about
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationDYX1C1 is required for axonemal dynein assembly and ciliary motilityThe coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formationSIX2 and BMP4 mutations associate with anomalous kidney developmentCCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms.Direct and indirect roles for Nodal signaling in two axis conversions during asymmetric morphogenesis of the zebrafish heartRASopathies: unraveling mechanisms with animal modelsIntegration of nodal and BMP signals in the heart requires FoxH1 to create left-right differences in cell migration rates that direct cardiac asymmetryThe exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypesZebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants.Mutations in zebrafish leucine-rich repeat-containing six-like affect cilia motility and result in pronephric cysts, but have variable effects on left-right patterning.Fluid dynamics in zebrafish Kupffer's vesicle.Regression-based identification of behavior-encoding neurons during large-scale optical imaging of neural activity at cellular resolution.Categorical data analysis in experimental biologyNodal-dependent mesendoderm specification requires the combinatorial activities of FoxH1 and Eomesodermin.Adeno-associated virus-mediated rescue of the cognitive defects in a mouse model for Angelman syndrome.Prolonged, brain-wide expression of nuclear-localized GCaMP3 for functional circuit mappingFunctional knowledge transfer for high-accuracy prediction of under-studied biological processesExamining the establishment of cellular axes using intrinsic chirality.Zebrafish pronephros: a model for understanding cystic kidney disease.c21orf59/kurly Controls Both Cilia Motility and PolarizationIn vivo severity ranking of Ras pathway mutations associated with developmental disorders.Two additional midline barriers function with midline lefty1 expression to maintain asymmetric Nodal signaling during left-right axis specification in zebrafish.Modeling Syndromic Congenital Heart Defects in Zebrafish.Left-Right Patterning: Breaking Symmetry to Asymmetric Morphogenesis.Divergent effects of intrinsically active MEK variants on developmental Ras signaling.Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature.Embedding, serial sectioning and staining of zebrafish embryos using JB-4 resin.Left-right asymmetry: lessons from Cancún.Quantitative differences in tissue surface tension influence zebrafish germ layer positioning.RASopathies: unraveling mechanisms with animal models.Zebrafish curly up encodes a Pkd2 ortholog that restricts left-side-specific expression of southpaw.pitx3 defines an equivalence domain for lens and anterior pituitary placode.Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151.Gdf3 is required for robust Nodal signaling during germ layer formation and left-right patterning.Antagonistic interactions in the zebrafish midline prior to the emergence of asymmetric gene expression are important for left-right patterning.ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signaling.More than Maintenance? A Role for IFT Genes in Planar Cell PolarityAlternative splicing affecting a novel domain in the C. elegans EGL-15 FGF receptor confers functional specificityOptimizing photoswitchable MEK
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P50
description
hulumtuese
@sq
onderzoeker
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researcher
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հետազոտող
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name
Rebecca D. Burdine
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Rebecca D. Burdine
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Rebecca D. Burdine
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Rebecca D. Burdine
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type
label
Rebecca D. Burdine
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Rebecca D. Burdine
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Rebecca D. Burdine
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Rebecca D. Burdine
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Becky
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prefLabel
Rebecca D. Burdine
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Rebecca D. Burdine
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Rebecca D. Burdine
@es
Rebecca D. Burdine
@sl
P106
P1153
6602681393
P21
P31
P496
0000-0001-6620-5015