S. Friess

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Contributions of Statistics to the Analysis of Environmental Health Problems Caused by Pollutants

S. Friess, 1977 .

Reactions of Peracids. VI. The Reaction of Acetylcyclanes with Perbenzoic Acid1

S. Friess, R. Pinson, 1952 .

Reactions of Peracids. V.1 The Reaction of Substituted Acetophenones with Perbenzoic Acid2

A. Soloway, S. Friess, 1951 .

Reactions of Peracids. IV. The Reaction of Cyclohexylphenyl Ketone with Perbenzoic Acid

S. Friess, N. Farnham, 1950 .

Reactions of Per Acids. II. The Reaction of Perbenzoic Acid with Simple Cyclic Ketones. Kinetic Studies

S. Friess, 1949 .

Reactions of Per Acids. I. The Reaction of Perbenzoic Acid with Some Simple Ketones

S. Friess, 1949 .

Further biological properties of the sea cucumber toxin holothurin A.

C. Thron, S. Friess, R. Patterson, 1963, Toxicology and applied pharmacology.

Analysis of the polydispersity of acetylcholinesterase by transport methods in the ultracentrifuge.

D. Millar, M. A. Grafius, S. Friess, 1968, Archives of biochemistry and biophysics.

Aryl esters and stimulus frequency as interdependent modulators of responses mediated at cholinergic receptors.

S. Friess, R. Durant, 1966, Toxicology and applied pharmacology.

Mode of action of marine saponins on neuromuscular tissues.

S. Friess, 1972, Federation proceedings.

Role of the sulphate charge center in irreversible interactions of holothurin A with chemoreceptors.

J. Chanley, F. J. Fash, S. Friess, 1967, Biochemical pharmacology.

Some structural requirements underlying holothurin A interactions with synaptic chemoreceptors.

J. Chanley, S. Friess, R. Durant, 1965, Biochemical pharmacology.

Some Observations on Certain Cycloöctatetraene Derivatives

V. Boekelheide, S. Friess, 1949 .

Some toxicologic properties of the alkaloids galanthamine and securinine.

E. Whitcomb, S. Friess, R. Durant, 1961, Toxicology and applied pharmacology.

A Rearrangement in the Nenitzescu Reaction of Cycloheptene with Acetyl Chloride and Aluminum Chloride

S. Friess, R. Pinson, 1951 .

Investigation of Rates and Mechanisms of Reactions

Arnold Weissberger, A. Weissberger, Myron L. Bender, 1974 .

Reactions of Peracids. III. Nuclear Oxidation of Aromatic Compounds with Perbenzoic Acid1

A. Miller, S. Friess, 1950 .

Nature of the Acetyl Cholinesterase Surface. III. Enzymatic Response to cis-trans Isomers in the Cyclohexane Series as Mapping Agents1,2

S. Friess, H. D. Baldridge, W. McCarville, 1955 .

Further response of acetylcholinesterase and of conduction in bullfrog sciatic nerve to the stereochemistry of amine inhibitors. II.

E. Whitcomb, S. Friess, R. Durant, 1959, Archives of biochemistry and biophysics.

Nature of the Acetyl Cholinesterase Surface. II. The Ring Effect in Enzymatic Inhibitors of the Substituted Ethylenediamine Type1

S. Friess, W. McCarville, 1954 .

The Energetics of Acid-catalyzed Hydrolysis of Triphosphoric and Pyrophosphoric Acids1

S. Friess, 1952 .

Reactions of Peracids. VII. Nuclear Oxidation of Aromatic Ethers with Perbenzoic Acid

A. Soloway, B. K. Morse, S. Friess, 1952 .

Polarography of Reduced Glutathione and Glutathione-Ascorbic Acid Mixtures Aperometric Method For Determination of Ascorbic Acid

D. M. Coulson, S. Friess, W. Crowell, 1950 .

Labilization of Ester Bonds in Aminocyclitol Derivatives. II. Polyacetates of Deoxystreptamine1

J. Daly, B. Witkop, G. Holland, 1960 .

Comparative Ganglion-blocking Potencies of the Geometric Isomers of Two Cyclic 1,2-Amino Alcohols

R. Doty, F. Standaert, S. Friess, 1959 .

Some pharmacologic properties of holothurin, an active neurotoxin from the sea cucumber.

R. Nigrelli, H. Sobotka, F. Standaert, 1959, The Journal of pharmacology and experimental therapeutics.

Tracer studies on the biosynthesis of cholesterol from C2 precursors in active bullfrog sciatic nerve.

J. Saunders, S. Friess, 1959, Archives of biochemistry and biophysics.

NEUROMUSCULAR AND CYTOTOXIC EFFECTS OF HOLOTHURIN A AND RELATED SAPONINS AT LOW CONCENTRATION LEVELS. III.

C. Thron, S. Friess, R. Durant, 1964, Therapie der Gegenwart.

Action of certain anticholinesterases on the spike potential of the desheathed sciatic nerve of the bullfrog.

J. Moore, E. Whitcomb, S. Friess, 1958, Journal of cellular and comparative physiology.

ATPase content of striated muscle stressed in O2-CO2 and hyperbaric N2-O2-CO2 atmospheres.

M. Cowan, S. Friess, 1969, Toxicology and applied pharmacology.

Rates and Energetics of Activation of the Acid-catalyzed Hydrolysis of Adenosine Triphosphate1a,b

S. Friess, 1953 .

The Betaines of 3-Hydroxyproline. Assignment of Configuration and Inhibition of Acetylcholinesterase

B. Witkop, F. Sakiyama, F. Irreverre, 1964 .

Chapter 4 - Toxicology of Hypobaric and Hyperbaric Environments*

S. Friess, A. Small, 1975 .

Blockade of the action current in single nodes of Ranvier from frog nerve by physostigmine and certain amino derivatives.

E. Whitcomb, S. Friess, 1960, Archives of biochemistry and biophysics.

The responses of acetylcholinesterase and conduction in bull-frog sciatic nerve to the stereochemistry of amino alcohol derivatives. III.

E. Whitcomb, S. Friess, R. Durant, 1959, Archives of biochemistry and biophysics.

Potency convergence and crossover in tertiary vs. quaternary tropine amino esters.

H. L. Martin, S. Friess, R. Durant, 1966, Toxicology and applied pharmacology.

Contribution of aryl groups to toxic interactions at chemoreceptors: 3-tropanol phenylacetates and their hexahydro derivatives as toxic agents.

S. Friess, R. Durant, L. Reber, 1966, Toxicology and applied pharmacology.

Interactions of aryl esters in the tropine and ψ-tropine series with tissue chemoreceptors. The ortho effect. VII☆☆☆

S. Friess, H. D. Baldridge, R. Durant, 1964 .

STRUCTURE VS. TOXICOLOGIC PARAMETERS IN NEW ESTERS OF TROPINE AND PSI-TROPINE. VI.

S. Friess, H. D. Baldridge, R. Durant, 1964, Toxicology and applied pharmacology.

Further elements of structural specificity in potentiation and blockade of excitable tissue preparations by aryl esters of tropine and pseudotropine. III.

C. Thron, S. Friess, R. Patterson, 1963, Toxicology and Applied Pharmacology.

Curare-binding macromolecules from medullated nerve tissue.

K. Neet, S. Friess, 1962, Archives of biochemistry and biophysics.

Central activity evoked in the cat by Cis-trans isomers of 1,2-aminocyclohexanol derivatives.

F. Standaert, S. Friess, W. C. Thommesen, 1961, Toxicology and Applied Pharmacology.

Studies on blockade of single nodes of Ranvier and of the acetylcholinesterase system by cyclic aromatic esters. II.

C. Thron, E. Whitcomb, S. Friess, 1961, Archives of biochemistry and biophysics.

Further toxicologic properties of aromatic esters in the tropine and psi-tropine series.

S. Friess, R. Durant, L. Reber, 1961, Toxicology and applied pharmacology.

Toxicologic properties and stereochemical configuration in derivatives of the tropanol series.

F. Standaert, S. Friess, L. Reber, 1960, Toxicology and applied pharmacology.

The action of some diamine optical antipodes on acetylcholinesterase inhibition and on conduction in desheathed bullfrog sciatic nerve.

E. Whitcomb, S. Friess, P. A. French, 1958, Archives of Biochemistry and Biophysics.

The Acetylcholinesterase Surface. VIII. Further Observations on Bifunctional Inhibition of the Enzyme1

S. Friess, 1957 .

The Acetylcholinesterase Surface. VI. Further Studies with Cyclic Isomers as Inhibitors and Substrates1,2

S. Friess, H. D. Baldridge, 1956 .

Irreversibility in nerve node inactivation by tertiary vs quaternary amino esters.

J. B. Anderson, S. Friess, 1972, Toxicology and applied pharmacology.

Further studies on node of Ranvier inactivation by electronegatively substituted tropanyl esters.

S. Friess, H. V. Kelly, P. M. Polaski, 1969, Toxicology and applied pharmacology.

Further studies of electronic influences on toxic interactions between aryl esters and tissue chemoreceptors

H. L. Martin, F. J. Fash, S. Friess, 1967 .

Some toxic properties of 2-α-tropine aryl esters

S. Friess, H. D. Baldridge, R. Durant, 1965 .

Stereospecific effects of tropanol aryl esters on normal and stressed neuromuscular receptors.

S. Friess, H. D. Baldridge, R. Durant, 1965, Toxicology and applied pharmacology.

Blockade of excitable nodes of Ranvier by stereoisomeric phenylacetate esters in the tropine and psi-tropine series. 3.

S. Friess, K. Minzghor, 1965, Archives of biochemistry and biophysics.

Structure vs. toxicity relationships in aryl esters of tropine and ψ-tropine. V☆

S. Friess, R. Durant, C. Allen, 1963 .

Blockade of superior cervical ganglionic transmission by tropine-p-tolylacetate and its quaternary methiodide derivative.

H. Weems, S. Friess, W. V. Hudak, 1969, Toxicology and applied pharmacology.

Ester and stimulus frequency mediated peturbations of response patterns from cat soleus tissues.

H. L. Martin, S. Friess, R. Durant, 1967, Toxicology and applied pharmacology.

Molecular conformation versus biological specificity in some simple cyclic amino alcohol derivatives.

S. Friess, R. Durant, L. Reber, 1961, Archives of biochemistry and biophysics.

Steric configuration and the activity at the mammalian neuromuscular junction of cyclic aminoalcohol derivatives.

F. Standaert, S. Friess, 1960, The Journal of pharmacology and experimental therapeutics.

Interference patterns in twitch potentiation of the rat phrenic nerve-diaphragm by aryl esters of tropine and psi-tropine. IV.

S. Friess, R. Durant, 1963, Toxicology and applied pharmacology.

Further aspects of stereospecificity in interaction of polyfunctional amine derivatives with bio-logical receptors.

B. Witkop, S. Friess, R. Durant, 1962, Archives of biochemistry and biophysics.

Some toxicologic properties of a new sries of aryl ethers derived from trans-2-aminocyclohexanol.

B. Witkop, F. Standaert, S. Friess, 1959, Toxicology and applied pharmacology.

Convulsant Activities of Aminocyclanol Derivatives as Influenced by Stereochemical Configurations.∗

F. Standaert, S. Friess, L. Reber, 1958, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Toxic effects of carbon dioxide and ternary nitrogen-oxygen-carbon dioxide hyperbaric atmospheres on the work function of cholinergic tissues

H. Weems, S. Friess, R. Durant, 1968 .

The Acetylcholinesterase Surface. IX. Dependence of Competitive Inhibition by Diaminocyclohexane Derivatives on Substrate Level1a

B. Witkop, D. Masterson, S. Friess, 1958 .

The Acetylcholinesterase Surface. V. Some New Competitive Inhibitors of Moderate Strength1,2

S. Friess, H. D. Baldridge, 1956 .

Nature of the Acetyl Cholinesterase Surface. I. Some Potent Competitive Inhibitors of the Enzyme1a,b

S. Friess, W. McCarville, 1954 .

Nature of the Acetylcholinesterase Surface. IV. The Control of Enzymatic Inhibition by Basicity in the Substituted Ethylenediamines1,2

S. Friess, H. D. Baldridge, 1956 .

Further studies on biological actions of steroidal saponins produced by poisonous echinoderms.

J. Chanley, S. Friess, R. Durant, 1968, Toxicon.

BLOCKADE PHENOMENA AT THE MAMMALIAN NEUROMUSCULAR SYNAPSE. COMPETITION BETWEEN REVERSIBLE ANTICHOLINESTERASES AND AN IRREVERSIBLE TOXIN.

S. Friess, R. Durant, 1965, Toxicology and Applied Pharmacology.

PHYSIOLOGICAL EFFECTS OF HOLOTHURIN, A SAPONIN OF ANIMAL ORIGIN

H. Sobotka, J. Chanley, S. Friess, 1964 .

Interactions of the echinoderm toxin holothurin A and its desulfated derivative with the cat superior cervical ganglion preparation.

J. Chanley, H. Weems, S. Friess, 1970, Toxicon : official journal of the International Society on Toxinology.

Carcinogenic risk assessment criteria associated with inhalation of airborne particulates containing chromium (VI/III).

S L Friess, S. Friess, 1989, The Science of the total environment.

Further Observations on the Reaction of Cyclanones with Perbenzoic Acid

S. Friess, P. E. Frankenburg, 1952 .

Acetylcholinesterase inhibitory activities of muscarine and muscarone derivatives

B. Witkop, S. Friess, R. Durant, 1959, Experientia.

Toxic effects induced in neuromuscular tissues by work in hyperbaric helium-oxygen-carbon dioxide environments.

H. L. Martin, M. Cowan, S. Friess, 1970, Toxicology and applied pharmacology.