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The CHARGE syndrome ortholog CHD-7 regulates TGF-β pathways in Caenorhabditis elegans. , Jofré DM., Proc Natl Acad Sci U S A. April 12, 2022; 119 (15): e2109508119.
A convergent molecular network underlying autism and congenital heart disease. , Rosenthal SB., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.
Modeling human congenital disorders with neural crest developmental defects using patient-derived induced pluripotent stem cells. , Okuno H., Regen Ther. August 24, 2021; 18 275-280.
HELLS and CDCA7 comprise a bipartite nucleosome remodeling complex defective in ICF syndrome. , Jenness C., Proc Natl Acad Sci U S A. January 30, 2018; 115 (5): E876-E885.
Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy. , Duncan AR., Semin Cell Dev Biol. March 1, 2016; 51 73-9.
CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance. , Schulz Y., Hum Genet. August 1, 2014; 133 (8): 997-1009.
CHD7 cooperates with PBAF to control multipotent neural crest formation. , Bajpai R ., Nature. February 18, 2010; 463 (7283): 958-62.
The SNF2 domain protein family in higher vertebrates displays dynamic expression patterns in Xenopus laevis embryos. , Linder B., Gene. February 4, 2004; 326 59-66.