2019
DOI: 10.1016/j.ydbio.2019.03.010
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Desmoplakin is required for epidermal integrity and morphogenesis in the Xenopus laevis embryo

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Cited by 19 publications
(15 citation statements)
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“…Desmoplakin is a unique and critical component of desmosomal cell-cell junctions and involved in integrity of the cytoskeletal intermediate filament network (Bendrick et al, 2019). It has been shown to be required for epidermal integrity and embryo morphogenesis (Bharathan and Dickinson, 2019), as well as in the coordination of cell migration (Bendrick et al, 2019). Mutations in desmoplakin have been linked to multiple allergies, severe dermatitis and metabolic wasting (SAM) syndrome (Liang et al, 2019).…”
Section: Discussionmentioning
confidence: 99%
“…Desmoplakin is a unique and critical component of desmosomal cell-cell junctions and involved in integrity of the cytoskeletal intermediate filament network (Bendrick et al, 2019). It has been shown to be required for epidermal integrity and embryo morphogenesis (Bharathan and Dickinson, 2019), as well as in the coordination of cell migration (Bendrick et al, 2019). Mutations in desmoplakin have been linked to multiple allergies, severe dermatitis and metabolic wasting (SAM) syndrome (Liang et al, 2019).…”
Section: Discussionmentioning
confidence: 99%
“…Desmoplakin is a unique and critical component of desmosomal cell-cell junctions and involved in integrity of the cytoskeletal intermediate filament network (Bendrick et al, 2019). It has been shown to be required for epidermal integrity and morphogenesis in the Xenopus laevis embryo (Bharathan and Dickinson, 2019) and novel roles in coordination of cell migration were recently established (Bendrick et al, 2019). Mutations in desmoplakin have been linked to multiple allergies, severe dermatitis and metabolic wasting (SAM) syndrome (Liang et al, 2019).…”
mentioning
confidence: 99%
“…Others merely monitored the breakdown of Sanger traces from directly amplified DNA at the target site, combined with a deconvolution algorithm to predict likely repairs [20,21]. Indels that cause reading frame-shifts are a frequent outcome, so analyses with basic DNA genotyping have instead emphasized the depletion of the targeted protein measured with specific antibody staining [21][22][23]. Reported mutation efficiencies have varied, which probably reflects differing Cas9-gRNA reagent activity.…”
Section: Published Xenopus Crispr/cas9 Research -Can the Mosaicism That Results From Repair Of Cas9 Dsbs Be Eliminated?mentioning
confidence: 99%