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Pregled bibliografske jedinice broj: 1123645

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


Racetin, Anita; Filipović, Natalija; Lozić, Mirela; Ogata, Masaki; Larissa, Gudelj Ensor; Kelam, Nela; Kovačević, Petra; Watanabe, Koichiro; Katsuyama, Yu; Saraga-Babić, Mirna et al.
A Homozygous Dab1−/− Is a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Mice Kidney and Urinary Tract // Biomolecules, 11 (2021), 609, 14 doi:10.3390/biom11040609 (međunarodna recenzija, članak, znanstveni)


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

Autori
Racetin, Anita ; Filipović, Natalija ; Lozić, Mirela ; Ogata, Masaki ; Larissa, Gudelj Ensor ; Kelam, Nela ; Kovačević, Petra ; Watanabe, Koichiro ; Katsuyama, Yu ; Saraga-Babić, Mirna ; Glavina Durdov, Merica ; Vukojević, Katarina

Izvornik
Biomolecules (2218-273X) 11 (2021); 609, 14

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
yotari ; kidney function ; postnatal kidney development ; immunofluorescence staining ; transmission electron microscopy

Sažetak
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 cause disorder in a wide spectrum of congenital anomalies of the kidney and urinary tract (CAKUT).

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Projekti:
HRZZ-IP-2016-06-2575 - Karakterizacija kandidat gena za kongenitalne anomalije bubrega i urotrakta (CAKUT) tijekom razvoja u miša i čovjeka (CAKUT) (Vukojević, Katarina, HRZZ - 2016-06) ( POIROT)

Ustanove:
KBC Split,
Medicinski fakultet, Split

Poveznice na cjeloviti tekst rada:

doi www.mdpi.com

Citiraj ovu publikaciju:

Racetin, Anita; Filipović, Natalija; Lozić, Mirela; Ogata, Masaki; Larissa, Gudelj Ensor; Kelam, Nela; Kovačević, Petra; Watanabe, Koichiro; Katsuyama, Yu; Saraga-Babić, Mirna et al.
A Homozygous Dab1−/− Is a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Mice Kidney and Urinary Tract // Biomolecules, 11 (2021), 609, 14 doi:10.3390/biom11040609 (međunarodna recenzija, članak, znanstveni)
Racetin, A., Filipović, N., Lozić, M., Ogata, M., Larissa, G., Kelam, N., Kovačević, P., Watanabe, K., Katsuyama, Y. & Saraga-Babić, M. (2021) A Homozygous Dab1−/− Is a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Mice Kidney and Urinary Tract. Biomolecules, 11, 609, 14 doi:10.3390/biom11040609.
@article{article, author = {Racetin, Anita and Filipovi\'{c}, Natalija and Lozi\'{c}, Mirela and Ogata, Masaki and Larissa, Gudelj Ensor and Kelam, Nela and Kova\v{c}evi\'{c}, Petra and Watanabe, Koichiro and Katsuyama, Yu and Saraga-Babi\'{c}, Mirna and Glavina Durdov, Merica and Vukojevi\'{c}, Katarina}, year = {2021}, pages = {14}, DOI = {10.3390/biom11040609}, chapter = {609}, keywords = {yotari, kidney function, postnatal kidney development, immunofluorescence staining, transmission electron microscopy}, journal = {Biomolecules}, doi = {10.3390/biom11040609}, volume = {11}, issn = {2218-273X}, title = {A Homozygous Dab1−/− Is a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Mice Kidney and Urinary Tract}, keyword = {yotari, kidney function, postnatal kidney development, immunofluorescence staining, transmission electron microscopy}, chapternumber = {609} }
@article{article, author = {Racetin, Anita and Filipovi\'{c}, Natalija and Lozi\'{c}, Mirela and Ogata, Masaki and Larissa, Gudelj Ensor and Kelam, Nela and Kova\v{c}evi\'{c}, Petra and Watanabe, Koichiro and Katsuyama, Yu and Saraga-Babi\'{c}, Mirna and Glavina Durdov, Merica and Vukojevi\'{c}, Katarina}, year = {2021}, pages = {14}, DOI = {10.3390/biom11040609}, chapter = {609}, keywords = {yotari, kidney function, postnatal kidney development, immunofluorescence staining, transmission electron microscopy}, journal = {Biomolecules}, doi = {10.3390/biom11040609}, volume = {11}, issn = {2218-273X}, title = {A Homozygous Dab1−/− Is a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Mice Kidney and Urinary Tract}, keyword = {yotari, kidney function, postnatal kidney development, immunofluorescence staining, transmission electron microscopy}, chapternumber = {609} }

Časopis indeksira:


  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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