Surveying the Down syndrome mouse model resource identifies critical regions responsible for chronic otitis media
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/article/10.1007/s00335-013-9475-x/fulltext.html
Reference52 articles.
1. Ait Yahya-Graison E, Aubert J et al (2007) Classification of human chromosome 21 gene-expression variations in Down syndrome: impact on disease phenotypes. Am J Hum Genet 81(3):475–491
2. American Academy of Pediatrics (2001) Health supervision for children with Down syndrome. Pediatrics 107(2):442–449
3. Antonarakis SE, Lyle R et al (2004) Chromosome 21 and Down syndrome: from genomics to pathophysiology. Nat Rev Genet 5(10):725–738
4. Balkany TJ, Downs MP et al (1979) Hearing loss in Down’s syndrome. A treatable handicap more common than generally recognized. Clin Pediatr (Phila) 18(2):116–118
5. Barr E, Dungworth J et al (2011) The prevalence of ear, nose and throat disorders in preschool children with Down’s syndrome in Glasgow. Scott Med J 56(2):98–103
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1. Hearing impairment in murine model of Down syndrome;Frontiers in Genetics;2022-08-04
2. Repeat tympanostomy tubes in children with Down syndrome;International Journal of Pediatric Otorhinolaryngology;2021-09
3. Mechanistic Analysis of Age-Related Clinical Manifestations in Down Syndrome;Frontiers in Aging Neuroscience;2021-07-01
4. Recent Perspectives on Gene-Microbe Interactions Determining Predisposition to Otitis Media;Frontiers in Genetics;2019-11-26
5. Triplications of human chromosome 21 orthologous regions in mice result in expansion of megakaryocyte-erythroid progenitors and reduction of granulocyte-macrophage progenitors;Oncotarget;2017-12-19
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