Rescue of the abnormal skeletal phenotype in Ts65Dn Down syndrome mice using genetic and therapeutic modulation of trisomicDyrk1a-Reference-Cited by-同舟云学术

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Rescue of the abnormal skeletal phenotype in Ts65Dn Down syndrome mice using genetic and therapeutic modulation of trisomicDyrk1a

Published:2015-07-23 Issue:20 Volume:24 Page:5687-5696
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Blazek Joshua D.,Abeysekera Irushi,Li Jiliang,Roper Randall J.

Funder

Jerome Lejuene Foundation

Blue River Community Foundation

National Science Foundation

Purdue Research Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/20/5687/13926671/ddv284.pdf

Reference57 articles.

1. Updated national birth prevalence estimates for selected birth defects in the United States, 2004-2006

2. The challenge of Down syndrome

3. Skeletal age of individuals with Down syndrome

4. Bone mass in young adults with Down syndrome

5. Bone mineral mass in males and females with and without Down syndrome

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1. Skeletal health in DYRK1A syndrome;Frontiers in Neuroscience;2024-09-06

2. Sex specific emergence of trisomicDyrk1a-related skeletal phenotypes in the development of a Down syndrome mouse model;2024-05-26

3. Endocrine, auxological and metabolic profile in children and adolescents with Down syndrome: from infancy to the first steps into adult life;Frontiers in Endocrinology;2024-04-08

4. Compromised femoral and lumbovertebral bone in the Dp(16)1Yey Down syndrome mouse model;Bone;2024-04

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