On trend extraction models: Interpretation,empirical evidence and forecasting performance

This paper deals with the economic interpretation of the unobserved components model in the light of the apparent problem posed by previous work in that several practiced methodologies seem to lead to very different models of certain economic variables. A detailed empirical analysis is carried out to show how the failure in obtaining quasi-orthogonal components can seriously bias the interpretation of some decomposition procedures. Finally, the forecasting performance (in both the short and long run) of these decomposition models is analyzed in comparison with other alternatives.     

Effect of carbon tetrachloride poisoning on the plasma levels of aspartate-aminotransferase isoenzymes in the rat

Riassunto Mediante frazionamento cromatografico su colonna di resina a scambio anionico, abbiamo potuto documentare nel siero di ratti intossicati con dosi diverse di CCl₄, incrementi assai significativi sia della componente mitocondriale che citoplasmatica della aspartato-aminotransferasi.     

La Rigenerazione del testicolo atrofico da Fluoroacetamide

Summary Morphological changes of atrophic testis, obtained by treating normal rats with fluoroacetamide, are studied at various times after treatment. The data show that the testicular germinal epithelium is fully regenerated 165 days after treatment.     

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13

Congenital generalized lipodystrophy, or Berardinelli-Seip syndrome (BSCL), is a rare autosomal recessive disease characterized by a near-absence of adipose tissue from birth or early infancy and severe insulin resistance. Other clinical and biological features include acanthosis nigricans, hyperandrogenism, muscular hypertrophy, hepatomegaly, altered glucose tolerance or diabetes mellitus, and hypertriglyceridemia. A locus (BSCL1) has been mapped to 9q34 with evidence of heterogeneity. Here, we report a genome screen of nine BSCL families from two geographical clusters (in Lebanon and Norway). We identified a new disease locus, designated BSCL2, within the 2.5-Mb interval flanked by markers D11S4076 and D11S480 on chromosome 11q13. Analysis of 20 additional families of various ethnic origins led to the identification of 11 families in which the disease cosegregates with the 11q13 locus; the remaining families provide confirmation of linkage to 9q34. Sequence analysis of genes located in the 11q13 interval disclosed mutations in a gene homologous to the murine guanine nucleotide-binding protein (G protein), gamma3-linked gene (Gng3lg) in all BSCL2-linked families. BSCL2 is most highly expressed in brain and testis and encodes a protein (which we have called seipin) of unknown function. Most of the variants are null mutations and probably result in a severe disruption of the protein. These findings are of general importance for understanding the molecular mechanisms underlying regulation of body fat distribution and insulin resistance.     

Dinemorphan N-demethylation by mouse liver microsomes

Dinemorphan, an antitussive drug, is N-demethylated in vitro by mouse liver microsomes with biphasic kinetics showing two apparent Km and Vmax. Moreover, dinemorphan N-demethylation is inhibited by CO, SKF-525A, metyrapone and it is specifically catalyzed by a phenobarbital-inducible form of cytochrome P-450.     

Efficacy of some histochemical techniques for acid mucopolysaccharides

Résumé L'efficacité relative de certaines méthodes histochimiques utilisées habituellement pour la mise en évidence des mucopolysaccharides acides a été étudiée sur des peaux de rats soumises à des conditions expérimentales diverses. Les différentes concentrations des substances en étude étaient connues, ayant été quantitativement déterminées par la méthode chimique dePearce etWatson. La réaction métachromatique, réalisée avec les précautions nécessaires et avec le concours de la digestion par l'hyaluronidase, nous a fourni une image fidèle de la concentration de mucopolysaccharides acides. Ce n'est pas le cas lorsqu'on emploie l'acide périodique-Schiff ou le fer colloïdal qui ne semblent pas être très utiles pour la mise en évidence des substances étudiées.     

Giant granules in adrenaline-secreting chromaffin cells of lizard adrenal glands after metyrapone administration

Summary Secretory granules of extraordinary size, some of them bigger than the cell nucleus, abound in the adrenaline cells of lizard adrenals after metyrapone injections during 7 days. In these granules, the bounding membrane is studded with ribosomes, and the core is formed by rounded small subunits. Some granules of this type are also found in noradrenaline cells. They may represent an exceptionally increased elaboration and storage of adrenaline, induced by metyrapone probably through its action on steroidogenic tissue.This research forms part of project No. 31.26.S1-1154 supported by the Consejo Nacional de Investigaciones Científícas y Tecnológicas.     

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium

The autosomal dominant, giant-platelet disorders, May-Hegglin anomaly (MHA; MIM 155100), Fechtner syndrome (FTNS; MIM 153640) and Sebastian syndrome (SBS), share the triad of thrombocytopenia, large platelets and characteristic leukocyte inclusions ('D?hle-like' bodies). MHA and SBS can be differentiated by subtle ultrastructural leukocyte inclusion features, whereas FTNS is distinguished by the additional Alport-like clinical features of sensorineural deafness, cataracts and nephritis. The similarities between these platelet disorders and our recent refinement of the MHA (ref. 6) and FTNS (ref. 7) disease loci to an overlapping region of 480 kb on chromosome 22 suggested that all three disorders are allelic. Among the identified candidate genes is the gene encoding nonmuscle myosin heavy chain 9 (MYH9; refs 8-10), which is expressed in platelets and upregulated during granulocyte differentiation. We identified six MYH9 mutations (one nonsense and five missense) in seven unrelated probands from MHA, SBS and FTNS families. On the basis of molecular modelling, the two mutations affecting the myosin head were predicted to impose electrostatic and conformational changes, whereas the truncating mutation deleted the unique carboxy-terminal tailpiece. The remaining missense mutations, all affecting highly conserved coiled-coil domain positions, imparted destabilizing electrostatic and polar changes. Thus, our results suggest that mutations in MYH9 result in three megakaryocyte/platelet/leukocyte syndromes and are important in the pathogenesis of sensorineural deafness, cataracts and nephritis.     

Analysis and prediction of the population in Spain: 1910-2000

"The starting hypothesis of this paper was the actual occurrence of important interactions between demographic and socio-economic factors when trying to reach population forecasts that may be more efficient than those obtained by mere extrapolative methods. In order to be able to implement this approach to the Spanish case it has been necessary to reconstruct first the Spanish population series by age and sex groups from 1910 to 1980. Later, we proceed to obtain population forecasts using alternative modeling strategies and comment on the potential problems that the new demographic situation may have for future public policy."