Proficiency of 38 HID-INDELS in kinship analysis and forensic parameters in a Mexican population

Author(s):  
J.A. Aguilar-Velázquez ◽  
E. Rojas-Prado ◽  
G. Martínez-Cortés ◽  
A.F. Favela-Mendoza ◽  
A. González-Martin ◽  
...  
2018 ◽  
Vol 14 (2) ◽  
Author(s):  
M.C. Ibarra

Abstract: To determine the frequency and distributionof dental anomalies of shape and numberin primary dentition. Methods: The study is retro-prolective, crosssectionaland descriptive. The sample was probabilistic,stratified for convenience by gender. Theclinical record of 1,568 patients was reviewed.These patients attended the Clinic of PediatricDentistry of FEBUAP during the period of 2012-2014, only 720 records of patients were includedin the study (321 girls and 399 boys) between theages of 1-10 years old, who provided complete,crisp radiographic studies with the presence ofdental anomalies of shape or number, the studywas divided into active and inactive patients.For inactive patients, photographs of x-rays withdental anomalies of shape and/or number weretaken. For cases with active patients, an interviewwith one of the parents was conducted andauthorization with informed consent was requested,also the child agreed to do a clinical examinationand take intraoral photographs. Results:A total of 63 children had anomalies (17girls and 46 boys). The total prevalence of dentalanomalies was 9%, of which 3.1% were (fusedand geminated teeth), 1.1% (agenesis) and 1.9%(supernumerary), 1.3% (supernumerary roots),0.27% (macrodontia), 0.11% (microdontia), andfinally 0.27% corresponded to (talon cusp). Conclusions: Although the prevalence of theseanomalies is not high, it is important to do a routineradiographic examination for early diagnosisand accordingly apply the correct preventivemeasures to establish the best treatment plan.


2017 ◽  
Author(s):  
Karen-Ivette Gutierrez-Aguirre ◽  
Maria-Luisa Lazo-de-la-Vega-Monroy ◽  
Yeniley Ruiz-Noa ◽  
Lorena-del-Rocio Ibarra-Reynoso ◽  
Juana-Rosalba Garcia-Ramirez ◽  
...  

Author(s):  
O. Palacio ◽  
A. Ibarra ◽  
Y. Posada ◽  
M. Camargo ◽  
J.D. Granda ◽  
...  
Keyword(s):  

Author(s):  
Andrei Semikhodskii ◽  
Yevgeniy Krassotkin ◽  
Tatiana Makarova ◽  
Vladislav Zavarin ◽  
Viktoria Ilina ◽  
...  

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Elizabeth Ruiz-Sánchez ◽  
Janet Jiménez-Genchi ◽  
Yessica M. Alcántara-Flores ◽  
Carlos J. Castañeda-González ◽  
Carlos L. Aviña-Cervantes ◽  
...  

Abstract Background Cognitive functions represent useful endophenotypes to identify the association between genetic variants and schizophrenia. In this sense, the NR4A2 gene has been implicated in schizophrenia and cognition in different animal models and clinical trials. We hypothesized that the NR4A2 gene is associated with working memory performance in schizophrenia. This study aimed to analyze two variants and the expression levels of the NR4A2 gene with susceptibility to schizophrenia, as well as to evaluate whether possession of NR4A2 variants influence the possible correlation between gene expression and working memory performance in schizophrenia. Methods The current study included 187 schizophrenia patients and 227 controls genotyped for two of the most studied NR4A2 genetic variants in neurological and neuropsychiatric diseases. Genotyping was performed using High Resolution Melt and sequencing techniques. In addition, mRNA expression of NR4A2 was performed in peripheral mononuclear cells of 112 patients and 118 controls. A group of these participants, 54 patients and 87 controls, performed the working memory index of the WAIS III test. Results Both genotypic frequencies of the two variants and expression levels of the NR4A2 gene showed no significant difference when in patients versus controls. However, patients homozygous for the rs34884856 promoter variant showed a positive correlation between expression levels and auditory working memory. Conclusions Our finding suggested that changes in expression levels of the NR4A2 gene could be associated with working memory in schizophrenia depending on patients’ genotype in a sample from a Mexican population.


2021 ◽  
Vol 160 (6) ◽  
pp. S-191
Author(s):  
Ricardo Flores Rendon ◽  
Francisco Alejandro Felix Tellez ◽  
Jose Maria Remes-Troche ◽  
Paulo C. Gomez-Castaños ◽  
Enrique Coss-Adame ◽  
...  
Keyword(s):  

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