Functional characterization of tissue-specific enhancers in the DLX5/6 locus-Reference-Cited by-同舟云学术

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Functional characterization of tissue-specific enhancers in the DLX5/6 locus

Published:2012-08-21 Issue:22 Volume:21 Page:4930-4938
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Birnbaum Ramon Y.,Everman David B.,Murphy Karl K.,Gurrieri Fiorella,Schwartz Charles E.,Ahituv Nadav

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/21/22/4930/17257393/dds336.pdf

Reference56 articles.

1. Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5;Acampora;Development,1999

2. Dlx genes pattern mammalian jaw primordium by regulating both lower jaw-specific and upper jaw-specific genetic programs;Jeong;Development,2008

3. Abnormal urethra formation in mouse models of split-hand/split-foot malformation type 1 and type 4;Suzuki;Eur. J. Hum. Genet.,2008

4. The Dlx5 and Dlx6 homeobox genes are essential for craniofacial, axial, and appendicular skeletal development;Robledo;Genes Dev.,2002

5. Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients;Elliott;Am. J. Med. Genet. A,2006

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4. Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits;Genetics in Medicine Open;2024

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