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1.
Nucleic Acids Res ; 52(D1): D1333-D1346, 2024 Jan 05.
Artículo en Inglés | MEDLINE | ID: mdl-37953324

RESUMEN

The Human Phenotype Ontology (HPO) is a widely used resource that comprehensively organizes and defines the phenotypic features of human disease, enabling computational inference and supporting genomic and phenotypic analyses through semantic similarity and machine learning algorithms. The HPO has widespread applications in clinical diagnostics and translational research, including genomic diagnostics, gene-disease discovery, and cohort analytics. In recent years, groups around the world have developed translations of the HPO from English to other languages, and the HPO browser has been internationalized, allowing users to view HPO term labels and in many cases synonyms and definitions in ten languages in addition to English. Since our last report, a total of 2239 new HPO terms and 49235 new HPO annotations were developed, many in collaboration with external groups in the fields of psychiatry, arthrogryposis, immunology and cardiology. The Medical Action Ontology (MAxO) is a new effort to model treatments and other measures taken for clinical management. Finally, the HPO consortium is contributing to efforts to integrate the HPO and the GA4GH Phenopacket Schema into electronic health records (EHRs) with the goal of more standardized and computable integration of rare disease data in EHRs.


Asunto(s)
Ontologías Biológicas , Humanos , Fenotipo , Genómica , Algoritmos , Enfermedades Raras
2.
Trends Genet ; 18(10): 499, 2002 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-12350347

RESUMEN

Genetically engineered strains of mice, modified by gene targeting (knockouts), are increasingly being employed as alternative effective research tools in elucidating the genetic basis of human deafness. An impressive array of auditory and vestibular mouse knockouts is already available as a valuable resource for studying the ontogenesis, morphogenesis and function of the mammalian inner ear. This article provides a current catalog of mouse knockouts with inner ear morphogenetic malformations and hearing or balance deficits resulting from ablation of genes that are regionally expressed in the inner ear and/or within surrounding tissues, such as the hindbrain, neural crest and mesenchyme.


Asunto(s)
Oído Interno/anomalías , Ratones Noqueados/anomalías , Animales , Sordera/genética , Humanos , Ratones , Ratones Noqueados/genética
3.
Trends Genet ; 18(1): 8-10, 2002 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11750688

RESUMEN

An increasing number of genetically engineered animals are produced worldwide for use in both basic and applied research. Here, I provide an update of some of the latest mouse knockouts in The Jackson Laboratory Transgenic/Targeted Mutation Database (TBASE), concentrating on those associated with male infertility and neuropathology.


Asunto(s)
Infertilidad Masculina/genética , Animales , Modelos Animales de Enfermedad , Femenino , Ingeniería Genética , Humanos , Infertilidad Masculina/patología , Masculino , Ratones , Ratones Noqueados , Síndrome de Rett/genética , Síndrome de Rett/patología
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