Study of neurosecretory cells ofHelix pomatia by intracellular dye injection

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Neurogenic responses of resistance and capacitance vessels

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Isoforms of baker's yeast transketolase

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The effect of chloramphenicol analogs on protein biosynthesis in a cell-freeEscherichia coli B system

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Laboratory of Biological Investigations.

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Laboratory for Chemistry of Antibiotics.     

Genetic control over the duration of G1 phase

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Mutual replaceability of amide and ester groups in biologically active peptides and depsipeptides

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A new synthetic method of coumestan derivatives

Zusammenfassung Die Synthese von 7-Hydroxy-5,6-dimethoxybenzofurano[3,2:3,4]coumarin aus 7,2-Dihydroxy-oder 7-Benzyloxy-2-hydroxy-4,5-dimethoxyisoflavon wird beschrieben.     

Studies on rII region of T2L phage

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Inhibition of sodium transport in frog skin by cardiac glycosides of different molecular structure

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Chromosomes and giemsa-bands of the Idaho spotted ground squirrel,Spermophilus brunneus (Howell)

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Supported by National Science Foundation Grants No. GB32114X and No. GB 29131X, and the Sprague Foundation. We thankD. Pozin for technical assistance.     

The role of the pentose-phosphate pathway in adjustment of the heart to a high load and the development of myocardial hypertrophy

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Temperature sensitivity in the respiratory-deficient mutants of yeast (Saccharomyces cerevisiae)

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Deamination by ‘Transformed’ mitochondrial amine oxidase of the ε-amino group of lysine and selective inhibition of this reaction by β-aminopropionitrile

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Mass spectrometric determination of the amino acid sequence in peptides: Desulfurization of sulfur-containing peptides

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16-β-methylprednisone from hecogenin

Zusammenfassung Es wird über die Herstellung des 16-Methylprednisons berichtet, welche vom Hecogenin ausgehend über ca. 15 Stufen durchgeführt wird. Als wichtige Zwischenstufe treten 5-Pregn-16-en-3-ol-11, 20-dion-Acetat und 16-Methylen-5-pregnan-3, 17-diol-11, 20-dion auf: letzteres wird durch eine stereospezifische katalytische Reduktion in das entsprechende 16-Methyl-derivat umgewandelt.     

Synthesis and pharmacological properties of [1-N4-dimethyl-asparagine]-angiotensin II

Summary [1-N⁴-Dimethyl-asparagine]-angiotensin II was synthesized by Merrifield's solid-phase procedure. The analogue gave rat blood pressure about 70% relative potency to Hypertensin (Ciba). Rabbit aorta strips gave intrinsic activity _E=1, a PD₂ of 6.92±0.09 and an affinity relative to [Asn¹]-angiotensin II of 6.5%.The editors do not hold themselves responsible for the opinions expressed in the authors' brief reports. — Les auteurs sont seuls responsables des opinions exprimées dans ces brèves communications. — Für die Kurzmitteilungen ist ausschliesslich der Autor verantwortlich. — Per le brevi comunicazioni è responsabile solo l'autore. — . — Solo los autores son responsables de las opiniones expresadas en estas comunicationes breves.Acknowledgment. The authors wish to express their appreciation to Dr Emanuel Escher, School of Medicine, Centre Hospitalier Universitaire, Sherbrooke, Quebec, for his help in providing the biological data and critical comments.     

IdentifyingY chromosome in interphase nuclei of the human brain

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The mechanism of blood vessel permeability derangement under the influence of histamine,serotonin and bradykinin

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Contribution to the method for approximation of X-ray diffraction line profile

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Interaction of polyene antibiotics and serum lipoproteins

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