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Molecular Pharmacology

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Index by author

February 01, 1989; Volume 35,Issue 2
  • A
  • B
  • C
  • D
  • E
  • F
  • G
  • H
  • I
  • J
  • K
  • L
  • M
  • N
  • O
  • P
  • Q
  • R
  • S
  • T
  • U
  • V
  • W
  • X
  • Y
  • Z

A

  1. Albuquerque, E X

    1. You have access
      N-methylanatoxinol isomers: derivatives of the agonist (+)-anatoxin-a block the nicotinic acetylcholine receptor ion channel.
      K L Swanson, Y Aracava, F J Sardina, H Rapoport, R S Aronstam and E X Albuquerque
      Molecular Pharmacology February 1989, 35 (2) 223-231;
  2. Aracava, Y

    1. You have access
      N-methylanatoxinol isomers: derivatives of the agonist (+)-anatoxin-a block the nicotinic acetylcholine receptor ion channel.
      K L Swanson, Y Aracava, F J Sardina, H Rapoport, R S Aronstam and E X Albuquerque
      Molecular Pharmacology February 1989, 35 (2) 223-231;
  3. Arcamone, F

    1. You have access
      Joint experimental and theoretical investigation of the comparative DNA binding affinities of intercalating anthracycline derivatives.
      N Gresh, B Pullman, F Arcamone, M Menozzi and R Tonani
      Molecular Pharmacology February 1989, 35 (2) 251-256;
  4. Aronstam, R S

    1. You have access
      N-methylanatoxinol isomers: derivatives of the agonist (+)-anatoxin-a block the nicotinic acetylcholine receptor ion channel.
      K L Swanson, Y Aracava, F J Sardina, H Rapoport, R S Aronstam and E X Albuquerque
      Molecular Pharmacology February 1989, 35 (2) 223-231;

B

  1. Beerman, T A

    1. You have access
      Modulation of topoisomerase II catalytic activity by DNA minor groove binding agents distamycin, Hoechst 33258, and 4',6-diamidine-2-phenylindole.
      J M Woynarowski, M McHugh, R D Sigmund and T A Beerman
      Molecular Pharmacology February 1989, 35 (2) 177-182;
  2. Bonner, F W

    1. You have access
      Investigations into the biochemical effects of region-specific nephrotoxins.
      K P Gartland, F W Bonner and J K Nicholson
      Molecular Pharmacology February 1989, 35 (2) 242-250;

C

  1. Canela, E I

    1. You have access
      Theoretical study of the protonation and tautomerization of adenosine, formycin, and their 2-NH2 and 2-F derivatives: functional implications in the mechanism of reaction of adenosine deaminase.
      M Orozco, E I Canela and R Franco
      Molecular Pharmacology February 1989, 35 (2) 257-264;
  2. Czajkowski, C

    1. You have access
      Identification of an intracellular pool of gamma-aminobutyric acidA/benzodiazepine receptors en route to the cell surface of brain neurons in culture.
      C Czajkowski and D H Farb
      Molecular Pharmacology February 1989, 35 (2) 183-188;

D

  1. de Costa, B R

    1. You have access
      meta- and para-isothiocyanato-t-butylbicycloorthobenzoate: irreversible ligands of the gamma-aminobutyric acid-regulated chloride ionophore.
      A H Lewin, B R de Costa, K C Rice and P Skolnick
      Molecular Pharmacology February 1989, 35 (2) 189-194;
  2. Domask, L M

    1. You have access
      Muscarinic receptor regulation of cytoplasmic Ca2+ concentrations in human SK-N-SH neuroblastoma cells: Ca2+ requirements for phospholipase C activation.
      S K Fisher, L M Domask and R M Roland
      Molecular Pharmacology February 1989, 35 (2) 195-204;

E

  1. Ellis, J

    1. You have access
      Gallamine exerts biphasic allosteric effects at muscarinic receptors.
      J Ellis and M Seidenberg
      Molecular Pharmacology February 1989, 35 (2) 173-176;

F

  1. Farb, D H

    1. You have access
      Identification of an intracellular pool of gamma-aminobutyric acidA/benzodiazepine receptors en route to the cell surface of brain neurons in culture.
      C Czajkowski and D H Farb
      Molecular Pharmacology February 1989, 35 (2) 183-188;
  2. Fisher, S K

    1. You have access
      Muscarinic receptor regulation of cytoplasmic Ca2+ concentrations in human SK-N-SH neuroblastoma cells: Ca2+ requirements for phospholipase C activation.
      S K Fisher, L M Domask and R M Roland
      Molecular Pharmacology February 1989, 35 (2) 195-204;
  3. Franco, R

    1. You have access
      Theoretical study of the protonation and tautomerization of adenosine, formycin, and their 2-NH2 and 2-F derivatives: functional implications in the mechanism of reaction of adenosine deaminase.
      M Orozco, E I Canela and R Franco
      Molecular Pharmacology February 1989, 35 (2) 257-264;

G

  1. Gago, F

    1. You have access
      The binding of nonintercalative drugs to alternating DNA sequences.
      F Gago, C A Reynolds and W G Richards
      Molecular Pharmacology February 1989, 35 (2) 232-241;
  2. Gannon, M N

    1. You have access
      A metactoid sensitization model to describe multiple receptors linked to a common response: application to histamine receptors coupled to [3H]cyclic AMP accumulation in guinea pig cortex.
      M N Gannon, L B Hough and H Weinstein
      Molecular Pharmacology February 1989, 35 (2) 205-213;
  3. Gartland, K P

    1. You have access
      Investigations into the biochemical effects of region-specific nephrotoxins.
      K P Gartland, F W Bonner and J K Nicholson
      Molecular Pharmacology February 1989, 35 (2) 242-250;
  4. Gresh, N

    1. You have access
      Joint experimental and theoretical investigation of the comparative DNA binding affinities of intercalating anthracycline derivatives.
      N Gresh, B Pullman, F Arcamone, M Menozzi and R Tonani
      Molecular Pharmacology February 1989, 35 (2) 251-256;

H

  1. Hough, L B

    1. You have access
      A metactoid sensitization model to describe multiple receptors linked to a common response: application to histamine receptors coupled to [3H]cyclic AMP accumulation in guinea pig cortex.
      M N Gannon, L B Hough and H Weinstein
      Molecular Pharmacology February 1989, 35 (2) 205-213;

K

  1. Kenakin, T P

    1. You have access
      Theoretical effects of single and multiple transducer receptor coupling proteins on estimates of the relative potency of agonists.
      T P Kenakin and P H Morgan
      Molecular Pharmacology February 1989, 35 (2) 214-222;

L

  1. Lewin, A H

    1. You have access
      meta- and para-isothiocyanato-t-butylbicycloorthobenzoate: irreversible ligands of the gamma-aminobutyric acid-regulated chloride ionophore.
      A H Lewin, B R de Costa, K C Rice and P Skolnick
      Molecular Pharmacology February 1989, 35 (2) 189-194;

M

  1. McHugh, M

    1. You have access
      Modulation of topoisomerase II catalytic activity by DNA minor groove binding agents distamycin, Hoechst 33258, and 4',6-diamidine-2-phenylindole.
      J M Woynarowski, M McHugh, R D Sigmund and T A Beerman
      Molecular Pharmacology February 1989, 35 (2) 177-182;
  2. Menozzi, M

    1. You have access
      Joint experimental and theoretical investigation of the comparative DNA binding affinities of intercalating anthracycline derivatives.
      N Gresh, B Pullman, F Arcamone, M Menozzi and R Tonani
      Molecular Pharmacology February 1989, 35 (2) 251-256;
  3. Morgan, P H

    1. You have access
      Theoretical effects of single and multiple transducer receptor coupling proteins on estimates of the relative potency of agonists.
      T P Kenakin and P H Morgan
      Molecular Pharmacology February 1989, 35 (2) 214-222;

N

  1. Nicholson, J K

    1. You have access
      Investigations into the biochemical effects of region-specific nephrotoxins.
      K P Gartland, F W Bonner and J K Nicholson
      Molecular Pharmacology February 1989, 35 (2) 242-250;

O

  1. Orozco, M

    1. You have access
      Theoretical study of the protonation and tautomerization of adenosine, formycin, and their 2-NH2 and 2-F derivatives: functional implications in the mechanism of reaction of adenosine deaminase.
      M Orozco, E I Canela and R Franco
      Molecular Pharmacology February 1989, 35 (2) 257-264;

P

  1. Pullman, B

    1. You have access
      Joint experimental and theoretical investigation of the comparative DNA binding affinities of intercalating anthracycline derivatives.
      N Gresh, B Pullman, F Arcamone, M Menozzi and R Tonani
      Molecular Pharmacology February 1989, 35 (2) 251-256;

R

  1. Rapoport, H

    1. You have access
      N-methylanatoxinol isomers: derivatives of the agonist (+)-anatoxin-a block the nicotinic acetylcholine receptor ion channel.
      K L Swanson, Y Aracava, F J Sardina, H Rapoport, R S Aronstam and E X Albuquerque
      Molecular Pharmacology February 1989, 35 (2) 223-231;
  2. Reynolds, C A

    1. You have access
      The binding of nonintercalative drugs to alternating DNA sequences.
      F Gago, C A Reynolds and W G Richards
      Molecular Pharmacology February 1989, 35 (2) 232-241;
  3. Rice, K C

    1. You have access
      meta- and para-isothiocyanato-t-butylbicycloorthobenzoate: irreversible ligands of the gamma-aminobutyric acid-regulated chloride ionophore.
      A H Lewin, B R de Costa, K C Rice and P Skolnick
      Molecular Pharmacology February 1989, 35 (2) 189-194;
  4. Richards, W G

    1. You have access
      The binding of nonintercalative drugs to alternating DNA sequences.
      F Gago, C A Reynolds and W G Richards
      Molecular Pharmacology February 1989, 35 (2) 232-241;
  5. Roland, R M

    1. You have access
      Muscarinic receptor regulation of cytoplasmic Ca2+ concentrations in human SK-N-SH neuroblastoma cells: Ca2+ requirements for phospholipase C activation.
      S K Fisher, L M Domask and R M Roland
      Molecular Pharmacology February 1989, 35 (2) 195-204;

S

  1. Sardina, F J

    1. You have access
      N-methylanatoxinol isomers: derivatives of the agonist (+)-anatoxin-a block the nicotinic acetylcholine receptor ion channel.
      K L Swanson, Y Aracava, F J Sardina, H Rapoport, R S Aronstam and E X Albuquerque
      Molecular Pharmacology February 1989, 35 (2) 223-231;
  2. Seidenberg, M

    1. You have access
      Gallamine exerts biphasic allosteric effects at muscarinic receptors.
      J Ellis and M Seidenberg
      Molecular Pharmacology February 1989, 35 (2) 173-176;
  3. Sigmund, R D

    1. You have access
      Modulation of topoisomerase II catalytic activity by DNA minor groove binding agents distamycin, Hoechst 33258, and 4',6-diamidine-2-phenylindole.
      J M Woynarowski, M McHugh, R D Sigmund and T A Beerman
      Molecular Pharmacology February 1989, 35 (2) 177-182;
  4. Skolnick, P

    1. You have access
      meta- and para-isothiocyanato-t-butylbicycloorthobenzoate: irreversible ligands of the gamma-aminobutyric acid-regulated chloride ionophore.
      A H Lewin, B R de Costa, K C Rice and P Skolnick
      Molecular Pharmacology February 1989, 35 (2) 189-194;
  5. Swanson, K L

    1. You have access
      N-methylanatoxinol isomers: derivatives of the agonist (+)-anatoxin-a block the nicotinic acetylcholine receptor ion channel.
      K L Swanson, Y Aracava, F J Sardina, H Rapoport, R S Aronstam and E X Albuquerque
      Molecular Pharmacology February 1989, 35 (2) 223-231;

T

  1. Tonani, R

    1. You have access
      Joint experimental and theoretical investigation of the comparative DNA binding affinities of intercalating anthracycline derivatives.
      N Gresh, B Pullman, F Arcamone, M Menozzi and R Tonani
      Molecular Pharmacology February 1989, 35 (2) 251-256;

W

  1. Weinstein, H

    1. You have access
      A metactoid sensitization model to describe multiple receptors linked to a common response: application to histamine receptors coupled to [3H]cyclic AMP accumulation in guinea pig cortex.
      M N Gannon, L B Hough and H Weinstein
      Molecular Pharmacology February 1989, 35 (2) 205-213;
  2. Woynarowski, J M

    1. You have access
      Modulation of topoisomerase II catalytic activity by DNA minor groove binding agents distamycin, Hoechst 33258, and 4',6-diamidine-2-phenylindole.
      J M Woynarowski, M McHugh, R D Sigmund and T A Beerman
      Molecular Pharmacology February 1989, 35 (2) 177-182;
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In this issue

Molecular Pharmacology
Vol. 35, Issue 2
1 Feb 1989
  • Table of Contents
  • Table of Contents (PDF)
  • Index by author
  • Back Matter (PDF)
  • Editorial Board (PDF)
  • Front Matter (PDF)
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  • Dehydrocrenatidine Is a Novel JAK Inhibitor
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