A Homozygous Dab1<sup>−/−</sup> Is a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Mice Kidney and Urinary Tract

A Homozygous Dab1<sup>−/−</sup> Is a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Mice Kidney and Urinary Tract

This study aimed to explore morphology changes in the kidneys of <i>Dab1<sup>−/−</sup></i> (<i>yotari)</i> mice, as well as expression patterns of reelin, NOTCH2, LC3B, and cleaved caspase3 (CASP3) proteins, as potential determinants of normal kidney formation and...

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Bibliographic Details
Main Authors: Anita Racetin, Natalija Filipović, Mirela Lozić, Masaki Ogata, Larissa Gudelj Ensor, Nela Kelam, Petra Kovačević, Koichiro Watanabe, Yu Katsuyama, Mirna Saraga-Babić, Merica Glavina Durdov, Katarina Vukojević
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Biomolecules
Subjects:
<i>yotari</i>
kidney function
postnatal kidney development
immunofluorescence staining
transmission electron microscopy
Online Access:https://www.mdpi.com/2218-273X/11/4/609

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