Lack of APOL1 in proximal tubules of normal human kidneys and proteinuric APOL1 transgenic mouse kidneys.
The mechanism of pathogenesis associated with APOL1 polymorphisms and risk for non-diabetic chronic kidney disease (CKD) is not fully understood. Prior studies have minimized a causal role for the circulating APOL1 protein, thus efforts to understand kidney pathogenesis have focused on APOL1 express...
Guardado en:
Autores principales: | Natalya A Blessing, Zhenzhen Wu, Sethu M Madhavan, Jonathan W Choy, Michelle Chen, Myung K Shin, Maarten Hoek, John R Sedor, John F O'Toole, Leslie A Bruggeman |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/fd5027d0c5714bc48fd1f7b797f2cb73 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Structures of the ApoL1 and ApoL2 N-terminal domains reveal a non-classical four-helix bundle motif
por: Mark Ultsch, et al.
Publicado: (2021) -
APOL1 variant alleles associate with reduced risk for opportunistic infections in HIV infection
por: Ping An, et al.
Publicado: (2021) -
Molecular patterns of isolated tubulitis differ from tubulitis with interstitial inflammation in early indication biopsies of kidney allografts
por: Petra Hruba, et al.
Publicado: (2020) -
Author Correction: Molecular patterns of isolated tubulitis differ from tubulitis with interstitial inflammation in early indication biopsies of kidney allografts
por: Petra Hruba, et al.
Publicado: (2021) -
Allostimulatory capacity of conditionally immortalized proximal tubule cell lines for bioartificial kidney application
por: Milos Mihajlovic, et al.
Publicado: (2017)