Author

D S Krafte

Observed names: D KRAFTE, D. S. KRAFTE, D. S. Krafte, D.S. Krafte, DS Krafte, Douglas S. Krafte

Observed institutions: California Institute of Technology, Pfizer (United States), University of Toronto, University of Rochester Medicine, Sterling Research Group, Boehringer Ingelheim (United States), University of Rochester

OpenAlex ID: A5110095955

Voltage-dependent modulation of Ca channel current in heart cells by Bay K8644.

1986 · M C Sanguinetti, D S Krafte, et al. · The Journal of General Physiology · 199

A neutral amino acid change in segment IIS4 dramatically alters the gating properties of the voltage-dependent sodium channel.

1990 · V J Auld, A L Goldin, et al. · Proceedings of the National Academy of Sciences · 183

Chemical synthesis and characterization of ShK toxin: a potent potassium channel inhibitor from a sea anemone

1995 · M. W. PENNINGTON, M. E. BYRNES, et al. · International journal of peptide & protein research · 103

Hydrogen ion modulation of Ca channel current in cardiac ventricular cells. Evidence for multiple mechanisms.

1988 · D S Krafte, R S Kass · The Journal of General Physiology · 102

Evidence for the involvement of more than one mRNA species in controlling the inactivation process of rat and rabbit brain Na channels expressed in Xenopus oocytes

1988 · DS Krafte, TP Snutch, et al. · Journal of Neuroscience · 93

Inactivation of cloned Na channels expressed in Xenopus oocytes.

1990 · D S Krafte, A L Goldin, et al. · The Journal of General Physiology · 87

Negative surface charge density near heart calcium channels. Relevance to block by dihydropyridines.

1987 · R S Kass, D S Krafte · The Journal of General Physiology · 73

Identification of Three Separate Binding Sites on SHK Toxin, a Potent Inhibitor of Voltage-Dependent Potassium Channels in Human T-Lymphocytes and Rat Brain

1996 · M.W. Pennington, V.M. Mahnir, et al. · Biochemical and Biophysical Research Communications · 64

Sodium channels and nociception: recent concepts and therapeutic opportunities

2007 · D KRAFTE, A BANNON · Current Opinion in Pharmacology · 60

Synthesis and Structure-Activity Relationships of 6-Heterocyclic-Substituted Purines as Inactivation Modifiers of Cardiac Sodium Channels

1995 · Kimberly G. Estep, Kurt A. Josef, et al. · Journal of Medicinal Chemistry · 47

Characterization of endogenous sodium channel gene expressed in Chinese hamster ovary cells

1993 · P. H. Lalik, D. S. Krafte, et al. · American Journal of Physiology-Cell Physiology · 30

Expression of cardiac Na channels with appropriate physiological and pharmacological properties in Xenopus oocytes.

1991 · D S Krafte, W A Volberg, et al. · Proceedings of the National Academy of Sciences · 27

Voltage-Dependent Modulation of Cardiac Ca-Channels by Dihydropyridines

1985 · R. S. Kass, M. C. Sanguinetti, et al. · Bayer-Symposium · 5

Identification of essential residues in the potassium channel inhibitor ShK toxin: analysis of monosubstituted analogs

1996 · W.R. Kem, M.W. Pennington, et al. · Toxicon · 4

ChemInform Abstract: Synthesis and Structure‐Activity Relationships of 6‐Heterocyclic‐ Substituted Purines as Inactivation Modifiers of Cardiac Sodium Channels.

1995 · K. G. ESTEP, K. A. JOSEF, et al. · ChemInform · 1

More than one rna species is involved in controlling inactivation of rat brain sodium channels expressed in xenopus oocytes

1987 · D S Krafte, T P Snutch, et al. · The Society for Neuroscience Abstracts · 1

ChemInform Abstract: 4,5‐Dihydro‐1‐phenyl‐1H‐2,4‐benzodiazepines: Novel Antiarrhythmic Agents.

1994 · R. E. JOHNSON, E. R. BAIZMAN, et al. · ChemInform

Works count: 17

Citation count: 1,079

H-index: 12

I10-index: 12