| Published Application/Species/Dilution | Reference |
|---|
- immunohistochemistry (knockout validation); mouse; 1:80; fig 2
- western blot (knockout validation); mouse; 1:2000; fig 3
| Jones K, Sarić N, Russell J, Andoniadou C, Scambler P, Basson M. CHD7 maintains neural stem cell quiescence and prevents premature stem cell depletion in the adult hippocampus. Stem Cells. 2015;33:196-210 pubmed publisher |
- immunoprecipitation; human; fig 2
| Laurette P, Strub T, Koludrovic D, Keime C, Le Gras S, Seberg H, et al. Transcription factor MITF and remodeller BRG1 define chromatin organisation at regulatory elements in melanoma cells. elife. 2015;4: pubmed publisher |
- immunohistochemistry - paraffin section; human
| Tahara T, Yamamoto E, Madireddi P, Suzuki H, Maruyama R, Chung W, et al. Colorectal carcinomas with CpG island methylator phenotype 1 frequently contain mutations in chromatin regulators. Gastroenterology. 2014;146:530-38.e5 pubmed publisher |
- immunohistochemistry; mouse; 1:50
| Batsukh T, Schulz Y, Wolf S, Rabe T, Oellerich T, Urlaub H, et al. Identification and characterization of FAM124B as a novel component of a CHD7 and CHD8 containing complex. PLoS ONE. 2012;7:e52640 pubmed publisher |
| Schnetz M, Bartels C, Shastri K, Balasubramanian D, Zentner G, Balaji R, et al. Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns. Genome Res. 2009;19:590-601 pubmed publisher |
| Yu T, Meiners L, Danielsen K, Wong M, Bowler T, Reinberg D, et al. Deregulated FGF and homeotic gene expression underlies cerebellar vermis hypoplasia in CHARGE syndrome. elife. 2013;2:e01305 pubmed publisher |
| Engelen E, Akinci U, Bryne J, Hou J, Gontan C, Moen M, et al. Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes. Nat Genet. 2011;43:607-11 pubmed publisher |
| Hurd E, Poucher H, Cheng K, Raphael Y, Martin D. The ATP-dependent chromatin remodeling enzyme CHD7 regulates pro-neural gene expression and neurogenesis in the inner ear. Development. 2010;137:3139-50 pubmed publisher |
| Layman W, McEwen D, Beyer L, Lalani S, Fernbach S, Oh E, et al. Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome. Hum Mol Genet. 2009;18:1909-23 pubmed publisher |
| Colin C, Tobaruella F, Correa R, Sogayar M, Demasi M. Cloning and characterization of a novel alternatively spliced transcript of the human CHD7 putative helicase. BMC Res Notes. 2010;3:252 pubmed publisher |
| Schnetz M, Handoko L, Akhtar-Zaidi B, Bartels C, Pereira C, Fisher A, et al. CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression. PLoS Genet. 2010;6:e1001023 pubmed publisher |
| Tian C, Yu H, Yang B, Han F, Zheng Y, Bartels C, et al. Otitis media in a new mouse model for CHARGE syndrome with a deletion in the Chd7 gene. PLoS ONE. 2012;7:e34944 pubmed publisher |
| Zentner G, Hurd E, Schnetz M, Handoko L, Wang C, Wang Z, et al. CHD7 functions in the nucleolus as a positive regulator of ribosomal RNA biogenesis. Hum Mol Genet. 2010;19:3491-501 pubmed publisher |
| Jiang X, Zhou Y, Xian L, Chen W, Wu H, Gao X. The mutation in Chd7 causes misexpression of Bmp4 and developmental defects in telencephalic midline. Am J Pathol. 2012;181:626-41 pubmed publisher |
| Bergman J, Bosman E, van Ravenswaaij-Arts C, Steel K. Study of smell and reproductive organs in a mouse model for CHARGE syndrome. Eur J Hum Genet. 2010;18:171-7 pubmed publisher |
| Layman W, Hurd E, Martin D. Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndrome. Hum Mol Genet. 2011;20:3138-50 pubmed publisher |
