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Design of a molecular method for subspecies specific identification of Klebsiella pneumoniae by using the 16S ribosomal subunit gene.
(2011-12-19)
Introduction: Rhinoscleroma is caused by Klebsiella pneumoniae rhinoscleromatis and the ozena infections caused by
K. pneumoniae ozaenae, both infections affect the upper respiratory tract. In the first clinical phases ...
Comparación de métodos de extracción de adn en tejidos parafinados y utilidad para amplificación por pcr
(Universidad Nacional de Colombia, 2013)
ResumenLos tejidos fijados en formol e incluidos en parafina son una fuente de material para hallazgos moleculares en el ámbito clínico y científico, demostrándose que el ADN extraído de éstos, es adecuado para amplificación ...
Molecular characterization of Chilean isolates of streptococcus agalactiae Caracterización molecular en aislados chilenos de Streptococcus agalactiae
(2008)
Background: Streptococcus agalactiae is the main causing organism of invasive infections such as sepsis and meningitis in the newborn. Aim: To perform a genotype characterization of Streptococcus agalactiae strains coming ...
Identificación morfológica y molecular de filarias caninas en una comuna semi-rural de la Región Metropolitana, Chile
(Sociedad Chilena de Infectologia, 2012)
Introduction: To date, there has been no definitive confirmation of the presence of zoonotic dirofilariasis in dogs in Chile. Objectives: To study the presence of dirofilarias in blood samples from dogs collected in a ...
FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile
(Cambridge University Press, 2016)
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability (ID) and co-morbid autism. It is caused by an amplification of the CGG repeat (>200), which is known as the full mutation, within the ...
Molecular analysis of exons 8, 9 and 10 of the fibroblast growth factor receptor 2 (FGFR2) gene in two families with index cases of Apert SyndromeAnálisis molecular de los exones 8, 9 y 10 del gen del factor de crecimiento de fibroblastos (FGFR2) en dos familias con casos índice de síndrome de Apert
(Universidad del ValleCali, Colombia, 2015-09-30)
Introduction: Apert syndrome (AS) is a craniosynostosis condition
caused by mutations in the Fibroblast Growth Factor Receptor 2
(FGFR2) gene. Clinical features include cutaneous and osseous
symmetric syndactily in hands ...
Comparación de tres métodos de extracción de ADN a partir de garrapatas duras (Acari: Ixodidae)
(Bogotá : Universidad de Ciencias Aplicadas y Ambientales, 2019, 2019-01)
Las garrapatas son el grupo de ectoparásitos de mayor relevancia en la transmisión de patógenos a los animales domésticos y a humanos. La detección de estos agentes, normalmente, se realiza por métodos basados en PCR y, ...
Caveolin-1-mediated suppression of cyclooxygenase-2 via a β-catenin-Tcf/Lef-dependent transcriptional mechanism reduced prostaglandin e2 production and survivin expression
(2009)
Augmented expression of cyclooxygenase-2 (COX-2) and enhanced production of prostaglandin E2 (PGE2) are associated
with increased tumor cell survival and malignancy. Caveolin-1 is a scaffold protein that has been proposed ...
Highly Toxic Microcystis aeruginosa Strain, Isolated from Sao Paulo—Brazil, Produce Hepatotoxins and Paralytic Shellfish Poison Neurotoxins
(Springer, 2011)
While evaluating several laboratory-cultured
cyanobacteria strains for the presence of paralytic shellfish
poison neurotoxins, the hydrophilic extract of Microcystis
aeruginosa strain SPC777—isolated from Billings’s ...
Porfiria variegata en Chile: identificación de mutaciones en el gen protoporfirinógeno oxidasa y su implicancia diagnóstica
(INST NACIONAL NUTRICION, 2006-08)
Variegate porphyria (VP) results from a hereditary deficiency of protoporphyrinogen oxidase (PPOX) that is transmitted in an autosomal dominan fashion. The diagnosis is based on the clinical symptoms and is confirmed ...