Search results for "CADA"

Pobrezas y exclusión social: el contexto de Andalucía

2011

Nueva pobreza y exclusión social de jóvenes en España: el caso de la Comunidad Valenciana

2011

Desigualdad, Pobreza y Exclusión Social: aproximación comparativa entre la Región de Murcia y España

2011

Nueva pobreza y exclusion social de jovenes y mujeres en España: el caso de Aragón

2011

Pobreza en España: jóvenes y mujeres en los espacios sociales de la vulnerabilidad

2011

This number of Quaderns presents the results of two research projects of the program I+D+i financed by the Spanish Ministry of Education for the period 2008 to 2011. The first project is called 'New poverty and social exclusion among youth in Spain' and was supervised by Ph. D. Ignasi Brunet. The second project was developed under the name of 'Poverty, social exclusion and gender inequality in Spain' and was supervised by Ph. D. Ángel Belzunegui. Both projects counted with a group formed by researchers from six Spanish universities from different regions where field work was carried out: Andalucía, Aragón, Cataluña, Comunidad Valenciana, Murcia y País Vasco. The first project has analyzed p…

Teoría de sistemas (2008/09)

2008

Conceptos fundamentales de la Teoría general de sistemas. Nociones básicas de estadística. Modelos cibernéticos. Sistemas caóticos.Asignatura optativa de Ciencias Ambientales. Primer ciclo. Segundo curso. Cuatrimestral: 6 créditos.

Core Histones Are Glutaminyl Substrates for Tissue Transglutaminase

1996

Chicken erythrocyte core histones are glutaminyl substrates in the transglutaminase (TGase) reaction with monodansylcadaverine (DNC) as donor amine. The modification is very fast when compared with that of many native substrates of TGase. Out of the 18 glutamines of the four histones, nine (namely glutamine 95 of H2B; glutamines 5, 19, and 125 of H3; glutamines 27 and 93 of H4; and glutamines 24, 104, and 112 of H2A) are the amine acceptors in free histones. The use of Gln112 of H2A requires a temperature-dependent partial unfolding of the histone, showing that structural determinants are decisive for the glutamine specificity. The structures of H2A and H2B do not appreciably change upon mo…

Structural characterisation of the natural membrane-bound state of melittin: a fluorescence study of a dansylated analogue

1997

Abstract The binding of a dansylated analogue of melittin (DNC–melittin) to natural membranes is described. The cytolytic peptide from honey bee venom melittin was enzymatically labelled in its glutamine-25 with the fluorescent probe monodansylcadaverine using guinea pig liver transglutaminase. The labelled peptide was characterised functionally in cytolytic assays, and spectroscopically by circular dichroism and fluorescence. The behaviour of DNC–melittin was, in all respects, indistinguishable from that of the naturally occurring peptide. We used resonance energy transfer to measure the state of aggregation of melittin on the membrane plane in synthetic and natural lipid bilayers. When bo…

A class of generalised finite T-groups

2011

Let F be a formation (of finite groups) containing all nilpotent groups such that any normal subgroup of any T-group in F and any subgroup of any soluble T-group in F belongs to F. A subgroup M of a finite group G is said to be F-normal in G if G/CoreG(M) belongs to F. Named after Kegel, a subgroup U of a finite group G is called a K- F-subnormal subgroup of G if either U=G or U=U0?U1???Un=G such that Ui?1 is either normal in Ui or Ui1 is F-normal in Ui, for i=1,2,...,n. We call a finite group G a TF-group if every K- F-subnormal subgroup of G is normal in G. When F is the class of all finite nilpotent groups, the TF-groups are precisely the T-groups. The aim of this paper is to analyse the…

Products of formations of finite groups

2006

[EN] In this paper criteria for a product of formations to be X-local, X a class of simple groups, are obtained. Some classical results on products of saturated formations appear as particular cases.