November 2015, 88 (5) 926-934; DOI: https://doi.org/10.1124/mol.115.100107

  8. Cui, Wenjun

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

D

  1. Diab, Sarah

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  2. Dong, Jin

    1. Critical Cysteine Residues in Both the Calcium-Sensing Receptor and the Allosteric Activator AMG 416 Underlie the Mechanism of Action
      Shawn T. Alexander, Thomas Hunter, Sarah Walter, Jin Dong, Derek Maclean, Amos Baruch, Raju Subramanian and James E. Tomlinson
      Molecular Pharmacology November 2015, 88 (5) 853-865; DOI: https://doi.org/10.1124/mol.115.098392

  3. Dugovic, Christine

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  4. Dvorak, Curt

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

E

  1. Eckert, William

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

F

  1. Farber, Joshua M.

    1. Selectivity in the Use of Gi/o Proteins Is Determined by the DRF Motif in CXCR6 and Is Cell-Type Specific
      Satya P. Singh, John F. Foley, Hongwei H. Zhang, Darrell E. Hurt, Jennifer L. Richards, Craig S. Smith, Fang Liao and Joshua M. Farber
      Molecular Pharmacology November 2015, 88 (5) 894-910; DOI: https://doi.org/10.1124/mol.115.099960

  2. Foley, John F.

    1. Selectivity in the Use of Gi/o Proteins Is Determined by the DRF Motif in CXCR6 and Is Cell-Type Specific
      Satya P. Singh, John F. Foley, Hongwei H. Zhang, Darrell E. Hurt, Jennifer L. Richards, Craig S. Smith, Fang Liao and Joshua M. Farber
      Molecular Pharmacology November 2015, 88 (5) 894-910; DOI: https://doi.org/10.1124/mol.115.099960

G

  1. Gawali, Vaibhavkumar S.

    1. Mechanism of Modification, by Lidocaine, of Fast and Slow Recovery from Inactivation of Voltage-Gated Na+ Channels
      Vaibhavkumar S. Gawali, Peter Lukacs, Rene Cervenka, Xaver Koenig, Lena Rubi, Karlheinz Hilber, Walter Sandtner and Hannes Todt
      Molecular Pharmacology November 2015, 88 (5) 866-879; DOI: https://doi.org/10.1124/mol.115.099580

  2. Gillam, Todd Alexander

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

H

  1. Harrington, Anthony

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  2. Henriques, Maria das Graças

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

  3. Hilber, Karlheinz

    1. Mechanism of Modification, by Lidocaine, of Fast and Slow Recovery from Inactivation of Voltage-Gated Na+ Channels
      Vaibhavkumar S. Gawali, Peter Lukacs, Rene Cervenka, Xaver Koenig, Lena Rubi, Karlheinz Hilber, Walter Sandtner and Hannes Todt
      Molecular Pharmacology November 2015, 88 (5) 866-879; DOI: https://doi.org/10.1124/mol.115.099580

  4. Hone, Arik J.

    1. α-Conotoxins Identify the α3β4* Subtype as the Predominant Nicotinic Acetylcholine Receptor Expressed in Human Adrenal Chromaffin Cells
      Arik J. Hone, J. Michael McIntosh, Layla Azam, Jon Lindstrom, Linda Lucero, Paul Whiteaker, Juan Passas, Jesús Blázquez and Almudena Albillos
      Molecular Pharmacology November 2015, 88 (5) 881-893; DOI: https://doi.org/10.1124/mol.115.100982

  5. Hou, Jianying

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

  6. Huang, Manna

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

  7. Huang, Yingchun

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

  8. Hunter, Thomas

    1. Critical Cysteine Residues in Both the Calcium-Sensing Receptor and the Allosteric Activator AMG 416 Underlie the Mechanism of Action
      Shawn T. Alexander, Thomas Hunter, Sarah Walter, Jin Dong, Derek Maclean, Amos Baruch, Raju Subramanian and James E. Tomlinson
      Molecular Pharmacology November 2015, 88 (5) 853-865; DOI: https://doi.org/10.1124/mol.115.098392

  9. Hurt, Darrell E.

    1. Selectivity in the Use of Gi/o Proteins Is Determined by the DRF Motif in CXCR6 and Is Cell-Type Specific
      Satya P. Singh, John F. Foley, Hongwei H. Zhang, Darrell E. Hurt, Jennifer L. Richards, Craig S. Smith, Fang Liao and Joshua M. Farber
      Molecular Pharmacology November 2015, 88 (5) 894-910; DOI: https://doi.org/10.1124/mol.115.099960

J

  1. Joseph, Victory

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

K

  1. Ke, Hengming

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

  2. Koenig, Xaver

    1. Mechanism of Modification, by Lidocaine, of Fast and Slow Recovery from Inactivation of Voltage-Gated Na+ Channels
      Vaibhavkumar S. Gawali, Peter Lukacs, Rene Cervenka, Xaver Koenig, Lena Rubi, Karlheinz Hilber, Walter Sandtner and Hannes Todt
      Molecular Pharmacology November 2015, 88 (5) 866-879; DOI: https://doi.org/10.1124/mol.115.099580

  3. Kuei, Chester

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

L

  1. Larsen, Aaron T.

    1. Breathing Stimulant Compounds Inhibit TASK-3 Potassium Channel Function Likely by Binding at a Common Site in the Channel Pore
      Rikki H. Chokshi, Aaron T. Larsen, Brijesh Bhayana and Joseph F. Cotten
      Molecular Pharmacology November 2015, 88 (5) 926-934; DOI: https://doi.org/10.1124/mol.115.100107

  2. Law, Brian K.

    1. Cyclin-Dependent Kinase Inhibitors as Anticancer Therapeutics
      Mary E. Law, Patrick E. Corsino, Satya Narayan and Brian K. Law
      Molecular Pharmacology November 2015, 88 (5) 846-852; DOI: https://doi.org/10.1124/mol.115.099325

  3. Law, Mary E.

    1. Cyclin-Dependent Kinase Inhibitors as Anticancer Therapeutics
      Mary E. Law, Patrick E. Corsino, Satya Narayan and Brian K. Law
      Molecular Pharmacology November 2015, 88 (5) 846-852; DOI: https://doi.org/10.1124/mol.115.099325

  4. Lee, Grace

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  5. Li, Peng

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  6. Li, Qingqin

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  7. Li, Zhe

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

  8. Liang, Beibei

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

  9. Liao, Fang

    1. Selectivity in the Use of Gi/o Proteins Is Determined by the DRF Motif in CXCR6 and Is Cell-Type Specific
      Satya P. Singh, John F. Foley, Hongwei H. Zhang, Darrell E. Hurt, Jennifer L. Richards, Craig S. Smith, Fang Liao and Joshua M. Farber
      Molecular Pharmacology November 2015, 88 (5) 894-910; DOI: https://doi.org/10.1124/mol.115.099960

  10. Lindstrom, Jon

    1. α-Conotoxins Identify the α3β4* Subtype as the Predominant Nicotinic Acetylcholine Receptor Expressed in Human Adrenal Chromaffin Cells
      Arik J. Hone, J. Michael McIntosh, Layla Azam, Jon Lindstrom, Linda Lucero, Paul Whiteaker, Juan Passas, Jesús Blázquez and Almudena Albillos
      Molecular Pharmacology November 2015, 88 (5) 881-893; DOI: https://doi.org/10.1124/mol.115.100982

  11. Liu, Changlu

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  12. Liu, Peiqing

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

  13. Lovenberg, Timothy W.

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  14. Lucero, Linda

    1. α-Conotoxins Identify the α3β4* Subtype as the Predominant Nicotinic Acetylcholine Receptor Expressed in Human Adrenal Chromaffin Cells
      Arik J. Hone, J. Michael McIntosh, Layla Azam, Jon Lindstrom, Linda Lucero, Paul Whiteaker, Juan Passas, Jesús Blázquez and Almudena Albillos
      Molecular Pharmacology November 2015, 88 (5) 881-893; DOI: https://doi.org/10.1124/mol.115.100982

  15. Lukacs, Peter

    1. Mechanism of Modification, by Lidocaine, of Fast and Slow Recovery from Inactivation of Voltage-Gated Na+ Channels
      Vaibhavkumar S. Gawali, Peter Lukacs, Rene Cervenka, Xaver Koenig, Lena Rubi, Karlheinz Hilber, Walter Sandtner and Hannes Todt
      Molecular Pharmacology November 2015, 88 (5) 866-879; DOI: https://doi.org/10.1124/mol.115.099580

  16. Luo, Hai-Bin

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

M

  1. Maclean, Derek

    1. Critical Cysteine Residues in Both the Calcium-Sensing Receptor and the Allosteric Activator AMG 416 Underlie the Mechanism of Action
      Shawn T. Alexander, Thomas Hunter, Sarah Walter, Jin Dong, Derek Maclean, Amos Baruch, Raju Subramanian and James E. Tomlinson
      Molecular Pharmacology November 2015, 88 (5) 853-865; DOI: https://doi.org/10.1124/mol.115.098392

  2. Maya-Monteiro, Clarissa Menezes

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

  3. McIntosh, J. Michael

    1. α-Conotoxins Identify the α3β4* Subtype as the Predominant Nicotinic Acetylcholine Receptor Expressed in Human Adrenal Chromaffin Cells
      Arik J. Hone, J. Michael McIntosh, Layla Azam, Jon Lindstrom, Linda Lucero, Paul Whiteaker, Juan Passas, Jesús Blázquez and Almudena Albillos
      Molecular Pharmacology November 2015, 88 (5) 881-893; DOI: https://doi.org/10.1124/mol.115.100982

  4. Moret, Katelim Hottz

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

N

  1. Narayan, Satya

    1. Cyclin-Dependent Kinase Inhibitors as Anticancer Therapeutics
      Mary E. Law, Patrick E. Corsino, Satya Narayan and Brian K. Law
      Molecular Pharmacology November 2015, 88 (5) 846-852; DOI: https://doi.org/10.1124/mol.115.099325

  2. Nepomuceno, Diane

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

P

  1. Pacheco, Patrícia

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

  2. Passas, Juan

    1. α-Conotoxins Identify the α3β4* Subtype as the Predominant Nicotinic Acetylcholine Receptor Expressed in Human Adrenal Chromaffin Cells
      Arik J. Hone, J. Michael McIntosh, Layla Azam, Jon Lindstrom, Linda Lucero, Paul Whiteaker, Juan Passas, Jesús Blázquez and Almudena Albillos
      Molecular Pharmacology November 2015, 88 (5) 881-893; DOI: https://doi.org/10.1124/mol.115.100982

  3. Peat, Tom

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  4. Penido, Carmen

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

R

  1. Richards, Jennifer L.

    1. Selectivity in the Use of Gi/o Proteins Is Determined by the DRF Motif in CXCR6 and Is Cell-Type Specific
      Satya P. Singh, John F. Foley, Hongwei H. Zhang, Darrell E. Hurt, Jennifer L. Richards, Craig S. Smith, Fang Liao and Joshua M. Farber
      Molecular Pharmacology November 2015, 88 (5) 894-910; DOI: https://doi.org/10.1124/mol.115.099960

  2. Rubi, Lena

    1. Mechanism of Modification, by Lidocaine, of Fast and Slow Recovery from Inactivation of Voltage-Gated Na+ Channels
      Vaibhavkumar S. Gawali, Peter Lukacs, Rene Cervenka, Xaver Koenig, Lena Rubi, Karlheinz Hilber, Walter Sandtner and Hannes Todt
      Molecular Pharmacology November 2015, 88 (5) 866-879; DOI: https://doi.org/10.1124/mol.115.099580

S

  1. Sandtner, Walter

    1. Mechanism of Modification, by Lidocaine, of Fast and Slow Recovery from Inactivation of Voltage-Gated Na+ Channels
      Vaibhavkumar S. Gawali, Peter Lukacs, Rene Cervenka, Xaver Koenig, Lena Rubi, Karlheinz Hilber, Walter Sandtner and Hannes Todt
      Molecular Pharmacology November 2015, 88 (5) 866-879; DOI: https://doi.org/10.1124/mol.115.099580

  2. Schmid, Raffaella

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  3. Shao, Yongxian

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

  4. Singh, Satya P.

    1. Selectivity in the Use of Gi/o Proteins Is Determined by the DRF Motif in CXCR6 and Is Cell-Type Specific
      Satya P. Singh, John F. Foley, Hongwei H. Zhang, Darrell E. Hurt, Jennifer L. Richards, Craig S. Smith, Fang Liao and Joshua M. Farber
      Molecular Pharmacology November 2015, 88 (5) 894-910; DOI: https://doi.org/10.1124/mol.115.099960

  5. Smith, Craig S.

    1. Selectivity in the Use of Gi/o Proteins Is Determined by the DRF Motif in CXCR6 and Is Cell-Type Specific
      Satya P. Singh, John F. Foley, Hongwei H. Zhang, Darrell E. Hurt, Jennifer L. Richards, Craig S. Smith, Fang Liao and Joshua M. Farber
      Molecular Pharmacology November 2015, 88 (5) 894-910; DOI: https://doi.org/10.1124/mol.115.099960

  6. Souza-Silva, Franklin

    1. Gedunin Binds to Myeloid Differentiation Protein 2 and Impairs Lipopolysaccharide-Induced Toll-Like Receptor 4 Signaling in Macrophages
      Perla Villani Borges, Katelim Hottz Moret, Clarissa Menezes Maya-Monteiro, Franklin Souza-Silva, Carlos Roberto Alves, Paulo Ricardo Batista, Ernesto Raúl Caffarena, Patrícia Pacheco, Maria das Graças Henriques and Carmen Penido
      Molecular Pharmacology November 2015, 88 (5) 949-961; DOI: https://doi.org/10.1124/mol.115.098970

  7. Subramanian, Raju

    1. Critical Cysteine Residues in Both the Calcium-Sensing Receptor and the Allosteric Activator AMG 416 Underlie the Mechanism of Action
      Shawn T. Alexander, Thomas Hunter, Sarah Walter, Jin Dong, Derek Maclean, Amos Baruch, Raju Subramanian and James E. Tomlinson
      Molecular Pharmacology November 2015, 88 (5) 853-865; DOI: https://doi.org/10.1124/mol.115.098392

  8. Sutton, Steven W.

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

T

  1. Teo, Theodosia

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  2. Todt, Hannes

    1. Mechanism of Modification, by Lidocaine, of Fast and Slow Recovery from Inactivation of Voltage-Gated Na+ Channels
      Vaibhavkumar S. Gawali, Peter Lukacs, Rene Cervenka, Xaver Koenig, Lena Rubi, Karlheinz Hilber, Walter Sandtner and Hannes Todt
      Molecular Pharmacology November 2015, 88 (5) 866-879; DOI: https://doi.org/10.1124/mol.115.099580

  3. Tomlinson, James E.

    1. Critical Cysteine Residues in Both the Calcium-Sensing Receptor and the Allosteric Activator AMG 416 Underlie the Mechanism of Action
      Shawn T. Alexander, Thomas Hunter, Sarah Walter, Jin Dong, Derek Maclean, Amos Baruch, Raju Subramanian and James E. Tomlinson
      Molecular Pharmacology November 2015, 88 (5) 853-865; DOI: https://doi.org/10.1124/mol.115.098392

W

  1. Walter, Sarah

    1. Critical Cysteine Residues in Both the Calcium-Sensing Receptor and the Allosteric Activator AMG 416 Underlie the Mechanism of Action
      Shawn T. Alexander, Thomas Hunter, Sarah Walter, Jin Dong, Derek Maclean, Amos Baruch, Raju Subramanian and James E. Tomlinson
      Molecular Pharmacology November 2015, 88 (5) 853-865; DOI: https://doi.org/10.1124/mol.115.098392

  2. Wan, Yiqian

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

  3. Wang, Shudong

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  4. Whiteaker, Paul

    1. α-Conotoxins Identify the α3β4* Subtype as the Predominant Nicotinic Acetylcholine Receptor Expressed in Human Adrenal Chromaffin Cells
      Arik J. Hone, J. Michael McIntosh, Layla Azam, Jon Lindstrom, Linda Lucero, Paul Whiteaker, Juan Passas, Jesús Blázquez and Almudena Albillos
      Molecular Pharmacology November 2015, 88 (5) 881-893; DOI: https://doi.org/10.1124/mol.115.100982

  5. Wu, Jiejun

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  6. Wu, Yinuo

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747

Y

  1. Yang, Yuchao

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  2. Yao, Xiang

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  3. Yieh, Lynn

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

  4. Yu, Mingfeng

    1. Identification of a Highly Conserved Allosteric Binding Site on Mnk1 and Mnk2
      Sunita K.C. Basnet, Sarah Diab, Raffaella Schmid, Mingfeng Yu, Yuchao Yang, Todd Alexander Gillam, Theodosia Teo, Peng Li, Tom Peat, Hugo Albrecht and Shudong Wang
      Molecular Pharmacology November 2015, 88 (5) 935-948; DOI: https://doi.org/10.1124/mol.115.100131

  5. Yun, Sujin

    1. GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine
      Changlu Liu, Pascal Bonaventure, Grace Lee, Diane Nepomuceno, Chester Kuei, Jiejun Wu, Qingqin Li, Victory Joseph, Steven W. Sutton, William Eckert, Xiang Yao, Lynn Yieh, Curt Dvorak, Nicholas Carruthers, Heather Coate, Sujin Yun, Christine Dugovic, Anthony Harrington and Timothy W. Lovenberg
      Molecular Pharmacology November 2015, 88 (5) 911-925; DOI: https://doi.org/10.1124/mol.115.100412

Z

  1. Zhang, Hongwei H.

    1. Selectivity in the Use of Gi/o Proteins Is Determined by the DRF Motif in CXCR6 and Is Cell-Type Specific
      Satya P. Singh, John F. Foley, Hongwei H. Zhang, Darrell E. Hurt, Jennifer L. Richards, Craig S. Smith, Fang Liao and Joshua M. Farber
      Molecular Pharmacology November 2015, 88 (5) 894-910; DOI: https://doi.org/10.1124/mol.115.099960

  2. Zhu, Xinhai

    1. Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Structural Asymmetry of Phosphodiesterase-9A and a Unique Pocket for Selective Binding of a Potent Enantiomeric Inhibitor
      Manna Huang, Yongxian Shao, Jianying Hou, Wenjun Cui, Beibei Liang, Yingchun Huang, Zhe Li, Yinuo Wu, Xinhai Zhu, Peiqing Liu, Yiqian Wan, Hengming Ke and Hai-Bin Luo
      Molecular Pharmacology November 2015, 88 (5) 836-845; DOI: https://doi.org/10.1124/mol.115.099747
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