Found: 12
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Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 6, p. 1752, doi. 10.1002/ajmg.a.62703
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- Article
Basal Keratinocytes Contribute to All Strata of the Adult Zebrafish Epidermis.
- Published in:
- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0084858
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- Article
A transparent electrode based on a metal nanotrough network.
- Published in:
- Nature Nanotechnology, 2013, v. 8, n. 6, p. 421, doi. 10.1038/nnano.2013.84
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- Article
Dolastatin 15 from a Marine Cyanobacterium Suppresses HIF‐1α Mediated Cancer Cell Viability and Vascularization.
- Published in:
- ChemBioChem, 2020, v. 21, n. 16, p. 2356, doi. 10.1002/cbic.202000180
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- Article
wnt10a is required for zebrafish median fin fold maintenance and adult unpaired fin metamorphosis.
- Published in:
- Developmental Dynamics, 2024, v. 253, n. 6, p. 566, doi. 10.1002/dvdy.672
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- Article
In vivo time-lapse imaging shows dynamic oligodendrocyte progenitor behavior during zebrafish development.
- Published in:
- Nature Neuroscience, 2006, v. 9, n. 12, p. 1506, doi. 10.1038/nn1803
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- Article
Highlight article: Use of zebrafish to model chemotherapy and targeted therapy gastrointestinal toxicity.
- Published in:
- Experimental Biology & Medicine, 2019, v. 244, n. 14, p. 1178, doi. 10.1177/1535370219855334
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- Article
p53 and TAp63 Promote Keratinocyte Proliferation and Differentiation in Breeding Tubercles of the Zebrafish.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 1, p. 1, doi. 10.1371/journal.pgen.1004048
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- Article
Genetic Analysis of Fin Development in Zebrafish Identifies Furin and Hemicentin1 as Potential Novel Fraser Syndrome Disease Genes.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 4, p. 1, doi. 10.1371/journal.pgen.1000907
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- Article
The Epithelial Cell Adhesion Molecule EpCAM Is Required for Epithelial Morphogenesis and Integrity during Zebrafish Epiboly and Skin Development.
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- PLoS Genetics, 2009, v. 5, n. 7, p. 1, doi. 10.1371/journal.pgen.1000563
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- Article
Leukocyte Tyrosine Kinase Functions in Pigment Cell Development.
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- PLoS Genetics, 2008, v. 4, n. 3, p. 1, doi. 10.1371/journal.pgen.1000026
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- Article
Identification and In Vivo Functional Characterization of Novel Compound Heterozygous BMP1 Variants in Osteogenesis Imperfecta.
- Published in:
- Human Mutation, 2015, v. 36, n. 2, p. 191, doi. 10.1002/humu.22731
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- Publication type:
- Article