A Homozygous Dab1(−/−) 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 Dab1(−/−) (yotari) mice, as well as expression patterns of reelin, NOTCH2, LC3B, and cleaved caspase3 (CASP3) proteins, as potential determinants of normal kidney formation and function. We assumed that Dab1 functional inactivation may...

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Detalles Bibliográficos
Autores principales: Racetin, Anita, Filipović, Natalija, Lozić, Mirela, Ogata, Masaki, Gudelj Ensor, Larissa, Kelam, Nela, Kovačević, Petra, Watanabe, Koichiro, Katsuyama, Yu, Saraga-Babić, Mirna, Glavina Durdov, Merica, Vukojević, Katarina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073787/
https://www.ncbi.nlm.nih.gov/pubmed/33924028
http://dx.doi.org/10.3390/biom11040609

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073787/
https://www.ncbi.nlm.nih.gov/pubmed/33924028
http://dx.doi.org/10.3390/biom11040609

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