Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Year range
1.
Rev. colomb. anestesiol ; 39(3): 308-313, ago.-oct. 2011.
Article in English, Spanish | LILACS | ID: lil-594625

ABSTRACT

El proyecto genoma humano, los avances y los desarrollos de las diferentes “omicas”, apoyados en la medicina traslacional, han permitido el conocimiento y avance en muchos de los mecanismos moleculares de la fisiología y la patología en el humano. Basado enestos conocimientos se tienen muchas evidencias de que la mayor parte de la terapia con medicamentos puede ser individualizada sobre los estudios de variación del genoma humano, ya que solo entre el 30 % y 60 % de los pacientes tienen una respuesta común a dichas terapias...


Subject(s)
Humans , Male , Female , Adolescent , Young Adult , Middle Aged , Anesthesia , Medicine , Pharmacogenetics , Drug Utilization , Genome, Human , Translational Research, Biomedical
2.
Rev. colomb. anestesiol ; 36(1): 11-18, ene.-mar. 2008. ilus, tab
Article in English | LILACS, COLNAL | ID: lil-636010

ABSTRACT

Objective : The purpose of the presera study was to devélop a molecular genotyping method test by using a real time PCR hybridization probé and applying it to the analysis of C1843T mutations of the Sus scrofa RYR1 gene. Animáis population Three PSS-susceptible and PSS non-susceptible crossbred swine races were used for the experiments: Pietrain X Landrace Belga, Pietrain X Large White and Pietrain X Duroc. Methods: We have devéloped a genotyping method by using a hybridization probé and applied it to the analysis of C1843T mutations of the RYR1 gene, associated with PSS susceptibility. Genotyping results obtained by hybridization probé strategies were confirmed by restriction analysis and sequencing. In addi-tion, phenotype/genotype correlation analyses were devéloped by using the in vitro contracture test and confirmed the in vivo hálothane-succinylcholine challenge. Results: The real-time PCR with fluorescent hybridization probé methodology was designed to identify ho-mozygous PSS-resistant, PSS-susceptible animáis as well as heterozygous carriers. All cases genotyped by fluorescent hybridization probes were in agreement with PCR restriction enzyme digestión and sequencing and showed a 100% concordance between the in vivo and in vitro porcine stress syndrome (PSS) susceptibility results. Conclusions and clinical relevance: The real-time PCR with fluorescent hybridization probé method described here provides a rapid, easily interpretable and réliáble tool for genotyping the C1843T (Arg615-Cys) polymorphism of the RYR1 gene. This new methodology may be useful in the wide-scale genotyping of PSS-susceptibility and genetic selection.

SELECTION OF CITATIONS
SEARCH DETAIL