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Immunofluorescence confocal micrographs (IF) from control (ctrl.) and foxi1 morphants (foxi1 MO; 3 or 0.5 pmol) at st. 32 stained for Acetylated-α-tubulin (Ac.-α-tub., cilia, gray), F-actin (Actin, cell borders and morphology, gray). Targeted cells were identified by membrane RFP expression (memRFP, magenta) and are outlined in blue. Strongly targeted areas targeted by 3 pmol of foxi1 MO fail to generate intercalating cell types. Location of insets is indicated by dashed yellow box in upper panels.

Immunofluorescence confocal micrographs (IF) from control (ctrl.) and foxi1 morphants (foxi1 MO; 3 or 0.5 pmol) at st. 32 stained for Acetylated-α-tubulin (Ac.-α-tub., cilia, gray), F-actin (Actin, cell borders and morphology, gray). Targeted cells were identified by membrane RFP expression (memRFP, magenta) and are outlined in blue. Strongly targeted areas targeted by 3 pmol of foxi1 MO fail to generate intercalating cell types. Location of insets is indicated by dashed yellow box in upper panels.

The TF Foxi1 regulates #ionocytes and is associated with several human diseases. @walenteklab.bsky.social &co show that low concentrations of Foxi1 in progenitor cells maintain #epidermal identity via the #NotchPathway, affecting #mucociliary cell fates in Xenopus @plosbiology.org 🧪 plos.io/3YLOhcp

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Immunofluorescence confocal micrographs (IF) from control (ctrl.) and foxi1 morphants (foxi1 MO; 3 or 0.5 pmol) at st. 32 stained for Acetylated-α-tubulin (Ac.-α-tub., cilia, gray), F-actin (Actin, cell borders and morphology, gray). Targeted cells were identified by membrane RFP expression (memRFP, magenta) and are outlined in blue. Strongly targeted areas targeted by 3 pmol of foxi1 MO fail to generate intercalating cell types. Location of insets is indicated by dashed yellow box in upper panels.

Immunofluorescence confocal micrographs (IF) from control (ctrl.) and foxi1 morphants (foxi1 MO; 3 or 0.5 pmol) at st. 32 stained for Acetylated-α-tubulin (Ac.-α-tub., cilia, gray), F-actin (Actin, cell borders and morphology, gray). Targeted cells were identified by membrane RFP expression (memRFP, magenta) and are outlined in blue. Strongly targeted areas targeted by 3 pmol of foxi1 MO fail to generate intercalating cell types. Location of insets is indicated by dashed yellow box in upper panels.

The TF Foxi1 regulates #ionocytes and is associated with several human diseases. @walenteklab.bsky.social &co show that low concentrations of Foxi1 in progenitor cells maintain #epidermal identity via the #NotchPathway, affecting #mucociliary cell fates in Xenopus @plosbiology.org 🧪 plos.io/3YLOhcp

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Immunofluorescence confocal micrographs (IF) from control (ctrl.) and foxi1 morphants (foxi1 MO; 3 or 0.5 pmol) at st. 32 stained for Acetylated-α-tubulin (Ac.-α-tub., cilia, gray), F-actin (Actin, cell borders and morphology, gray). Targeted cells were identified by membrane RFP expression (memRFP, magenta) and are outlined in blue. Strongly targeted areas targeted by 3 pmol of foxi1 MO fail to generate intercalating cell types. Location of insets is indicated by dashed yellow box in upper panels.

Immunofluorescence confocal micrographs (IF) from control (ctrl.) and foxi1 morphants (foxi1 MO; 3 or 0.5 pmol) at st. 32 stained for Acetylated-α-tubulin (Ac.-α-tub., cilia, gray), F-actin (Actin, cell borders and morphology, gray). Targeted cells were identified by membrane RFP expression (memRFP, magenta) and are outlined in blue. Strongly targeted areas targeted by 3 pmol of foxi1 MO fail to generate intercalating cell types. Location of insets is indicated by dashed yellow box in upper panels.

The TF Foxi1 regulates #ionocytes and is associated with several human diseases. @walenteklab.bsky.social &co show that low concentrations of Foxi1 in progenitor cells maintain #epidermal identity via the #NotchPathway, affecting #mucociliary cell fates in Xenopus @plosbiology.org 🧪 plos.io/3YLOhcp

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