Listar por tema "Genetics"
Mostrando ítems 1-9 de 9
-
Estudio de la expresión y variabilidad genética del gen PDZK1 en piel normal, y el papel que desempeña en la pigmentación humana.
Universitat Jaume I (2018-07-11)Introduction: The expression of the PDZK1 gene has s een to be increased in melasma via t he action of estrogens, causing an increase in the activity of tyrosinase and the synthesis of melanin. The aim of this ... -
Gender is a major factor explaining discrepancies in eye colour prediction based on HERC2/OCA2 genotype and the IrisPlex model
Elsevier (2013)In recent years, several studies have greatly increased our understanding of the genetic basis underlying human eye colour variation. A large percentage of the eye colour diversity present in humans can already be genetically ... -
Genética de la pigmentación humana: diferencias entre sexos
Universitat Jaume I (2017-06-13)Introducción: En estudios previos se han observado diferencias fenotípicas en la pigmentación humana y en la sensibilidad solar entre sexos. También se ha podido ver que parte de estas diferencias no solo obedecen a razones ... -
Genética y Derecho. La medicina genómica en el sistema nacional de salud
Diputación General de Aragón. Departamento de Presidencia (2019-12)La medicina genética o genómica es una realidad, su integración en nuestra sociedad y en los sistemas de salud es imparable. Las posibilidades que ofrece esta tecnología para el diagnóstico y el tratamiento de enfermedades ... -
Impact of the -1438G>A polymorphism in the serotonin 2A receptor gene on anthropometric profile and obesity risk: A case-control study in a Spanish Mediterranean population
(2008)Research into the genetic factors that regulate food intake is arousing great interest. The polymorphism -1438G>A in the serotonin 2A receptor or 5-hydroxytriptamine (5-HT) type 2A receptor (5-HTR2A) gene has been ... -
Marcadores genéticos comórbidos en el trastorno específico del lenguaje y las dificultades en la lectura
Universitat Jaume I (2017-07-18)In recent years there have been many studies on language disorders. Specific Language Impairment and Reading Disabilities are common disorders in childhood that show considerable comorbidity and diagnosis, overlaps that ... -
Neurofilament-lysosomal genetic intersections in the cortical network of stuttering
Elsevier (2019-10-24)The neurobiological underpinnings of stuttering, a speech disorder characterized by disrupted speech fluency, remain unclear. While recent developments in the field have afforded researchers the ability to pinpoint several ... -
New insights in primary ciliary dyskinesia
Taylor & Francis (2017)Introduction: Primary ciliary dyskinesia (PCD) is a rare genetic disease with an estimated prevalence of 1:20.000 births. It is characterized by abnormal motility of cilia, leading to impaired mucociliary clearance, and ... -
Psychosis-inducing effects of cannabis are related to both childhood abuse and COMT genotypes
Wiley (2014-01)OBJECTIVE: To test whether the association between childhood abuse, cannabis use and psychotic experiences (PEs) was moderated by the COMT (catechol-O-methyltransferase) gene. METHOD: Psychotic experiences (PEs), ...