Stereospecificity of allantoin degradation inStreptococcus allantoicus

Zusammenfassung Die Stereospezifität der Enzyme des Allantoinabbaus inStreptococcus allantoicus und die optische Drehung der Reaktionsprodukte wurde bestimmt. Allantoinase war aspezifisch, während Allantoate-amidohydrolase ausschliesslich (-)-Ureidoglykolate bildete. Diese Substanz wurde durch (-)-Ureidoglykolase hydrolysiert.     

Effect of aluminium phosphate gel on whole-body retention of simultaneously administered226Ra,85Sr and47Ca in mice

Résumé L'administration presque simultanée d'un gel de phosphate d'alumine et de²²⁶RaCl₂ réduit de 800 fois l'absorption intestinale du²²⁶Ra chez la souris. La charge corporelle en⁸⁵Sr et⁴⁷Ca est réduite d'environ 10 resp. 3 fois.     

Suppression of immunization to tuberculosis and diphtheria by an extract of lymphoid tissue

Zusammenfassung Dank einer neuen Anwendung von Lymphknotenextrakten (statt Röntgenextrakten, Corticosteroiden, Antilymphozytenserum usw.) wird eine erhebliche Reduktion der immunologischen Reaktion erzielt, wenn die Tiere mit diesen Extrakten vorbehandelt und gleichzeitig mit Antigenen behandelt werden.

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This investigation was supported in part by U.S.P.H.S. Research Grant No. CA-02624 from National Cancer Institute; and in part by an institutional grant to Detroit Institute of Cancer Research from United Foundation of greater Detroit allocated through Michigan Cancer Foundation and the Detroit General Hospital Research Corporation, and Newaygo County Cancer Society.     

Granular physics: creating a dry variety of quicksand

Sand can normally support a weight by relying on internal force chains. Here we weaken this force-chain structure in very fine sand by allowing air to flow through it: we find that the sand can then no longer support weight, even when the air is turned off and the bed has settled--a ball sinks into the sand to a depth of about five diameters. The final depth of the ball scales linearly with its mass and, above a threshold mass, a jet is formed that shoots sand violently into the air.     

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

CHARGE syndrome is a common cause of congenital anomalies affecting several tissues in a nonrandom fashion. We report a 2.3-Mb de novo overlapping microdeletion on chromosome 8q12 identified by array comparative genomic hybridization in two individuals with CHARGE syndrome. Sequence analysis of genes located in this region detected mutations in the gene CHD7 in 10 of 17 individuals with CHARGE syndrome without microdeletions, accounting for the disease in most affected individuals.