Why not Post-Political?

This commentary on Gert Goeminne’s paper “Postphenomenology and the politics of sustainable technology” elaborates on the subpolitics of technology as a basis for dealing with sustainability issues. It questions the “sustainable technology” phrasing of the issue and focuses on the political/post-political debate to eventually suggest that the politics of sustainable technology is a possible post-political question. Minor disagreements on some philosophy of science references are briefly expressed.     

Network Visualization in Cell Biology

Many of the processes known to take place in biological cells are analyzed in the form of different types of network.The complexity of these networks increases along with our knowledge of these processes,making their analysis more difficult.Network visualization is a powerful analysis method that will have to be developed further to deal with this complexity.This survey provides a brief overview of network visualization in general,followed by an in-depth discussion of its application to three network types specific to cell biology,namely gene regulatory,protein interaction,and metabolic networks.Finally,we discuss the difficulty of visually integrating these network types and trying to compare networks of cells that belong to different organisms.     

Adhesion and aggregation of human platelets to rabbit subendothelium. A new approach for investigation: Specific antibodies

Summary An IgG antibody occurring in a recently transfused thrombasthenic patient inhibited all the ADP-mediated aggregations and platelet-platelet interaction (thrombus formation) on rabbit aorta subendothelium; another IgG antibody occurring in a multitransfused Bernard-Soulier patient inhibited ristocetin and bovine factor VIII mediated aggregation and platelet-subendothelium interaction.     

Sur le mycoside Cm,nouveau peptido-glycolipide isolé deMycobacterium marianum

Summary Mycoside C_m, m.p. 198–200° []_D = – 31° (CHCl₃), a new peptido-glycolipid isolated fromMycobacterium marianum, has the approximate molecular formula C₁₀₈H₁₈₅N₇O₂₈ and gives on hydrolysis seven molecules ofd-amino acids (oned-phenylalanine, threed-allo-threonine, threed-alanine), three molecules of 6-deoxyhexoses (one 6-deoxy-talose of as yet undetermined configuration and two molecules of 3,4-di-O-methyl-l-rhamnose); the lipid moiety of mycoside C_m is a hydroxy-acid of approximate formula C₅₀H₉₆O₃; three O-acetyl groups are also present. The preliminary formula (I) is proposed for mycoside C_m.

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60ème communication sur les constitutants des Mycobactéries; 59ème comm. voir: ref. 7.

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Ce travail a bénéficié d'une subvention de la Fondation Waksman pour le développement des Études microbiologiques en France, et d'une subvention du National Institute of Allergy and Infectious Diseases (Grant E 28 38).     

Mixture Model Analysis of Complex Samples

We investigate the effects of a complex sampling design on the estimation of mixture models. An approximate or pseudo likelihood approach is proposed to obtain consistent estimates of class-specific parameters when the sample arises from such a complex design. The effects of ignoring the sample design are demonstrated empirically in the context of an international value segmentation study in which a multinomial mixture model is applied to identify segment-level value rankings. The analysis reveals that ignoring the sample design results in both an incorrect number of segments as identified by information criteria and biased estimates of segment-level parameters.     

TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome

A predisposition for thoracic aortic aneurysms leading to acute aortic dissections can be inherited in families in an autosomal dominant manner. Genome-wide linkage analysis of two large unrelated families with thoracic aortic disease followed by whole-exome sequencing of affected relatives identified causative mutations in TGFB2. These mutations-a frameshift mutation in exon 6 and a nonsense mutation in exon 4-segregated with disease with a combined logarithm of odds (LOD) score of 7.7. Sanger sequencing of 276 probands from families with inherited thoracic aortic disease identified 2 additional TGFB2 mutations. TGFB2 encodes transforming growth factor (TGF)-β2, and the mutations are predicted to cause haploinsufficiency for TGFB2; however, aortic tissue from cases paradoxically shows increased TGF-β2 expression and immunostaining. Thus, haploinsufficiency for TGFB2 predisposes to thoracic aortic disease, suggesting that the initial pathway driving disease is decreased cellular TGF-β2 levels leading to a secondary increase in TGF-β2 production in the diseased aorta.