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Diverse coactivator recruitment through differential PPARγ nuclear receptor agonism
(Genetics and Molecular Biology, 2013-03-04)
The PPARγ nuclear receptor regulates the expression of genes involved in lipid and carbohydrate metabolism, and it has protective effects in some patients with type 2 diabetes. Nevertheless, the therapeutic value of the ...
Clinical and Descriptive Study of Orofacial Clefts in Colombia: 2069 Patients From Operation Smile Foundation
(Cleft Palate Craniofac J., 2022)
Objective: To describe the population of patients with cleft lip and/or palate (CL/P) in terms of cleft phenotypes, gender, age, ethnic group, family history, clinical presentation (syndromic vs nonsyndromic), some ...
Flores Morales : vestuario a partir del perfil de cada una de las mujeres de mi Familia Morales
(Universidad de los AndesDiseñoFacultad de Arquitectura y DiseñoDepartamento de Diseño, 2019)
Este proyecto nació de un sentimiento personal de querer mostrar, por medio del vestuario, las mujeres que me hicieron lo que soy hoy. Por el lado de mi mamá, es decir el lado Morales, somos 7 mujeres: mi abuelita, mi mamá, ...
Origin and dynamics of a hybrid zone between Ramphocelus tanagers (Thraupidae) in Colombia
(UniandesMaestría en Ciencias BiológicasFacultad de CienciasDepartamento de Biología, 2010)
Characterizations of hybrid zones are of importance in evolutionary biology because they can give insights about the characters and processes implied in population divergence. Here, we characterize a hybrid zone between ...
Trastornos del neurodesarrollo (síndrome X frágil) y neurodegenerativos (síndrome de temblor/ataxia) asociados al ‘crecimiento’ de un gen
(Revista de Neurología 40 (7) p. 431-437, 2005-04-01)
To present the latest findings on fragile X syndrome, the first genetic disorder identified to be caused by a new type of mutation called trinucleotide repeat expansion. Development. Fragile X syndrome is the most common ...
The gene for an inherited form of deafness maps to chromosome 5q31
(1992-06-01)
Primary-i.e., nonsyndromal-postlingual deafness is inherited as an autosomal dominant phenotype in a large kindred in Costa Rica. Genetically susceptible individuals begin to lose hearing at low frequencies at about age ...
Audiologic Features of Norrie Disease
(Ann Otol Rhinol Laryngol 114 (7) p. 533-538, 2005)
Objectives: Norrie disease is an X-linked recessive disorder in which patients are born blind and develop sensory hearing
loss in adolescence. The hearing loss associated with Norrie disease has been shown in a genetically ...
The gene for an inherited form of deafness maps to chromosome 5q31
(1992-06-01)
Primary-i.e., nonsyndromal-postlingual deafness is inherited as an autosomal dominant phenotype in a large kindred in Costa Rica. Genetically susceptible individuals begin to lose hearing at low frequencies at about age ...
Behavioural characterisation of chronic unpredictable stress based on ethologically relevant paradigms in rats
(2019-11)
The chronic unpredictable stress (CUS) paradigm is extensively used in preclinical research. However,
CUS exhibits translational inconsistencies, some of them resulting from the use of adult rodents,
despite the evidence ...
Expanding the Trichoderma harzianum species complex: Three new species from Argentine natural and cultivated ecosystems
(2021-06-22)
A study was performed on a collection of 84 isolates from decaying plant tissues and soils in
Argentina previously identified as Trichoderma harzianum. Based on multiple phenotypic characters
and multilocus phylogenetic ...