Similar articles for PMID: 25119037

Year	Number of Results
1998	1
2000	1
2002	1
2005	4
2006	5
2007	6
2008	2
2009	5
2010	8
2011	9
2012	7
2013	7
2014	15
2015	9
2016	8
2017	10
2018	10
2019	7
2020	6
2021	11
2022	17
2023	6
2024	0

1

Inappropriate p53 activation during development induces features of CHARGE syndrome.

Van Nostrand JL, Brady CA, Jung H, Fuentes DR, Kozak MM, Johnson TM, Lin CY, Lin CJ, Swiderski DL, Vogel H, Bernstein JA, Attié-Bitach T, Chang CP, Wysocka J, Martin DM, Attardi LD. Van Nostrand JL, et al. Nature. 2014 Oct 9;514(7521):228-32. doi: 10.1038/nature13585. Epub 2014 Aug 3. Nature. 2014. PMID: 25119037 Free PMC article.

2

The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.

Sperry ED, Hurd EA, Durham MA, Reamer EN, Stein AB, Martin DM. Sperry ED, et al. Dev Dyn. 2014 Sep;243(9):1055-66. doi: 10.1002/dvdy.24156. Epub 2014 Jul 10. Dev Dyn. 2014. PMID: 24975120 Free PMC article.

3

Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome.

Balow SA, Pierce LX, Zentner GE, Conrad PA, Davis S, Sabaawy HE, McDermott BM Jr, Scacheri PC. Balow SA, et al. Dev Biol. 2013 Oct 1;382(1):57-69. doi: 10.1016/j.ydbio.2013.07.026. Epub 2013 Aug 3. Dev Biol. 2013. PMID: 23920116 Free PMC article.

4

CHD7 regulates cardiovascular development through ATP-dependent and -independent activities.

Yan S, Thienthanasit R, Chen D, Engelen E, Brühl J, Crossman DK, Kesterson R, Wang Q, Bouazoune K, Jiao K. Yan S, et al. Proc Natl Acad Sci U S A. 2020 Nov 17;117(46):28847-28858. doi: 10.1073/pnas.2005222117. Epub 2020 Oct 30. Proc Natl Acad Sci U S A. 2020. PMID: 33127760 Free PMC article.

5

Guilty as CHARGED: p53's expanding role in disease.

Van Nostrand JL, Attardi LD. Van Nostrand JL, et al. Cell Cycle. 2014;13(24):3798-807. doi: 10.4161/15384101.2014.987627. Cell Cycle. 2014. PMID: 25483057 Free PMC article.

6

CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance.

Schulz Y, Wehner P, Opitz L, Salinas-Riester G, Bongers EM, van Ravenswaaij-Arts CM, Wincent J, Schoumans J, Kohlhase J, Borchers A, Pauli S. Schulz Y, et al. Hum Genet. 2014 Aug;133(8):997-1009. doi: 10.1007/s00439-014-1444-2. Epub 2014 Apr 13. Hum Genet. 2014. PMID: 24728844

7

Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.

Lalani SR, Safiullah AM, Fernbach SD, Harutyunyan KG, Thaller C, Peterson LE, McPherson JD, Gibbs RA, White LD, Hefner M, Davenport SL, Graham JM, Bacino CA, Glass NL, Towbin JA, Craigen WJ, Neish SR, Lin AE, Belmont JW. Lalani SR, et al. Am J Hum Genet. 2006 Feb;78(2):303-14. doi: 10.1086/500273. Epub 2005 Dec 29. Am J Hum Genet. 2006. PMID: 16400610 Free PMC article.

8

CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.

Micucci JA, Layman WS, Hurd EA, Sperry ED, Frank SF, Durham MA, Swiderski DL, Skidmore JM, Scacheri PC, Raphael Y, Martin DM. Micucci JA, et al. Hum Mol Genet. 2014 Jan 15;23(2):434-48. doi: 10.1093/hmg/ddt435. Epub 2013 Sep 10. Hum Mol Genet. 2014. PMID: 24026680 Free PMC article.

9

Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE Syndrome.

Gage PJ, Hurd EA, Martin DM. Gage PJ, et al. Invest Ophthalmol Vis Sci. 2015 Dec;56(13):7923-30. doi: 10.1167/iovs.15-18069. Invest Ophthalmol Vis Sci. 2015. PMID: 26670829 Free PMC article.

10

CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development.

Yao H, Hill SF, Skidmore JM, Sperry ED, Swiderski DL, Sanchez GJ, Bartels CF, Raphael Y, Scacheri PC, Iwase S, Martin DM. Yao H, et al. JCI Insight. 2018 Feb 22;3(4):e97440. doi: 10.1172/jci.insight.97440. eCollection 2018 Feb 22. JCI Insight. 2018. PMID: 29467333 Free PMC article.

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