<p>Kidneys of wild-type (A) and mutant genotypes (B–D), carrying <i>Hoxb7/myrVenus</i>, were excised at E12.5, cultured <i>in vitro</i>, and photographed at the indicated times. The <i>Ret−/−</i> Wolffian duct (B) failed to develop a ureter or kidney, while the <i>Spry1−/−</i> kidney (C) has multiple ureters (arrowheads), swollen UB tips and an enlarged common nephric duct (cnd). (D), in two examples of <i>Gdnf−/−</i>;<i>Spry1−/−</i> mutant kidneys, UB branching is retarded at E12.5, and subsequent branching in culture displays abnormal patterns (asterisks and arrowheads – see text) compared to wild-type.</p
<p>(A) Newborn kidneys with <i>Mek1</i> deleted specifically in ureteric bud (UB) derivatives are co...
<p>(A–J) Sections of P0 kidneys stained using late nephron markers confirm abnormal nephron formatio...
<p>A–B: E11.5 H&E staining shows no renal abnormalities in Foxd1DTA mutants (B) compared to controls...
<p>(A–D) Newborn stage kidneys, all carrying the <i>Hoxb7/myrVenus</i> transgene to label the UB bra...
<p>(A,B) Podocalyxin staining of nascent glomeruli in wild-type (A) and <i>Ret−/−;Spry1−/−</i> (B) k...
<p>A–B: E18.5 PECAM and Six2 immunofluorescence staining. Mutant kidneys (B) showed irregular vessel...
AbstractWhile it is clear that the normal branching morphogenesis of the ureteric bud (UB) is critic...
<p>(A–F) Time lapse imaging of kidneys cultured for 48 h, and ureteric buds visualized by the green ...
<p>A–B. E16.5 NCAM staining. In mutant kidneys (B), we observed a lack of organization in differenti...
<p>A–B: Six2 immunofluorescence staining showed that mutant kidneys (B) had gaps in Six2 expression ...
Early defect in branching morphogenesis of the ureteric bud in induced nephron deficit. Development ...
<p>38 somite stage E10.5 embryos were stained with the epithelial markers Pax2 (red) and E-cadherin ...
<p>All frames are from E14 organs. <b>A</b>, <b>C</b> and <b>E</b> are from wild type mice (-/-) and...
AbstractWhile it is clear that the normal branching morphogenesis of the ureteric bud (UB) is critic...
<p>A–B: E13.5 Six2 staining reveals that mutant kidneys (B) have thicker nephron progenitors and wid...
<p>(A) Newborn kidneys with <i>Mek1</i> deleted specifically in ureteric bud (UB) derivatives are co...
<p>(A–J) Sections of P0 kidneys stained using late nephron markers confirm abnormal nephron formatio...
<p>A–B: E11.5 H&E staining shows no renal abnormalities in Foxd1DTA mutants (B) compared to controls...
<p>(A–D) Newborn stage kidneys, all carrying the <i>Hoxb7/myrVenus</i> transgene to label the UB bra...
<p>(A,B) Podocalyxin staining of nascent glomeruli in wild-type (A) and <i>Ret−/−;Spry1−/−</i> (B) k...
<p>A–B: E18.5 PECAM and Six2 immunofluorescence staining. Mutant kidneys (B) showed irregular vessel...
AbstractWhile it is clear that the normal branching morphogenesis of the ureteric bud (UB) is critic...
<p>(A–F) Time lapse imaging of kidneys cultured for 48 h, and ureteric buds visualized by the green ...
<p>A–B. E16.5 NCAM staining. In mutant kidneys (B), we observed a lack of organization in differenti...
<p>A–B: Six2 immunofluorescence staining showed that mutant kidneys (B) had gaps in Six2 expression ...
Early defect in branching morphogenesis of the ureteric bud in induced nephron deficit. Development ...
<p>38 somite stage E10.5 embryos were stained with the epithelial markers Pax2 (red) and E-cadherin ...
<p>All frames are from E14 organs. <b>A</b>, <b>C</b> and <b>E</b> are from wild type mice (-/-) and...
AbstractWhile it is clear that the normal branching morphogenesis of the ureteric bud (UB) is critic...
<p>A–B: E13.5 Six2 staining reveals that mutant kidneys (B) have thicker nephron progenitors and wid...
<p>(A) Newborn kidneys with <i>Mek1</i> deleted specifically in ureteric bud (UB) derivatives are co...
<p>(A–J) Sections of P0 kidneys stained using late nephron markers confirm abnormal nephron formatio...
<p>A–B: E11.5 H&E staining shows no renal abnormalities in Foxd1DTA mutants (B) compared to controls...