El sistema verbal español según Samuel Gili Gaya

En este artículo nos centramos en uno de los temas de la gramática española más complejos: la conjugación verbal. A partir de la obra de Samuel Gili Gaya (1961), Curso superior de sintaxis española, analizamos en obras gramaticales representativas de la segunda mitad del siglo XX el estudio de este tema considerando la presencia de las teorías de Gili Gaya. Con ello, pretendemos comprobar nuestra hipótesis inicial: las ideas lingüísticas de este autor suponen, en gran medida, la unión de la Gramática tradicional con enfoques posteriores.

Toponimia documental del Valle Medio del Ésera, III: Toponimia del Ayuntamiento de Foradada del Toscar (Huesca)

En este artículo se analiza lingüísticamente la toponimia documental que pertenece a los núcleos de población del Ayuntamiento de Foradada del Toscar. Para ello partimos, principalmente, de la lectura de dos fuentes documentales inéditas: los Amillaramientos con rectificaciones hasta el año 1879 (Am.) conservados en el Archivo Histórico Provincial de Huesca (AHPH) y, sobre todo, los Protocolos Notariales de Pedro de Guart (Protocolos) conservados en el Archivo Capitular de Lérida (ACL). El análisis se realiza desde el punto de vista tradicional de la toponimia diacrónica. La mayoría de los topónimos estudiados proceden de una base lingüística latina; otros, en cambio, están relacionados con las lenguas prerromanas (barza, clot, coma, por ejemplo) y con el elemento lingüistico vasco (Gabessaco).

V0 production in p+A collisions at √s = 41.6 GeV

Inclusive doubly differential cross sections d 2 σ pA /dx F   dp T 2 as a function of Feynman-x (x F ) and transverse momentum (p T ) for the production of K S 0 , Λ and Λ¯ in proton-nucleus interactions at 920 GeV are presented. The measurements were performed by HERA-B in the negative x F range (−0.12EPOS 1.67 and PYTHIA 6.3. EPOS reproduces the data to within ≈20% except at very low transverse momentum.

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens

Background: Congenital bilateral absence of the vas deferens (CBAVD) is a form of male infertility in which mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene have been identified. The molecular basis of CBAVD is not completely understood. Although patients with cystic fibrosis have mutations in both copies of the CFTR gene, most patients with CBAVD have mutations in only one copy of the gene. Methods: To investigate CBAVD at the molecular level, we have characterized the mutations in the CFTR gene in 102 patients with this condition. None had clinical manifestations of cystic fibrosis. We also analyzed a DNA variant (the 5T allele) in a noncoding region of CFTR that causes reduced levels of the normal CFTR protein. Parents of patients with cystic fibrosis, patients with types of infertility other than CBAVD, and normal subjects were studied as controls. Results: Nineteen of the 102 patients with CBAVD had mutations in both copies of the CFTR gene, and none of them had the 5T allele. Fifty-four patients had a mutation in one copy of CFTR, and 34 of them (63 percent) had the 5T allele in the other CFTR gene. In 29 patients no CFTR mutations were found, but 7 of them (24 percent) had the 5T allele. In contrast, the frequency of this allele in the general population was about 5 percent. Conclusions: Most patients with CBAVD have mutations in the CFTR gene. The combination of the 5T allele in one copy of the CFTR gene with a cystic fibrosis mutation in the other copy is the most common cause of CBAVD. The 5T allele mutation has a wide range of clinical presentations, occurring in patients with CBAVD or moderate forms of cystic fibrosis and in fertile men.