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Published in 2017 at "Developmental Dynamics"
DOI: 10.1002/dvdy.24511
Abstract: Background: Zebrafish visual function depends on quality optics. An F3 screen for developmental mutations in the Zebrafish nervous system was conducted in wild‐type (wt) AB Zebrafish exposed to 3 mM of N‐ethyl‐N‐nitrosourea (ENU). Results: Mutant…
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Keywords:
occhiolino occ;
model;
mutant zebrafish;
function ... See more keywords
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Published in 2020 at "Stem Cell Reports"
DOI: 10.1016/j.stemcr.2020.07.020
Abstract: Summary Cell transplantation into immunodeficient recipients is a widely used approach to study stem cell and cancer biology; however, studying cell states post transplantation in vivo is inconvenient in mammals. Here, we generated a foxn1/Casper…
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Keywords:
foxn1 casper;
casper;
casper mutant;
mutant zebrafish ... See more keywords
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Published in 2017 at "Journal of Lipid Research"
DOI: 10.1194/jlr.d081521
Abstract: Elevated plasma LDL cholesterol is the dominant risk factor for the development of atherosclerosis and cardiovascular disease. Deficiency in the LDL receptor (LDLR) is a major cause of familial hypercholesterolemia in humans, and the LDLR…
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Keywords:
ldl receptor;
accumulation;
hypercholesterolemia;
mutant zebrafish ... See more keywords
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Published in 2021 at "eNeuro"
DOI: 10.1523/eneuro.0493-20.2021
Abstract: Abstract Autism spectrum disorders (ASDs) are characterized by abnormal behavioral traits arising from neural circuit dysfunction. While a number of genes have been implicated in ASDs, in most cases, a clear understanding of how mutations…
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Keywords:
excitability;
mutant zebrafish;
escape;
variability ... See more keywords
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1
Published in 2022 at "Frontiers in Cell and Developmental Biology"
DOI: 10.3389/fcell.2022.952832
Abstract: Tuberous sclerosis complex (TSC) is a multisystem genetic disorder caused by pathogenic variants in TSC1 and TSC2 genes. TSC patients present with seizures and brain abnormalities such as tubers and subependymal giant cells astrocytoma (SEGA).…
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Keywords:
mutant zebrafish;
hit;
model;
tsc2 ... See more keywords
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Published in 2020 at "International Journal of Biological Sciences"
DOI: 10.7150/ijbs.47510
Abstract: A previous study suggested that human Coffin-Siris syndrome is related to the mutation of SOX11. Since the homozygous SOX11 mutant mice died soon after birth, no suitable model was available for the study of the…
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Keywords:
developmental defects;
coffin siris;
sox11am mutant;
multiple developmental ... See more keywords