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1.
West J Emerg Med ; 18(1): 60-68, 2017 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-28116010

RESUMEN

INTRODUCTION: Dissemination of educational research is critical to improving medical education, promotion of faculty and ultimately patient care. The objective of this study was to identify the top 25 cited education articles in the emergency medicine (EM) literature and the top 25 cited EM education articles in all journals, as well as report on the characteristics of the articles. METHODS: Two searches were conducted in the Web of Science in June 2016 using a list of education-related search terms. We searched 19 EM journals for education articles as well as all other literature for EM education-related articles. Articles identified were reviewed for citation count, article type, journal, authors, and publication year. RESULTS: With regards to EM journals, the greatest number of articles were classified as articles/reviews, followed by research articles on topics such as deliberate practice (cited 266 times) and cognitive errors (cited 201 times). In contrast in the non-EM journals, research articles were predominant. Both searches found several simulation and ultrasound articles to be included. The most common EM journal was Academic Emergency Medicine (n = 18), and Academic Medicine was the most common non-EM journal (n=5). A reasonable number of articles included external funding sources (6 EM articles and 13 non-EM articles.). CONCLUSION: This study identified the most frequently cited medical education articles in the field of EM education, published in EM journals as well as all other journals indexed in Web of Science. The results identify impactful articles to medical education, providing a resource to educators while identifying trends that may be used to guide EM educational research and publishing efforts.


Asunto(s)
Medicina de Emergencia/educación , Publicaciones Periódicas como Asunto/estadística & datos numéricos , Bibliometría , Educación Médica , Factor de Impacto de la Revista , Literatura de Revisión como Asunto
2.
Am J Med Genet B Neuropsychiatr Genet ; 147B(7): 1126-37, 2008 Oct 05.
Artículo en Inglés | MEDLINE | ID: mdl-18361432

RESUMEN

The etiology of mental disorders remains largely unclear. Complex interactions between genetic and environmental factors are key to the development of such disorders. Puerperal psychosis is the most extreme form of postnatal mood disorder in women. Similarly, parturition in the pig can trigger extreme behavioral disturbances, including maternal infanticide. In this study, we have used a targeted cDNA microarray approach using the pig as a model to understand the genes and genetic pathways that are involved in these processes. Two subtracted cDNA libraries from porcine hypothalamus were constructed, which were enriched for genes that were over-expressed and under-expressed in the aberrant behavioral phenotype, compared to the matched control. In addition to this, a normalized library was constructed from hypothalamus and pituitary samples taken from pigs in a variety of reproductive states. The libraries were partially sequenced and combined represented approximately 5,159 different genes. Microarray analysis determined differences in gene expression between hypothalamus samples from nine matched pairs of infanticidal versus control animals, using a common reference design. Microarray analysis of variance (MAANOVA) identified 52 clones as being differentially expressed (P

Asunto(s)
Conducta Animal , Perfilación de la Expresión Génica , Trastornos Puerperales/genética , Animales , Animales Recién Nacidos , Modelos Animales de Enfermedad , Femenino , Biblioteca de Genes , Humanos , Hipotálamo , Recién Nacido , Infanticidio , Análisis de Secuencia por Matrices de Oligonucleótidos , Hipófisis , Porcinos
3.
J Med Genet ; 44(8): 498-508, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17496197

RESUMEN

INTRODUCTION: Microarray gene-expression profiling is a powerful tool for global analysis of the transcriptional consequences of disease phenotypes. Understanding the genetic correlates of particular pathological states is important for more accurate diagnosis and screening of patients, and thus for suggesting appropriate avenues of treatment. As yet, there has been little research describing gene-expression profiling of infertile and subfertile men, and thus the underlying transcriptional events involved in loss of spermatogenesis remain unclear. Here we present the results of an initial screen of 33 patients with differing spermatogenic phenotypes. METHODS: Oligonucleotide array expression profiling was performed on testis biopsies for 33 patients presenting for testicular sperm extraction. Significantly regulated genes were selected using a mixed model analysis of variance. Principle components analysis and hierarchical clustering were used to interpret the resulting dataset with reference to the patient history, clinical findings and histological composition of the biopsies. RESULTS: Striking patterns of coordinated gene expression were found. The most significant contains multiple germ cell-specific genes and corresponds to the degree of successful spermatogenesis in each patient, whereas a second pattern corresponds to inflammatory activity within the testis. Smaller-scale patterns were also observed, relating to unique features of the individual biopsies.


Asunto(s)
Infertilidad Masculina/genética , Transcripción Genética , Azoospermia/genética , Biopsia , Regulador de Conductancia de Transmembrana de Fibrosis Quística/genética , Citocinas/sangre , Exones , Regulación de la Expresión Génica , Humanos , Infertilidad Masculina/patología , Masculino , Análisis de Secuencia por Matrices de Oligonucleótidos , Fenotipo , Receptores de Interferón/genética , Técnicas Reproductivas Asistidas , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Motilidad Espermática , Conducto Deferente/patología , Vasectomía , Receptor de Interferón gamma
4.
Mamm Genome ; 17(9): 956-75, 2006 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-16964443

RESUMEN

A gene expression time course in the juvenile mouse testis was established using cDNA microarrays derived from a variety of isolated testis cell types. In conjunction with the use of four germ cell-deficient mouse models, a stage and cell-type classification over nine time points has been obtained and analyzed for differential expression of genes. The expression profiles have been clustered into nine groups and subjected to detailed analysis of associated gene ontology. This has allowed the correlation of particular cellular processes and functions with different expression clusters. Focused analysis of transcripts involved in cell number regulation (apoptosis and proliferation) and their spatiotemporal expression patterns are presented. The findings indicate that for genes involved in both apoptosis and proliferation, several distinct pathways regulating these processes are active in somatic and germ cell lineages.


Asunto(s)
Regulación del Desarrollo de la Expresión Génica , Transducción de Señal/genética , Espermatogénesis/genética , Testículo/metabolismo , Animales , Apoptosis/genética , Proliferación Celular , Perfilación de la Expresión Génica , Células Germinativas/citología , Células Germinativas/metabolismo , Masculino , Ratones , Ratones Endogámicos C57BL , Células de Sertoli/citología , Células de Sertoli/metabolismo , Transducción de Señal/fisiología , Espermátides/citología , Espermátides/metabolismo , Espermatocitos/citología , Espermatocitos/metabolismo , Testículo/citología , Testículo/crecimiento & desarrollo
5.
Mamm Genome ; 14(7): 437-47, 2003 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12925892

RESUMEN

Sequences complementary to the X-linked ubiquitin-specific protease gene Usp9x (Dffrx) have been shown to map to the Sxr(b) interval of the mouse Y Chromosome (chr) and to be expressed in a testis-specific manner. In humans, ubiquitously expressed functional homologues (USP9Y and USP9X DFFRY/DFFRX) are present on both sex chromosomes, whereas in mouse it remains to be demonstrated that the Y-linked sequences encode a functional protein. In this paper, it is shown that the Usp9y gene encodes a potentially functional ubiquitin-specific protease possessing a core promoter region that shares several features characteristic of other testis-specific genes. Analysis of synonymous and nonsynonymous nucleotide changes suggests that there is constraint on the amino acid sequence of both the mouse Usp9x and Usp9y genes, a finding that mirrors similar analysis of the human orthologs. Thus, in both mouse and human, selection is acting to maintain the amino acid sequence of the X and Y-linked genes. This indicates that in both species the genes on each sex chromosome continue to encode an important function.


Asunto(s)
Endopeptidasas/genética , Regiones Promotoras Genéticas , Selección Genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Humanos , Ratones , Antígenos de Histocompatibilidad Menor , Datos de Secuencia Molecular , ARN Mensajero , Ubiquitina Tiolesterasa
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