2019
DOI: 10.1080/19768354.2018.1557744
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Znf76 is associated with development of the eyes, midbrain, MHB, and hindbrain in zebrafish embryos

Abstract: ZNF76 is a transcriptional repressor that targets the TATA-binding protein (TBP) and plays an essential role during brain development; however, its function during embryogenesis remains unclear. Here, we report the expression pattern and potential functions of znf76 in zebrafish embryos. Maternal transcripts of znf76 were detected at low levels in embryos at the 1-cell stage, with zygotic transcripts appearing at the sphere stage. At the bud stage, the distribution… Show more

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Cited by 5 publications
(5 citation statements)
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“…The zebrafish genome contains about 26,000 protein-coding genes and shows approximately 70% of homology with the human genome, including 82% of orthologous human disease-related genes ( Howe et al, 2013 ). The transparent model organism is particularly useful in studies directly observing ongoing events inside the live vertebrate animal body, providing detailed information in organ and neural development ( Choe et al, 2020 ; Jung et al, 2019 ; 2020b ; Lee et al, 2020c ; Oh and Park, 2019 ).…”
Section: Hervs In Transgenic Animal Modelsmentioning
confidence: 99%
“…The zebrafish genome contains about 26,000 protein-coding genes and shows approximately 70% of homology with the human genome, including 82% of orthologous human disease-related genes ( Howe et al, 2013 ). The transparent model organism is particularly useful in studies directly observing ongoing events inside the live vertebrate animal body, providing detailed information in organ and neural development ( Choe et al, 2020 ; Jung et al, 2019 ; 2020b ; Lee et al, 2020c ; Oh and Park, 2019 ).…”
Section: Hervs In Transgenic Animal Modelsmentioning
confidence: 99%
“…By SNP-array, no relevant de novo copy number variants (CNV) were evidenced. By WES, one rare de novo missense variant predicted to be deleterious in silico was identified for one trio in the ZNF76 gene, playing a role in cerebral and ocular development [6]. With the hypothesis of an autosomic dominant trait with incomplete penetrance, we selected too many variants.…”
Section: Hunting For the Genetic Basis Of Susac Syndromementioning
confidence: 99%
“…Clemence David 1,2 Thomas Papo 1,2 Ibrahima Ba 3,4 Emmanuelle Ollivier 5 Catherine Boileau 3,4,6 Philippe Dieudé 4,7 Boris Keren 8 Caroline Kannengiesser 3,4 Karim Sacre…”
Section: Co N Fli C T O F I Nte R E S T Sunclassified
“…Whole-mount in situ hybridization (WISH) was performed following a standard procedure with minor modifications as described in (Thisse et al 1993;Jung et al 2019). After confirming the sequences in the plasmid construct, cloned trim46a construct was linearized with restriction enzyme.…”
Section: Whole-mount In Situ Hybridizationmentioning
confidence: 99%