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Mostrando ítems 2181-2190 de 2854
Estudo da imunoexpressão do VEGF165 e do VEGF165B em lesões orais de líquen plano e pênfigo vulgar
(BrasilUFRNPROGRAMA DE PÓS-GRADUAÇÃO EM PATOLOGIA ORAL, 2018-06-28)
Oral Lichen Planus is an immunologically mediated mucocutaneous disease of
relatively unknown etiology with prevalences in the world population varying from 0.22 to
5%. Pemphigus vulgaris is a chronic autoimmune disease ...
Genetic diversity at the FMR1 locus in Mexican population
(2005)
Background. Fragile X syndrome is the most frequent cause of inherited mental retardation; it is caused by expansion of CGG repeats in the first exon of the FMR1 gene. Number of CGG repeats varies between 6 and 50 triplets ...
Analysis of linkage disequilibrium between the 5′ and 3′ haplotypes of the β-globin gene cluster in Mexican afromestizos
(2010)
Analysis of the 5′ and 3′ haplotypes (Hps) of the β-globin gene cluster was performed in 110 βA chromosomes from unrelated Mexican afromestizo individuals in order to determine Hardy-Weinberg equilibrium, allelic frequencies, ...
HB Fannin-Lubbock-I with a single GGC>GAC mutation at β119(GH2)Gly→Asp in a homozygous mexican patient
(2009)
We studied a fast-moving, abnormal hemoglobin (Hb) identified as FanninLubbock-I [β119(GH2)Gly→Asp] in a homozygous Mexican girl. To date, homozygosity for the Hb Fannin-Lubbock-I variant has not been reported. Her parents ...
Evaluación del gen FANCA mediante técnica MLPA (Multiplex Ligand-Probe Amplification) en pacientes con Anemia de Fanconi
(Biblioteca Digital wdg.biblioUniversidad de Guadalajara, 2016-02-01)
Introducción. La anemia de Fanconi (AF) es un trastorno hereditario, considerado dentro del grupo de los síndromes de inestabilidad cromosómica, ya que presenta falla en la reparación del ADN. La AF es una enfermedad ...
Revealing stage-specific expression patterns of long noncoding RNAs along mouse spermatogenesis
(Taylor and Francis, 2020)
The discovery of a large number of long noncoding RNAs (lncRNAs), and the finding that they may play
key roles in different biological processes, have started to provide a new perspective in the understanding of gene ...
Analysis of the SLC4A1 gene in three Mexican patients with hereditary spherocytosis: Report of a novel mutation
(2010)
We analyzed the SLC4A1 gene in three Mexican patients with Hereditary Spherocytosis (HS). The promoter and all 20 exons were investigated through heteroduplex analysis and DNA sequencing. No DNA changes were detected in ...
Shorter CAG repeat in the AR gene is associated with atypical hyperplasia and breast carcinoma
(2007-03-01)
Background: Previous reports into the role of [CAG]n repeat lengths in the androgen receptor (AR) gene indicate that these may play an important part in the development and progression of breast cancer, however, knowledge ...
The Vampirome: Transcriptome and proteome analysis of the principal and accessory submaxillary glands of the vampire bat Desmodus rotundus, a vector of human rabies
(2013-04-06)
Vampire bats are notorious for being the sole mammals that strictly feed on fresh blood for their survival. While their saliva has been historically associated with anticoagulants, only one antihemostatic (plasminogen ...
A phylogenetic analysis of Pleurodema (Anura: Leptodactylidae: Leiuperinae) based on mitochondrial and nuclear gene sequences, with comments on the evolution of anuran foam nests
(Wiley-Blackwell, 2012-10-01)
Species of the genus Pleurodema are relatively small, plump frogs that mostly occur in strong-seasonal and dry environments. The genus currently comprises 14 species distributed from Panama to southern Patagonia. Here we ...