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1.
Prensa méd. argent ; 106(7): 419-424, 20200000. graf
Article in Spanish | LILACS, BINACIS | ID: biblio-1366939

ABSTRACT

Estudio descriptivo sobre la prevalencia e incidencia de Síndrome de Down en los Certificados Médicos Oficiales firmados en nuestro servicio en el período comprendido entre los años 2017- 2019, la prevalencia de cardiopatías congénitas en los mismos y la prevalencia de nacimientos con esta anomalía genética en nuestro hospital. Comparación con estadística nacional e internacional


Descriptive study on prevalence and incidence in Down Syndrome in the Official Medical Certificates signed by our service between years 2017-2019, the prevalence of con genital heart disease on these and the prevalence of birth with this genetic anomaly on our hospital. National and International comparison of statistics


Subject(s)
Humans , Birth Certificates , Epidemiology, Descriptive , Incidence , Prevalence , Retrospective Studies , Down Syndrome/pathology , Heart Defects, Congenital/diagnosis
2.
Health Policy and Management ; : 207-220, 2015.
Article in Korean | WPRIM | ID: wpr-157811

ABSTRACT

BACKGROUND: The purpose of this exploratory study is to explain where, when and how the introduction of user fee system works in low and middle income countries using context, mechanism, and outcome configuration. METHODS: Considering advanced research in realist review approach, we made a review process including those following 4 steps. They are identifying the review question, initial theory and mechanism, searching and selecting primary studies, and extracting, analyzing, and synthesizing relevant data. RESULTS: User fee had a detrimental effect on medical utilization in low and middle income countries. Also previous and current interventions and community participation were critical context in user fee system. Those contexts were associated with intervention initiation and recognition and coping strategies. Such contexts and mechanisms were critical explanatory factors in medical utilization. CONCLUSION: User fee is a series of interventions that are fragile and dynamic. So the introduction of user fee system needs a comprehensive understanding of previous and new intervention, policy infrastructure, and other factors that can influence on medical utilization.


Subject(s)
Community Participation , Fees and Charges
3.
Rev. colomb. biotecnol ; 13(1): 42-51, jul. 2011. graf, ilus, tab
Article in Spanish | LILACS | ID: lil-600572

ABSTRACT

Los modelos experimentales en rata han sido de gran utilidad en las evaluaciones terapéuticas o de reemplazo de células en enfermedades neurodegenerativas. Se ha comprobado que las células de la médula ósea (CMO) de ratas pueden diferenciarse en células que no forman parte de sus linajes normales. Hay evidencias de estos procesos de trans-diferenciación, pero aún no se conocen los mecanismos moleculares que activan estos procesos. El propósito de nuestro trabajo fue estudiar el polimorfismo genético del ADN de los tipos celulares que conforman las CMO y las células del sistema nervioso central (SNC), estríatales y de la corteza de ratas mediante la técnica de RAPD. Las CMO, las células mononucleares (CMMO), las células estromales (CEMO) y las del SNC fueron obtenidas de ratas, y su ADN genómico fue purificado y amplificado mediante la técnica de RAPD, utilizando 15 cebadores al azar. Se construyó un dendograma de las bandas de amplificación generadas utilizando el método de UPGMA. Las células estudiadas según el análisis del RAPD quedaron en 2 grupos bien definidos, pudiéndose diferenciar las CEMO del resto de las células estudiadas. Los cebadores OPA-6, 7 y 12, mostraron el polimorfismo genético de los linajes de células estudiadas. Mediante la técnica de RAPD se demostró la variabilidad genética entre las CEMO y las CMMO, células estriadas y de corteza que mostraron una homogeneidad genética, proponiéndose marcadores específicos de RAPD para cada grupo de células. Este es el primer estudio del polimorfismo genético de las CMO y del SNC de ratas.


Experimental models have been of grate usefulness in the therapeutic or replacement cells in neurodegenerative diseases. It has been demonstrated that bone marrow cells (BMC), can be difefferentiated in cells that do not form part of their normal lineage. There is evidence of these trans-differentiation processes in these cells, but nevertheless, molecular mechanisms that activate these differentiation process still not known. The purpose of our work was to study the genetic polymorphism of those cellular types; that conform the rat bone marrow cells (BMC) as well as those of the central nervous system (CNS), striatum cells and cortex ones, trough RAPD technique. BM, mononuclear cells (BMMC), estromal cells (BMSC) and the CNS cells were obtained from rats and genomic ADN was purified and amplified through RAPD technique, using 15 random primers. A dendogram was constructed according to UPGMA method of the amplifying RAPD bands. Studied cells as- according to the RAPD analysis- were grouped into 2 well- defined groups, as CEMO coud be differentiated from the rest of studied cells. OPA-6, 7 and 12 primers showed the genetic polymorphism of the studied lineages cells. Also will be proposed specific RAPD genetic markers. Through RAPD technique permitted the genetic variability was demonstrated betwen BMEC and BMMC of striated cells and of cortex, which demonstratd a genetic homogeneity through RAPD technique so specific genetic markers of RAPD were thus propose for each group of cells. These constitute the first study on genetic polymorphism of BMC and CNS.


Subject(s)
Bone Marrow/abnormalities , Bone Marrow/growth & development , Bone Marrow/immunology , Bone Marrow/ultrastructure , Polymorphism, Genetic/physiology , Polymorphism, Genetic/genetics , Random Amplified Polymorphic DNA Technique , Central Nervous System/abnormalities , Central Nervous System/injuries , Central Nervous System/metabolism , Central Nervous System/microbiology , Central Nervous System/ultrastructure
4.
China Biotechnology ; (12)2006.
Article in Chinese | WPRIM | ID: wpr-685121

ABSTRACT

BADH-CMO double gene,CMO gene and DREB1A gene were transformed respectively to embryonic callus of Kentucky bluegrass by particle bombardment. Then the embryonic callas of kentucky bluegrass were put in meclium for subculture which is mixed with 100mg/L hygromycin and the meclium for plantlet regeneration which mixell with 50mg/L hy gromycin about one month. Thus,the hygromycin-selectecl plants were obtained and were transplantecl into tlowerpots. The results of the PCR and Southern blot analysis indicated that the DREB1A gene,CMO gene and BADH-CMO double-gene were integrated into the genomic DNA of Kentucky bluegrass.

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