Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome-Reference-Cited by-同舟云学术

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

Published:2013-10 Issue:1 Volume:382 Page:57-69
ISSN:0012-1606
Container-title:Developmental Biology
language:en
Short-container-title:Developmental Biology

Author:

Balow Stephanie A.,Pierce Lain X.,Zentner Gabriel E.,Conrad Patricia A.,Davis Stephani,Sabaawy Hatem E.,McDermott Brian M.,Scacheri Peter C.

Funder

The CHARGE Syndrome Foundation (PCS)

the Office of Research Infrastructure Program of the National Institutes of Health

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,Molecular Biology

Reference53 articles.

1. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs;Altschul;Nucleic Acids Res.,1997

2. Perturbation of rRNA synthesis in the bap28 mutation leads to apoptosis mediated by p53 in the zebrafish central nervous system;Azuma;J. Biol. Chem.,2006

3. CHD7 cooperates with PBAF to control multipotent neural crest formation;Bajpai;Nature,2010

4. Mutations in the CHD7 gene: the experience of a commercial laboratory;Bartels;Genet. Test. Mol. Biomarkers,2010

5. Multiple mutations in mouse Chd7 provide models for CHARGE syndrome;Bosman;Hum. Mol. Genet.,2005

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4. Mutual Regulation of ncRNAs and Chromatin Remodeling Complexes in Normal and Pathological Conditions;International Journal of Molecular Sciences;2023-04-25

5. Morphological and sensorimotor phenotypes in a zebrafish CHARGE syndrome model are domain‐dependent;Genes, Brain and Behavior;2023-01-30

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