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1.
Anim Genet ; 47(3): 334-44, 2016 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-26932307

RESUMEN

We explored the involvement of genomic copy number variants (CNVs) in susceptibility to recurrent airway obstruction (RAO), or heaves-an asthmalike inflammatory disease in horses. Analysis of 16 RAO-susceptible (cases) and six RAO-resistant (control) horses on a custom-made whole-genome 400K equine tiling array identified 245 CNV regions (CNVRs), 197 previously known and 48 new, distributed on all horse autosomes and the X chromosome. Among the new CNVRs, 30 were exclusively found in RAO cases and were further analyzed by quantitative PCR, including additional cases and controls. Suggestive association (P = 0.03; corrected P = 0.06) was found between RAO and a loss on chromosome 5 involving NME7, a gene necessary for ciliary functions in lungs and involved in primary ciliary dyskinesia in humans. The CNVR could be a potential marker for RAO susceptibility but needs further study in additional RAO cohorts. Other CNVRs were not associated with RAO, although several involved genes of interest, such as SPI2/SERPINA1 from the serpin gene family, which are associated with chronic obstructive pulmonary disease and asthma in humans. The SPI2/SERPINA1 CNVR showed striking variation among horses, but it was not significantly different between RAO cases and controls. The findings provide baseline information on the relationship between CNVs and RAO susceptibility. Discovery of new CNVs and the use of a larger population of RAO-affected and control horses are needed to shed more light on their significance in modulating this complex and heterogeneous disease.


Asunto(s)
Obstrucción de las Vías Aéreas/veterinaria , Variaciones en el Número de Copia de ADN , Enfermedades de los Caballos/genética , Caballos/genética , Obstrucción de las Vías Aéreas/genética , Animales , Hibridación Genómica Comparativa , Fenotipo , Reacción en Cadena en Tiempo Real de la Polimerasa , Serpinas/genética
2.
J Vet Intern Med ; 29(6): 1648-59, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26340305

RESUMEN

Rhodococcus equi pneumonia is a major cause of morbidity and mortality in neonatal foals. Much effort has been made to identify preventative measures and new treatments for R. equi with limited success. With a growing focus in the medical community on understanding the genetic basis of disease susceptibility, investigators have begun to evaluate the interaction of the genetics of the foal with R. equi. This review describes past efforts to understand the genetic basis underlying R. equi susceptibility and tolerance. It also highlights the genetic technology available to study horses and describes the use of this technology in investigating R. equi. This review provides readers with a foundational understanding of candidate gene approaches, single nucleotide polymorphism-based, and copy number variant-based genome-wide association studies, and next generation sequencing (both DNA and RNA).


Asunto(s)
Infecciones por Actinomycetales/veterinaria , Predisposición Genética a la Enfermedad , Enfermedades de los Caballos/microbiología , Rhodococcus equi , Infecciones por Actinomycetales/genética , Infecciones por Actinomycetales/microbiología , Animales , Enfermedades de los Caballos/genética , Caballos
3.
s.l; Instituto Panmericano de Geografía e Historia; Oct. 1997. 15 p. tab, mapas.
No convencional en En | Desastres | ID: des-10013
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