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Absence of the c.169+50delTAAACAG mutation of SOD1 gene in a sample of keratoconus patients in Brazilian population
(2020-07-09)
Objective: To determine the presence of the 7-bp deletion c.169+50delTAAACAG in intron 2 of Superoxide Dismutase-1 gene in keratoconic patients from the State of São Paulo, Brazil, which promotes splicing variations, ...
Allelic polymorphism in the serotonin transporter gene in major depression patients
(Calí : Universidad del Valle, 2011-04-11)
Introduction: Major depression (MD), like other mood disorders, is considered a worldwide endemic pathology, becoming one of the biggest public health problems. The hereditary factors of mood disorders have been studied ...
Allelic polymorphism in the serotonin transporter gene in major depression patients.
(2011-11-10)
Introduction: Major depression (MD), like other mood disorders, is considered a worldwide endemic pathology,
becoming one of the biggest public health problems. The hereditary factors of mood disorders have been studied ...
Caracterização de polimorfismos do gene AMH e sua associação com características indicadoras de precocidade sexual em novilhas da raça Nelore
(Universidade Estadual Paulista (Unesp), 2017-04-25)
O hormônio anti-Mülleriano (AMH) é uma glicoproteína de 140 kDa exclusivamente expressa nas gônadas e que pertence à família de fatores de crescimento transformantes (TGF)-ß e está relacionada ao desenvolvimento folicular ...
Nuevos aportes a la genética del hipotiroidismo congénito y de la resistencia a hormonas tiroideas : identificación y caracterización molecular de las mutaciones responsables
(Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica, 2014)